| Year |
Citation |
Score |
| 2023 |
Gunasekaran TI, Reyes-Dumeyer D, Faber KM, Goate A, Boeve B, Cruchaga C, Pericak-Vance M, Haines JL, Rosenberg R, Tsuang D, Mejia DR, Medrano M, Lantigua RA, Sweet RA, Bennett DA, et al. Identification of Rare Damaging Missense and Loss of Function Variants in GWAS Loci Using Genome Sequencing Data from Two Cohorts of Familial Late-Onset Alzheimer's Disease. Medrxiv : the Preprint Server For Health Sciences. PMID 38196599 DOI: 10.1101/2023.12.18.23300145 |
0.348 |
|
| 2023 |
Nuytemans K, Rajabli F, Jean-Francois M, Kurup JT, Adams LD, Starks TD, Whitehead PL, Kunkle BW, Caban-Holt A, Haines JL, Cuccaro ML, Vance JM, Byrd GS, Beecham GW, Reitz C, ... Pericak-Vance MA, et al. Genetic analyses in multiplex families confirms chromosome 5q35 as a risk locus for Alzheimer's Disease in individuals of African Ancestry. Neurobiology of Aging. 133: 125-133. PMID 37952397 DOI: 10.1016/j.neurobiolaging.2023.10.010 |
0.373 |
|
| 2023 |
Lee WP, Choi SH, Shea MG, Cheng PL, Dombroski BA, Pitsillides AN, Heard-Costa NL, Wang H, Bulekova K, Kuzma AB, Leung YY, Farrell JJ, Lin H, Naj A, Blue EE, ... ... Pericak-Vance M, et al. Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project. Medrxiv : the Preprint Server For Health Sciences. PMID 37693521 DOI: 10.1101/2023.09.01.23294953 |
0.315 |
|
| 2023 |
Rajabli F, Benchek P, Tosto G, Kushch N, Sha J, Bazemore K, Zhu C, Lee WP, Haut J, Hamilton-Nelson KL, Wheeler NR, Zhao Y, Farrell JJ, Grunin MA, Leung YY, ... ... Pericak-Vance MA, et al. Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences. PMID 37461624 DOI: 10.1101/2023.07.06.23292311 |
0.36 |
|
| 2023 |
Reitz C, Pericak-Vance MA, Foroud T, Mayeux R. A global view of the genetic basis of Alzheimer disease. Nature Reviews. Neurology. PMID 37024647 DOI: 10.1038/s41582-023-00789-z |
0.308 |
|
| 2022 |
Rajabli F, Beecham GW, Hendrie HC, Baiyewu O, Ogunniyi A, Gao S, Kushch NA, Lipkin-Vasquez M, Hamilton-Nelson KL, Young JI, Dykxhoorn DM, Nuytemans K, Kunkle BW, Wang L, Jin F, ... ... Pericak-Vance MA, et al. A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry. Plos Genetics. 18: e1009977. PMID 35788729 DOI: 10.1371/journal.pgen.1009977 |
0.335 |
|
| 2022 |
Bellenguez C, Küçükali F, Jansen IE, Kleineidam L, Moreno-Grau S, Amin N, Naj AC, Campos-Martin R, Grenier-Boley B, Andrade V, Holmans PA, Boland A, Damotte V, van der Lee SJ, Costa MR, ... ... Pericak-Vance MA, et al. New insights into the genetic etiology of Alzheimer's disease and related dementias. Nature Genetics. PMID 35379992 DOI: 10.1038/s41588-022-01024-z |
0.309 |
|
| 2022 |
Reyes-Dumeyer D, Faber K, Vardarajan B, Goate A, Renton A, Chao M, Boeve B, Cruchaga C, Pericak-Vance M, Haines JL, Rosenberg R, Tsuang D, Sweet RA, Bennett DA, Wilson RS, et al. The National Institute on Aging Late-Onset Alzheimer's Disease Family Based Study: A resource for genetic discovery. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 34978149 DOI: 10.1002/alz.12514 |
0.303 |
|
| 2021 |
Xue D, Bush WS, Renton AE, Marcora EA, Bis JC, Kunkle BW, Boerwinkle E, DeStefano AL, Farrer L, Goate A, Mayeux R, Pericak-Vance M, Schellenberg G, Seshadri S, et al. Large-scale sequencing studies expand the known genetic architecture of Alzheimer's disease. Alzheimer's & Dementia (Amsterdam, Netherlands). 13: e12255. PMID 35005195 DOI: 10.1002/dad2.12255 |
0.309 |
|
| 2021 |
Rajabli F, Feliciano-Astacio BE, Cukier HN, Wang L, Griswold AJ, Hamilton-Nelson KL, Adams LD, Rodriguez VC, Mena PR, Tejada S, Celis K, Whitehead PL, Van Booven DJ, Hofmann NK, Bussies PL, ... ... Pericak-Vance MA, et al. Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus. Neurobiology of Aging. PMID 33902942 DOI: 10.1016/j.neurobiolaging.2021.02.019 |
0.376 |
|
| 2020 |
Lancour D, Dupuis J, Mayeux R, Haines JL, Pericak-Vance MA, Schellenberg GC, Crovella M, Farrer LA, Kasif S. Analysis of brain region-specific co-expression networks reveals clustering of established and novel genes associated with Alzheimer disease. Alzheimer's Research & Therapy. 12: 103. PMID 32878640 DOI: 10.1186/S13195-020-00674-7 |
0.403 |
|
| 2020 |
Dumitrescu L, Mahoney ER, Mukherjee S, Lee ML, Bush WS, Engelman CD, Lu Q, Fardo DW, Trittschuh EH, Mez J, Kaczorowski C, Hernandez Saucedo H, Widaman KF, Buckley R, Properzi M, ... ... Pericak-Vance MA, et al. Genetic variants and functional pathways associated with resilience to Alzheimer's disease. Brain : a Journal of Neurology. 143: 2561-2575. PMID 32844198 DOI: 10.1093/Brain/Awaa209 |
0.404 |
|
| 2020 |
Griswold AJ, Sivasankaran SK, Van Booven D, Gardner OK, Rajabli F, Whitehead PL, Hamilton-Nelson KL, Adams LD, Scott AM, Hofmann NK, Vance JM, Cuccaro ML, Bush WS, Martin ER, Byrd GS, ... ... Pericak-Vance MA, et al. Immune and Inflammatory Pathways Implicated by Whole Blood Transcriptomic Analysis in a Diverse Ancestry Alzheimer's Disease Cohort. Journal of Alzheimer's Disease : Jad. PMID 32597797 DOI: 10.3233/Jad-190855 |
0.39 |
|
| 2020 |
Knopman D, Lemere CA, Lamb BT, Craft S, Gitlin LN, Golde TE, Pericak-Vance M, Sano M, Schellenberg G, Schneider JA, Zheng H, Khachaturian Z, Snyder HM, Carrillo MC. Scientific Advising and Reviewing: On strengthening the bond between the Alzheimer's Association and the scientific community. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 32426924 DOI: 10.1002/Alz.12059 |
0.321 |
|
| 2020 |
Bussies PL, Rajabli F, Griswold A, Dorfsman DA, Whitehead P, Adams LD, Mena PR, Cuccaro M, Haines JL, Byrd GS, Beecham GW, Pericak-Vance MA, Young JI, Vance JM. Use of local genetic ancestry to assess -523' and risk for Alzheimer disease. Neurology. Genetics. 6: e404. PMID 32337333 DOI: 10.1212/Nxg.0000000000000404 |
0.39 |
|
| 2020 |
Reiman EM, Arboleda-Velasquez JF, Quiroz YT, Huentelman MJ, Beach TG, Caselli RJ, Chen Y, Su Y, Myers AJ, Hardy J, Paul Vonsattel J, Younkin SG, Bennett DA, De Jager PL, Larson EB, ... ... Pericak-Vance MA, et al. Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study. Nature Communications. 11: 667. PMID 32015339 DOI: 10.1038/S41467-019-14279-8 |
0.378 |
|
| 2019 |
Hauser MA, Allingham RR, Aung T, Van Der Heide CJ, Taylor KD, Rotter JI, Wang SJ, Bonnemaijer PWM, Williams SE, Abdullahi SM, Abu-Amero KK, Anderson MG, Akafo S, Alhassan MB, ... ... Pericak-Vance MA, et al. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry. Jama. 322: 1682-1691. PMID 31688885 DOI: 10.1001/Jama.2019.16161 |
0.327 |
|
| 2019 |
Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Bush WS, Gifford KA, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, Montine TJ, ... ... Pericak-Vance MA, et al. Sex differences in the genetic predictors of Alzheimer's pathology. Brain : a Journal of Neurology. 142: 2581-2589. PMID 31497858 DOI: 10.1093/Brain/Awz206 |
0.414 |
|
| 2019 |
Fan BJ, Bailey JC, Igo RP, Kang JH, Boumenna T, Brilliant MH, Budenz DL, Fingert JH, Gaasterland T, Gaasterland D, Hauser MA, Kraft P, Lee RK, Lichter PR, Liu Y, ... ... Pericak-Vance MA, et al. Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis. Jama Ophthalmology. PMID 31436842 DOI: 10.1001/Jamaophthalmol.2019.3109 |
0.39 |
|
| 2019 |
Choi KY, Lee JJ, Gunasekaran TI, Kang S, Lee W, Jeong J, Lim HJ, Zhang X, Zhu C, Won SY, Choi YY, Seo EH, Lee SC, Gim J, Chung JY, ... ... Pericak-Vance MA, et al. Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of ε4 on Alzheimer's Disease Risk in a Multiracial Sample. Journal of Clinical Medicine. 8. PMID 31426376 DOI: 10.3390/Jcm8081236 |
0.402 |
|
| 2019 |
Waksmunski AR, Igo RP, Song YE, Cooke Bailey JN, Laux R, Fuzzell D, Fuzzell S, Adams LD, Caywood L, Prough M, Stambolian D, Scott WK, Pericak-Vance MA, Haines JL. Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish. Human Genetics. PMID 31367973 DOI: 10.1007/S00439-019-02050-4 |
0.45 |
|
| 2019 |
Feliciano-Astacio BE, Celis K, Ramos J, Rajabli F, Adams LD, Rodriguez A, Rodriguez V, Bussies PL, Sierra C, Manrique P, Mena PR, Grana A, Prough M, Hamilton-Nelson KL, Feliciano N, ... ... Pericak-Vance MA, et al. The Puerto Rico Alzheimer Disease Initiative (PRADI): A Multisource Ascertainment Approach. Frontiers in Genetics. 10: 538. PMID 31275353 DOI: 10.3389/Fgene.2019.00538 |
0.369 |
|
| 2019 |
Ma Y, Jun GR, Zhang X, Chung J, Naj AC, Chen Y, Bellenguez C, Hamilton-Nelson K, Martin ER, Kunkle BW, Bis JC, Debette S, DeStefano AL, Fornage M, Nicolas G, ... ... Pericak-Vance MA, et al. Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype. Jama Neurology. PMID 31180460 DOI: 10.1001/Jamaneurol.2019.1456 |
0.442 |
|
| 2019 |
Goldschmidt-Clermont PJ, Volinsky FG, LaRosa SP, Gilbert JR, Periçak-Vance MA. Time for Well-Powered Controlled Prospective Studies to test a Causal Role for Herpes Viruses in Alzheimer Using Anti-Herpes Drugs. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. PMID 31175818 DOI: 10.1093/Gerona/Glz150 |
0.305 |
|
| 2019 |
Gardner OK, Wang L, Van Booven D, Whitehead PL, Hamilton-Nelson KL, Adams LD, Starks TD, Hofmann NK, Vance JM, Cuccaro ML, Martin ER, Byrd GS, Haines JL, Bush WS, Beecham GW, ... Pericak-Vance MA, et al. RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways. Human Molecular Genetics. PMID 31162550 DOI: 10.1093/Hmg/Ddz110 |
0.32 |
|
| 2019 |
Ma Y, Jun GR, Chung J, Zhang X, Kunkle BW, Naj AC, White CC, Bennett DA, De Jager PL, Mayeux R, Haines JL, Pericak-Vance MA, Schellenberg GD, Farrer LA, et al. CpG-related SNPs in the MS4A region have a dose-dependent effect on risk of late-onset Alzheimer disease. Aging Cell. e12964. PMID 31144443 DOI: 10.1111/Acel.12964 |
0.415 |
|
| 2019 |
Patel D, Mez J, Vardarajan BN, Staley L, Chung J, Zhang X, Farrell JJ, Rynkiewicz MJ, Cannon-Albright LA, Teerlink CC, Stevens J, Corcoran C, Gonzalez Murcia JD, Lopez OL, Mayeux R, ... ... Pericak-Vance MA, et al. Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry. Jama Network Open. 2: e191350. PMID 30924900 DOI: 10.1001/Jamanetworkopen.2019.1350 |
0.402 |
|
| 2019 |
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Pericak-Vance MA, et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. 51: 414-430. PMID 30820047 DOI: 10.1038/s41588-019-0358-2 |
0.335 |
|
| 2019 |
Deng HX, Pericak-Vance MA, Siddique T. Reply to 'TMEM230 variants in Parkinson's disease' and 'Doubts about TMEM230 as a gene for parkinsonism'. Nature Genetics. PMID 30804556 DOI: 10.1038/S41588-019-0355-5 |
0.353 |
|
| 2019 |
Martin ER, Gao XR, Haines JL, Pericak-Vance MA, Li Y. P1-139: TESTS OF DISEASE RISK VERSUS AGE AT ONSET: A POWER COMPARISON Alzheimer's & Dementia. 15: P290-P290. DOI: 10.1016/J.Jalz.2019.06.694 |
0.307 |
|
| 2019 |
Mena PR, Kunkle BW, Faber K, Celis K, Adams LD, Foroud TM, Reyes-Dumeyer D, Kuzma AB, Naj A, Martin ER, Dalgard C, Schellenberg GD, Wang L, Vance JM, Cuccaro ML, ... ... Pericak-Vance MA, et al. P2-151: THE ALZHEIMER'S DISEASE SEQUENCING PROJECT - FOLLOW UP STUDY (ADSP-FUS): INCREASING ETHNIC DIVERSITY IN ALZHEIMER'S GENETICS RESEARCH Alzheimer's & Dementia. 15: P634-P634. DOI: 10.1016/J.Jalz.2019.06.4961 |
0.364 |
|
| 2019 |
Gardner OK, Wang L, Booven DV, Whitehead PL, Hamilton-Nelson KL, Adams LD, Starks TD, Hofmann NK, Vance JM, Cuccaro ML, Martin ER, Byrd GS, Haines JL, Bush WS, Beecham GW, ... Pericak-Vance MA, et al. O3-13-04: Genetic Variants In Alzheimer'S Disease-Associated Regions Have Different Effects On Rna Editing Rates In African-American And Non-Hispanic White Populations Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4699 |
0.348 |
|
| 2019 |
Jaworski J, Kunkle BW, Rajabli F, Adams LD, Starks TD, Goate AM, Cuccaro ML, Vance JM, Martin ER, Foroud TM, Mayeux R, Reitz C, Byrd GS, Beecham GW, Pericak-Vance MA. O3-13-02: Genome-Wide Linkage Analysis Of African-American Alzheimer Disease Families Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4697 |
0.375 |
|
| 2019 |
Patel D, Mez J, Vardarajan BN, Staley L, Chung J, Zhang X, Farrell J, Rynkiewicz MJ, Cannon-Albright L, Teerlink C, Stevens J, Corcoran C, Murcia JDG, Lopez OL, Mayeux R, ... ... Pericak-Vance MA, et al. O3-13-01: Highly Penetrant Late-Onset Alzheimer Disease Variants In Notch3 In Ashkenazi Jews Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4696 |
0.341 |
|
| 2019 |
Naj A, Sha J, Leonenko G, Chen Y, Chouraki V, Leber M, Sims R, Grenier-Boley B, Bis JC, Zhao Y, Kuzma AB, Kunkle BW, Karamujić-Čomić H, Lee SJVD, Bellenguez C, ... ... Pericak-Vance MA, et al. O2‐10‐06: Genome‐Wide Meta‐Analysis Of Late‐Onset Alzheimer'S Disease Using Rare Variant Imputation In 64,859 Subjects Identifies Risk Loci With Roles In Innate Immunity And Cardiovascular Traits: The International Genomics Of Alzheimer'S Project (Igap) Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4510 |
0.375 |
|
| 2019 |
Zhang X, Farrell J, Zhu C, Mayeux R, Haines JL, Pericak-Vance MA, Schellenberg GD, Lunetta KL, Farrer LAA, Sequencing AD. O2-10-04: Mitochondrial Variants And Haplogroups Associated With Late-Onset Alzheimer'S Disease Identified By Whole Exome Sequencing Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4508 |
0.345 |
|
| 2019 |
Griswold AJ, Gardner OK, Booven DV, Jean-Francois M, Hamilton-Nelson KL, Whitehead PL, Adams LD, Starks TD, Hofmann NK, Cuccaro ML, Martin ER, Vance JM, Byrd GS, Haines JL, Bush WS, ... ... Pericak-Vance MA, et al. P4-114: Eqtl Analysis Identifies Ancestry Specific Regulatory Effects Of Alzheimer Disease Associated Variants Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3775 |
0.418 |
|
| 2019 |
Vardarajan BN, Jaworski J, Beecham GW, Barral S, Reyes-Dumeyer D, Medrano M, Lantigua R, Leung YY, Wang L, Naj A, Martin ER, Haines JL, Bush WS, Farrer LA, Schellenberg GD, ... Pericak-Vance MA, et al. P4-097: Rare Variants In Familial Late-Onset Alzheimer'S Disease Identified From Large Scale Whole Genome Sequencing Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3757 |
0.398 |
|
| 2019 |
Kunkle BW, Hamilton-Nelson KL, Gomez L, Jean-Francois M, Naj A, Wang L, Kuzma AB, Beecham GW, Bush WS, Hohman TJ, Vardarajan BN, Wang L, Mayeux R, Haines JL, Farrer LA, ... ... Pericak-Vance MA, et al. P4-094: Exome-Wide Analysis Identifies Novel Sex-Specific Candidate Genes For Alzheimer Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3754 |
0.416 |
|
| 2019 |
Cuccaro ML, Celis K, Adams LD, Scott AM, Ayodele T, Martinez I, Starks TD, Vance JM, Byrd GS, Haines JL, Reitz C, Beecham GW, Pericak-Vance MA. P3-311: Neuropsychiatric Features In African American (Aa) And Caucasian (Ca) Individuals With Alzheimer Disease (Ad) Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3343 |
0.328 |
|
| 2019 |
Main LR, Disher MC, Song Y, Laux R, Miskimen K, Cuccaro ML, Ogrocki P, Lerner AJ, Vance JM, Fuzzell MD, Fuzzell S, Sewell J, Caywood LJ, Prough M, Scott B, ... Pericak-Vance MA, et al. P3-135: Protective Genetic Variants In The Midwestern Amish Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3163 |
0.335 |
|
| 2019 |
Jean-Francois M, Johnson FS, Baez P, Martinez I, Adams LD, Vance JM, Martin ER, Ayodele T, Pericak-Vance MA, Cuccaro ML, Beecham GW, Reitz C. P2-150: Degree Of Inbreeding In Multiplex Caribbean Hispanic Families Loaded For Early-Onset Alzheimer'S Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2557 |
0.372 |
|
| 2019 |
Celis K, Hamilton-Nelson KL, Hofmann NK, Pericak-Vance MA, Vance JM, Wang L. P2-149: IDENTIFICATION OF FUNCTIONAL VARIANTS IN THE AFRICAN LOCAL ANCESTRY REGION SURROUNDING APOE ε4 Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2556 |
0.311 |
|
| 2019 |
Nuytemans K, Booven DJv, Hofmann NK, Rajabli F, Griswold AJ, Brown CD, Pericak-Vance MA, Vance JM. P2-143: Using Massively Parallel Reporter Assays To Identify Protective Functional Variants In The Apoe Region Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2550 |
0.31 |
|
| 2019 |
Rajabli F, Feliciano-Astacio BE, Celis K, Hamilton-Nelson KL, Adams LD, Rodriguez VC, Mena PR, Whitehead PL, Hofmann NK, Bussies P, Prough M, Sierra-Lopez CB, Acosta H, Chinea A, Feliciano NI, ... ... Pericak-Vance MA, et al. P2-140: Genome-Wide Linkage Analysis Of Caribbean Hispanic Puerto Rican Families Supports Evidence Of Linkage To C9Orf72 Region Of Chromosome 9 Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2547 |
0.396 |
|
| 2019 |
Bussies P, Rajabli F, Hamilton-Nelson KL, Whitehead PL, Cuccaro ML, Griswold AJ, Haines JL, Byrd GS, Pericak-Vance MA, Vance JM, Young J. P2-135: The Tomm40 Repeat Does Not Provide Protection For Ad For Apoe4 Carriers With Local Genomic African Ancestry (Lga) Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2542 |
0.332 |
|
| 2019 |
Starks TD, Byfield G, Naney KB, Luther R, King V, Dykxhoorn DM, Cukier HN, Edwards C, Adams LD, Haines JL, Cuccaro ML, Vance JM, Mayeux R, Reitz C, Beecham GW, ... Pericak-Vance MA, et al. P1‐558: Mitigating Complexities In Recruiting And Retaining African American (Aa) Multiplex Families For Alzheimer Disease Research Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.1163 |
0.344 |
|
| 2018 |
Beecham GW, Vardarajan B, Blue E, Bush W, Jaworski J, Barral S, DeStefano A, Hamilton-Nelson K, Kunkle B, Martin ER, Naj A, Rajabli F, Reitz C, Thornton T, van Duijn C, ... ... Pericak-Vance MA, et al. Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease. Neurology. Genetics. 4: e286. PMID 30569016 DOI: 10.1212/Nxg.0000000000000286 |
0.415 |
|
| 2018 |
Rajabli F, Feliciano BE, Celis K, Hamilton-Nelson KL, Whitehead PL, Adams LD, Bussies PL, Manrique CP, Rodriguez A, Rodriguez V, Starks T, Byfield GE, Sierra Lopez CB, McCauley JL, Acosta H, ... ... Pericak-Vance MA, et al. Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations. Plos Genetics. 14: e1007791. PMID 30517106 DOI: 10.1371/Journal.Pgen.1007791 |
0.382 |
|
| 2018 |
Zhang X, Zhu C, Beecham G, Vardarajan BN, Ma Y, Lancour D, Farrell JJ, Chung J, Mayeux R, Haines JL, Schellenberg GD, Pericak-Vance MA, Lunetta KL, Farrer LA. A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 30503768 DOI: 10.1016/j.jalz.2018.10.005 |
0.319 |
|
| 2018 |
Broce IJ, Tan CH, Fan CC, Jansen I, Savage JE, Witoelar A, Wen N, Hess CP, Dillon WP, Glastonbury CM, Glymour M, Yokoyama JS, Elahi FM, Rabinovici GD, Miller BL, ... ... Pericak-Vance M, et al. Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer's disease. Acta Neuropathologica. PMID 30413934 DOI: 10.1007/S00401-018-1928-6 |
0.447 |
|
| 2018 |
Gusareva ES, Twizere JC, Sleegers K, Dourlen P, Abisambra JF, Meier S, Cloyd R, Weiss B, Dermaut B, Bessonov K, van der Lee SJ, Carrasquillo MM, Katsumata Y, Cherkaoui M, Asselbergh B, ... ... Pericak-Vance MA, et al. Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease. Neurobiology of Aging. PMID 30201328 DOI: 10.1016/J.Neurobiolaging.2018.08.001 |
0.427 |
|
| 2018 |
Bis JC, Jian X, Kunkle BW, Chen Y, Hamilton-Nelson KL, Bush WS, Salerno WJ, Lancour D, Ma Y, Renton AE, Marcora E, Farrell JJ, Zhao Y, Qu L, Ahmad S, ... ... Pericak-Vance MA, et al. Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry. PMID 30108311 DOI: 10.1038/S41380-018-0112-7 |
0.459 |
|
| 2018 |
Vardarajan BN, Barral S, Jaworski J, Beecham GW, Blue E, Tosto G, Reyes-Dumeyer D, Medrano M, Lantigua R, Naj A, Thornton T, DeStefano A, Martin E, Wang LS, Brown L, ... ... Pericak-Vance MA, et al. Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease. Annals of Clinical and Translational Neurology. 5: 406-417. PMID 29688227 DOI: 10.1002/Acn3.537 |
0.312 |
|
| 2018 |
Lancour D, Naj A, Mayeux R, Haines JL, Pericak-Vance MA, Schellenberg GC, Crovella M, Farrer LA, Kasif S. One for all and all for One: Improving replication of genetic studies through network diffusion. Plos Genetics. 14: e1007306. PMID 29684019 DOI: 10.1371/Journal.Pgen.1007306 |
0.389 |
|
| 2018 |
Blue EE, Bis JC, Dorschner MO, Tsuang DW, Barral SM, Beecham G, Below JE, Bush WS, Butkiewicz M, Cruchaga C, DeStefano A, Farrer LA, Goate A, Haines J, Jaworski J, ... ... Pericak-Vance MA, et al. Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. Dementia and Geriatric Cognitive Disorders. 45: 1-17. PMID 29486463 DOI: 10.1159/000485503 |
0.414 |
|
| 2018 |
Chung J, Zhang X, Allen M, Wang X, Ma Y, Beecham G, Montine TJ, Younkin SG, Dickson DW, Golde TE, Price ND, Ertekin-Taner N, Lunetta KL, Mez J, ... ... Pericak-Vance MA, et al. Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease. Alzheimer's Research & Therapy. 10: 22. PMID 29458411 DOI: 10.1186/S13195-018-0349-Z |
0.393 |
|
| 2018 |
Bailey JNC, Gharahkhani P, Kang JH, Butkiewicz M, Sullivan DA, Weinreb RN, Aschard H, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert JH, ... ... Pericak-Vance MA, et al. Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets. Investigative Ophthalmology & Visual Science. 59: 629-636. PMID 29392307 DOI: 10.1167/Iovs.17-22708 |
0.341 |
|
| 2018 |
Nuytemans K, Ortel TL, Gomez L, Hofmann N, Alves N, Dueker N, Beecham A, Whitehead P, Hahn Estabrooks S, Kitchens CS, Erkan D, Brandão LR, James AH, Kulkarni R, Manco-Johnson MJ, ... Pericak-Vance MA, et al. Variants in chondroitin sulfate metabolism genes in thrombotic storm. Thrombosis Research. 161: 43-51. PMID 29178990 DOI: 10.1016/J.Thromres.2017.11.016 |
0.308 |
|
| 2018 |
Patel D, Chung J, Mez J, Zhang X, Haines JL, Pericak-Vance MA, Schellenberg G, Lunetta KL, Farrer LA. O5-04-02: Rare Coding Mutations Associated With Alzheimer Disease And Other Dementias Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.3014 |
0.322 |
|
| 2018 |
Rajabli F, Vance JM, Feliciano-Astacio BE, Celis K, Adams LD, Hamilton-Nelson KL, Wang L, Nuytemans K, Whitehead PL, Hofmann NK, Rolati S, Haines JL, Byrd GS, Reitz C, Beecham GW, ... Pericak-Vance MA, et al. O3-06-06: Identifying A Protective Variant That Lowers The Risk For Developing Ad In Apoe-E4 Carriers Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.2805 |
0.307 |
|
| 2018 |
Vardarajan BN, Barral S, Jaworski J, Beecham GW, Blue E, Tosto G, Reyes-Dumeyer D, Medrano M, Lantigua R, Naj AC, Thornton TA, Destefano AL, Martin ER, Wang L, Brown L, ... ... Pericak-Vance MA, et al. P1-156: Gene-Based Analyses In Whole Genome Sequencing Of Familial Late-Onset Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.160 |
0.419 |
|
| 2018 |
Kunkle BW, Jaworski J, Rajabli F, Adams LD, Cuccaro ML, Vance JM, Goate AM, Martin ER, Foroud TM, Reitz C, Beecham GW, Mayeux R, Pericak-Vance MA. P1-154: Genome-Wide Linkage Analyses Of African American Families Supports Evidence Of Linkage To Chromosome 12 Alzheimers & Dementia. 14: 336. DOI: 10.1016/J.Jalz.2018.06.158 |
0.382 |
|
| 2018 |
Griswold AJ, Sivasankaran SK, Gardner OK, Rajabli F, Hamilton-Nelson KL, Rolati S, Hofmann NK, Whitehead PL, Adams LD, Byrd GS, Martin ER, Cuccaro ML, Bush WS, Haines JL, Vance JM, ... ... Pericak-Vance MA, et al. P1-144: Transcriptomic Analysis Of Whole Blood In African American And Non-Hispanic White Alzheimer Disease Cases And Controls Alzheimers & Dementia. 14: 331. DOI: 10.1016/J.Jalz.2018.06.147 |
0.314 |
|
| 2017 |
Beecham GW, Bis JC, Martin ER, Choi SH, DeStefano AL, van Duijn CM, Fornage M, Gabriel SB, Koboldt DC, Larson DE, Naj AC, Psaty BM, Salerno W, Bush WS, Foroud TM, ... ... Pericak-Vance MA, et al. The Alzheimer's Disease Sequencing Project: Study design and sample selection. Neurology. Genetics. 3: e194. PMID 29184913 DOI: 10.1212/Nxg.0000000000000194 |
0.411 |
|
| 2017 |
Cukier HN, Kunkle BK, Hamilton KL, Rolati S, Kohli MA, Whitehead PL, Jaworski J, Vance JM, Cuccaro ML, Carney RM, Gilbert JR, Farrer LA, Martin ER, Beecham GW, Haines JL, ... Pericak-Vance MA, et al. Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function. Journal of Alzheimer's Disease & Parkinsonism. 7. PMID 29177109 DOI: 10.4172/2161-0460.1000355 |
0.34 |
|
| 2017 |
Griswold AJ, Van Booven D, Cuccaro ML, Haines JL, Gilbert JR, Pericak-Vance MA. Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder. Neurogenetics. PMID 29151244 DOI: 10.1007/S10048-017-0529-1 |
0.38 |
|
| 2017 |
Rehker J, Rodhe J, Nesbitt RR, Boyle EA, Martin BK, Lord J, Karaca I, Naj A, Jessen F, Helisalmi S, Soininen H, Hiltunen M, Ramirez A, Scherer M, Farrer LA, ... ... Pericak-Vance MA, et al. Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants. Plos One. 12: e0185777. PMID 28985224 DOI: 10.1371/Journal.Pone.0185777 |
0.391 |
|
| 2017 |
Aschard H, Kang JH, Iglesias AI, Hysi P, Cooke Bailey JN, Khawaja AP, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert JH, Budenz DL, ... ... Pericak-Vance MA, et al. Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis. European Journal of Human Genetics : Ejhg. PMID 28853718 DOI: 10.1038/Ejhg.2017.136 |
0.341 |
|
| 2017 |
Persad PJ, Heid IM, Weeks DE, Baird PN, de Jong EK, Haines JL, Pericak-Vance MA, Scott WK. Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Investigative Ophthalmology & Visual Science. 58: 4027-4038. PMID 28813576 DOI: 10.1167/Iovs.17-21734 |
0.367 |
|
| 2017 |
Kunkle BW, Vardarajan BN, Naj AC, Whitehead PL, Rolati S, Slifer S, Carney RM, Cuccaro ML, Vance JM, Gilbert JR, Wang LS, Farrer LA, Reitz C, Haines JL, Beecham GW, ... ... Pericak-Vance MA, et al. Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport. Jama Neurology. PMID 28738127 DOI: 10.1001/Jamaneurol.2017.1518 |
0.41 |
|
| 2017 |
Hou L, Kember RL, Roach JC, O'Connell JR, Craig DW, Bucan M, Scott WK, Pericak-Vance M, Haines JL, Crawford MH, Shuldiner AR, McMahon FJ. A population-specific reference panel empowers genetic studies of Anabaptist populations. Scientific Reports. 7: 6079. PMID 28729679 DOI: 10.1038/S41598-017-05445-3 |
0.355 |
|
| 2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Pericak-Vance MA, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.437 |
|
| 2017 |
Huang KL, Marcora E, Pimenova AA, Di Narzo AF, Kapoor M, Jin SC, Harari O, Bertelsen S, Fairfax BP, Czajkowski J, Chouraki V, Grenier-Boley B, Bellenguez C, Deming Y, McKenzie A, ... ... Pericak-Vance MA, et al. A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease. Nature Neuroscience. PMID 28628103 DOI: 10.1038/Nn.4587 |
0.387 |
|
| 2017 |
Aung T, Ozaki M, Lee MC, Schlötzer-Schrehardt U, Thorleifsson G, Mizoguchi T, Igo RP, Haripriya A, Williams SE, Astakhov YS, Orr AC, Burdon KP, Nakano S, Mori K, Abu-Amero K, ... ... Pericak-Vance MA, et al. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nature Genetics. PMID 28553957 DOI: 10.1038/Ng.3875 |
0.427 |
|
| 2017 |
Kunkle BW, Carney RM, Kohli MA, Naj AC, Hamilton-Nelson KL, Whitehead PL, Wang L, Lang R, Cuccaro ML, Vance JM, Byrd GS, Beecham GW, Gilbert JR, Martin ER, Haines JL, ... Pericak-Vance MA, et al. Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease. Neuroscience Letters. PMID 28400126 DOI: 10.1016/J.Neulet.2017.04.014 |
0.301 |
|
| 2017 |
Desikan RS, Fan CC, Wang Y, Schork AJ, Cabral HJ, Cupples LA, Thompson WK, Besser L, Kukull WA, Holland D, Chen CH, Brewer JB, Karow DS, Kauppi K, Witoelar A, ... ... Pericak-Vance M, et al. Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score. Plos Medicine. 14: e1002258. PMID 28323831 DOI: 10.1371/Journal.Pmed.1002258 |
0.427 |
|
| 2017 |
Deming Y, Li Z, Kapoor M, Harari O, Del-Aguila JL, Black K, Carrell D, Cai Y, Fernandez MV, Budde J, Ma S, Saef B, Howells B, Huang KL, Bertelsen S, ... ... Pericak-Vance MA, et al. Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers. Acta Neuropathologica. PMID 28247064 DOI: 10.1007/s00401-017-1685-y |
0.324 |
|
| 2017 |
Jun GR, Chung J, Mez J, Barber R, Beecham GW, Bennett DA, Buxbaum JD, Byrd GS, Carrasquillo MM, Crane PK, Cruchaga C, De Jager P, Ertekin-Taner N, Evans D, Fallin MD, ... ... Pericak-Vance MA, et al. Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 28183528 DOI: 10.1016/J.Jalz.2016.12.012 |
0.416 |
|
| 2017 |
Haddick PC, Larson JL, Rathore N, Bhangale TR, Phung QT, Srinivasan K, Hansen DV, Lill JR, Pericak-Vance MA, Haines J, Farrer LA, Kauwe JS, Schellenberg GD, Cruchaga C, et al. A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains. Journal of Alzheimer's Disease : Jad. PMID 28106546 DOI: 10.3233/Jad-160524 |
0.326 |
|
| 2017 |
Pericak-Vance M, Rajabli F, Feliciano-Astacio B, Celis K, Hamilton-Nelson K, Adams L, Rodgriguez A, Byrd G, Vance J, Cuccuro M, Haines J, Beecham G. African haplotypic background mitigates the effect of apoe ε4 risk allele in alzheimer disease Journal of the Neurological Sciences. 381: 1137. DOI: 10.1016/J.Jns.2017.08.3201 |
0.392 |
|
| 2017 |
Zhang X, Ma Y, Lancour D, Farrell J, Chung J, Mayeux R, Haines JL, Schellenberg GD, Pericak-Vance MA, Lunetta KL, Farrer LA. Novel Genetic Variants Associated With Familial Late-Onset Alzheimer Disease In The Alzheimer’S Disease Sequencing Project Alzheimers & Dementia. 13: 572. DOI: 10.1016/J.Jalz.2017.07.189 |
0.422 |
|
| 2017 |
Beecham GW, Vardarajan BN, Blue E, Barral S, Haines JL, Bush WS, Duijn CMv, Martin ER, Schellenberg GD, Mayeux R, Wijsman E, Pericak-Vance MA. Whole-Genome Sequencing In Familial Late-Onset Alzheimer’S Disease Identifies Rare Variation In Ad Candidate Genes Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.07.188 |
0.421 |
|
| 2017 |
Deming Y, Kapoor M, Li Z, Harari O, Black K, Del-Aguila JL, Carrell D, Cai Y, Fernandez MV, Budde JP, Ma S, Saef B, Howells B, Huang K, Bertelsen S, ... ... Pericak-Vance MA, et al. CEREBROSPINAL FLUID ENDOPHENOTYPES PROVIDE INSIGHT INTO BIOLOGY UNDERLYING ALZHEIMER'S DISEASE Alzheimer's & Dementia. 13: P218-P219. DOI: 10.1016/J.Jalz.2017.07.096 |
0.317 |
|
| 2017 |
Chung J, Ma Y, Zhang X, Yang Q, Beecham GW, Lunetta KL, Mez J, Haines JL, Pericak-Vance MA, Schellenberg GD, Jun GR, Farrer LA. Bivariate Genome-Wide Association Study Of Neuropathologic Features Of Alzheimer’S Disease Alzheimers & Dementia. 13: 217. DOI: 10.1016/J.Jalz.2017.07.094 |
0.342 |
|
| 2017 |
Naj AC, Below J, Zhao Y, Chen H, Lee SJvd, Hamilton-Nelson KL, Petty L, Kunkle BW, Kuzma AB, Valladares O, Reitz C, Beecham GW, Martin ER, Wang L, Haines JL, ... ... Pericak-Vance MA, et al. Genome-Wide Rare Variant Imputation And Tissue-Specific Transcriptomic Analysis Identify Novel Rare Variant Candidate Loci In Late-Onset Alzheimer’S Disease: The Alzheimer’S Disease Genetics Consortium Alzheimers & Dementia. 13: 189. DOI: 10.1016/J.Jalz.2017.07.045 |
0.413 |
|
| 2017 |
Celis K, Feliciano-Astacio BE, Adams LD, Bussies P, Sierra C, Hamilton-Nelson KL, Rajabli F, Acosta H, Chinea A, McCauley JL, Vance JM, Cuccaro ML, Beecham GW, Pericak-Vance MA. The Puerto Rican Alzheimer Disease Initiative (Pradi): Initial Clinical Findings Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.774 |
0.32 |
|
| 2017 |
Cukier HN, Mehta N, Ramirez J, Rolati S, Whitehead PL, Deon Adams L, Celis K, Carney R, Vance JM, Cuccaro ML, Byrd GS, Pericak-Vance MA, Dykxhoorn DM. [P2-114]: PATIENT-DERIVED IPSC MODEL OF AN ABCA7
FRAMESHIFT DELETION ASSOCIATED WITH ALZHEIMER's DISEASE IN AFRICAN AMERICANS Alzheimer's & Dementia. 13: P650-P650. DOI: 10.1016/J.Jalz.2017.06.764 |
0.363 |
|
| 2017 |
Rajabli F, Hamilton-Nelson KL, Feliciano-Astacio BE, Celis K, Adams LD, Bussies P, Sierra C, Chinea A, Acosta H, McCauley JL, Vance JM, Cuccaro ML, Haines JL, Bush WS, Beecham GW, ... Pericak-Vance MA, et al. The Relevance Of Apoe4 To Alzheimer’S Disease In The Presence Of Local Ancestry Differences Alzheimers & Dementia. 13: 650. DOI: 10.1016/J.Jalz.2017.06.763 |
0.312 |
|
| 2017 |
Reitz C, Tang M, Reyes-Dumeyer D, Kunkle BW, Hamilton-Nelson KL, Lantigua R, Medrano M, Martin ER, Jimenez-Velazquez IZ, Pericak-Vance MA, Mayeux R, Beecham GW. [P2-105]: COLLECTION OF MULTIPLEX FAMILIES WITH UNEXPLAINED EARLY-ONSET ALZHEIMER's DISEASE FOR GENOMIC RESEARCH Alzheimer's & Dementia. 13: P647-P647. DOI: 10.1016/J.Jalz.2017.06.755 |
0.393 |
|
| 2017 |
Byfield G, Starks T, Byrd GS, Cuccaro ML, Adams LD, Whitehead PL, Reitz C, Beecham GW, Reyes-Dumeyer D, Haines JL, Mayeux R, Vance JM, Pericak-Vance MA, Edwards C, Hamilton-Nelson KL. Influence Of Community Engaged Family Connector In Recruiting And Ascertaining African Americans’ Family Members For Genomic Research Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.724 |
0.303 |
|
| 2016 |
Sardell RJ, Persad PJ, Pan SS, Whitehead P, Adams LD, Laux RA, Fortun JA, Brantley MA, Kovach JL, Schwartz SG, Agarwal A, Haines JL, Scott WK, Pericak-Vance MA. Progression Rate From Intermediate to Advanced Age-Related Macular Degeneration Is Correlated With the Number of Risk Alleles at the CFH Locus. Investigative Ophthalmology & Visual Science. 57: 6107-6115. PMID 27832277 DOI: 10.1167/Iovs.16-19519 |
0.336 |
|
| 2016 |
Cuccaro ML, Carney RM, Zhang Y, Bohm C, Kunkle BW, Vardarajan BN, Whitehead PL, Cukier HN, Mayeux R, St George-Hyslop P, Pericak-Vance MA. SORL1 mutations in early- and late-onset Alzheimer disease. Neurology. Genetics. 2: e116. PMID 27822510 DOI: 10.1212/Nxg.0000000000000116 |
0.323 |
|
| 2016 |
Mez J, Chung J, Jun G, Kriegel J, Bourlas AP, Sherva R, Logue MW, Barnes LL, Bennett DA, Buxbaum JD, Byrd GS, Crane PK, Ertekin-Taner N, Evans D, Fallin MD, ... ... Pericak-Vance MA, et al. Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 27770636 DOI: 10.1016/J.Jalz.2016.09.002 |
0.391 |
|
| 2016 |
Pasquale LR, Aschard H, Kang JH, Bailey JN, Lindström S, Chasman DI, Christen WG, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert J, ... ... Pericak-Vance MA, et al. Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample. Menopause (New York, N.Y.). PMID 27760082 DOI: 10.1097/Gme.0000000000000741 |
0.314 |
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| 2016 |
Hussman JP, Beecham AH, Schmidt M, Martin ER, McCauley JL, Vance JM, Haines JL, Pericak-Vance MA. GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis. Genes and Immunity. PMID 27278126 DOI: 10.1038/Gene.2016.23 |
0.328 |
|
| 2016 |
Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, ... ... Pericak-Vance MA, et al. Identification of TMEM230 mutations in familial Parkinson's disease. Nature Genetics. PMID 27270108 DOI: 10.1038/Ng.3589 |
0.392 |
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| 2016 |
Beecham AH, Wang L, Vasudeva N, Liu Z, Dong C, Goldschmidt-Clermont PJ, Pericak-Vance MA, Rundek T, Seo D, Blanton SH, Sacco RL, Beecham GW. Utility of blood pressure genetic risk score in admixed Hispanic samples. Journal of Human Hypertension. PMID 27251080 DOI: 10.1038/Jhh.2016.29 |
0.32 |
|
| 2016 |
Cukier HN, Kunkle BW, Vardarajan BN, Rolati S, Hamilton-Nelson KL, Kohli MA, Whitehead PL, Dombroski BA, Van Booven D, Lang R, Dykxhoorn DM, Farrer LA, Cuccaro ML, Vance JM, Gilbert JR, ... ... Pericak-Vance MA, et al. ABCA7 frameshift deletion associated with Alzheimer disease in African Americans. Neurology. Genetics. 2: e79. PMID 27231719 DOI: 10.1016/J.Jalz.2016.06.305 |
0.406 |
|
| 2016 |
Hoffman JD, van Grinsven MJ, Li C, Brantley M, McGrath J, Agarwal A, Scott WK, Schwartz SG, Kovach J, Pericak-Vance M, Sanchez CI, Haines JL. Genetic Association Analysis of Drusen Progression. Investigative Ophthalmology & Visual Science. 57: 2225-2231. PMID 27116550 DOI: 10.1167/Iovs.15-18571 |
0.357 |
|
| 2016 |
Kohli MA, Cukier HN, Hamilton-Nelson KL, Rolati S, Kunkle BW, Whitehead PL, Züchner SL, Farrer LA, Martin ER, Beecham GW, Haines JL, Vance JM, Cuccaro ML, Gilbert JR, Schellenberg GD, ... ... Pericak-Vance MA, et al. Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease. Neurology. Genetics. 2: e41. PMID 27066578 DOI: 10.1212/Nxg.0000000000000041 |
0.43 |
|
| 2016 |
Ridge PG, Hoyt KB, Boehme K, Mukherjee S, Crane PK, Haines JL, Mayeux R, Farrer LA, Pericak-Vance MA, Schellenberg GD, Kauwe JS. Assessment of the genetic variance of late-onset Alzheimer's disease. Neurobiology of Aging. PMID 27036079 DOI: 10.1016/J.Neurobiolaging.2016.02.024 |
0.423 |
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| 2016 |
Cooke Bailey JN, Hoffman JD, Sardell RJ, Scott WK, Pericak-Vance MA, Haines JL. The Application of Genetic Risk Scores in Age-Related Macular Degeneration: A Review. Journal of Clinical Medicine. 5. PMID 26959068 DOI: 10.3390/Jcm5030031 |
0.332 |
|
| 2016 |
Hohman TJ, Bush WS, Jiang L, Brown-Gentry KD, Torstenson ES, Dudek SM, Mukherjee S, Naj A, Kunkle BW, Ritchie MD, Martin ER, Schellenberg GD, Mayeux R, Farrer LA, Pericak-Vance MA, et al. Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium. Neurobiology of Aging. 38: 141-50. PMID 26827652 DOI: 10.1016/J.Neurobiolaging.2015.10.031 |
0.452 |
|
| 2016 |
Bailey JN, Loomis SJ, Kang JH, Allingham RR, Gharahkhani P, Khor CC, Burdon KP, Aschard H, Chasman DI, Igo RP, Hysi PG, Glastonbury CA, Ashley-Koch A, Brilliant M, Brown AA, ... ... Pericak-Vance MA, et al. Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nature Genetics. PMID 26752265 DOI: 10.1038/Ng.3482 |
0.361 |
|
| 2016 |
Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, ... ... Pericak-Vance MA, et al. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics. 48: 134-43. PMID 26691988 DOI: 10.1038/Ng.3448 |
0.422 |
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| 2016 |
Cuccaro ML, Carney RM, Cukier HN, Kunkle BW, Vardarajan BN, Bohm C, Zhang Y, St George-Hyslop P, Mayeux R, Pericak-Vance MA. P1-126: Pathogenic SORL1 Mutations and Parkinsonian Features in Alzheimer's Disease Alzheimer's & Dementia. 12: P451-P452. DOI: 10.1016/J.Jalz.2016.06.874 |
0.334 |
|
| 2016 |
Chung J, Ma Y, Lunetta KL, Mez J, Beecham GW, Pericak-Vance MA, Haines JL, Mayeux R, Schellenberg GD, Jun GR, Farrer LA. Multivariate Phenotypes Association Study Of Neuropathological Features Of Alzheimer'S Disease And Related Dementias Alzheimers & Dementia. 12: 450. DOI: 10.1016/J.Jalz.2016.06.838 |
0.368 |
|
| 2016 |
Huang K, Jin SC, Harari O, Kapoor M, Bertelsen S, Czajkowski J, Lambert j, Chouraki V, Bellenguez C, Grenier-Boley B, Deming Y, McKenzie A, Renton AE, Budde J, Del-Aguila JL, ... ... Pericak-Vance MA, et al. A Common Allele In Spi1 Lowers Risk And Delays Age At Onset For Alzheimer'S Disease Alzheimers & Dementia. 12: 253. DOI: 10.1016/J.Jalz.2016.06.453 |
0.38 |
|
| 2016 |
Below J, Petty L, Hu H, Huff C, DeStefano AL, Fornage M, Bis JC, Haines JL, Pericak-Vance MA, Mayeux R, Schellenberg GD, van Duijn CM, Wijsman E, Seshadri S, Boerwinkle E. O2-06-03: Tissue-Specific Genome-Wide Predictions of Genetically Regulated Expression in Alzheimer's Disease Alzheimer's & Dementia. 12: P239-P240. DOI: 10.1016/J.Jalz.2016.06.426 |
0.343 |
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| 2016 |
Beecham GW, Vardarajan BN, Blue E, Barral S, Haines JL, Bush WS, Duijn CMv, Martin ER, Schellenberg GD, Mayeux R, Wijsman E, Pericak-Vance MA. Whole Genome Sequencing In Familial Late-Onset Alzheimer’S Disease Identifies Variations In Ttc3 And Fsip2 Alzheimers & Dementia. 12: 197. DOI: 10.1016/J.Jalz.2016.06.343 |
0.369 |
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| 2016 |
Cukier HN, Kunkle BW, Rolati S, Whitehead PL, Vance JM, Cuccaro ML, Carney RM, Gilbert JR, Martin ER, Beecham GW, Haines JL, Pericak-Vance MA, Hamilton-Nelson KL. O1-09-02: Whole Exome Sequencing of Late Onset Multiplex Families Identifies Rare Coding Variants in Known and Novel Alzheimer’s Disease Genes Alzheimer's & Dementia. 12: P196-P197. DOI: 10.1016/J.Jalz.2016.06.342 |
0.37 |
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| 2016 |
Naj AC, Zhao Y, Lee SJvd, Hamilton KL, Kunkle BW, Partch AB, Valladares O, Beecham GW, Martin ER, Wang L, Haines JL, Mayeux R, Farrer LA, Pericak-Vance MA, Schellenberg GD. High-Resolution Imputation In Genome-Wide Association Studies Of Late-Onset Alzheimer'S Disease Identifies Novel Rare Variant Associations Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.308 |
0.397 |
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| 2016 |
Kunkle BW, Vardarajan BN, Naj AC, Cukier HN, Dykxhoorn DM, Rolati S, Whitehead PL, Carney RM, Cuccaro ML, Vance JM, Genetics Consortium AD, Farrer LA, Haines JL, Schellenberg GD, Martin ER, ... ... Pericak-Vance MA, et al. O1-03-03: Identification of Novel Candidate Genes for Early-Onset Alzheimer's Disease Through Integrated Whole-Exome Sequencing and Exome Chip Array Association Analysis Alzheimer's & Dementia. 12: P177-P178. DOI: 10.1016/J.Jalz.2016.06.306 |
0.37 |
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| 2016 |
Marcora E, Renton AE, Beecham GW, Boerwinkle E, Cantwell L, Cruchaga C, Cweibel R, Felsenfeld A, Fornage M, Kapoor M, Kauwe K, Khaladkar M, Kobolt D, Ma Y, Mayeux R, ... ... Pericak-Vance MA, et al. F1-01-02: Alzheimer's Disease Sequencing Project: Search for Alzheimer's Disease Resilience Genes That May Modify Disease Susceptibility in Specific Apoe Genotype Backgrounds Alzheimer's & Dementia. 12: P162-P163. DOI: 10.1016/J.Jalz.2016.06.272 |
0.38 |
|
| 2016 |
Mukherjee S, Boehme KL, Fardo DW, Kunkle BW, Kauwe J, Lambert J, Amouyel P, Pericak-Vance MA, Schellenberg GD, Crane PK. P3-096: Secondary Analyses of International Genomics of Alzheimer's Project Stage I GWAS Summary Data Identifies Additional Variants Associated With Late-Onset Alzheimer's Disease Alzheimer's & Dementia. 12: P856-P857. DOI: 10.1016/J.Jalz.2016.06.1755 |
0.391 |
|
| 2016 |
Jun GR, Chung J, Lunetta KL, Haines JL, Pericak-Vance MA, Mayeux R, Schellenberg GD, Farrer LA. Further Stratification Of Apoe E4-Negative Subjects Identifies Novel Genes For Alzheimer'S Disease Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.1290 |
0.36 |
|
| 2015 |
Hall JB, Cooke Bailey JN, Hoffman JD, Pericak-Vance MA, Scott WK, Kovach JL, Schwartz SG, Agarwal A, Brantley MA, Haines JL, Bush WS. Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models. Bmc Bioinformatics. 16: 329. PMID 26467978 DOI: 10.1186/S12859-015-0760-4 |
0.327 |
|
| 2015 |
Barral S, Cheng R, Reitz C, Vardarajan B, Lee J, Kunkle B, Beecham G, Cantwell LS, Pericak-Vance MA, Farrer LA, Haines JL, Goate AM, Foroud T, Boerwinkle E, Schellenberg GD, et al. Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26433351 DOI: 10.1016/J.Jalz.2015.07.487 |
0.44 |
|
| 2015 |
Ghani M, Reitz C, Cheng R, Vardarajan BN, Jun G, Sato C, Naj A, Rajbhandary R, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, ... ... Pericak-Vance MA, et al. Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. Jama Neurology. PMID 26366463 DOI: 10.1001/Jamaneurol.2015.1700 |
0.428 |
|
| 2015 |
Kunkle BW, Jaworski J, Barral S, Vardarajan B, Beecham GW, Martin ER, Cantwell LS, Partch A, Bird TD, Raskind WH, DeStefano AL, Carney RM, Cuccaro M, Vance JM, Farrer LA, ... ... Pericak-Vance MA, et al. Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26365416 DOI: 10.1016/J.Jalz.2015.05.020 |
0.429 |
|
| 2015 |
Tosto G, Fu H, Vardarajan BN, Lee JH, Cheng R, Reyes-Dumeyer D, Lantigua R, Medrano M, Jimenez-Velazquez IZ, Elkind MS, Wright CB, Sacco RL, Pericak-Vance M, Farrer L, Rogaeva E, et al. F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease. Annals of Clinical and Translational Neurology. 2: 810-20. PMID 26339675 DOI: 10.1002/Acn3.223 |
0.45 |
|
| 2015 |
Griswold AJ, Dueker ND, Van Booven D, Rantus JA, Jaworski JM, Slifer SH, Schmidt MA, Hulme W, Konidari I, Whitehead PL, Cuccaro ML, Martin ER, Haines JL, Gilbert JR, Hussman JP, ... Pericak-Vance MA, et al. Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Molecular Autism. 6: 43. PMID 26185613 DOI: 10.1186/S13229-015-0034-Z |
0.388 |
|
| 2015 |
Hohman TJ, Cooke-Bailey JN, Reitz C, Jun G, Naj A, Beecham GW, Liu Z, Carney RM, Vance JM, Cuccaro ML, Rajbhandary R, Vardarajan BN, Wang LS, Valladares O, Lin CF, ... ... Pericak-Vance MA, et al. Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26092349 DOI: 10.1016/J.Jalz.2015.02.012 |
0.406 |
|
| 2015 |
Humphries C, Kohli MA, Whitehead P, Mash DC, Pericak-Vance MA, Gilbert J. Alzheimer disease (AD) specific transcription, DNA methylation and splicing in twenty AD associated loci. Molecular and Cellular Neurosciences. 67: 37-45. PMID 26004081 DOI: 10.1016/J.Mcn.2015.05.003 |
0.391 |
|
| 2015 |
Kozol RA, Cukier HN, Zou B, Mayo V, De Rubeis S, Cai G, Griswold AJ, Whitehead PL, Haines JL, Gilbert JR, Cuccaro ML, Martin ER, Baker JD, Buxbaum JD, Pericak-Vance MA, et al. Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis. Human Molecular Genetics. 24: 4006-23. PMID 25882707 DOI: 10.1093/Hmg/Ddv138 |
0.317 |
|
| 2015 |
Desikan RS, Schork AJ, Wang Y, Thompson WK, Dehghan A, Ridker PM, Chasman DI, McEvoy LK, Holland D, Chen CH, Karow DS, Brewer JB, Hess CP, Williams J, Sims R, ... ... Pericak-Vance MA, et al. Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease. Circulation. 131: 2061-9. PMID 25862742 DOI: 10.1161/Circulationaha.115.015489 |
0.384 |
|
| 2015 |
Jun G, Ibrahim-Verbaas CA, Vronskaya M, Lambert JC, Chung J, Naj AC, Kunkle BW, Wang LS, Bis JC, Bellenguez C, Harold D, Lunetta KL, Destefano AL, Grenier-Boley B, Sims R, ... ... Pericak-Vance MA, et al. A novel Alzheimer disease locus located near the gene encoding tau protein. Molecular Psychiatry. PMID 25778476 DOI: 10.1038/Mp.2015.23 |
0.428 |
|
| 2015 |
Desikan RS, Schork AJ, Wang Y, Witoelar A, Sharma M, McEvoy LK, Holland D, Brewer JB, Chen CH, Thompson WK, Harold D, Williams J, Owen MJ, O'Donovan MC, Pericak-Vance MA, et al. Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus. Molecular Psychiatry. PMID 25687773 DOI: 10.1038/Mp.2015.6 |
0.428 |
|
| 2015 |
D'Aoust LN, Cummings AC, Laux R, Fuzzell D, Caywood L, Reinhart-Mercer L, Scott WK, Pericak-Vance MA, Haines JL. Examination of candidate exonic variants for association to Alzheimer disease in the Amish. Plos One. 10: e0118043. PMID 25668194 DOI: 10.1371/Journal.Pone.0118043 |
0.48 |
|
| 2015 |
Beecham GW, Dickson DW, Scott WK, Martin ER, Schellenberg G, Nuytemans K, Larson EB, Buxbaum JD, Trojanowski JQ, Van Deerlin VM, Hurtig HI, Mash DC, Beach TG, Troncoso JC, Pletnikova O, ... ... Pericak-Vance MA, et al. PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease. Neurology. 84: 972-80. PMID 25663231 DOI: 10.1212/Wnl.0000000000001332 |
0.343 |
|
| 2015 |
Wang LS, Naj AC, Graham RR, Crane PK, Kunkle BW, Cruchaga C, Murcia JD, Cannon-Albright L, Baldwin CT, Zetterberg H, Blennow K, Kukull WA, Faber KM, Schupf N, Norton MC, ... ... Pericak-Vance MA, et al. Rarity of the Alzheimer disease-protective APP A673T variant in the United States. Jama Neurology. 72: 209-16. PMID 25531812 DOI: 10.1001/Jamaneurol.2014.2157 |
0.389 |
|
| 2015 |
Humphries CE, Kohli MA, Nathanson L, Whitehead P, Beecham G, Martin E, Mash DC, Pericak-Vance MA, Gilbert J. Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 44: 977-87. PMID 25380588 DOI: 10.3233/Jad-141989 |
0.303 |
|
| 2015 |
Kunkle BW, Grenier-Boley B, Vronskaya M, Chouraki V, Lee SJvd, Hamilton-Nelson KL, Toeglhofer AM, Sims R, Jakobsdottir J, Bis JC, Dombroski BA, Martin ER, Mayeux R, Farrer LA, Duijn CMv, ... ... Pericak-Vance MA, et al. Low-frequency variant imputation identifies rare variant candidate loci in a gwas of late-onset Alzheimer’s disease in the igap consortium Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.08.158 |
0.388 |
|
| 2015 |
Beecham GW, Kunkle BW, Vardarajan B, Whitehead PL, Rolati S, Martin ER, Gilbert JR, Mayeux R, Haines JL, Pericak-Vance MA. O3-13-02: Whole-exome sequencing in early-onset Alzheimer disease cases identifies novel candidate genes Alzheimer's & Dementia. 11: P251-P251. DOI: 10.1016/J.Jalz.2015.07.310 |
0.362 |
|
| 2015 |
Jun G, Chung J, Tosto G, Vardarajan B, Reitz C, Lunetta KL, Manly JJ, Byrd GS, Haines JL, Pericak-Vance MA, Kuwano R, Mayeux R, Schellenberg GD, Farrer LA. Transethnic genome-wide meta-analysis for Alzheimer disease Alzheimers & Dementia. 11: 230. DOI: 10.1016/J.Jalz.2015.07.266 |
0.366 |
|
| 2015 |
Butkiewicz M, Pericak-Vance MA, Mayeux R, Farrer LA, Wang L, Schellenberg GD, Bush WS, Haines JL. Analyzing pathway specificity of variants associated with Alzheimer’s disease from the scientific literature corpus Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.06.875 |
0.361 |
|
| 2015 |
Cukier HN, Kunkle BW, Rolati S, Hamilton-Nelson KL, Kohli MA, Dombroski BA, Vardarajan BN, Whitehead PL, Booven DJV, Martin ER, Beecham GW, Farrer LA, Cuccaro ML, Vance JM, Mayeux R, ... ... Pericak-Vance MA, et al. ABCA7 deletion associated with Alzheimer's disease in african americans Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.06.549 |
0.365 |
|
| 2014 |
Wetzel-Smith MK, Hunkapiller J, Bhangale TR, Srinivasan K, Maloney JA, Atwal JK, Sa SM, Yaylaoglu MB, Foreman O, Ortmann W, Rathore N, Hansen DV, Tessier-Lavigne M, Mayeux R, ... Pericak-Vance M, et al. A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death. Nature Medicine. 20: 1452-7. PMID 25419706 DOI: 10.1038/Nm.3736 |
0.379 |
|
| 2014 |
Crawford DC, Dumitrescu L, Goodloe R, Brown-Gentry K, Boston J, McClellan B, Sutcliffe C, Wiseman R, Baker P, Pericak-Vance MA, Scott WK, Allen M, Mayo P, Schnetz-Boutaud N, Dilks HH, et al. Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study. Circulation. Cardiovascular Genetics. 7: 848-53. PMID 25363704 DOI: 10.1161/Circgenetics.113.000369 |
0.31 |
|
| 2014 |
Allen M, Kachadoorian M, Quicksall Z, Zou F, Chai HS, Younkin C, Crook JE, Pankratz VS, Carrasquillo MM, Krishnan S, Nguyen T, Ma L, Malphrus K, Lincoln S, Bisceglio G, ... ... Pericak-Vance MA, et al. Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels. Alzheimer's Research & Therapy. 6: 39. PMID 25324900 DOI: 10.1186/Alzrt268 |
0.398 |
|
| 2014 |
Cooke Bailey JN, Pericak-Vance MA, Haines JL. Genome-wide association studies: getting to pathogenesis, the role of inflammation/complement in age-related macular degeneration. Cold Spring Harbor Perspectives in Medicine. 4: a017186. PMID 25213188 DOI: 10.1101/Cshperspect.A017186 |
0.392 |
|
| 2014 |
Naj AC, Jun G, Reitz C, Kunkle BW, Perry W, Park YS, Beecham GW, Rajbhandary RA, Hamilton-Nelson KL, Wang LS, Kauwe JS, Huentelman MJ, Myers AJ, Bird TD, Boeve BF, ... ... Pericak-Vance MA, et al. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. Jama Neurology. 71: 1394-404. PMID 25199842 DOI: 10.1001/Jamaneurol.2014.1491 |
0.423 |
|
| 2014 |
Beecham GW, Hamilton K, Naj AC, Martin ER, Huentelman M, Myers AJ, Corneveaux JJ, Hardy J, Vonsattel JP, Younkin SG, Bennett DA, De Jager PL, Larson EB, Crane PK, Kamboh MI, ... ... Pericak-Vance MA, et al. Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Plos Genetics. 10: e1004606. PMID 25188341 DOI: 10.1371/Journal.Pgen.1004606 |
0.404 |
|
| 2014 |
Cuccaro ML, Czape K, Alessandri M, Lee J, Deppen AR, Bendik E, Dueker N, Nations L, Pericak-Vance M, Hahn S. Genetic testing and corresponding services among individuals with autism spectrum disorder (ASD). American Journal of Medical Genetics. Part A. 164: 2592-600. PMID 25131847 DOI: 10.1002/Ajmg.A.36698 |
0.313 |
|
| 2014 |
Jun G, Asai H, Zeldich E, Drapeau E, Chen C, Chung J, Park JH, Kim S, Haroutunian V, Foroud T, Kuwano R, Haines JL, Pericak-Vance MA, Schellenberg GD, Lunetta KL, et al. PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation. Annals of Neurology. 76: 379-92. PMID 25043464 DOI: 10.1002/Ana.24219 |
0.425 |
|
| 2014 |
Bailey JN, Yaspan BL, Pasquale LR, Hauser MA, Kang JH, Loomis SJ, Brilliant M, Budenz DL, Christen WG, Fingert J, Gaasterland D, Gaasterland T, Kraft P, Lee RK, Lichter PR, ... ... Pericak-Vance MA, et al. Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma. Human Genetics. 133: 1319-30. PMID 25037249 DOI: 10.1007/S00439-014-1468-7 |
0.302 |
|
| 2014 |
Bailey JN, Pericak-Vance MA, Haines JL. The impact of the human genome project on complex disease. Genes. 5: 518-35. PMID 25032678 DOI: 10.3390/Genes5030518 |
0.424 |
|
| 2014 |
Courtenay MD, Cade W, Schwartz SG, Kovach JL, Agarwal A, Wang G, Haines JL, Pericak-Vance MA, Scott WK. Set-based joint test of interaction between SNPs in the VEGF pathway and exogenous estrogen finds association with age-related macular degeneration. Investigative Ophthalmology & Visual Science. PMID 25015356 DOI: 10.1167/Iovs.14-14494 |
0.392 |
|
| 2014 |
Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, ... ... Pericak-Vance MA, et al. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Plos One. 9: e94661. PMID 24922517 DOI: 10.1371/Journal.Pone.0094661 |
0.454 |
|
| 2014 |
Hoffman JD, Cooke Bailey JN, D'Aoust L, Cade W, Ayala-Haedo J, Fuzzell D, Laux R, Adams LD, Reinhart-Mercer L, Caywood L, Whitehead-Gay P, Agarwal A, Wang G, Scott WK, Pericak-Vance MA, et al. Rare complement factor H variant associated with age-related macular degeneration in the Amish. Investigative Ophthalmology & Visual Science. 55: 4455-60. PMID 24906858 DOI: 10.1167/Iovs.13-13684 |
0.322 |
|
| 2014 |
Ratnapriya R, Zhan X, Fariss RN, Branham KE, Zipprer D, Chakarova CF, Sergeev YV, Campos MM, Othman M, Friedman JS, Maminishkis A, Waseem NH, Brooks M, Rajasimha HK, Edwards AO, ... ... Pericak-Vance MA, et al. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Human Molecular Genetics. 23: 5827-37. PMID 24899048 DOI: 10.1093/Hmg/Ddu276 |
0.445 |
|
| 2014 |
Nelson PT, Estus S, Abner EL, Parikh I, Malik M, Neltner JH, Ighodaro E, Wang WX, Wilfred BR, Wang LS, Kukull WA, Nandakumar K, Farman ML, Poon WW, Corrada MM, ... ... Pericak-Vance MA, et al. ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. Acta Neuropathologica. 127: 825-43. PMID 24770881 DOI: 10.1007/S00401-014-1282-2 |
0.419 |
|
| 2014 |
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, ... ... Pericak-Vance M, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/J.Ajhg.2014.03.018 |
0.367 |
|
| 2014 |
Loomis SJ, Kang JH, Weinreb RN, Yaspan BL, Cooke Bailey JN, Gaasterland D, Gaasterland T, Lee RK, Lichter PR, Budenz DL, Liu Y, Realini T, Friedman DS, McCarty CA, Moroi SE, ... ... Pericak-Vance MA, et al. Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss. Ophthalmology. 121: 508-16. PMID 24572674 DOI: 10.1016/J.Ophtha.2013.09.012 |
0.361 |
|
| 2014 |
Ruiz A, Heilmann S, Becker T, Hernández I, Wagner H, Thelen M, Mauleón A, Rosende-Roca M, Bellenguez C, Bis JC, Harold D, Gerrish A, Sims R, Sotolongo-Grau O, Espinosa A, ... ... Pericak-Vance MA, et al. Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene. Translational Psychiatry. 4: e358. PMID 24495969 DOI: 10.1038/Tp.2014.2 |
0.441 |
|
| 2014 |
Benitez BA, Jin SC, Guerreiro R, Graham R, Lord J, Harold D, Sims R, Lambert JC, Gibbs JR, Bras J, Sassi C, Harari O, Bertelsen S, Lupton MK, Powell J, ... ... Pericak-Vance MA, et al. Missense variant in TREML2 protects against Alzheimer's disease. Neurobiology of Aging. 35: 1510.e19-26. PMID 24439484 DOI: 10.1016/J.Neurobiolaging.2013.12.010 |
0.454 |
|
| 2014 |
Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, ... ... Pericak-Vance MA, et al. Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders. Molecular Autism. 5: 1. PMID 24410847 DOI: 10.1186/2040-2392-5-1 |
0.424 |
|
| 2014 |
Veatch OJ, Veenstra-Vanderweele J, Potter M, Pericak-Vance MA, Haines JL. Genetically meaningful phenotypic subgroups in autism spectrum disorders. Genes, Brain, and Behavior. 13: 276-85. PMID 24373520 DOI: 10.1111/Gbb.12117 |
0.384 |
|
| 2014 |
Carney RM, Kohli MA, Kunkle BW, Naj AC, Gilbert JR, Züchner S, Pericak-Vance MA. Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 360-5. PMID 23727082 DOI: 10.1016/J.Jalz.2013.02.011 |
0.361 |
|
| 2014 |
Pericak-Vance M, Reitz C, Kunkle BW, Vardarajan BN, Kohli MA, Naj AC, Whitehead PL, Perry W, Martin E, Beecham G, Gilbert J, Farrer LA, Haines J, Schellenberg GD, Mayeux R. P2-131: WHOLE-EXOME SEQUENCING OF HISPANIC EARLY-ONSET ALZHEIMER DISEASE FAMILIES IDENTIFIES RARE VARIANTS IN MULTIPLE ALZHEIMER'S-RELATED GENES Alzheimer's & Dementia. 10: P518-P519. DOI: 10.1016/J.Jalz.2014.05.806 |
0.441 |
|
| 2014 |
Haines J, D'Aoust LN, Laux R, Fuzzell D, Caywood L, Reinhart-Mercer L, Scott W, Pericak-Vance M. P2-032: THE GENETIC ARCHITECTURE OF ALZHEIMER DISEASE IN THE MID-WESTERN U.S. AMISH Alzheimer's & Dementia. 10: P481-P482. DOI: 10.1016/J.Jalz.2014.05.705 |
0.374 |
|
| 2014 |
Naj AC, Cruchaga C, Kunkle BW, Mukherjee S, Graham R, Wang L, Behrens T, Mayeux R, Haines J, Farrer LA, Pericak-Vance M, Schellenberg GD. Exome Array Analysis Identifies Novel Risk Variants For Alzheimer'S Disease With Onset Before 65 Years Alzheimers & Dementia. 10: 319. DOI: 10.1016/J.Jalz.2014.05.280 |
0.385 |
|
| 2014 |
Carney R, Kohli MA, Kunkle BW, Martin ER, Beecham GW, Gilbert JR, Pericak-Vance MA. P1-036: CLINICAL CHARACTERISTICS OF LATE ONSET ALZHEIMER DISEASE IN AN EXTENDED FAMILY WITH A MISSENSE VARIANT IN TTC3 Alzheimer's & Dementia. 10: P316-P316. DOI: 10.1016/J.Jalz.2014.05.271 |
0.401 |
|
| 2014 |
Kunkle BW, Naj AC, Hamilton-Nelson K, Perry WR, Partch A, Valladares O, Chung J, Jun G, Schmidt M, Beecham G, Wang L, Martin E, Mayeux R, Haines J, Farrer LA, ... ... Pericak-Vance M, et al. Low-Frequency Variant Imputation Identifies Novel Disease-Associated Loci In A Genome-Wide Association Study Of Late-Onset Alzheimer'S Disease Alzheimers & Dementia. 10: 135. DOI: 10.1016/J.Jalz.2014.04.076 |
0.412 |
|
| 2013 |
Murdock DG, Bradford Y, Schnetz-Boutaud N, Mayo P, Allen MJ, D'Aoust LN, Liang X, Mitchell SL, Zuchner S, Small GW, Gilbert JR, Pericak-Vance MA, Haines JL. KIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriers. Plos One. 8: e82194. PMID 24349219 DOI: 10.1371/Journal.Pone.0082194 |
0.434 |
|
| 2013 |
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-Wells TA, Jones N, Smith AV, Chouraki V, ... ... Pericak-Vance MA, et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nature Genetics. 45: 1452-8. PMID 24162737 DOI: 10.1038/Ng.2802 |
0.443 |
|
| 2013 |
Beecham AH, Patsopoulos NA, Xifara DK, Davis MF, Kemppinen A, Cotsapas C, Shah TS, Spencer C, Booth D, Goris A, Oturai A, Saarela J, Fontaine B, Hemmer B, ... ... Pericak-Vance MA, et al. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nature Genetics. 45: 1353-60. PMID 24076602 DOI: 10.1038/Ng.2770 |
0.391 |
|
| 2013 |
Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, ... ... Pericak-Vance MA, et al. Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nature Genetics. 45: 1375-9. PMID 24036949 DOI: 10.1038/Ng.2758 |
0.373 |
|
| 2013 |
Park YS, Schmidt M, Martin ER, Pericak-Vance MA, Chung RH. Pathway-PDT: a flexible pathway analysis tool for nuclear families. Bmc Bioinformatics. 14: 267. PMID 24006871 DOI: 10.1186/1471-2105-14-267 |
0.332 |
|
| 2013 |
Cooke Bailey JN, Sobrin L, Pericak-Vance MA, Haines JL, Hammond CJ, Wiggs JL. Advances in the genomics of common eye diseases. Human Molecular Genetics. 22: R59-65. PMID 23962718 DOI: 10.1093/Hmg/Ddt396 |
0.388 |
|
| 2013 |
Nuytemans K, Bademci G, Kohli MM, Beecham GW, Wang L, Young JI, Nahab F, Martin ER, Gilbert JR, Benatar M, Haines JL, Scott WK, Züchner S, Pericak-Vance MA, Vance JM. C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Annals of Human Genetics. 77: 351-63. PMID 23845100 DOI: 10.1111/Ahg.12033 |
0.302 |
|
| 2013 |
Davis MF, Cummings AC, D'Aoust LN, Jiang L, Velez Edwards DR, Laux R, Reinhart-Mercer L, Fuzzell D, Scott WK, Pericak-Vance MA, Lee SL, Haines JL. Parkinson disease loci in the mid-western Amish. Human Genetics. 132: 1213-21. PMID 23793441 DOI: 10.1007/S00439-013-1316-1 |
0.36 |
|
| 2013 |
Reitz C, Tosto G, Vardarajan B, Rogaeva E, Ghani M, Rogers RS, Conrad C, Haines JL, Pericak-Vance MA, Fallin MD, Foroud T, Farrer LA, Schellenberg GD, George-Hyslop PS, Mayeux R, et al. Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Translational Psychiatry. 3: e256. PMID 23673467 DOI: 10.1038/Tp.2013.13 |
0.414 |
|
| 2013 |
Cummings AC, Torstenson E, Davis MF, D'Aoust LN, Scott WK, Pericak-Vance MA, Bush WS, Haines JL. Evaluating power and type 1 error in large pedigree analyses of binary traits. Plos One. 8: e62615. PMID 23658753 DOI: 10.1371/Journal.Pone.0062615 |
0.319 |
|
| 2013 |
Wang G, Dubovy SR, Kovach JL, Schwartz SG, Agarwal A, Scott WK, Haines JL, Pericak-Vance MA. Variants at chromosome 10q26 locus and the expression of HTRA1 in the retina. Experimental Eye Research. 112: 102-5. PMID 23644223 DOI: 10.1016/J.Exer.2013.04.019 |
0.392 |
|
| 2013 |
Naj AC, Scott WK, Courtenay MD, Cade WH, Schwartz SG, Kovach JL, Agarwal A, Wang G, Haines JL, Pericak-Vance MA. Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis. Annals of Human Genetics. 77: 215-31. PMID 23577725 DOI: 10.1111/Ahg.12011 |
0.373 |
|
| 2013 |
Wang G, Scott WK, Agarwal A, Haines JL, Pericak-Vance MA. Coding variants in ARMS2 and the risk of age-related macular degeneration. Jama Ophthalmology. 131: 804-5. PMID 23572227 DOI: 10.1001/Jamaophthalmol.2013.589 |
0.385 |
|
| 2013 |
Reitz C, Jun G, Naj A, Rajbhandary R, Vardarajan BN, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, Crane PK, Buxbaum JD, Murrell JR, ... ... Pericak-Vance MA, et al. Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. Jama. 309: 1483-92. PMID 23571587 DOI: 10.1001/Jama.2013.2973 |
0.49 |
|
| 2013 |
Miyashita A, Koike A, Jun G, Wang LS, Takahashi S, Matsubara E, Kawarabayashi T, Shoji M, Tomita N, Arai H, Asada T, Harigaya Y, Ikeda M, Amari M, Hanyu H, ... ... Pericak-Vance MA, et al. SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians. Plos One. 8: e58618. PMID 23565137 DOI: 10.1371/Journal.Pone.0058618 |
0.426 |
|
| 2013 |
Cruchaga C, Kauwe JS, Harari O, Jin SC, Cai Y, Karch CM, Benitez BA, Jeng AT, Skorupa T, Carrell D, Bertelsen S, Bailey M, McKean D, Shulman JM, De Jager PL, ... ... Pericak-Vance MA, et al. GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease. Neuron. 78: 256-68. PMID 23562540 DOI: 10.1016/J.Neuron.2013.02.026 |
0.4 |
|
| 2013 |
Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GH, Sim X, Weeks DE, Guymer RH, ... ... Pericak-Vance MA, et al. Seven new loci associated with age-related macular degeneration. Nature Genetics. 45: 433-9, 439e1-2. PMID 23455636 DOI: 10.1038/Ng.2578 |
0.423 |
|
| 2013 |
Holton P, Ryten M, Nalls M, Trabzuni D, Weale ME, Hernandez D, Crehan H, Gibbs JR, Mayeux R, Haines JL, Farrer LA, Pericak-Vance MA, Schellenberg GD, Ramirez-Restrepo M, et al. Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci. Annals of Human Genetics. 77: 85-105. PMID 23360175 DOI: 10.1111/Ahg.12000 |
0.309 |
|
| 2013 |
Rampersaud E, Nathanson L, Farmer J, Meshbane K, Belton RL, Dressen A, Cuccaro M, Musto A, Daunert S, Deo S, Hudson N, Vance JM, Seo D, Mendez A, Dykxhoorn DM, ... Pericak-Vance MA, et al. Genomic signatures of a global fitness index in a multi-ethnic cohort of women. Annals of Human Genetics. 77: 147-57. PMID 23289938 DOI: 10.1111/Ahg.12006 |
0.311 |
|
| 2013 |
Pasquale LR, Loomis SJ, Kang JH, Yaspan BL, Abdrabou W, Budenz DL, Chen TC, Delbono E, Friedman DS, Gaasterland D, Gaasterland T, Grosskreutz CL, Lee RK, Lichter PR, Liu Y, ... ... Pericak-Vance MA, et al. CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States. American Journal of Ophthalmology. 155: 342-353.e5. PMID 23111177 DOI: 10.1016/J.Ajo.2012.07.023 |
0.369 |
|
| 2013 |
Kohli MA, John-Williams K, Rajbhandary R, Naj A, Whitehead P, Hamilton K, Carney RM, Wright C, Crocco E, Gwirtzman HE, Lang R, Beecham G, Martin ER, Gilbert J, Benatar M, ... ... Pericak-Vance MA, et al. Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians. Neurobiology of Aging. 34: 1519.e5-12. PMID 23107433 DOI: 10.1016/J.Neurobiolaging.2012.10.003 |
0.411 |
|
| 2013 |
Wiggs JL, Hauser MA, Abdrabou W, Allingham RR, Budenz DL, Delbono E, Friedman DS, Kang JH, Gaasterland D, Gaasterland T, Lee RK, Lichter PR, Loomis S, Liu Y, McCarty C, ... ... Pericak-Vance M, et al. The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variables. Journal of Glaucoma. 22: 517-25. PMID 22828004 DOI: 10.1097/Ijg.0B013E31824D4Fd8 |
0.365 |
|
| 2013 |
Edwards DR, Gilbert JR, Hicks JE, Myers JL, Jiang L, Cummings AC, Guo S, Gallins PJ, Konidari I, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Laux R, Jackson CE, ... Pericak-Vance MA, et al. Linkage and association of successful aging to the 6q25 region in large Amish kindreds. Age (Dordrecht, Netherlands). 35: 1467-77. PMID 22773346 DOI: 10.1007/S11357-012-9447-1 |
0.397 |
|
| 2013 |
D'Aoust L, Cummings A, Jiang L, Laux R, Fuzzell D, Caywood L, Reinhart-Mercer L, Scott W, Pericak-Vance M, Haines J. P1-064: Identification of variants that confer susceptibility to Alzheimer's disease in the Amish through exome sequencing Alzheimer's & Dementia. 9: P175-P175. DOI: 10.1016/J.Jalz.2013.05.285 |
0.385 |
|
| 2013 |
Humphries C, Whitehead PL, Mash D, Beecham G, Pericak-Vance M, Gilbert J. P1-053: Genome-wide analysis of DNA methylation differentiates late-onset Alzheimer's disease from dementia with Lewy bodies Alzheimer's & Dementia. 9: P171-P172. DOI: 10.1016/J.Jalz.2013.05.274 |
0.343 |
|
| 2013 |
Chung J, Sherva R, Koesterer R, Haines J, Pericak-Vance M, Schellenberg G, Mayeux R, Farrer L. Genome-wide association study identifies susceptibility loci associated with the rate of cognitive decline Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.1100 |
0.314 |
|
| 2013 |
Pericak-Vance M, Kunkle B, Kholi M, Naj A, Perry W, Hamilton K, Whitehead PL, Levin B, Carney R, Crocco E, Wright C, Beecham G, Martin E, Wang L, Gilbert J, et al. P3-021: Variant-domain mapping in confirmed late-onset Alzheimer disease (LOAD) loci identifies multiple genomic regions with potentially functional variants Alzheimer's & Dementia. 9: P557-P557. DOI: 10.1016/J.Jalz.2013.05.1090 |
0.401 |
|
| 2013 |
Martin E, Kunkle B, Haines J, Farrer L, Pericak-Vance M, Schellenberg G. ADGC+: An expanded Alzheimer's Disease Genetics Consortium (ADGC) genome-wide association study Alzheimers & Dementia. 9: 557. DOI: 10.1016/J.Jalz.2013.05.1089 |
0.411 |
|
| 2013 |
Naj A, Cruchaga C, Kunkle B, Mukherjee S, Graham R, Behrens T, Mayeux R, Haines J, Farrer L, Pericak-Vance M, Schellenberg G, Wang L. Exome array analysis identifies novel risk variants for non-familial early-onset Alzheimer’s disease Alzheimers & Dementia. 9: 517. DOI: 10.1016/J.Jalz.2013.04.237 |
0.396 |
|
| 2012 |
Whitcomb DC, LaRusch J, Krasinskas AM, Klei L, Smith JP, Brand RE, Neoptolemos JP, Lerch MM, Tector M, Sandhu BS, Guda NM, Orlichenko L, Alkaade S, Amann ST, ... ... Pericak-Vance MA, et al. Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nature Genetics. 44: 1349-54. PMID 23143602 DOI: 10.1038/Ng.2466 |
0.355 |
|
| 2012 |
Cukier HN, Lee JM, Ma D, Young JI, Mayo V, Butler BL, Ramsook SS, Rantus JA, Abrams AJ, Whitehead PL, Wright HH, Abramson RK, Haines JL, Cuccaro ML, Pericak-Vance MA, et al. The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1. Autism Research : Official Journal of the International Society For Autism Research. 5: 385-97. PMID 23055267 DOI: 10.1002/Aur.1251 |
0.396 |
|
| 2012 |
Schnetz-Boutaud NC, Hoffman J, Coe JE, Murdock DG, Pericak-Vance MA, Haines JL. Identification and confirmation of an exonic splicing enhancer variation in exon 5 of the Alzheimer disease associated PICALM gene. Annals of Human Genetics. 76: 448-53. PMID 22943764 DOI: 10.1111/J.1469-1809.2012.00727.X |
0.444 |
|
| 2012 |
Cummings AC, Jiang L, Velez Edwards DR, McCauley JL, Laux R, McFarland LL, Fuzzell D, Knebusch C, Caywood L, Reinhart-Mercer L, Nations L, Gilbert JR, Konidari I, Tramontana M, Cuccaro ML, ... ... Pericak-Vance MA, et al. Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. Annals of Human Genetics. 76: 342-51. PMID 22881374 DOI: 10.1111/J.1469-1809.2012.00721.X |
0.446 |
|
| 2012 |
Jun G, Vardarajan BN, Buros J, Yu CE, Hawk MV, Dombroski BA, Crane PK, Larson EB, Mayeux R, Haines JL, Lunetta KL, Pericak-Vance MA, Schellenberg GD, Farrer LA. Comprehensive search for Alzheimer disease susceptibility loci in the APOE region. Archives of Neurology. 69: 1270-9. PMID 22869155 DOI: 10.1001/Archneurol.2012.2052 |
0.449 |
|
| 2012 |
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... ... Pericak-Vance MA, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/Hmg/Dds301 |
0.41 |
|
| 2012 |
Kamboh MI, Demirci FY, Wang X, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ, Jun G, Baldwin C, Logue MW, Buros J, Farrer L, Pericak-Vance MA, et al. Genome-wide association study of Alzheimer's disease. Translational Psychiatry. 2: e117. PMID 22832961 DOI: 10.1038/Tp.2012.45 |
0.359 |
|
| 2012 |
Allen M, Zou F, Chai HS, Younkin CS, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN, Nair AA, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus KG, Palusak R, ... ... Pericak-Vance MA, et al. Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology. 79: 221-8. PMID 22722634 DOI: 10.1212/Wnl.0B013E3182605801 |
0.408 |
|
| 2012 |
Zou F, Chai HS, Younkin CS, Allen M, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN, Nair AA, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus KG, Palusak R, ... ... Pericak-Vance MA, et al. Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants. Plos Genetics. 8: e1002707. PMID 22685416 DOI: 10.1371/Journal.Pgen.1002707 |
0.433 |
|
| 2012 |
Ulmer M, Li J, Yaspan BL, Ozel AB, Richards JE, Moroi SE, Hawthorne F, Budenz DL, Friedman DS, Gaasterland D, Haines J, Kang JH, Lee R, Lichter P, Liu Y, ... ... Pericak-Vance M, et al. Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia. Investigative Ophthalmology & Visual Science. 53: 4468-74. PMID 22661486 DOI: 10.1167/Iovs.12-9784 |
0.378 |
|
| 2012 |
Wiggs JL, Yaspan BL, Hauser MA, Kang JH, Allingham RR, Olson LM, Abdrabou W, Fan BJ, Wang DY, Brodeur W, Budenz DL, Caprioli J, Crenshaw A, Crooks K, Delbono E, ... ... Pericak-Vance M, et al. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. Plos Genetics. 8: e1002654. PMID 22570617 DOI: 10.1371/Journal.Pgen.1002654 |
0.36 |
|
| 2012 |
Coppola G, Chinnathambi S, Lee JJ, Dombroski BA, Baker MC, Soto-Ortolaza AI, Lee SE, Klein E, Huang AY, Sears R, Lane JR, Karydas AM, Kenet RO, Biernat J, Wang LS, ... ... Pericak-Vance MA, et al. Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases. Human Molecular Genetics. 21: 3500-12. PMID 22556362 DOI: 10.1093/Hmg/Dds161 |
0.415 |
|
| 2012 |
Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, Jaworski JM, Salyakina D, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Martin ER, ... ... Pericak-Vance MA, et al. Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human Molecular Genetics. 21: 3513-23. PMID 22543975 DOI: 10.1093/Hmg/Dds164 |
0.403 |
|
| 2012 |
Schwartz SG, Agarwal A, Kovach JL, Gallins PJ, Cade W, Postel EA, Wang G, Ayala-Haedo J, Spencer KM, Haines JL, Pericak-Vance MA, Scott WK. The ARMS2 A69S variant and bilateral advanced age-related macular degeneration. Retina (Philadelphia, Pa.). 32: 1486-91. PMID 22481475 DOI: 10.1097/Iae.0B013E318240A540 |
0.308 |
|
| 2012 |
Hedges DJ, Hamilton-Nelson KL, Sacharow SJ, Nations L, Beecham GW, Kozhekbaeva ZM, Butler BL, Cukier HN, Whitehead PL, Ma D, Jaworski JM, Nathanson L, Lee JM, Hauser SL, Oksenberg JR, ... ... Pericak-Vance MA, et al. Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci. Molecular Autism. 3: 2. PMID 22472195 DOI: 10.1186/2040-2392-3-2 |
0.347 |
|
| 2012 |
Wang L, Hara K, Van Baaren JM, Price JC, Beecham GW, Gallins PJ, Whitehead PL, Wang G, Lu C, Slifer MA, Züchner S, Martin ER, Mash D, Haines JL, Pericak-Vance MA, et al. Vitamin D receptor and Alzheimer's disease: a genetic and functional study. Neurobiology of Aging. 33: 1844.e1-9. PMID 22306846 DOI: 10.1016/J.Neurobiolaging.2011.12.038 |
0.391 |
|
| 2012 |
Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, ... ... Pericak-Vance MA, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. 131: 565-79. PMID 21996756 DOI: 10.1007/S00439-011-1094-6 |
0.404 |
|
| 2012 |
Courtenay MD, Gilbert JR, Jiang L, Cummings AC, Gallins PJ, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Laux R, McCauley JL, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK. Mitochondrial haplogroup X is associated with successful aging in the Amish. Human Genetics. 131: 201-8. PMID 21750925 DOI: 10.1007/S00439-011-1060-3 |
0.316 |
|
| 2012 |
Cai G, Atzmon G, Naj AC, Beecham GW, Barzilai N, Haines JL, Sano M, Pericak-Vance M, Buxbaum JD. Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease. Neurobiology of Aging. 33: 416-417.e3. PMID 20381196 DOI: 10.1016/J.Neurobiolaging.2010.03.003 |
0.363 |
|
| 2012 |
Pericak-Vance M, Zuchner S, Kohli M, John-Williams K, Naj A, Rajbhandary R, Whitehead PL, Hamilton-Nelson K, Carney R, Wright C, Crocco E, Gwirtzman H, Lang R, Beecham G, Martin E, et al. Large repeat expansions in the C9ORF72 gene contribute to a spectrum of neurodegenerative disorders including Alzheimer's disease in Caucasians, but not African-Americans Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2013.08.277 |
0.379 |
|
| 2012 |
Kuwano R, Miyashita A, Koike A, Nishida N, Tokunaga K, Yamamoto K, Ihara Y, Kim J, Pericak-Vance M, Farrer L, Schellenberg G. Genome-wide association study of Alzheimer's disease: A collaborative genetic study on Alzheimer's disease with Japan, Korea and the Alzheimer's Disease Genetics Consortium Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.2111 |
0.409 |
|
| 2012 |
Haines J, Naj A, Kohli M, Hamilton-Nelson K, Rajbhandary R, Whitehead PL, Carney R, Crocco E, Wright C, Beecham G, Martin E, Gilbert J, Zuchner S, Pericak-Vance M, Levin B. O5-03-01: Deep resequencing of 9 confirmed late-onset Alzheimer's disease (LOAD) loci identifies multiple genomic regions with potentially functional variants Alzheimer's & Dementia. 8: P734-P735. DOI: 10.1016/J.Jalz.2012.05.1981 |
0.382 |
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| 2012 |
Zuchner S, Kohli M, Naj A, Hamilton K, Rajbhandary R, Plitnik T, John-Williams K, Whitehead PL, Gilbert J, Martin E, Beecham G, Haines J, Pericak-Vance M. Exome sequencing of extended late-onset Alzheimer's disease families identifies a variant in the TTC3 gene Alzheimers & Dementia. 8: 679. DOI: 10.1016/J.Jalz.2012.05.1839 |
0.429 |
|
| 2012 |
Carney R, Kohli M, Naj A, Beecham G, Hamilton-Nelson K, Haines J, Gilbert J, Zuchner S, Pericak-Vance M. Parkinsonian symptoms and lack of prominent frontal atrophy in a family with early-onset dementia and the MAPT R406W mutation Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1832 |
0.3 |
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| 2012 |
Beecham G, Montine T, Rajbhandary R, Hamilton-Nelson K, Naj A, Martin E, Mayeux R, Haines J, Farrer L, Schellenberg G, Pericak-Vance M. P4-102: APP associated with late-onset Alzheimer's disease in an autopsy-confirmed dataset Alzheimer's & Dementia. 8: P668-P668. DOI: 10.1016/J.Jalz.2012.05.1805 |
0.384 |
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| 2012 |
Cummings A, Shaffer C, Jiang L, Laux R, Fuzzell D, Knebusch C, Reinhart-Mercer L, Caywood L, Jackson C, Scott W, Pericak-Vance M, Haines J. Sequence analysis of CTNNA2 and LRRTM1 for late-onset Alzheimer's disease in the Amish Alzheimers & Dementia. 8: 664. DOI: 10.1016/J.Jalz.2012.05.1790 |
0.369 |
|
| 2012 |
Allen M, Zou F, Chai HS, Younkin C, Crook J, Pankratz V, Carrasquillo M, Rowley C, Nair A, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus K, Palusak R, ... ... Pericak-Vance M, et al. Genetic association of variants with late-onset Alzheimer's disease risk and brain gene expression Alzheimers & Dementia. 8: 451. DOI: 10.1016/J.Jalz.2012.05.1202 |
0.415 |
|
| 2011 |
Patsopoulos NA, Esposito F, Reischl J, Lehr S, Bauer D, Heubach J, Sandbrink R, Pohl C, Edan G, Kappos L, ... ... Pericak-Vance M, et al. Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. Annals of Neurology. 70: 897-912. PMID 22190364 DOI: 10.1002/Ana.22609 |
0.41 |
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| 2011 |
Chung RH, Ma D, Wang K, Hedges DJ, Jaworski JM, Gilbert JR, Cuccaro ML, Wright HH, Abramson RK, Konidari I, Whitehead PL, Schellenberg GD, Hakonarson H, Haines JL, Pericak-Vance MA, et al. An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males. Molecular Autism. 2: 18. PMID 22050706 DOI: 10.1186/2040-2392-2-18 |
0.401 |
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| 2011 |
Salyakina D, Cukier HN, Lee JM, Sacharow S, Nations LD, Ma D, Jaworski JM, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Haines JL, Gilbert JR, ... ... Pericak-Vance MA, et al. Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk. Plos One. 6: e26049. PMID 22016809 DOI: 10.1371/Journal.Pone.0026049 |
0.431 |
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| 2011 |
Sawcer S, Hellenthal G, Pirinen M, Spencer CC, Patsopoulos NA, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt SE, Edkins S, Gray E, Booth DR, ... ... Pericak-Vance MA, et al. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature. 476: 214-9. PMID 21833088 DOI: 10.1038/Nature10251 |
0.446 |
|
| 2011 |
Edwards DR, Gilbert JR, Jiang L, Gallins PJ, Caywood L, Creason M, Fuzzell D, Knebusch C, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK. Successful aging shows linkage to chromosomes 6, 7, and 14 in the Amish. Annals of Human Genetics. 75: 516-28. PMID 21668908 DOI: 10.1111/J.1469-1809.2011.00658.X |
0.387 |
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| 2011 |
Zuvich RL, Bush WS, McCauley JL, Beecham AH, De Jager PL, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Sawcer SJ, Pericak-Vance MA, Barcellos LF, Mortlock DP, Haines JL. Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex. Human Molecular Genetics. 20: 3517-24. PMID 21653641 DOI: 10.1093/Hmg/Ddr250 |
0.401 |
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| 2011 |
Cummings AC, Lee SL, McCauley JL, Jiang L, Crunk A, McFarland LL, Gallins PJ, Fuzzell D, Knebusch C, Jackson CE, Scott WK, Pericak-Vance MA, Haines JL. A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6. Annals of Human Genetics. 75: 351-8. PMID 21488853 DOI: 10.1111/J.1469-1809.2011.00643.X |
0.451 |
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| 2011 |
Cukier HN, Salyakina D, Blankstein SF, Robinson JL, Sacharow S, Ma D, Wright HH, Abramson RK, Menon R, Williams SM, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 493-501. PMID 21480499 DOI: 10.1002/Ajmg.B.31188 |
0.402 |
|
| 2011 |
Naj AC, Jun G, Beecham GW, Wang LS, Vardarajan BN, Buros J, Gallins PJ, Buxbaum JD, Jarvik GP, Crane PK, Larson EB, Bird TD, Boeve BF, Graff-Radford NR, De Jager PL, ... ... Pericak-Vance MA, et al. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nature Genetics. 43: 436-41. PMID 21460841 DOI: 10.1038/Ng.801 |
0.319 |
|
| 2011 |
Spencer KL, Olson LM, Schnetz-Boutaud N, Gallins P, Agarwal A, Iannaccone A, Kritchevsky SB, Garcia M, Nalls MA, Newman AB, Scott WK, Pericak-Vance MA, Haines JL. Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration. Plos One. 6: e17784. PMID 21455292 DOI: 10.1371/Journal.Pone.0017784 |
0.328 |
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| 2011 |
Edwards YJ, Beecham GW, Scott WK, Khuri S, Bademci G, Tekin D, Martin ER, Jiang Z, Mash DC, ffrench-Mullen J, Pericak-Vance MA, Tsinoremas N, Vance JM. Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach. Plos One. 6: e16917. PMID 21364952 DOI: 10.1371/Journal.Pone.0016917 |
0.351 |
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| 2011 |
Griswold AJ, Ma D, Sacharow SJ, Robinson JL, Jaworski JM, Wright HH, Abramson RK, Lybaek H, Øyen N, Cuccaro ML, Gilbert JR, Pericak-Vance MA. A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis. Autism Research : Official Journal of the International Society For Autism Research. 4: 221-7. PMID 21360829 DOI: 10.1002/Aur.186 |
0.392 |
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| 2011 |
Reitz C, Tokuhiro S, Clark LN, Conrad C, Vonsattel JP, Hazrati LN, Palotás A, Lantigua R, Medrano M, Z Jiménez-Velázquez I, Vardarajan B, Simkin I, Haines JL, Pericak-Vance MA, Farrer LA, et al. SORCS1 alters amyloid precursor protein processing and variants may increase Alzheimer's disease risk. Annals of Neurology. 69: 47-64. PMID 21280075 DOI: 10.1002/Ana.22308 |
0.389 |
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| 2011 |
Yaspan BL, Bush WS, Torstenson ES, Ma D, Pericak-Vance MA, Ritchie MD, Sutcliffe JS, Haines JL. Genetic analysis of biological pathway data through genomic randomization. Human Genetics. 129: 563-71. PMID 21279722 DOI: 10.1007/S00439-011-0956-2 |
0.382 |
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| 2011 |
Hussman JP, Chung RH, Griswold AJ, Jaworski JM, Salyakina D, Ma D, Konidari I, Whitehead PL, Vance JM, Martin ER, Cuccaro ML, Gilbert JR, Haines JL, Pericak-Vance MA. A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism. Molecular Autism. 2: 1. PMID 21247446 DOI: 10.1186/2040-2392-2-1 |
0.346 |
|
| 2011 |
Reitz C, Cheng R, Rogaeva E, Lee JH, Tokuhiro S, Zou F, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Arai H, Kamboh MI, Prince JA, Maier W, ... ... Pericak-Vance MA, et al. Meta-analysis of the association between variants in SORL1 and Alzheimer disease. Archives of Neurology. 68: 99-106. PMID 21220680 DOI: 10.1001/Archneurol.2010.346 |
0.415 |
|
| 2011 |
Spencer KL, Olson LM, Schnetz-Boutaud N, Gallins P, Wang G, Scott WK, Agarwal A, Jakobsdottir J, Conley Y, Weeks DE, Gorin MB, Pericak-Vance MA, Haines JL. Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility. Investigative Ophthalmology & Visual Science. 52: 1748-54. PMID 21169531 DOI: 10.1167/Iovs.09-5112 |
0.393 |
|
| 2011 |
Sherva R, Baldwin CT, Inzelberg R, Vardarajan B, Cupples LA, Lunetta K, Bowirrat A, Naj A, Pericak-Vance M, Friedland RP, Farrer LA. Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data. Journal of Alzheimer's Disease : Jad. 23: 349-59. PMID 21098978 DOI: 10.3233/Jad-2010-100714 |
0.457 |
|
| 2011 |
McCorquodale DS, Ozomaro U, Huang J, Montenegro G, Kushman A, Citrigno L, Price J, Speziani F, Pericak-Vance MA, Züchner S. Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia. Clinical Genetics. 79: 523-30. PMID 20718791 DOI: 10.1111/J.1399-0004.2010.01501.X |
0.322 |
|
| 2011 |
Saunders AM, Strittmatter WJ, Schmechel D, St. George-Hyslop PH, Pericak-Vance MA, Joo SH, Rosi BL, Gusella JF, Crapper-MacLachlan DR, Alberts MJ, Hulette C, Crain B, Goldgaber D, Roses AD. Association of apolipoprotein E allele 4 with late-onset familial and sporadic Alzheimer's disease Neurology. 77: 950-950. DOI: 10.1212/01.wnl.0000405291.74999.10 |
0.301 |
|
| 2011 |
Ortel TL, Beecham G, Hedges D, Whitehead P, Beecham A, Hahn S, Lawson JW, Erkan D, Brandao LR, James AH, Manco-Johnson MJ, Kulkarni R, Kitchens CS, Pericak-Vance M, Vance JM. Whole-Exome Sequencing Identifies Novel Risk Variant for Thrombotic Storm Blood. 118: 1229-1229. DOI: 10.1182/Blood.V118.21.1229.1229 |
0.372 |
|
| 2011 |
Thornton-Wells T, Torstenson E, Dudek S, Ritchie M, Martin E, Pericak-Vance M, Haines J. Discovery and Replication of Gene-Gene Interactions in Multiple Independent Datasets from the Alzheimer Disease Genetics Consortium Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.548 |
0.402 |
|
| 2011 |
Schnetz-Boutaud N, Hoffman J, Coe J, Murdock D, Pericak-Vance M, Haines J. P1-261: Identification of An Exonic Splicing Enhancer Variation in Exon 5 of the Alzheimer Disease Associated PICALM Gene Alzheimer's & Dementia. 7: S194-S195. DOI: 10.1016/J.Jalz.2011.05.541 |
0.42 |
|
| 2011 |
Naj A, Jun G, Buros J, Gallins P, Farrer L, Haines J, Pericak-Vance M, Schellenberg G. Genome-Wide Association Study of Late-Onset Alzheimer Disease Identifies Disease-Associated Variants in MS4A4/MS4A6E, CD2AP, CD33, and EPHA1 Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.530 |
0.381 |
|
| 2011 |
Martin E, Naj A, Park YS, Gallins P, Hamilton K, Rajbhandary R, Haines J, Pericak-Vance M. Genome-Wide Association Analysis Identifies Novel Loci Associated with the Onset Age Among Cases with Late-Onset Alzheimer’s Disease Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.526 |
0.394 |
|
| 2011 |
Cummings A, Haines J, Pericak-Vance M, Laux R, Jiang L, Edwards DV, McFarland L, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Jackson C, McCauley J, Scott W. O1-01-01: Genome-wide study for Alzheimer's disease in the Amish Alzheimer's & Dementia. 7: S92-S92. DOI: 10.1016/J.Jalz.2011.05.225 |
0.333 |
|
| 2010 |
Salyakina D, Ma DQ, Jaworski JM, Konidari I, Whitehead PL, Henson R, Martinez D, Robinson JL, Sacharow S, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Variants in several genomic regions associated with asperger disorder. Autism Research : Official Journal of the International Society For Autism Research. 3: 303-10. PMID 21182207 DOI: 10.1002/Aur.158 |
0.417 |
|
| 2010 |
Naj AC, Beecham GW, Martin ER, Gallins PJ, Powell EH, Konidari I, Whitehead PL, Cai G, Haroutunian V, Scott WK, Vance JM, Slifer MA, Gwirtsman HE, Gilbert JR, Haines JL, ... ... Pericak-Vance MA, et al. Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. Plos Genetics. 6: e1001130. PMID 20885792 DOI: 10.1371/Journal.Pgen.1001130 |
0.412 |
|
| 2010 |
Christianson CA, Powell KP, Hahn SE, Bartz D, Roxbury T, Blanton SH, Vance JM, Pericak-Vance M, Telfair J, Henrich VC. Findings from a community education needs assessment to facilitate the integration of genomic medicine into primary care. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 12: 587-93. PMID 20860071 DOI: 10.1097/Gim.0B013E3181Ed3F97 |
0.348 |
|
| 2010 |
Lambert JC, Sleegers K, González-Pérez A, Ingelsson M, Beecham GW, Hiltunen M, Combarros O, Bullido MJ, Brouwers N, Bettens K, Berr C, Pasquier F, Richard F, Dekosky ST, Hannequin D, ... ... Pericak-Vance MA, et al. The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. Journal of Alzheimer's Disease : Jad. 22: 247-55. PMID 20847397 DOI: 10.3233/Jad-2010-100933 |
0.45 |
|
| 2010 |
Briggs FB, Bartlett SE, Goldstein BA, Wang J, McCauley JL, Zuvich RL, De Jager PL, Rioux JD, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Oksenberg JR, Sawcer SJ, Pericak-Vance MA, et al. Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals. Human Molecular Genetics. 19: 4286-95. PMID 20699326 DOI: 10.1093/Hmg/Ddq328 |
0.341 |
|
| 2010 |
Jun G, Naj AC, Beecham GW, Wang LS, Buros J, Gallins PJ, Buxbaum JD, Ertekin-Taner N, Fallin MD, Friedland R, Inzelberg R, Kramer P, Rogaeva E, St George-Hyslop P, ... ... Pericak-Vance MA, et al. Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. Archives of Neurology. 67: 1473-84. PMID 20697030 DOI: 10.1001/Archneurol.2010.201 |
0.384 |
|
| 2010 |
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Pericak-Vance MA, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/Hmg/Ddq307 |
0.418 |
|
| 2010 |
Beecham GW, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. APOE is not associated with Alzheimer disease: a cautionary tale of genotype imputation. Annals of Human Genetics. 74: 189-94. PMID 20529013 DOI: 10.1111/J.1469-1809.2010.00573.X |
0.408 |
|
| 2010 |
Beecham GW, Naj AC, Gilbert JR, Haines JL, Buxbaum JD, Pericak-Vance MA. PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility. Psychiatric Genetics. 20: 321-4. PMID 20523261 DOI: 10.1097/Ypg.0B013E32833B635D |
0.385 |
|
| 2010 |
Briggs FB, Goldstein BA, McCauley JL, Zuvich RL, De Jager PL, Rioux JD, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Oksenberg JR, Sawcer SJ, Pericak-Vance MA, Haines JL, Barcellos LF, et al. Variation within DNA repair pathway genes and risk of multiple sclerosis. American Journal of Epidemiology. 172: 217-24. PMID 20522537 DOI: 10.1093/Aje/Kwq086 |
0.374 |
|
| 2010 |
Booth DR, Heard RN, Stewart GJ, Cox M, Scott RJ, Lechner-Scott J, Goris A, Dobosi R, Dubois B, Saarela J, Leppä V, Peltonen L, Pirttila T, Cournu-Rebeix I, ... ... Pericak-Vance MA, et al. Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Nature Genetics. 42: 469-70; author reply. PMID 20502484 DOI: 10.1038/Ng0610-469 |
0.306 |
|
| 2010 |
Chen W, Stambolian D, Edwards AO, Branham KE, Othman M, Jakobsdottir J, Tosakulwong N, Pericak-Vance MA, Campochiaro PA, Klein ML, Tan PL, Conley YP, Kanda A, Kopplin L, Li Y, et al. Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 107: 7401-6. PMID 20385819 DOI: 10.1073/Pnas.0912702107 |
0.392 |
|
| 2010 |
Ayala-Haedo JA, Gallins PJ, Whitehead PL, Schwartz SG, Kovach JL, Postel EA, Agarwal A, Wang G, Haines JL, Pericak-Vance MA, Scott WK. Analysis of single nucleotide polymorphisms in the NOS2A gene and interaction with smoking in age-related macular degeneration. Annals of Human Genetics. 74: 195-201. PMID 20374233 DOI: 10.1111/J.1469-1809.2010.00570.X |
0.333 |
|
| 2010 |
Bush WS, Sawcer SJ, de Jager PL, Oksenberg JR, McCauley JL, Pericak-Vance MA, Haines JL. Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come. American Journal of Human Genetics. 86: 621-5. PMID 20362272 DOI: 10.1016/J.Ajhg.2010.02.027 |
0.395 |
|
| 2010 |
Bronson PG, Caillier S, Ramsay PP, McCauley JL, Zuvich RL, De Jager PL, Rioux JD, Ivinson AJ, Compston A, Hafler DA, Sawcer SJ, Pericak-Vance MA, Haines JL, Hauser SL, et al. CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis. Human Molecular Genetics. 19: 2331-40. PMID 20211854 DOI: 10.1093/Hmg/Ddq101 |
0.342 |
|
| 2010 |
Wang G, Spencer KL, Scott WK, Whitehead P, Court BL, Ayala-Haedo J, Mayo P, Schwartz SG, Kovach JL, Gallins P, Polk M, Agarwal A, Postel EA, Haines JL, Pericak-Vance MA. Analysis of the indel at the ARMS2 3'UTR in age-related macular degeneration. Human Genetics. 127: 595-602. PMID 20182747 DOI: 10.1007/S00439-010-0805-8 |
0.374 |
|
| 2010 |
Zuvich RL, McCauley JL, Oksenberg JR, Sawcer SJ, De Jager PL, Aubin C, Cross AH, Piccio L, Aggarwal NT, Evans D, Hafler DA, Compston A, Hauser SL, Pericak-Vance MA, et al. Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility. Human Genetics. 127: 525-35. PMID 20112030 DOI: 10.1007/S00439-010-0789-4 |
0.415 |
|
| 2010 |
Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, Beecham GW, Wang L, Züchner S, Konidari I, Wang G, Singer C, Nahab F, Scott B, Stajich JM, Pericak-Vance M, et al. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Annals of Human Genetics. 74: 97-109. PMID 20070850 DOI: 10.1111/J.1469-1809.2009.00560.X |
0.393 |
|
| 2010 |
Edwards DR, Gallins P, Polk M, Ayala-Haedo J, Schwartz SG, Kovach JL, Spencer K, Wang G, Agarwal A, Postel EA, Haines JL, Pericak-Vance M, Scott WK. Inverse association of female hormone replacement therapy with age-related macular degeneration and interactions with ARMS2 polymorphisms. Investigative Ophthalmology & Visual Science. 51: 1873-9. PMID 19933179 DOI: 10.1167/Iovs.09-4000 |
0.361 |
|
| 2010 |
Cukier HN, Rabionet R, Konidari I, Rayner-Evans MY, Baltos ML, Wright HH, Abramson RK, Martin ER, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Novel variants identified in methyl-CpG-binding domain genes in autistic individuals. Neurogenetics. 11: 291-303. PMID 19921286 DOI: 10.1007/S10048-009-0228-7 |
0.654 |
|
| 2010 |
Ma DQ, Rabionet R, Konidari I, Jaworski J, Cukier HN, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA, Martin ER. Association and gene-gene interaction of SLC6A4 and ITGB3 in autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 477-83. PMID 19588468 DOI: 10.1002/Ajmg.B.31003 |
0.663 |
|
| 2010 |
Reitz C, Tokuhiro S, Clark L, Conrad C, Vonsattel J, Lantigua R, Medrano M, Simkin I, Haines J, Pericak-Vance M, Farrer L, Lee J, Rogaeva E, George-Hyslop PS, Mayeux R. Sorcs1 Alters APP Processing and Variants may Increase Alzheimer's Disease Risk Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.08.091 |
0.357 |
|
| 2010 |
Kohli MA, Griswold A, Naj AC, Beecham G, Haines JL, Gilbert J, Pericak-Vance MA. Comprehensive variant discovery in the Late-Onset Alzheimer Disease susceptibility gene Clusterin using next generation sequencing technology Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.610 |
0.38 |
|
| 2010 |
Reitz C, Cheng R, Rogaeva E, Lee J, Tokuhiro S, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Kamboh IM, Prince J, Maier W, Riemenschneider M, Owen M, ... ... Pericak-Vance MA, et al. Meta-analysis of the association between SORL1 variants and Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.351 |
0.394 |
|
| 2010 |
Beecham GW, Schnetz-Boutaud N, Bartlett J, Naj A, Gilbert J, Martin ER, Buxbaum J, Haines JL, Pericak-Vance MA. Copy number polymorphism at chromosome 19 locus associated with late-onset Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.349 |
0.384 |
|
| 2010 |
Cummings AC, Jiang L, Edwards DV, Laux R, McFarland LL, Gallins PJ, Caywood L, Creason M, Fuzzell D, Knebusch C, Tramontana MG, Slifer MA, Jackson CE, Scott WK, Pericak-Vance MA, et al. Genome-wide linkage study in the Amish shows evidence for a chromosome 3 locus in late-onset Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.220 |
0.306 |
|
| 2010 |
Naj AC, Beecham GW, Martin ER, Gallins PJ, Powell EH, Konidari I, Whitehead PL, Cai G, Kajiwara Y, Haroutunian V, Scott WK, Vance JM, Slifer MA, Gwirtsman HE, Gilbert JR, ... ... Pericak-Vance MA, et al. O1‐03‐03: Dementia revealed: Novel chromosome 6 locus for late‐onset Alzheimer's disease provides genetic evidence for folate‐pathway abnormalities Alzheimer's & Dementia. 6. DOI: 10.1016/j.jalz.2010.05.219 |
0.309 |
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| 2010 |
Zuchner S, Beecham G, Haines J, Pericak-Vance M. O1-03-02: Exome sequencing of late-onset extended Alzheimer families Alzheimer's & Dementia. 6: S74-S74. DOI: 10.1016/J.Jalz.2010.05.218 |
0.309 |
|
| 2010 |
Pericak-Vance MA. Genome-wide association studies and neuropsychological phenotypes Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.195 |
0.316 |
|
| 2009 |
Hedges DJ, Hedges D, Burges D, Powell E, Almonte C, Huang J, Young S, Boese B, Schmidt M, Pericak-Vance MA, Martin E, Zhang X, Harkins TT, Züchner S. Exome sequencing of a multigenerational human pedigree. Plos One. 4: e8232. PMID 20011588 DOI: 10.1371/Journal.Pone.0008232 |
0.375 |
|
| 2009 |
Cukier HN, Skaar DA, Rayner-Evans MY, Konidari I, Whitehead PL, Jaworski JM, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility. Autism Research : Official Journal of the International Society For Autism Research. 2: 258-66. PMID 19877165 DOI: 10.1002/Aur.96 |
0.411 |
|
| 2009 |
Gregory SG, Connelly JJ, Towers AJ, Johnson J, Biscocho D, Markunas CA, Lintas C, Abramson RK, Wright HH, Ellis P, Langford CF, Worley G, Delong GR, Murphy SK, Cuccaro ML, ... ... Pericak-Vance MA, et al. Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. Bmc Medicine. 7: 62. PMID 19845972 DOI: 10.1186/1741-7015-7-62 |
0.337 |
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| 2009 |
Pericak-Vance MA, Haines JL. Beyond proof of principle: new genes for Alzheimer's disease through collaboration. The Lancet. Neurology. 8: 977-9. PMID 19833292 DOI: 10.1016/S1474-4422(09)70277-7 |
0.426 |
|
| 2009 |
Zuvich RL, McCauley JL, Pericak-Vance MA, Haines JL. Genetics and pathogenesis of multiple sclerosis. Seminars in Immunology. 21: 328-33. PMID 19775910 DOI: 10.1016/J.Smim.2009.08.003 |
0.372 |
|
| 2009 |
McCauley JL, Zuvich RL, Bradford Y, Kenealy SJ, Schnetz-Boutaud N, Gregory SG, Hauser SL, Oksenberg JR, Mortlock DP, Pericak-Vance MA, Haines JL. Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis. Genes and Immunity. 10: 624-30. PMID 19626040 DOI: 10.1038/Gene.2009.53 |
0.44 |
|
| 2009 |
De Jager PL, Jia X, Wang J, de Bakker PI, Ottoboni L, Aggarwal NT, Piccio L, Raychaudhuri S, Tran D, Aubin C, Briskin R, Romano S, Baranzini SE, McCauley JL, ... Pericak-Vance MA, et al. Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. Nature Genetics. 41: 776-82. PMID 19525953 DOI: 10.1038/Ng.401 |
0.341 |
|
| 2009 |
Beecham GW, Schnetz-Boutaud N, Haines JL, Pericak-Vance MA. CALHM1 polymorphism is not associated with late-onset Alzheimer disease. Annals of Human Genetics. 73: 379-81. PMID 19472444 DOI: 10.1111/J.1469-1809.2009.00509.X |
0.383 |
|
| 2009 |
Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, ... ... Pericak-Vance MA, et al. A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Annals of Human Genetics. 73: 263-73. PMID 19456320 DOI: 10.1111/J.1469-1809.2009.00523.X |
0.436 |
|
| 2009 |
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, ... ... Pericak-Vance MA, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999 |
0.384 |
|
| 2009 |
Slifer MA, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. Resolving the relationship between ApolipoproteinE and depression. Neuroscience Letters. 455: 116-9. PMID 19368858 DOI: 10.1016/J.Neulet.2009.03.007 |
0.312 |
|
| 2009 |
Kajiwara Y, Akram A, Katsel P, Haroutunian V, Schmeidler J, Beecham G, Haines JL, Pericak-Vance MA, Buxbaum JD. FE65 binds Teashirt, inhibiting expression of the primate-specific caspase-4. Plos One. 4: e5071. PMID 19343227 DOI: 10.1371/Journal.Pone.0005071 |
0.357 |
|
| 2009 |
Ban M, Goris A, Lorentzen AR, Baker A, Mihalova T, Ingram G, Booth DR, Heard RN, Stewart GJ, Bogaert E, Dubois B, Harbo HF, Celius EG, Spurkland A, Strange R, ... ... Pericak-Vance M, et al. Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. European Journal of Human Genetics : Ejhg. 17: 1309-13. PMID 19293837 DOI: 10.1038/Ejhg.2009.41 |
0.396 |
|
| 2009 |
Kwiatkowski TJ, Bosco DA, Leclerc AL, Tamrazian E, Vanderburg CR, Russ C, Davis A, Gilchrist J, Kasarskis EJ, Munsat T, Valdmanis P, Rouleau GA, Hosler BA, Cortelli P, de Jong PJ, ... ... Pericak-Vance MA, et al. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science (New York, N.Y.). 323: 1205-8. PMID 19251627 DOI: 10.1126/Science.1166066 |
0.33 |
|
| 2009 |
Liang X, Slifer M, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Gilbert JR, Pericak-Vance MA, Haines JL. Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10. Human Mutation. 30: 463-71. PMID 19241460 DOI: 10.1002/Humu.20953 |
0.487 |
|
| 2009 |
Anderson BM, Schnetz-Boutaud NC, Bartlett J, Wotawa AM, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Examination of association of genes in the serotonin system to autism. Neurogenetics. 10: 209-16. PMID 19184136 DOI: 10.1007/S10048-009-0171-7 |
0.425 |
|
| 2009 |
Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, Haines JL, Pericak-Vance MA. Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. American Journal of Human Genetics. 84: 35-43. PMID 19118814 DOI: 10.1016/J.Ajhg.2008.12.008 |
0.429 |
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| 2009 |
Edwards TL, Pericak-Vance M, Gilbert JR, Haines JL, Martin ER, Ritchie MD. An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 721-35. PMID 19105203 DOI: 10.1002/Ajmg.B.30899 |
0.45 |
|
| 2009 |
Züchner S, Wendland JR, Ashley-Koch AE, Collins AL, Tran-Viet KN, Quinn K, Timpano KC, Cuccaro ML, Pericak-Vance MA, Steffens DC, Krishnan KR, Feng G, Murphy DL. Multiple rare SAPAP3 missense variants in trichotillomania and OCD. Molecular Psychiatry. 14: 6-9. PMID 19096451 DOI: 10.1038/Mp.2008.83 |
0.389 |
|
| 2009 |
Afshari NA, Li YJ, Pericak-Vance MA, Gregory S, Klintworth GK. Genome-wide linkage scan in fuchs endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. 50: 1093-7. PMID 18502986 DOI: 10.1167/Iovs.08-1839 |
0.398 |
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| 2009 |
Ortel TL, Sarikaya FC, Alptekin A, Hansen KE, Roubey RAS, Sharathkumar A, Hoffman RW, Pericak-Vance M, Vance J, Hahn S, Schmidt S. Antiphospholipid Syndrome: Clinical Characteristics of Patients and Affected Family Members From Multiplex Families. Blood. 114: 2972-2972. DOI: 10.1182/Blood.V114.22.2972.2972 |
0.326 |
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| 2009 |
Naj AC, Beecham GW, Slifer MA, Martin ER, Gallins PJ, Konidari I, Whitehead PL, Cai G, Kajiwara Y, Haroutunian V, Gwirtsman HE, Gilbert JR, Haines JL, Buxbaum JD, Pericak-Vance MA. Genome-wide association study validates associations in APOE, VDR, SORL1, WWC1, and ELAVL4 and identifies novel candidate genes for late-onset Alzheimer's disease Alzheimers & Dementia. 5. DOI: 10.1016/J.Jalz.2009.05.519 |
0.428 |
|
| 2009 |
Beecham GW, Naj AC, Cai G, Kajiwara Y, Haroutunian V, Konidari I, Gallins P, Whitehead P, Gilbert JR, Slifer MA, Gwirstman H, Martin ER, Buxbaum J, Haines JL, Pericak-Vance MA. GRB-associated binding protein 2 (GAB2) interacts with APOE to alter risk of late-onset Alzheimer's disease Alzheimers & Dementia. 5: 111. DOI: 10.1016/J.Jalz.2009.05.348 |
0.347 |
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| 2009 |
Slifer MA, Naj A, Beecham G, Martin E, Konidari I, Whitehead P, Gallins P, Cai G, Kajiwara Y, Haroutunian V, Vance J, Haines J, Buxbaum J, Pericak-Vance M. ELAVL4 locus confirmed in depression of Alzheimer's disease Alzheimers & Dementia. 5: 468. DOI: 10.1016/J.Jalz.2009.04.793 |
0.307 |
|
| 2009 |
Haines JL, Davis AC, McCauley JL, Jiang L, Gallins PJ, Jackson CE, Scott WK, Pericak-Vance MA. P4-114: Genome-wide association study for dementia in the midwestern US Amish Alzheimer's & Dementia. 5: P464-P465. DOI: 10.1016/J.Jalz.2009.04.782 |
0.333 |
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| 2009 |
Byrd GS, Pericak-Vance M, Edwards CL, Taylor A, Kelkar V, Byrd JR, Starks TD, Pimpong DS, Li Y. Ascertaining older african americans for genetic studies in Alzheimer's disease Alzheimers & Dementia. 5: 234. DOI: 10.1016/J.Jalz.2009.04.201 |
0.366 |
|
| 2008 |
Anderson BM, Schnetz-Boutaud N, Bartlett J, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Examination of association to autism of common genetic variationin genes related to dopamine. Autism Research : Official Journal of the International Society For Autism Research. 1: 364-9. PMID 19360691 DOI: 10.1002/Aur.55 |
0.441 |
|
| 2008 |
Züchner S, Gilbert JR, Martin ER, Leon-Guerrero CR, Xu PT, Browning C, Bronson PG, Whitehead P, Schmechel DE, Haines JL, Pericak-Vance MA. Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3. Annals of Human Genetics. 72: 725-31. PMID 18761660 DOI: 10.1111/J.1469-1809.2008.00474.X |
0.374 |
|
| 2008 |
Barcellos LF, Ramsay PP, Caillier SJ, Sawcer S, Haines J, Schmidt S, Pericak-Vance M, Compston DA, Gabatto P, Hauser SL, Oksenberg JR. Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis. Genes and Immunity. 9: 493-500. PMID 18580885 DOI: 10.1038/Gene.2008.41 |
0.397 |
|
| 2008 |
Canter JA, Olson LM, Spencer K, Schnetz-Boutaud N, Anderson B, Hauser MA, Schmidt S, Postel EA, Agarwal A, Pericak-Vance MA, Sternberg P, Haines JL. Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration. Plos One. 3: e2091. PMID 18461138 DOI: 10.1371/Journal.Pone.0002091 |
0.364 |
|
| 2008 |
Spencer KL, Olson LM, Anderson BM, Schnetz-Boutaud N, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. C3 R102G polymorphism increases risk of age-related macular degeneration. Human Molecular Genetics. 17: 1821-4. PMID 18325906 DOI: 10.1093/Hmg/Ddn075 |
0.399 |
|
| 2008 |
Beetz C, Schüle R, Deconinck T, Tran-Viet KN, Zhu H, Kremer BP, Frints SG, van Zelst-Stams WA, Byrne P, Otto S, Nygren AO, Baets J, Smets K, Ceulemans B, Dan B, ... ... Pericak-Vance M, et al. REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31. Brain : a Journal of Neurology. 131: 1078-86. PMID 18321925 DOI: 10.1093/Brain/Awn026 |
0.338 |
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| 2008 |
Wang L, Hauser ER, Shah SH, Seo D, Sivashanmugam P, Exum ST, Gregory SG, Granger CB, Haines JL, Jones CJ, Crossman D, Haynes C, Kraus WE, Freedman NJ, Pericak-Vance MA, et al. Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease. Annals of Human Genetics. 72: 443-53. PMID 18318786 DOI: 10.1111/J.1469-1809.2008.00433.X |
0.393 |
|
| 2008 |
Spencer KL, Hauser MA, Olson LM, Schmidt S, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration. Human Molecular Genetics. 17: 971-7. PMID 18084039 DOI: 10.1093/Hmg/Ddm369 |
0.405 |
|
| 2008 |
Thornton-Wells TA, Moore JH, Martin ER, Pericak-Vance MA, Haines JL. Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis. Genetic Epidemiology. 32: 187-203. PMID 18076107 DOI: 10.1002/Gepi.20294 |
0.419 |
|
| 2008 |
Shuler RK, Schmidt S, Gallins P, Hauser MA, Scott WK, Caldwell J, Agarwal A, Haines JL, Pericak-Vance MA, Postel EA. Peripheral reticular pigmentary change is associated with complement factor H polymorphism (Y402H) in age-related macular degeneration. Ophthalmology. 115: 520-4. PMID 18067970 DOI: 10.1016/J.Ophtha.2007.06.021 |
0.362 |
|
| 2008 |
Shuler RK, Schmidt S, Gallins P, Hauser MA, Scott WK, Caldwell J, Agarwal A, Haines JL, Pericak-Vance MA, Postel EA. Phenotype analysis of patients with the risk variant LOC387715 (A69S) in age-related macular degeneration. American Journal of Ophthalmology. 145: 303-307. PMID 18061132 DOI: 10.1016/J.Ajo.2007.09.027 |
0.356 |
|
| 2008 |
Liang X, Schnetz-Boutaud N, Bartlett J, Allen MJ, Gwirtsman H, Schmechel DE, Carney RM, Gilbert JR, Pericak-Vance MA, Haines JL. No association between SNP rs498055 on chromosome 10 and late-onset Alzheimer disease in multiple datasets. Annals of Human Genetics. 72: 141-4. PMID 17725684 DOI: 10.1111/J.1469-1809.2007.00394.X |
0.462 |
|
| 2008 |
Pericak-Vance MA. PL-03-01: Genetics of Alzheimer's disease: What's real, what's not, what's hot Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.367 |
0.316 |
|
| 2008 |
Slifer MA, Beecham GW, Martin ER, Wang G, Gilbert JR, Haines JL, Vance J, Pericak-Vance MA. O2-06-02: A genetic susceptibility locus for depression of Alzheimer's disease and Parkinson's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.350 |
0.351 |
|
| 2008 |
Martin ER, Turner SD, Beecham GW, Gilbert JR, Haines JL, Pericak-Vance MA, Ritchie MD. P3-240: Genome-wide analysis of gene-gene interaction in Alzheimer's disease Alzheimer's & Dementia. 4: T591-T591. DOI: 10.1016/J.Jalz.2008.05.1807 |
0.39 |
|
| 2008 |
Hara K, Gilbert J, Gallins P, Whitehead P, Beecham G, Slifer M, Martin E, Haines J, Pericak-Vance M. P3-228: Genetic association of vitamin D receptor gene on chromosome 12q with late-onset Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1795 |
0.409 |
|
| 2008 |
Haines J, McCauley JL, Davis AC, Crunk AE, McFarland LL, Jiang L, Gallins PJ, Jackson CE, Scott WK, Pericak-Vance MA. P3-225: Whole-genome SNP linkage screen for dementia in the midwestern U.S. Amish Alzheimer's & Dementia. 4: T586-T587. DOI: 10.1016/J.Jalz.2008.05.1792 |
0.336 |
|
| 2008 |
Gilbert JR, Beecham G, Gallins P, Slifer M, Martin ER, Haines J, Pericak-Vance MA. P3-223: Genome-wide association analysis of the age-at-onset for individuals with Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1790 |
0.4 |
|
| 2008 |
Beecham GW, Slifer MA, Martin ER, Li Y, Carney RM, Gilbert JR, Haines JL, Pericak-Vance MA. P3-200: Genomic convergence of late-onset Alzheimer's disease candidate genes Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1766 |
0.406 |
|
| 2008 |
Lin PI, Vance JM, Pericak-Vance MA, Martin ER. Response to Zaykin and Shibata American Journal of Human Genetics. 82: 796-797. DOI: 10.1016/J.Ajhg.2008.02.004 |
0.377 |
|
| 2007 |
Haines JL, Spencer KM, Pericak-Vance MA. Bringing the genetics of macular degeneration into focus. Proceedings of the National Academy of Sciences of the United States of America. 104: 16725-6. PMID 17940012 DOI: 10.1073/Pnas.0708151104 |
0.384 |
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| 2007 |
Xu PT, Li YJ, Qin XJ, Kroner C, Green-Odlum A, Xu H, Wang TY, Schmechel DE, Hulette CM, Ervin J, Hauser M, Haines J, Pericak-Vance MA, Gilbert JR. A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease. Molecular and Cellular Neurosciences. 36: 313-31. PMID 17822919 DOI: 10.1016/J.Mcn.2007.06.009 |
0.376 |
|
| 2007 |
Spencer KL, Hauser MA, Olson LM, Schnetz-Boutaud N, Scott WK, Schmidt S, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration. Investigative Ophthalmology & Visual Science. 48: 4277-83. PMID 17724217 DOI: 10.1167/Iovs.06-1427 |
0.388 |
|
| 2007 |
McCauley JL, Kenealy SJ, Margulies EH, Schnetz-Boutaud N, Gregory SG, Hauser SL, Oksenberg JR, Pericak-Vance MA, Haines JL, Mortlock DP. SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approach. Bmc Genomics. 8: 266. PMID 17683615 DOI: 10.1186/1471-2164-8-266 |
0.421 |
|
| 2007 |
Cuccaro ML, Brinkley J, Abramson RK, Hall A, Wright HH, Hussman JP, Gilbert JR, Pericak-Vance MA. Autism in African American families: clinical-phenotypic findings. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 1022-6. PMID 17671983 DOI: 10.1002/Ajmg.B.30535 |
0.325 |
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| 2007 |
Gregory SG, Schmidt S, Seth P, Oksenberg JR, Hart J, Prokop A, Caillier SJ, Ban M, Goris A, Barcellos LF, Lincoln R, McCauley JL, Sawcer SJ, Compston DA, Dubois B, ... ... Pericak-Vance MA, et al. Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis. Nature Genetics. 39: 1083-91. PMID 17660817 DOI: 10.1038/Ng2103 |
0.435 |
|
| 2007 |
Hafler DA, Compston A, Sawcer S, Lander ES, Daly MJ, De Jager PL, de Bakker PI, Gabriel SB, Mirel DB, Ivinson AJ, Pericak-Vance MA, Gregory SG, Rioux JD, McCauley JL, et al. Risk alleles for multiple sclerosis identified by a genomewide study. The New England Journal of Medicine. 357: 851-62. PMID 17660530 DOI: 10.1056/Nejmoa073493 |
0.4 |
|
| 2007 |
Ashley-Koch AE, Jaworski J, Ma de Q, Mei H, Ritchie MD, Skaar DA, Robert Delong G, Worley G, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA. Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk. Psychiatric Genetics. 17: 221-6. PMID 17621165 DOI: 10.1097/Ypg.0B013E32809C2F75 |
0.438 |
|
| 2007 |
Spencer KL, Hauser MA, Olson LM, Schmidt S, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration. Human Molecular Genetics. 16: 1986-92. PMID 17576744 DOI: 10.1093/Hmg/Ddm146 |
0.399 |
|
| 2007 |
Liang X, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease. Human Mutation. 28: 1065-73. PMID 17573676 DOI: 10.1002/Humu.20567 |
0.487 |
|
| 2007 |
Beetz C, Zuchner S, Ashley-Koch A, Auer-Grumbach M, Byrne P, Chinnery PF, Hutchinson M, McDermott CJ, Meijer IA, Nygren AO, Pericak-Vance M, Pyle A, Rouleau GA, Schickel J, Shaw PJ, et al. Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause. Human Mutation. 28: 739-40. PMID 17345589 DOI: 10.1002/Humu.20508 |
0.331 |
|
| 2007 |
Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Pericak-Vance MA, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985 |
0.422 |
|
| 2007 |
Lin PI, Vance JM, Pericak-Vance MA, Martin ER. No gene is an island: the flip-flop phenomenon. American Journal of Human Genetics. 80: 531-8. PMID 17273975 DOI: 10.1086/512133 |
0.389 |
|
| 2007 |
Haines JL, Pericak-Vance MA. Rapid dissection of the genetic risk of age-related macular degeneration: achieving the promise of the genomic era. Jama. 297: 401-2. PMID 17252632 DOI: 10.1001/Jama.297.4.401 |
0.344 |
|
| 2007 |
Yeo TW, De Jager PL, Gregory SG, Barcellos LF, Walton A, Goris A, Fenoglio C, Ban M, Taylor CJ, Goodman RS, Walsh E, Wolfish CS, Horton R, Traherne J, Beck S, ... ... Pericak-Vance MA, et al. A second major histocompatibility complex susceptibility locus for multiple sclerosis. Annals of Neurology. 61: 228-36. PMID 17252545 DOI: 10.1002/Ana.21063 |
0.383 |
|
| 2007 |
Shuler RK, Hauser MA, Caldwell J, Gallins P, Schmidt S, Scott WK, Agarwal A, Haines JL, Pericak-Vance MA, Postel EA. Neovascular age-related macular degeneration and its association with LOC387715 and complement factor H polymorphism. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 63-7. PMID 17210853 DOI: 10.1001/Archopht.125.1.63 |
0.334 |
|
| 2007 |
Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14. Molecular Psychiatry. 12: 376-84. PMID 17179998 DOI: 10.1038/Sj.Mp.4001927 |
0.417 |
|
| 2007 |
Liang X, Schnetz-Boutaud N, Bartlett J, Anderson BM, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer disease. Dementia and Geriatric Cognitive Disorders. 23: 126-32. PMID 17159347 DOI: 10.1159/000097857 |
0.492 |
|
| 2007 |
Motsinger AA, Brassat D, Caillier SJ, Erlich HA, Walker K, Steiner LL, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD. Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes. Neurogenetics. 8: 11-20. PMID 17024427 DOI: 10.1007/S10048-006-0058-9 |
0.386 |
|
| 2007 |
Hauser SL, Barcellos LF, Pericak-Vance M, Haines JL, Oksenberg JR. Clustering of autoimmune disease in families at high risk for multiple sclerosis? - Authors' reply Lancet Neurology. 6: 207. DOI: 10.1016/S1474-4422(07)70044-3 |
0.315 |
|
| 2006 |
Li YJ, Xu P, Qin X, Schmechel DE, Hulette CM, Haines JL, Pericak-Vance MA, Gilbert JR. A comparative analysis of the information content in long and short SAGE libraries. Bmc Bioinformatics. 7: 504. PMID 17109755 DOI: 10.1186/1471-2105-7-504 |
0.321 |
|
| 2006 |
Barcellos LF, Kamdar BB, Ramsay PP, DeLoa C, Lincoln RR, Caillier S, Schmidt S, Haines JL, Pericak-Vance MA, Oksenberg JR, Hauser SL. Clustering of autoimmune diseases in families with a high-risk for multiple sclerosis: a descriptive study. The Lancet. Neurology. 5: 924-31. PMID 17052659 DOI: 10.1016/S1474-4422(06)70552-X |
0.354 |
|
| 2006 |
Zuchner S, Cuccaro ML, Tran-Viet KN, Cope H, Krishnan RR, Pericak-Vance MA, Wright HH, Ashley-Koch A. SLITRK1 mutations in trichotillomania. Molecular Psychiatry. 11: 887-9. PMID 17003809 DOI: 10.1038/Sj.Mp.4001898 |
0.313 |
|
| 2006 |
de Bakker PI, McVean G, Sabeti PC, Miretti MM, Green T, Marchini J, Ke X, Monsuur AJ, Whittaker P, Delgado M, Morrison J, Richardson A, Walsh EC, Gao X, Galver L, ... ... Pericak-Vance M, et al. A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nature Genetics. 38: 1166-72. PMID 16998491 DOI: 10.1038/Ng1885 |
0.371 |
|
| 2006 |
Hauser MA, Sena DF, Flor J, Walter J, Auguste J, Larocque-Abramson K, Graham F, Delbono E, Haines JL, Pericak-Vance MA, Rand Allingham R, Wiggs JL. Distribution of optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United States. Journal of Glaucoma. 15: 358-63. PMID 16988596 DOI: 10.1097/01.Ijg.0000212255.17950.42 |
0.33 |
|
| 2006 |
Barcellos LF, Sawcer S, Ramsay PP, Baranzini SE, Thomson G, Briggs F, Cree BC, Begovich AB, Villoslada P, Montalban X, Uccelli A, Savettieri G, Lincoln RR, DeLoa C, Haines JL, ... Pericak-Vance MA, et al. Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis. Human Molecular Genetics. 15: 2813-24. PMID 16905561 DOI: 10.1093/Hmg/Ddl223 |
0.382 |
|
| 2006 |
Chen W, Saeed M, Mao H, Siddique N, Dellefave L, Hung WY, Deng HX, Sufit RL, Heller SL, Haines JL, Pericak-Vance M, Siddique T. Lack of association of VEGF promoter polymorphisms with sporadic ALS. Neurology. 67: 508-10. PMID 16894118 DOI: 10.1212/01.Wnl.0000227926.42370.04 |
0.301 |
|
| 2006 |
Lin PI, Martin ER, Bronson PG, Browning-Large C, Small GW, Schmechel DE, Welsh-Bohmer KA, Haines JL, Gilbert JR, Pericak-Vance MA. Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease. Neurology. 67: 64-8. PMID 16832079 DOI: 10.1212/01.Wnl.0000223438.90113.4E |
0.451 |
|
| 2006 |
Postel EA, Agarwal A, Caldwell J, Gallins P, Toth C, Schmidt S, Scott WK, Hauser MA, Haines JL, Pericak-Vance MA. Complement factor H increases risk for atrophic age-related macular degeneration. Ophthalmology. 113: 1504-7. PMID 16828512 DOI: 10.1016/J.Ophtha.2006.02.049 |
0.33 |
|
| 2006 |
Züchner S, Wang G, Tran-Viet KN, Nance MA, Gaskell PC, Vance JM, Ashley-Koch AE, Pericak-Vance MA. Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. American Journal of Human Genetics. 79: 365-9. PMID 16826527 DOI: 10.1086/505361 |
0.342 |
|
| 2006 |
Saeed M, Siddique N, Hung WY, Usacheva E, Liu E, Sufit RL, Heller SL, Haines JL, Pericak-Vance M, Siddique T. Paraoxonase cluster polymorphisms are associated with sporadic ALS. Neurology. 67: 771-6. PMID 16822964 DOI: 10.1212/01.Wnl.0000227187.52002.88 |
0.366 |
|
| 2006 |
Collins AL, Ma D, Whitehead PL, Martin ER, Wright HH, Abramson RK, Hussman JP, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Investigation of autism and GABA receptor subunit genes in multiple ethnic groups. Neurogenetics. 7: 167-74. PMID 16770606 DOI: 10.1007/S10048-006-0045-1 |
0.381 |
|
| 2006 |
Lin PI, Martin ER, Browning-Large CA, Schmechel DE, Welsh-Bohmer KA, Doraiswamy PM, Gilbert JR, Haines JL, Pericak-Vance MA. Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis. Neurogenetics. 7: 157-65. PMID 16770605 DOI: 10.1007/S10048-006-0047-Z |
0.45 |
|
| 2006 |
Schmidt S, Pericak-Vance MA, Sawcer S, Barcellos LF, Hart J, Sims J, Prokop AM, van der Walt J, DeLoa C, Lincoln RR, Oksenberg JR, Compston A, Hauser SL, Haines JL, Gregory SG, et al. Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis. Genes and Immunity. 7: 384-92. PMID 16738668 DOI: 10.1038/Sj.Gene.6364311 |
0.389 |
|
| 2006 |
Hauser MA, Allingham RR, Linkroum K, Wang J, LaRocque-Abramson K, Figueiredo D, Santiago-Turla C, del Bono EA, Haines JL, Pericak-Vance MA, Wiggs JL. Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma. Investigative Ophthalmology & Visual Science. 47: 2542-6. PMID 16723468 DOI: 10.1167/Iovs.05-1476 |
0.404 |
|
| 2006 |
Burwick RM, Ramsay PP, Haines JL, Hauser SL, Oksenberg JR, Pericak-Vance MA, Schmidt S, Compston A, Sawcer S, Cittadella R, Savettieri G, Quattrone A, Polman CH, Uitdehaag BM, Zwemmer JN, et al. APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers. Neurology. 66: 1373-83. PMID 16682670 DOI: 10.1212/01.Wnl.0000210531.19498.3F |
0.389 |
|
| 2006 |
Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA. An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder. Annals of Human Genetics. 70: 281-92. PMID 16674551 DOI: 10.1111/J.1469-1809.2006.00253.X |
0.416 |
|
| 2006 |
Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Lack of association between autism and SLC25A12. The American Journal of Psychiatry. 163: 929-31. PMID 16648338 DOI: 10.1176/Ajp.2006.163.5.929 |
0.701 |
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| 2006 |
Schmidt S, Hauser MA, Scott WK, Postel EA, Agarwal A, Gallins P, Wong F, Chen YS, Spencer K, Schnetz-Boutaud N, Haines JL, Pericak-Vance MA. Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration. American Journal of Human Genetics. 78: 852-64. PMID 16642439 DOI: 10.1086/503822 |
0.396 |
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| 2006 |
Brassat D, Motsinger AA, Caillier SJ, Erlich HA, Walker K, Steiner LL, Cree BA, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD. Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans. Genes and Immunity. 7: 310-5. PMID 16625214 DOI: 10.1038/Sj.Gene.6364299 |
0.385 |
|
| 2006 |
Züchner S, Kail ME, Nance MA, Gaskell PC, Svenson IK, Marchuk DA, Pericak-Vance MA, Ashley-Koch AE. A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12. Neurogenetics. 7: 127-9. PMID 16565863 DOI: 10.1007/S10048-006-0029-1 |
0.31 |
|
| 2006 |
Slifer MA, Martin ER, Bronson PG, Browning-Large C, Doraiswamy PM, Welsh-Bohmer KA, Gilbert JR, Haines JL, Pericak-Vance MA. Lack of association between UBQLN1 and Alzheimer disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 208-13. PMID 16526030 DOI: 10.1002/Ajmg.B.30298 |
0.417 |
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| 2006 |
McCauley JL, Hahs DW, Jiang L, Scott WK, Welsh-Bohmer KA, Jackson CE, Vance JM, Pericak-Vance MA, Haines JL. Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish. Bmc Medical Genetics. 7: 19. PMID 16515697 DOI: 10.1186/1471-2350-7-19 |
0.386 |
|
| 2006 |
Pillai SG, Chiano MN, White NJ, Speer M, Barnes KC, Carlsen K, Gerritsen J, Helms P, Lenney W, Silverman M, Sly P, Sundy J, Tsanakas J, von Berg A, Whyte M, ... ... Pericak-Vance M, et al. A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p. European Journal of Human Genetics : Ejhg. 14: 307-16. PMID 16391567 DOI: 10.1038/Sj.Ejhg.5201532 |
0.371 |
|
| 2006 |
Hahs DW, McCauley JL, Crunk AE, McFarland LL, Gaskell PC, Jiang L, Slifer SH, Vance JM, Scott WK, Welsh-Bohmer KA, Johnson SR, Jackson CE, Pericak-Vance MA, Haines JL. A genome-wide linkage analysis of dementia in the Amish. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 160-6. PMID 16389594 DOI: 10.1002/Ajmg.B.30257 |
0.449 |
|
| 2006 |
Haines JL, Schnetz-Boutaud N, Schmidt S, Scott WK, Agarwal A, Postel EA, Olson L, Kenealy SJ, Hauser M, Gilbert JR, Pericak-Vance MA. Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6. Investigative Ophthalmology & Visual Science. 47: 329-35. PMID 16384981 DOI: 10.1167/Iovs.05-0116 |
0.438 |
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| 2006 |
Kenealy SJ, Herrel LA, Bradford Y, Schnetz-Boutaud N, Oksenberg JR, Hauser SL, Barcellos LF, Schmidt S, Gregory SG, Pericak-Vance MA, Haines JL. Examination of seven candidate regions for multiple sclerosis: strong evidence of linkage to chromosome 1q44. Genes and Immunity. 7: 73-6. PMID 16341055 DOI: 10.1038/Sj.Gene.6364275 |
0.386 |
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| 2006 |
Liang X, Schnetz-Boutaud N, Kenealy SJ, Jiang L, Bartlett J, Lynch B, Gaskell PC, Gwirtsman H, McFarland L, Bembe ML, Bronson P, Gilbert JR, Martin ER, Pericak-Vance MA, Haines JL. Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus. Molecular Psychiatry. 11: 280-5. PMID 16222332 DOI: 10.1038/Sj.Mp.4001766 |
0.449 |
|
| 2006 |
Xu PT, Li YJ, Qin XJ, Scherzer CR, Xu H, Schmechel DE, Hulette CM, Ervin J, Gullans SR, Haines J, Pericak-Vance MA, Gilbert JR. Differences in apolipoprotein E3/3 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease. Neurobiology of Disease. 21: 256-75. PMID 16198584 DOI: 10.1016/J.Nbd.2005.07.004 |
0.383 |
|
| 2006 |
Li YJ, Scott WK, Zhang L, Lin PI, Oliveira SA, Skelly T, Doraiswamy MP, Welsh-Bohmer KA, Martin ER, Haines JL, Pericak-Vance MA, Vance JM. Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases. Neurobiology of Aging. 27: 1087-93. PMID 15985314 DOI: 10.1016/J.Neurobiolaging.2005.05.013 |
0.422 |
|
| 2006 |
Yan J, Siddique N, Slifer S, Bigio E, Mao H, Chen W, Liu E, Shi Y, Khan S, Haines J, Pericak-Vance M, Siddique T. A Major Novel Locus for ALS/FTD on Chromosome 9p21 and its Pathological Correlates: S61.006 Neurology. 67: 186-186. DOI: 10.1212/01.Wnl.0000234887.27166.69 |
0.416 |
|
| 2006 |
Cuccaro ML, Carney RM, Slifer M, Gaskell PC, Schmechel DM, Vance JM, Hulette CM, Pericak-Vance MA. P2-129: Benefits of follow-up in Alzheimer disease genetics research Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.967 |
0.372 |
|
| 2006 |
Zuchner S, Xu P, Browning C, Bronson PG, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. P1-362: Genetic evaluation of the Alzheimer’s disease locus on chromosome 9p21.3 Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.740 |
0.379 |
|
| 2006 |
Vance JM, Deng J, Mayhew G, Grimsley J, Pericak-Vance MA, Li Y. AbstractPoster presentation: Sunday posterP1-361: Mapping genes affecting age-at-onset of Alzheimer’s disease in the chromosome 8 Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.739 |
0.369 |
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| 2006 |
Martin E, Thornton-Wells T, Edwards T, Hahn L, Bronson P, Gilbert J, Haines J, Pericak-Vance M, Ritchie M. P1-355: Joint analysis of candidate genes in AD through data reduction Alzheimer's & Dementia. 2: S201-S202. DOI: 10.1016/J.Jalz.2006.05.733 |
0.334 |
|
| 2006 |
Bronson PG, Wall NN, Haines JL, Schmechel DE, Gilbert JR, Pericak-Vance MA, Martin ER. P1-345: Evidence for association between late-onset Alzheimer's disease and MTHFR on chromosome 1 Alzheimer's & Dementia. 2: S198-S198. DOI: 10.1016/J.Jalz.2006.05.723 |
0.412 |
|
| 2006 |
Slifer MA, Gilbert JR, Lin P, Liang X, Haines JL, Pericak-Vance MA. P1-330: Large scale candidate gene association studies in Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.708 |
0.359 |
|
| 2006 |
Schnetz-Boutaud N, Liang X, Martin ER, Anderson BM, Zuchner S, Gilbert JR, Pericak-Vance MA, Haines JL. P1-313: Examination of the effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.691 |
0.373 |
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| 2006 |
Byrd GS, Pericak-Vance M, Edwards C, Johnson S, Taylor A, Boswell G, Caldwell D, Williams I, Li Y. P4-197: Community investment and recruitment of African Americans for Alzheimer’s disease genetics research Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1936 |
0.318 |
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| 2005 |
Martin ER, Bronson PG, Li YJ, Wall N, Chung RH, Schmechel DE, Small G, Xu PT, Bartlett J, Schnetz-Boutaud N, Haines JL, Gilbert JR, Pericak-Vance MA. Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease. Journal of Medical Genetics. 42: 787-92. PMID 16199552 DOI: 10.1136/Jmg.2004.029553 |
0.489 |
|
| 2005 |
Xu H, Gregory SG, Hauser ER, Stenger JE, Pericak-Vance MA, Vance JM, Züchner S, Hauser MA. SNPselector: a web tool for selecting SNPs for genetic association studies. Bioinformatics (Oxford, England). 21: 4181-6. PMID 16179360 DOI: 10.1093/Bioinformatics/Bti682 |
0.377 |
|
| 2005 |
Boyles AL, Scott WK, Martin ER, Schmidt S, Li YJ, Ashley-Koch A, Bass MP, Schmidt M, Pericak-Vance MA, Speer MC, Hauser ER. Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing. Human Heredity. 59: 220-7. PMID 16093727 DOI: 10.1159/000087122 |
0.317 |
|
| 2005 |
Sawcer S, Ban M, Maranian M, Yeo TW, Compston A, Kirby A, Daly MJ, De Jager PL, Walsh E, Lander ES, Rioux JD, Hafler DA, Ivinson A, Rimmler J, Gregory SG, ... ... Pericak-Vance MA, et al. A high-density screen for linkage in multiple sclerosis. American Journal of Human Genetics. 77: 454-67. PMID 16080120 DOI: 10.1086/444547 |
0.302 |
|
| 2005 |
Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA. Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism. American Journal of Human Genetics. 77: 377-88. PMID 16080114 DOI: 10.1086/433195 |
0.42 |
|
| 2005 |
van der Walt JM, Scott WK, Slifer S, Gaskell PC, Martin ER, Welsh-Bohmer K, Creason M, Crunk A, Fuzzell D, McFarland L, Kroner CC, Jackson CE, Haines JL, Pericak-Vance MA. Maternal lineages and Alzheimer disease risk in the Old Order Amish. Human Genetics. 118: 115-22. PMID 16078048 DOI: 10.1007/S00439-005-0032-X |
0.386 |
|
| 2005 |
Slifer MA, Martin ER, Haines JL, Pericak-Vance MA. The ubiquilin 1 gene and Alzheimer's disease. The New England Journal of Medicine. 352: 2752-3; author reply. PMID 15987928 DOI: 10.1056/Nejm200506303522618 |
0.374 |
|
| 2005 |
Fisher SA, Abecasis GR, Yashar BM, Zareparsi S, Swaroop A, Iyengar SK, Klein BE, Klein R, Lee KE, Majewski J, Schultz DW, Klein ML, Seddon JM, Santangelo SL, Weeks DE, ... ... Pericak-Vance MA, et al. Meta-analysis of genome scans of age-related macular degeneration. Human Molecular Genetics. 14: 2257-64. PMID 15987700 DOI: 10.1093/Hmg/Ddi230 |
0.416 |
|
| 2005 |
Oliveira SA, Li YJ, Noureddine MA, Zuchner S, Qin X, Pericak-Vance MA, Vance JM. Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease. American Journal of Human Genetics. 77: 252-64. PMID 15986317 DOI: 10.1086/432588 |
0.42 |
|
| 2005 |
Allingham RR, Wiggs JL, Hauser ER, Larocque-Abramson KR, Santiago-Turla C, Broomer B, Del Bono EA, Graham FL, Haines JL, Pericak-Vance MA, Hauser MA. Early adult-onset POAG linked to 15q11-13 using ordered subset analysis. Investigative Ophthalmology & Visual Science. 46: 2002-5. PMID 15914615 DOI: 10.1167/Iovs.04-1477 |
0.467 |
|
| 2005 |
Winn MP, Conlon PJ, Lynn KL, Farrington MK, Creazzo T, Hawkins AF, Daskalakis N, Kwan SY, Ebersviller S, Burchette JL, Pericak-Vance MA, Howell DN, Vance JM, Rosenberg PB. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. Science (New York, N.Y.). 308: 1801-4. PMID 15879175 DOI: 10.1126/Science.1106215 |
0.325 |
|
| 2005 |
Postel EA, Agarwal A, Schmidt S, Fan YT, Scott WK, Gilbert JR, Haines JL, Pericak-Vance MA. Comparing age-related macular degeneration phenotype in probands from singleton and multiplex families. American Journal of Ophthalmology. 139: 820-5. PMID 15860286 DOI: 10.1016/J.Ajo.2004.12.029 |
0.36 |
|
| 2005 |
Ashley-Koch AE, Shao Y, Rimmler JB, Gaskell PC, Welsh-Bohmer KA, Jackson CE, Scott WK, Haines JL, Pericak-Vance MA. An autosomal genomic screen for dementia in an extended Amish family. Neuroscience Letters. 379: 199-204. PMID 15843063 DOI: 10.1016/J.Neulet.2004.12.065 |
0.437 |
|
| 2005 |
Noureddine MA, Qin XJ, Oliveira SA, Skelly TJ, van der Walt J, Hauser MA, Pericak-Vance MA, Vance JM, Li YJ. Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease. Human Genetics. 117: 27-33. PMID 15827745 DOI: 10.1007/S00439-005-1259-2 |
0.398 |
|
| 2005 |
Stenger JE, Xu H, Haynes C, Hauser ER, Pericak-Vance M, Goldschmidt-Clermont PJ, Vance JM. Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browser. Bmc Bioinformatics. 6: 95. PMID 15826305 DOI: 10.1186/1471-2105-6-95 |
0.33 |
|
| 2005 |
Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA. Complement factor H variant increases the risk of age-related macular degeneration. Science (New York, N.Y.). 308: 419-21. PMID 15761120 DOI: 10.1126/Science.1110359 |
0.394 |
|
| 2005 |
Ma DQ, Jaworski J, Menold MM, Donnelly S, Abramson RK, Wright HH, Delong GR, Gilbert JR, Pericak-Vance MA, Cuccaro ML. Ordered-subset analysis of savant skills in autism for 15q11-q13. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 135: 38-41. PMID 15756693 DOI: 10.1002/Ajmg.B.30166 |
0.368 |
|
| 2005 |
Züchner S, Noureddine M, Kennerson M, Verhoeven K, Claeys K, De Jonghe P, Merory J, Oliveira SA, Speer MC, Stenger JE, Walizada G, Zhu D, Pericak-Vance MA, Nicholson G, Timmerman V, et al. Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease. Nature Genetics. 37: 289-94. PMID 15731758 DOI: 10.1038/Ng1514 |
0.387 |
|
| 2005 |
Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA. Analysis of the RELN gene as a genetic risk factor for autism. Molecular Psychiatry. 10: 563-71. PMID 15558079 DOI: 10.1038/Sj.Mp.4001614 |
0.469 |
|
| 2004 |
Li YJ, Pericak-Vance MA, Haines JL, Siddique N, McKenna-Yasek D, Hung WY, Sapp P, Allen CI, Chen W, Hosler B, Saunders AM, Dellefave LM, Brown RH, Siddique T. Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis. Neurogenetics. 5: 209-13. PMID 15657798 DOI: 10.1007/S10048-004-0193-0 |
0.405 |
|
| 2004 |
Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes. Neuroscience Letters. 372: 209-14. PMID 15542242 DOI: 10.1016/J.Neulet.2004.09.037 |
0.708 |
|
| 2004 |
Kenealy SJ, Babron MC, Bradford Y, Schnetz-Boutaud N, Haines JL, Rimmler JB, Schmidt S, Pericak-Vance MA, Barcellos LF, Lincoln RR, Oksenberg JR, Hauser SL, Clanet M, Brassat D, Edan G, et al. A second-generation genomic screen for multiple sclerosis. American Journal of Human Genetics. 75: 1070-8. PMID 15494893 DOI: 10.1086/426459 |
0.394 |
|
| 2004 |
Oliveira SA, Scott WK, Zhang F, Stajich JM, Fujiwara K, Hauser M, Scott BL, Pericak-Vance MA, Vance JM, Martin ER. Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype. Neurogenetics. 5: 147-55. PMID 15459824 DOI: 10.1007/S10048-004-0180-5 |
0.387 |
|
| 2004 |
Nicodemus KK, Stenger JE, Schmechel DE, Welsh-Bohmer KA, Saunders AM, Roses AD, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA, Martin ER. Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease. Neurogenetics. 5: 201-8. PMID 15455263 DOI: 10.1007/S10048-004-0189-9 |
0.438 |
|
| 2004 |
Hauser ER, Crossman DC, Granger CB, Haines JL, Jones CJ, Mooser V, McAdam B, Winkelmann BR, Wiseman AH, Muhlestein JB, Bartel AG, Dennis CA, Dowdy E, Estabrooks S, Eggleston K, ... ... Pericak-Vance MA, et al. A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study. American Journal of Human Genetics. 75: 436-47. PMID 15272420 DOI: 10.1086/423900 |
0.407 |
|
| 2004 |
Svenson IK, Kloos MT, Gaskell PC, Nance MA, Garbern JY, Hisanaga S, Pericak-Vance MA, Ashley-Koch AE, Marchuk DA. Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations. Neurogenetics. 5: 157-64. PMID 15248095 DOI: 10.1007/S10048-004-0186-Z |
0.355 |
|
| 2004 |
Sawcer SJ, Maranian M, Singlehurst S, Yeo T, Compston A, Daly MJ, De Jager PL, Gabriel S, Hafler DA, Ivinson AJ, Lander ES, Rioux JD, Walsh E, Gregory SG, Schmidt S, ... Pericak-Vance MA, et al. Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping. Human Molecular Genetics. 13: 1943-9. PMID 15238506 DOI: 10.1093/Hmg/Ddh202 |
0.343 |
|
| 2004 |
Schmidt S, Scott WK, Postel EA, Agarwal A, Hauser ER, De La Paz MA, Gilbert JR, Weeks DE, Gorin MB, Haines JL, Pericak-Vance MA. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12. Bmc Genetics. 5: 18. PMID 15238159 DOI: 10.1186/1471-2156-5-18 |
0.408 |
|
| 2004 |
van der Walt JM, Dementieva YA, Martin ER, Scott WK, Nicodemus KK, Kroner CC, Welsh-Bohmer KA, Saunders AM, Roses AD, Small GW, Schmechel DE, Murali Doraiswamy P, Gilbert JR, Haines JL, Vance JM, ... Pericak-Vance MA, et al. Analysis of European mitochondrial haplogroups with Alzheimer disease risk. Neuroscience Letters. 365: 28-32. PMID 15234467 DOI: 10.1016/J.Neulet.2004.04.051 |
0.386 |
|
| 2004 |
Li YJ, Hauser MA, Scott WK, Martin ER, Booze MW, Qin XJ, Walter JW, Nance MA, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Goetz CG, ... ... Pericak-Vance MA, et al. Apolipoprotein E controls the risk and age at onset of Parkinson disease. Neurology. 62: 2005-9. PMID 15184605 DOI: 10.1212/01.Wnl.0000128089.53030.Ac |
0.357 |
|
| 2004 |
Weeks DE, Conley YP, Tsai HJ, Mah TS, Schmidt S, Postel EA, Agarwal A, Haines JL, Pericak-Vance MA, Rosenfeld PJ, Paul TO, Eller AW, Morse LS, Dailey JP, Ferrell RE, et al. Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions. American Journal of Human Genetics. 75: 174-89. PMID 15168325 DOI: 10.1086/422476 |
0.349 |
|
| 2004 |
van der Walt JM, Noureddine MA, Kittappa R, Hauser MA, Scott WK, McKay R, Zhang F, Stajich JM, Fujiwara K, Scott BL, Pericak-Vance MA, Vance JM, Martin ER. Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease. American Journal of Human Genetics. 74: 1121-7. PMID 15122513 DOI: 10.1086/421052 |
0.346 |
|
| 2004 |
Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, Rochelle J, Dadali EL, Zappia M, Nelis E, Patitucci A, Senderek J, Parman Y, Evgrafov O, Jonghe PD, Takahashi Y, Tsuji S, ... Pericak-Vance MA, et al. Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A. Nature Genetics. 36: 449-51. PMID 15064763 DOI: 10.1038/Ng1341 |
0.3 |
|
| 2004 |
Kenealy SJ, Schmidt S, Agarwal A, Postel EA, De La Paz MA, Pericak-Vance MA, Haines JL. Linkage analysis for age-related macular degeneration supports a gene on chromosome 10q26. Molecular Vision. 10: 57-61. PMID 14758336 DOI: 10.1016/J.Ajo.2004.02.050 |
0.421 |
|
| 2004 |
Raiford KL, Shao Y, Allen IC, Martin ER, Menold MM, Wright HH, Abramson RK, Worley G, DeLong GR, Vance JM, Cuccaro ML, Gilbert JR, Pericak-Vance MA. No association between the APOE gene and autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 57-60. PMID 14755445 DOI: 10.1002/Ajmg.B.20104 |
0.371 |
|
| 2004 |
Oksenberg JR, Barcellos LF, Cree BA, Baranzini SE, Bugawan TL, Khan O, Lincoln RR, Swerdlin A, Mignot E, Lin L, Goodin D, Erlich HA, Schmidt S, Thomson G, Reich DE, ... Pericak-Vance MA, et al. Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans. American Journal of Human Genetics. 74: 160-7. PMID 14669136 DOI: 10.1086/380997 |
0.365 |
|
| 2004 |
Pericak-Vance MA, Rimmler JB, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Hauser SL, Cournu-Rebeix I, Azoulay-Cayla A, Lyon-Caen O, Fontaine B, Duhamel E, Coppin H, Brassat D, et al. Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study. Neurogenetics. 5: 45-8. PMID 14595552 DOI: 10.1007/S10048-003-0163-Y |
0.385 |
|
| 2004 |
Lee SL, Lynch B, Wang J, Schnetz-Boutaud N, Pericak-Vance MA, Blakely RD, Haines JL. P4-144 The high-affinity choline transporter (CHT) functional variant 189V in Alzheimer's disease: an association study Neurobiology of Aging. 25: S516. DOI: 10.1016/S0197-4580(04)81702-0 |
0.345 |
|
| 2004 |
Quan H, Haines JL, Sanchez-Boutard N, Small G, Roses A, Schmechel D, Welsh-Bohmer K, Xu P, Li Y, Gilbert JR, Vance JM, Pericak-Vance MA. P4-138 Genomic convergence on chromosome 12 in Alzheimer's disease Neurobiology of Aging. 25: S514. DOI: 10.1016/S0197-4580(04)81696-8 |
0.386 |
|
| 2004 |
Martin E, Bronson P, Jiang L, Welsh-Bohmer K, Schmechel D, Small G, Haines J, Gilbert J, Pericak-Vance M, Moore J. P4-134 A multilocus association analysis of APOE, LRP1 and A2M in Alzheimer disease Neurobiology of Aging. 25: S513. DOI: 10.1016/S0197-4580(04)81692-0 |
0.391 |
|
| 2004 |
Gilbert JR, Xu P, Li Y, Qin X, Schmechel D, Hulette C, McLaurin A, Scherzer C, Gullans SR, Haines JL, Pericak-Vance MA. P4-103 APOE allele specific gene expression in Alzheimer's and control hippocampus Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81661-0 |
0.364 |
|
| 2004 |
Li Y, Oliveira SA, Qin X, Roses AD, Schmechel D, Welsh-Bohmer KA, Haines JL, Pericak-Vance MA, Vance JM. P4-088 Association analysis of interleukin 1 (IL-1) polymorphisms with age-at-onset and risk of Alzheimer disease Neurobiology of Aging. 25: S499. DOI: 10.1016/S0197-4580(04)81646-4 |
0.36 |
|
| 2004 |
Pericak-Vance MA, Bronson P, Martin ER, Browning C, Rayner M, Xu P, Small GW, Roses AD, Schmechel DE, Doraiswamy PM, Welsh-Bohmer KA, Haines JL, Gilbert JR. P4-080 Genetic studies of Alzheimer disease on chromosome 9P Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81638-5 |
0.399 |
|
| 2004 |
Browning C, Vance DD, Bronson PG, Schmechel D, Welsh-Bohmer K, Scott W, Haines JL, Vance JM, Pericak-Vance MA. P4-072 Follow-up analysis of chromosome 2 linkage in early-onset Alzheimer disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81630-0 |
0.406 |
|
| 2004 |
Xu P, Hulette C, Hauser M, Schmechel DE, Pericak-Vance MA, Gilbert JR. O1-03-06 Transcription analysis of APOE specific hippocampus in Alzheimer's disease (AD) using serial analysis of gene expression (SAGE) and long-SAGE Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80049-6 |
0.348 |
|
| 2003 |
Kenealy SJ, Pericak-Vance MA, Haines JL. The genetic epidemiology of multiple sclerosis. Journal of Neuroimmunology. 143: 7-12. PMID 14575907 DOI: 10.1016/J.Jneuroim.2003.08.005 |
0.368 |
|
| 2003 |
Li YJ, Oliveira SA, Xu P, Martin ER, Stenger JE, Scherzer CR, Hauser MA, Scott WK, Small GW, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, ... ... Pericak-Vance MA, et al. Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease. Human Molecular Genetics. 12: 3259-67. PMID 14570706 DOI: 10.1093/Hmg/Ddg357 |
0.428 |
|
| 2003 |
Scott WK, Hauser ER, Schmechel DE, Welsh-Bohmer KA, Small GW, Roses AD, Saunders AM, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA. Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22. American Journal of Human Genetics. 73: 1041-51. PMID 14564669 DOI: 10.1086/379083 |
0.433 |
|
| 2003 |
Martin ER, Bass MP, Gilbert JR, Pericak-Vance MA, Hauser ER. Genotype-based association test for general pedigrees: the genotype-PDT. Genetic Epidemiology. 25: 203-13. PMID 14557988 DOI: 10.1002/Gepi.10258 |
0.41 |
|
| 2003 |
Wiggs JL, Auguste J, Allingham RR, Flor JD, Pericak-Vance MA, Rogers K, LaRocque KR, Graham FL, Broomer B, Del Bono E, Haines JL, Hauser M. Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma. Archives of Ophthalmology (Chicago, Ill. : 1960). 121: 1181-3. PMID 12912697 DOI: 10.1001/Archopht.121.8.1181 |
0.35 |
|
| 2003 |
Oliveira SA, Martin ER, Scott WK, Nicodemus KK, Small GW, Schmechel DE, Doraiswamy PM, Roses AD, Saunders AM, Gilbert JR, Haines JL, Vance JM, Pericak-Vance MA. The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease. Neuroscience Letters. 347: 143-6. PMID 12875906 DOI: 10.1016/S0304-3940(03)00670-0 |
0.425 |
|
| 2003 |
Oliveira SA, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons KE, Pahwa R, Stern MB, Hiner BC, Jankovic J, Ondo WG, Allen FH, Scott BL, Goetz CG, ... ... Pericak-Vance MA, et al. Association study of Parkin gene polymorphisms with idiopathic Parkinson disease. Archives of Neurology. 60: 975-80. PMID 12873854 DOI: 10.1001/Archneur.60.7.975 |
0.373 |
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| 2003 |
Sapp PC, Hosler BA, McKenna-Yasek D, Chin W, Gann A, Genise H, Gorenstein J, Huang M, Sailer W, Scheffler M, Valesky M, Haines JL, Pericak-Vance M, Siddique T, Horvitz HR, et al. Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis. American Journal of Human Genetics. 73: 397-403. PMID 12858291 DOI: 10.1086/377158 |
0.352 |
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| 2003 |
Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, Kakol J, Buyske S, Chui B, Cohen P, de Toma C, Ehm M, Glanowski S, He C, Heil J, Markianos K, ... ... Pericak-Vance MA, et al. A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. American Journal of Human Genetics. 73: 271-84. PMID 12844283 DOI: 10.1086/377137 |
0.335 |
|
| 2003 |
Schmidt S, Postel EA, Agarwal A, Allen IC, Walters SN, De la Paz MA, Scott WK, Haines JL, Pericak-Vance MA, Gilbert JR. Detailed analysis of allelic variation in the ABCA4 gene in age-related maculopathy. Investigative Ophthalmology & Visual Science. 44: 2868-75. PMID 12824224 DOI: 10.1167/Iovs.02-0957 |
0.437 |
|
| 2003 |
Caillier S, Barcellos LF, Baranzini SE, Swerdlin A, Lincoln RR, Steinman L, Martin E, Haines JL, Pericak-Vance M, Hauser SL, Oksenberg JR. Osteopontin polymorphisms and disease course in multiple sclerosis. Genes and Immunity. 4: 312-5. PMID 12761568 DOI: 10.1038/Sj.Gene.6363952 |
0.357 |
|
| 2003 |
Oliveira SA, Scott WK, Martin ER, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Ondo WG, Allen FH, Scott BL, Goetz CG, Small GW, ... ... Pericak-Vance MA, et al. Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. Annals of Neurology. 53: 624-9. PMID 12730996 DOI: 10.1002/Ana.10524 |
0.346 |
|
| 2003 |
Cuccaro ML, Shao Y, Bass MP, Abramson RK, Ravan SA, Wright HH, Wolpert CM, Donnelly SL, Pericak-Vance MA. Behavioral comparisons in autistic individuals from multiplex and singleton families. Journal of Autism and Developmental Disorders. 33: 87-91. PMID 12708583 DOI: 10.1023/A:1022286622534 |
0.395 |
|
| 2003 |
van der Walt JM, Martin ER, Scott WK, Zhang F, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, ... ... Pericak-Vance MA, et al. Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease. Neurology. 60: 1189-91. PMID 12682333 DOI: 10.1212/01.Wnl.0000055929.84668.9A |
0.388 |
|
| 2003 |
Hauser ER, Mooser V, Crossman DC, Haines JL, Jones CH, Winkelmann BR, Schmidt S, Scott WK, Roses AD, Pericak-Vance MA, Granger CB, Kraus WE. Design of the Genetics of Early Onset Cardiovascular Disease (GENECARD) study. American Heart Journal. 145: 602-13. PMID 12679755 DOI: 10.1067/Mhj.2003.13 |
0.316 |
|
| 2003 |
Trembath Y, Rosenberg C, Ervin JF, Schmechel DE, Gaskell P, Pericak-Vance M, Vance J, Hulette CM. Lewy body pathology is a frequent co-pathology in familial Alzheimer's disease. Acta Neuropathologica. 105: 484-8. PMID 12677449 DOI: 10.1007/S00401-003-0670-9 |
0.372 |
|
| 2003 |
van der Walt JM, Nicodemus KK, Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, ... ... Pericak-Vance MA, et al. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. American Journal of Human Genetics. 72: 804-11. PMID 12618962 DOI: 10.1086/373937 |
0.308 |
|
| 2003 |
Shao Y, Cuccaro ML, Hauser ER, Raiford KL, Menold MM, Wolpert CM, Ravan SA, Elston L, Decena K, Donnelly SL, Abramson RK, Wright HH, DeLong GR, Gilbert JR, Pericak-Vance MA. Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. American Journal of Human Genetics. 72: 539-48. PMID 12567325 DOI: 10.1086/367846 |
0.424 |
|
| 2003 |
Barcellos LF, Oksenberg JR, Begovich AB, Martin ER, Schmidt S, Vittinghoff E, Goodin DS, Pelletier D, Lincoln RR, Bucher P, Swerdlin A, Pericak-Vance MA, Haines JL, Hauser SL. HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course. American Journal of Human Genetics. 72: 710-6. PMID 12557126 DOI: 10.1086/367781 |
0.312 |
|
| 2002 |
Schmidt S, Klaver C, Saunders A, Postel E, De La Paz M, Agarwal A, Small K, Udar N, Ong J, Chalukya M, Nesburn A, Kenney C, Domurath R, Hogan M, Mah T, ... ... Pericak-Vance M, et al. A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy. Ophthalmic Genetics. 23: 209-23. PMID 12567264 DOI: 10.1076/Opge.23.4.209.13883 |
0.371 |
|
| 2002 |
Speer MC, Graham FL, Bonner E, Collier K, Stajich JM, Gaskell PC, Pericak-Vance MA, Vance JM. Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432. Neurogenetics. 4: 83-5. PMID 12481986 DOI: 10.1007/S10048-002-0139-3 |
0.405 |
|
| 2002 |
Hauser MA, Conde CB, Kowaljow V, Zeppa G, Taratuto AL, Torian UM, Vance J, Pericak-Vance MA, Speer MC, Rosa AL. myotilin Mutation found in second pedigree with LGMD1A. American Journal of Human Genetics. 71: 1428-32. PMID 12428213 DOI: 10.1086/344532 |
0.329 |
|
| 2002 |
Haines JL, Bradford Y, Garcia ME, Reed AD, Neumeister E, Pericak-Vance MA, Rimmler JB, Menold MM, Martin ER, Oksenberg JR, Barcellos LF, Lincoln R, Hauser SL. Multiple susceptibility loci for multiple sclerosis. Human Molecular Genetics. 11: 2251-6. PMID 12217953 DOI: 10.1093/Hmg/11.19.2251 |
0.404 |
|
| 2002 |
Neary JJ, Conlon PJ, Croke D, Dorman A, Keogan M, Zhang FY, Vance JM, Pericak-Vance MA, Scott WK, Winn MP. Linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1. Journal of the American Society of Nephrology : Jasn. 13: 2052-7. PMID 12138136 DOI: 10.1097/01.Asn.0000022006.49966.F8 |
0.413 |
|
| 2002 |
Li YJ, Scott WK, Hedges DJ, Zhang F, Gaskell PC, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Allen FA, Goetz CG, ... ... Pericak-Vance MA, et al. Age at onset in two common neurodegenerative diseases is genetically controlled. American Journal of Human Genetics. 70: 985-93. PMID 11875758 DOI: 10.1086/339815 |
0.423 |
|
| 2002 |
Shao Y, Raiford KL, Wolpert CM, Cope HA, Ravan SA, Ashley-Koch AA, Abramson RK, Wright HH, DeLong RG, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. American Journal of Human Genetics. 70: 1058-61. PMID 11875756 DOI: 10.1086/339765 |
0.411 |
|
| 2002 |
McCoy PA, Shao Y, Wolpert CM, Donnelly SL, Ashley-Koch A, Abel HL, Ravan SA, Abramson RK, Wright HH, DeLong GR, Cuccaro ML, Gilbert JR, Pericak-Vance MA. No association between the WNT2 gene and autistic disorder. American Journal of Medical Genetics. 114: 106-9. PMID 11840514 DOI: 10.1002/Ajmg.10182 |
0.389 |
|
| 2002 |
Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, Bass MP, McClain C, von Wendt L, Vance JM, Abramson RH, Wright HH, Ashley-Koch A, Gilbert JR, DeLong RG, ... ... Pericak-Vance MA, et al. Genomic screen and follow-up analysis for autistic disorder. American Journal of Medical Genetics. 114: 99-105. PMID 11840513 DOI: 10.1002/Ajmg.10153 |
0.401 |
|
| 2002 |
Schmidt S, Barcellos LF, DeSombre K, Rimmler JB, Lincoln RR, Bucher P, Saunders AM, Lai E, Martin ER, Vance JM, Oksenberg JR, Hauser SL, Pericak-Vance MA, Haines JL. Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis. American Journal of Human Genetics. 70: 708-17. PMID 11836653 DOI: 10.1086/339269 |
0.452 |
|
| 2002 |
Barcellos LF, Oksenberg JR, Green AJ, Bucher P, Rimmler JB, Schmidt S, Garcia ME, Lincoln RR, Pericak-Vance MA, Haines JL, Hauser SL. Genetic basis for clinical expression in multiple sclerosis. Brain : a Journal of Neurology. 125: 150-8. PMID 11834600 DOI: 10.1093/Brain/Awf009 |
0.393 |
|
| 2002 |
Baxter RV, Ben Othmane K, Rochelle JM, Stajich JE, Hulette C, Dew-Knight S, Hentati F, Ben Hamida M, Bel S, Stenger JE, Gilbert JR, Pericak-Vance MA, Vance JM. Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21. Nature Genetics. 30: 21-2. PMID 11743579 DOI: 10.1038/Ng796 |
0.342 |
|
| 2001 |
Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, van der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC. Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy. Journal of Clinical Neuromuscular Disease. 3: 1-7. PMID 19078645 DOI: 10.1097/00131402-200109000-00001 |
0.319 |
|
| 2001 |
Pericak-Vance MA. Analysis of genetic linkage data for Mendelian traits. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 1.4. PMID 18428236 DOI: 10.1002/0471142905.Hg0104S09 |
0.403 |
|
| 2001 |
Menold MM, Shao Y, Wolpert CM, Donnelly SL, Raiford KL, Martin ER, Ravan SA, Abramson RK, Wright HH, Delong GR, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder. Journal of Neurogenetics. 15: 245-59. PMID 12092907 DOI: 10.3109/01677060109167380 |
0.401 |
|
| 2001 |
Schmidt S, Shao Y, Hauser ER, Slifer SH, Martin ER, Scott WK, Speer MC, Pericak-Vance MA. Life after the screen: making sense of many P-values. Genetic Epidemiology. 21: S546-51. PMID 11793734 DOI: 10.1002/Gepi.2001.21.S1.S546 |
0.304 |
|
| 2001 |
Jones KW, Ehm MG, Pericak-Vance MA, Haines JL, Boyd PR, Peroutka SJ. Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus. Genomics. 78: 150-4. PMID 11735221 DOI: 10.1006/Geno.2001.6665 |
0.432 |
|
| 2001 |
Pericak-Vance MA, Rimmler JB, Martin ER, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Goodkin DE, Hauser SL. Linkage and association analysis of chromosome 19q13 in multiple sclerosis. Neurogenetics. 3: 195-201. PMID 11714099 DOI: 10.1007/S100480100119 |
0.407 |
|
| 2001 |
Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH, Goetz CG, ... ... Pericak-Vance MA, et al. Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease. Jama. 286: 2245-50. PMID 11710889 DOI: 10.1001/Jama.286.18.2245 |
0.411 |
|
| 2001 |
Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH, Goetz CG, Small GW, ... ... Pericak-Vance MA, et al. Complete genomic screen in Parkinson disease: evidence for multiple genes. Jama. 286: 2239-44. PMID 11710888 DOI: 10.1001/Jama.286.18.2239 |
0.374 |
|
| 2001 |
Svenson IK, Ashley-Koch AE, Pericak-Vance MA, Marchuk DA. A second leaky splice-site mutation in the spastin gene. American Journal of Human Genetics. 69: 1407-9. PMID 11704932 DOI: 10.1086/324593 |
0.308 |
|
| 2001 |
Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vance M, et al. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nature Genetics. 29: 160-5. PMID 11586297 DOI: 10.1038/Ng1001-160 |
0.369 |
|
| 2001 |
Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner MB, Hutcheson HB, Gilbert JR, Pericak-Vance MA, Copeland-Yates SA, Michaelis RC, Wassink TH, Santangelo SL, Sheffield VC, Piven J, et al. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics. 77: 105-13. PMID 11543639 DOI: 10.1006/Geno.2001.6617 |
0.425 |
|
| 2001 |
Barcellos LF, Caillier S, Dragone L, Elder M, Vittinghoff E, Bucher P, Lincoln RR, Pericak-Vance M, Haines JL, Weiss A, Hauser SL, Oksenberg JR. PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients. Nature Genetics. 29: 23-4. PMID 11528386 DOI: 10.1038/Ng722 |
0.358 |
|
| 2001 |
Rampoldi L, Dobson-Stone C, Rubio JP, Danek A, Chalmers RM, Wood NW, Verellen C, Ferrer X, Malandrini A, Fabrizi GM, Brown R, Vance J, Pericak-Vance M, Rudolf G, Carrè S, et al. A conserved sorting-associated protein is mutant in chorea-acanthocytosis. Nature Genetics. 28: 119-20. PMID 11381253 DOI: 10.1038/88821 |
0.338 |
|
| 2001 |
Ashley-Koch A, Bonner ER, Gaskell PC, West SG, Tim R, Wolpert CM, Jones R, Farrell CD, Nance M, Svenson IK, Marchuk DA, Boustany RM, Vance JM, Scott WK, Pericak-Vance MA. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia. Neurogenetics. 3: 91-7. PMID 11354831 DOI: 10.1007/S100480000098 |
0.389 |
|
| 2001 |
Wolpert CM, Donnelly SL, Cuccaro ML, Hedges DJ, Poole CP, Wright HH, Gilbert JR, Pericak-Vance MA. De novo partial duplication of chromosome 7p in a male with autistic disorder. American Journal of Medical Genetics. 105: 222-5. PMID 11353439 DOI: 10.1002/Ajmg.1258 |
0.334 |
|
| 2001 |
Green AJ, Barcellos LF, Rimmler JB, Garcia ME, Caillier S, Lincoln RR, Bucher P, Pericak-Vance MA, Haines JL, Hauser SL, Oksenberg JR. Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility. Journal of Neuroimmunology. 116: 116-24. PMID 11311337 DOI: 10.1016/S0165-5728(01)00283-1 |
0.43 |
|
| 2001 |
Svenson IK, Ashley-Koch AE, Gaskell PC, Riney TJ, Cumming WJ, Kingston HM, Hogan EL, Boustany RM, Vance JM, Nance MA, Pericak-Vance MA, Marchuk DA. Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia. American Journal of Human Genetics. 68: 1077-85. PMID 11309678 DOI: 10.1086/320111 |
0.331 |
|
| 2001 |
Allingham RR, Seo B, Rampersaud E, Bembe M, Challa P, Liu N, Parrish T, Karolak L, Gilbert J, Pericak-Vance MA, Klintworth GK, Vance JM. A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis. American Journal of Human Genetics. 68: 491-4. PMID 11170897 DOI: 10.1086/318194 |
0.424 |
|
| 2001 |
Oliveira SA, Scott WK, Pericak-Vance MA, Vance JM. Dissecting a complex disease using modern techniques of molecular biology Laboratory Medicine. 32: 594-598. DOI: 10.1309/Uj8W-H1Ht-4B21-Bjxh |
0.326 |
|
| 2000 |
Pericak-Vance MA, Grubber J, Bailey LR, Hedges D, West S, Santoro L, Kemmerer B, Hall JL, Saunders AM, Roses AD, Small GW, Scott WK, Conneally PM, Vance JM, Haines JL. Identification of novel genes in late-onset Alzheimer's disease. Experimental Gerontology. 35: 1343-52. PMID 11113612 DOI: 10.1016/S0531-5565(00)00196-0 |
0.442 |
|
| 2000 |
Hosler BA, Siddique T, Sapp PC, Sailor W, Huang MC, Hossain A, Daube JR, Nance M, Fan C, Kaplan J, Hung WY, McKenna-Yasek D, Haines JL, Pericak-Vance MA, Horvitz HR, et al. Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. Jama. 284: 1664-9. PMID 11015796 DOI: 10.1001/Jama.284.13.1664 |
0.412 |
|
| 2000 |
Hauser ER, Pericak-Vance MA. Genetic analysis for common complex disease. American Heart Journal. 140: S36-44. PMID 11011322 DOI: 10.1067/Mhj.2000.108946 |
0.358 |
|
| 2000 |
Bass MP, Menold MM, Wolpert CM, Donnelly SL, Ravan SA, Hauser ER, Maddox LO, Vance JM, Abramson RK, Wright HH, Gilbert JR, Cuccaro ML, DeLong GR, Pericak-Vance MA. Genetic studies in autistic disorder and chromosome 15. Neurogenetics. 2: 219-26. PMID 10983717 DOI: 10.1007/S100489900081 |
0.41 |
|
| 2000 |
Rosenberg CK, Pericak-Vance MA, Saunders AM, Gilbert JR, Gaskell PC, Hulette CM. Lewy body and Alzheimer pathology in a family with the amyloid-beta precursor protein APP717 gene mutation. Acta Neuropathologica. 100: 145-52. PMID 10963361 DOI: 10.1007/S004019900155 |
0.356 |
|
| 2000 |
Hauser MA, Horrigan SK, Salmikangas P, Torian UM, Viles KD, Dancel R, Tim RW, Taivainen A, Bartoloni L, Gilchrist JM, Stajich JM, Gaskell PC, Gilbert JR, Vance JM, Pericak-Vance MA, et al. Myotilin is mutated in limb girdle muscular dystrophy 1A. Human Molecular Genetics. 9: 2141-7. PMID 10958653 DOI: 10.1093/Hmg/9.14.2141 |
0.319 |
|
| 2000 |
Bookheimer SY, Strojwas MH, Cohen MS, Saunders AM, Pericak-Vance MA, Mazziotta JC, Small GW. Patterns of brain activation in people at risk for Alzheimer's disease. The New England Journal of Medicine. 343: 450-6. PMID 10944562 DOI: 10.1056/Nejm200008173430701 |
0.352 |
|
| 2000 |
Wolpert CM, Menold MM, Bass MP, Qumsiyeh MB, Donnelly SL, Ravan SA, Vance JM, Gilbert JR, Abramson RK, Wright HH, Cuccaro ML, Pericak-Vance MA. Three probands with autistic disorder and isodicentric chromosome 15. American Journal of Medical Genetics. 96: 365-72. PMID 10898916 DOI: 10.1002/1096-8628(20000612)96:3<365::Aid-Ajmg25>3.0.Co;2-X |
0.349 |
|
| 2000 |
Donnelly SL, Wolpert CM, Menold MM, Bass MP, Gilbert JR, Cuccaro ML, Delong GR, Pericak-Vance MA. Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome. American Journal of Medical Genetics. 96: 312-6. PMID 10898907 DOI: 10.1002/1096-8628(20000612)96:3<312::Aid-Ajmg16>3.0.Co;2-8 |
0.319 |
|
| 2000 |
Martin ER, Lai EH, Gilbert JR, Rogala AR, Afshari AJ, Riley J, Finch KL, Stevens JF, Livak KJ, Slotterbeck BD, Slifer SH, Warren LL, Conneally PM, Schmechel DE, Purvis I, ... Pericak-Vance MA, et al. SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease. American Journal of Human Genetics. 67: 383-94. PMID 10869235 DOI: 10.1086/303003 |
0.453 |
|
| 2000 |
Nance MA, Nuttall FQ, Econs MJ, Lyles KW, Viles KD, Vance JM, Pericak-Vance MA, Speer MC. Heterogeneity in Paget disease of the bone American Journal of Medical Genetics. 92: 303-307. PMID 10861657 DOI: 10.1002/1096-8628(20000619)92:5<303::Aid-Ajmg2>3.0.Co;2-E |
0.379 |
|
| 2000 |
Small GW, Ercoli LM, Silverman DH, Huang SC, Komo S, Bookheimer SY, Lavretsky H, Miller K, Siddarth P, Rasgon NL, Mazziotta JC, Saxena S, Wu HM, Mega MS, Cummings JL, ... ... Pericak-Vance MA, et al. Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 97: 6037-42. PMID 10811879 DOI: 10.1073/Pnas.090106797 |
0.325 |
|
| 2000 |
Barcellos LF, Schito AM, Rimmler JB, Vittinghoff E, Shih A, Lincoln R, Callier S, Elkins MK, Goodkin DE, Haines JL, Pericak-Vance MA, Hauser SL, Oksenberg JR. CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group. Immunogenetics. 51: 281-8. PMID 10803840 DOI: 10.1007/S002510050621 |
0.395 |
|
| 2000 |
Wiggs JL, Allingham RR, Hossain A, Kern J, Auguste J, DelBono EA, Broomer B, Graham FL, Hauser M, Pericak-Vance M, Haines JL. Genome-wide scan for adult onset primary open angle glaucoma. Human Molecular Genetics. 9: 1109-17. PMID 10767336 DOI: 10.1093/Hmg/9.7.1109 |
0.436 |
|
| 2000 |
Melvin EC, George TM, Worley G, Franklin A, Mackey J, Viles K, Shah N, Drake CR, Enterline DS, McLone D, Nye J, Oakes WJ, McLaughlin C, Walker ML, Peterson P, ... ... Pericak-Vance MA, et al. Genetic studies in neural tube defects. NTD Collaborative Group. Pediatric Neurosurgery. 32: 1-9. PMID 10765131 DOI: 10.1159/000028889 |
0.387 |
|
| 2000 |
Scott WK, Grubber JM, Conneally PM, Small GW, Hulette CM, Rosenberg CK, Saunders AM, Roses AD, Haines JL, Pericak-Vance MA. Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity. American Journal of Human Genetics. 66: 922-32. PMID 10712207 DOI: 10.1086/302828 |
0.463 |
|
| 2000 |
Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL, Ravan SA, Zimmerman A, Gilbert JR, Vance JM, Maddox LO, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. American Journal of Medical Genetics. 96: 43-8. PMID 10686550 DOI: 10.1002/(Sici)1096-8628(20000207)96:1<43::Aid-Ajmg9>3.0.Co;2-3 |
0.386 |
|
| 2000 |
Gilbert JR, Kumar A, Newey S, Rao N, Ioannou P, Qiu H, Lin D, Xu P, Pettenati MJ, Pericak-Vance MA. Physical and cDNA mapping in the DBH region of human chromosome 9q34. Human Heredity. 50: 151-7. PMID 10686491 DOI: 10.1159/000022905 |
0.33 |
|
| 2000 |
Martin ER, Gilbert JR, Lai EH, Riley J, Rogala AR, Slotterbeck BD, Sipe CA, Grubber JM, Warren LL, Conneally PM, Saunders AM, Schmechel DE, Purvis I, Pericak-Vance MA, Roses AD, et al. Analysis of association at single nucleotide polymorphisms in the APOE region. Genomics. 63: 7-12. PMID 10662539 DOI: 10.1006/Geno.1999.6057 |
0.404 |
|
| 2000 |
Pericak-Vance MA. Screening for novel Alzheimer's disease genes Neurobiology of Aging. 21: 211. DOI: 10.1016/S0197-4580(00)83278-9 |
0.355 |
|
| 2000 |
Scott WK, Grubber JM, Conneally P, Small GW, Gilbert JR, Haines JL, Pericak-Vance MA. Fine-mapping of the chromosome 12 Alzheimer disease locus using family-based association tests of microsatellite markers Neurobiology of Aging. 21: 129. DOI: 10.1016/S0197-4580(00)82380-5 |
0.404 |
|
| 1999 |
Haines JL, Pericak-Vance MA. Genetics of multiple sclerosis. Current Directions in Autoimmunity. 1: 273-88. PMID 11791446 DOI: 10.1159/000060491 |
0.306 |
|
| 1999 |
Fontaine B, Cournu I, Arnaud I, Babron MC, Eichenbaum-Voline S, Oksenberg JR, Pericak-Vance MA, Haines JL, Semama G, Liblau R, Lyon-Caen O, Clerget-Darpoux F, Clanet M, Hauser SL. Chromosome 17q22-q24 and multiple sclerosis genetic susceptibility. American-French Multiple Sclerosis Genetic Group. Genes and Immunity. 1: 149-50. PMID 11196661 DOI: 10.1038/Sj.Gene.6363646 |
0.414 |
|
| 1999 |
Othmane KB, Johnson E, Menold M, Graham FL, Hamida MB, Hasegawa O, Rogala AD, Ohnishi A, Pericak-Vance M, Hentati F, Vance JM. Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15. Genomics. 62: 344-9. PMID 10644431 DOI: 10.1006/Geno.1999.6028 |
0.395 |
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