| Year |
Citation |
Score |
| 2024 |
Abu-Amara H, Zhao W, Li Z, Leung YY, Schellenberg GD, Wang LS, Moorjani P, Dey AB, Dey S, Zhou X, Gross AL, Lee J, Kardia SLR, Smith JA. Region-based analysis with functional annotation identifies genes associated with cognitive function in South Asians from India. Medrxiv : the Preprint Server For Health Sciences. PMID 38293024 DOI: 10.1101/2024.01.18.24301482 |
0.309 |
|
| 2024 |
Ho PC, Yu WH, Tee BL, Lee WP, Li C, Gu Y, Yokoyama JS, Reyes-Dumeyer D, Choi YB, Yang HS, Vardarajan BN, Tzuang M, Lieu K, Lu A, Faber KM, ... ... Schellenberg GD, et al. Asian Cohort for Alzheimer's Disease (ACAD) pilot study on genetic and non-genetic risk factors for Alzheimer's disease among Asian Americans and Canadians. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 38215053 DOI: 10.1002/alz.13611 |
0.339 |
|
| 2024 |
Vance JM, Farrer LA, Huang Y, Cruchaga C, Hyman BT, Pericak-Vance MA, Goate AM, Greicius MD, Griswold AJ, Haines JL, Tcw J, Schellenberg GD, Tsai LH, Herz J, Holtzman DM. Report of the APOE4 National Institute on Aging/Alzheimer Disease Sequencing Project Consortium Working Group: Reducing APOE4 in Carriers is a Therapeutic Goal for Alzheimer's Disease. Annals of Neurology. PMID 38180638 DOI: 10.1002/ana.26864 |
0.364 |
|
| 2023 |
Wang H, Chang TS, Dombroski BA, Cheng PL, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Rajput A, Paul De Deyn P, Le Bastard N, Gearing M, Donker Kaat L, Van Swieten JC, ... ... Schellenberg GD, et al. Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. Medrxiv : the Preprint Server For Health Sciences. PMID 38234807 DOI: 10.1101/2023.12.28.23300612 |
0.374 |
|
| 2023 |
Guo MH, Lee WP, Vardarajan B, Schellenberg GD, Phillips-Cremins J. Polygenic burden of short tandem repeat expansions promote risk for Alzheimer's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 38014121 DOI: 10.1101/2023.11.16.23298623 |
0.37 |
|
| 2023 |
Lee WP, Wang H, Dombroski B, Cheng PL, Tucci A, Si YQ, Farrell J, Tzeng JY, Leung YY, Malamon J, Wang LS, Vardarajan B, Farrer L, Schellenberg G, Project TADSPTAD. Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. Research Square. PMID 37886469 DOI: 10.21203/rs.3.rs-3353179/v1 |
0.377 |
|
| 2023 |
Greenfest-Allen E, Valladares O, Kuksa PP, Gangadharan P, Lee WP, Cifello J, Katanic Z, Kuzma AB, Wheeler N, Bush WS, Leung YY, Schellenberg G, Stoeckert CJ, Wang LS. NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37881831 DOI: 10.1002/alz.13509 |
0.343 |
|
| 2023 |
Wang H, Dombroski BA, Cheng PL, Tucci A, Si YQ, Farrell JJ, Tzeng JY, Leung YY, Malamon JS, Wang LS, Vardarajan BN, Farrer LA, Schellenberg GD, Lee WP. Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. Medrxiv : the Preprint Server For Health Sciences. PMID 37745545 DOI: 10.1101/2023.09.13.23295505 |
0.373 |
|
| 2023 |
Ray NR, Kunkle BW, Hamilton-Nelson K, Kurup JT, Rajabli F, Cosacak MI, Kizil C, Jean-Francois M, Cuccaro M, Reyes-Dumeyer D, Cantwell L, Kuzma A, Vance JM, Gao S, Hendrie HC, ... ... Schellenberg GD, et al. Extended genome-wide association study employing the African Genome Resources Panel identifies novel susceptibility loci for Alzheimer's Disease in individuals of African ancestry. Medrxiv : the Preprint Server For Health Sciences. PMID 37693582 DOI: 10.1101/2023.08.29.23294774 |
0.329 |
|
| 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, ... ... Schellenberg GD, 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 |
0.35 |
|
| 2023 |
Tejeda M, Farrell J, Zhu C, Wetzler L, Lunetta KL, Bush WS, Martin ER, Wang LS, Schellenberg GD, Pericak-Vance MA, Haines JL, Farrer LA, Sherva R. DNA from multiple viral species is associated with Alzheimer's disease risk. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37578203 DOI: 10.1002/alz.13414 |
0.307 |
|
| 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, ... ... Schellenberg GD, 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 |
0.353 |
|
| 2023 |
Ray NR, Ayodele T, Jean-Francois M, Baez P, Fernandez V, Bradley J, Crane PK, Dalgard CL, Kuzma A, Nicaretta H, Sims R, Williams J, Cuccaro ML, Pericak-Vance MA, Mayeux R, ... ... Schellenberg GD, et al. The Early-Onset Alzheimer's Disease Whole-Genome Sequencing Project: Study design and methodology. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37390458 DOI: 10.1002/alz.13370 |
0.362 |
|
| 2023 |
Kang M, Ang TFA, Devine SA, Sherva R, Mukherjee S, Trittschuh EH, Gibbons LE, Scollard P, Lee M, Choi SE, Klinedinst B, Nakano C, Dumitrescu LC, Durant A, Hohman TJ, ... ... Schellenberg GD, et al. A genome-wide search for pleiotropy in more than 100,000 harmonized longitudinal cognitive domain scores. Molecular Neurodegeneration. 18: 40. PMID 37349795 DOI: 10.1186/s13024-023-00633-4 |
0.335 |
|
| 2023 |
Li D, Farrell JJ, Mez J, Martin ER, Bush WS, Ruiz A, Boada M, de Rojas I, Mayeux R, Haines JL, Vance MAP, Wang LS, Schellenberg GD, Lunetta KL, Farrer LA. Novel loci for Alzheimer's disease identified by a genome-wide association study in Ashkenazi Jews. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37260021 DOI: 10.1002/alz.13117 |
0.379 |
|
| 2023 |
Bai H, Naj AC, Benchek P, Dumitrescu L, Hohman T, Hamilton-Nelson K, Kallianpur AR, Griswold AJ, Vardarajan B, Martin ER, Beecham GW, Below JE, Schellenberg G, Mayeux R, Farrer L, et al. A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37051669 DOI: 10.1002/alz.13050 |
0.305 |
|
| 2023 |
Wang H, Wang LS, Schellenberg G, Lee WP. The role of structural variations in Alzheimer's disease and other neurodegenerative diseases. Frontiers in Aging Neuroscience. 14: 1073905. PMID 36846102 DOI: 10.3389/fnagi.2022.1073905 |
0.347 |
|
| 2022 |
Holstege H, Hulsman M, Charbonnier C, Grenier-Boley B, Quenez O, Grozeva D, van Rooij JGJ, Sims R, Ahmad S, Amin N, Norsworthy PJ, Dols-Icardo O, Hummerich H, Kawalia A, Amouyel P, ... ... Schellenberg GD, et al. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genetics. PMID 36411364 DOI: 10.1038/s41588-022-01208-7 |
0.366 |
|
| 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, ... ... Schellenberg GD, 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 |
0.363 |
|
| 2022 |
Chung J, Das A, Sun X, Sobreira DR, Leung YY, Igartua C, Mozaffari S, Chou YF, Thiagalingam S, Mez J, Zhang X, Jun GR, Stein TD, Kunkle BW, Martin ER, ... ... Schellenberg GD, et al. Genome-wide association and multi-omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 35770850 DOI: 10.1002/alz.12719 |
0.33 |
|
| 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, ... ... Schellenberg GD, 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 |
0.376 |
|
| 2022 |
Vardarajan BN, Reyes-Dumeyer D, Piriz AL, Lantigua RA, Medrano M, Rivera D, Jiménez-Velázquez IZ, Martin E, Pericak-Vance MA, Bush W, Farrer L, Haines JL, Wang LS, Leung YY, Schellenberg G, et al. Progranulin mutations in clinical and neuropathological Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 35258170 DOI: 10.1002/alz.12567 |
0.329 |
|
| 2022 |
Jin B, Capra JA, Benchek P, Wheeler NR, Naj AC, Hamilton-Nelson KL, Farrell JJ, Leung YY, Kunkle BW, Vardarajan BN, Schellenberg GD, Mayeux R, Wang LS, Farrer LA, Pericak-Vance M, et al. An association test of the spatial distribution of rare missense variants within protein structures identify Alzheimer's disease-related patterns. Genome Research. PMID 35210353 DOI: 10.1101/gr.276069.121 |
0.314 |
|
| 2022 |
Jun GR, You Y, Zhu C, Meng G, Chung J, Panitch R, Hu J, Xia W, Bennett DA, Foroud TM, Wang LS, Haines JL, Mayeux R, Pericak-Vance MA, Schellenberg GD, et al. Protein phosphatase 2A and complement component 4 are linked to the protective effect of APOE ɛ2 for Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 35142023 DOI: 10.1002/alz.12607 |
0.336 |
|
| 2022 |
Kuksa PP, Liu CL, Fu W, Qu L, Zhao Y, Katanic Z, Clark K, Kuzma AB, Ho PC, Tzeng KT, Valladares O, Chou SY, Naj AC, Schellenberg GD, Wang LS, et al. Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. PMID 35068457 DOI: 10.3233/JAD-215055 |
0.367 |
|
| 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 |
0.363 |
|
| 2021 |
Lee WP, Tucci AA, Conery M, Leung YY, Kuzma AB, Valladares O, Chou YF, Lu W, Wang LS, Schellenberg GD, Tzeng JY. Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project. Frontiers in Genetics. 12: 752390. PMID 34804120 DOI: 10.3389/fgene.2021.752390 |
0.37 |
|
| 2021 |
de Rojas I, Moreno-Grau S, Tesi N, Grenier-Boley B, Andrade V, Jansen IE, Pedersen NL, Stringa N, Zettergren A, Hernández I, Montrreal L, Antúnez C, Antonell A, Tankard RM, Bis JC, ... ... Schellenberg GD, et al. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nature Communications. 12: 3417. PMID 34099642 DOI: 10.1038/s41467-021-22491-8 |
0.35 |
|
| 2020 |
Kunkle BW, Schmidt M, Klein HU, Naj AC, Hamilton-Nelson KL, Larson EB, Evans DA, De Jager PL, Crane PK, Buxbaum JD, Ertekin-Taner N, Barnes LL, Fallin MD, Manly JJ, Go RCP, ... ... Schellenberg GD, et al. Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis. Jama Neurology. PMID 33074286 DOI: 10.1001/jamaneurol.2020.3536 |
0.302 |
|
| 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, ... ... Schellenberg G, 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 |
0.417 |
|
| 2020 |
Weitzman SA, Narasimhan S, He Z, Changolkar L, McBride JD, Zhang B, Schellenberg GD, Trojanowski JQ, Lee VMY. Insoluble Tau From Human FTDP-17 Cases Exhibit Unique Transmission Properties In Vivo. Journal of Neuropathology and Experimental Neurology. 79: 941-949. PMID 32838419 DOI: 10.1093/Jnen/Nlaa086 |
0.379 |
|
| 2020 |
Fan CC, Banks SJ, Thompson WK, Chen CH, McEvoy LK, Tan CH, Kukull W, Bennett DA, Farrer LA, Mayeux R, Schellenberg GD, Andreassen OA, Desikan R, Dale AM. Sex-dependent autosomal effects on clinical progression of Alzheimer's disease. Brain : a Journal of Neurology. PMID 32591829 DOI: 10.1093/Brain/Awaa164 |
0.437 |
|
| 2020 |
Vergouw LJM, Melhem S, Donker Kaat L, Chiu WZ, Kuipers DJS, Breedveld G, Boon AJW, Wang LS, Naj AC, Mlynarksi E, Cantwell L, Quadri M, Ross OA, Dickson DW, Schellenberg GD, et al. LRP10 variants in progressive supranuclear palsy. Neurobiology of Aging. PMID 32527607 DOI: 10.1016/J.Neurobiolaging.2020.04.016 |
0.333 |
|
| 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 |
0.354 |
|
| 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, ... ... Schellenberg GD, 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 |
0.461 |
|
| 2019 |
Wheeler JM, McMillan P, Strovas TJ, Liachko NF, Amlie-Wolf A, Kow RL, Klein RL, Szot P, Robinson L, Guthrie C, Saxton A, Kanaan NM, Raskind M, Peskind E, Trojanowski JQ, ... ... Schellenberg GD, et al. Activity of the poly(A) binding protein MSUT2 determines susceptibility to pathological tau in the mammalian brain. Science Translational Medicine. 11. PMID 31852801 DOI: 10.1126/Scitranslmed.Aao6545 |
0.386 |
|
| 2019 |
Amlie-Wolf A, Tang M, Way J, Dombroski B, Jiang M, Vrettos N, Chou YF, Zhao Y, Kuzma A, Mlynarski EE, Leung YY, Brown CD, Wang LS, Schellenberg GD. Inferring the Molecular Mechanisms of Noncoding Alzheimer's Disease-Associated Genetic Variants. Journal of Alzheimer's Disease : Jad. PMID 31561366 DOI: 10.3233/Jad-190568 |
0.396 |
|
| 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, ... Schellenberg GD, 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 |
0.435 |
|
| 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, ... ... Schellenberg GD, 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 |
0.421 |
|
| 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, ... ... Schellenberg GD, et al. Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. PMID 31417202 DOI: 10.1038/s41588-019-0495-7 |
0.307 |
|
| 2019 |
Cali CP, Patino M, Tai YK, Ho WY, McLean CA, Morris CM, Seeley WW, Miller BL, Gaig C, Vonsattel JPG, White CL, Roeber S, Kretzschmar H, Troncoso JC, Troakes C, ... ... Schellenberg GD, et al. C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy. Acta Neuropathologica. PMID 31327044 DOI: 10.1007/S00401-019-02045-5 |
0.416 |
|
| 2019 |
Baker E, Sims R, Leonenko G, Frizzati A, Harwood JC, Grozeva D, Morgan K, Passmore P, Holmes C, Powell J, ... ... Schellenberg GD, et al. Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease. Plos One. 14: e0218111. PMID 31283791 DOI: 10.1371/Journal.Pone.0218111 |
0.471 |
|
| 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, ... ... Schellenberg GD, 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 |
0.489 |
|
| 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 |
0.443 |
|
| 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, ... ... Schellenberg G, 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 |
0.464 |
|
| 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, ... ... Schellenberg GD, 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 |
0.358 |
|
| 2019 |
Tan CH, Bonham LW, Fan CC, Mormino EC, Sugrue LP, Broce IJ, Hess CP, Yokoyama JS, Rabinovici GD, Miller BL, Yaffe K, Schellenberg GD, Kauppi K, Holland D, McEvoy LK, et al. Polygenic hazard score, amyloid deposition and Alzheimer's neurodegeneration. Brain : a Journal of Neurology. PMID 30689776 DOI: 10.1093/Brain/Awy327 |
0.421 |
|
| 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, 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 |
0.426 |
|
| 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, ... ... Schellenberg GD, 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 |
0.391 |
|
| 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, ... ... Schellenberg GD, 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 |
0.424 |
|
| 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 |
0.387 |
|
| 2019 |
Reiman EM, Arboleda-Velasquez JF, Quiroz YT, Huentelman MJ, Beach TG, Farrer LA, Mayeux R, Haines JL, Schellenberg GD, Beecham GW, Montine TJ, Jun GR. P4-259: Exceptionally Low Risk Of Alzheimer'S Dementia In Apoe2 Homozygotes Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3928 |
0.394 |
|
| 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, 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 |
0.412 |
|
| 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, ... Schellenberg GD, 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 |
0.434 |
|
| 2019 |
Vogel B, Kuzma AB, Valladares O, Greenfest-Allen E, Gangadharan P, Zhao Y, Katanic Z, Qu L, Lin H, Moon MK, Leung YY, Issen H, Klamann C, Naj A, Stoeckert CJ, ... Schellenberg GD, et al. P4-090: NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITE (NIAGADS): UPDATE 2019 Alzheimer's & Dementia. 15: P1309-P1309. DOI: 10.1016/J.Jalz.2019.06.3750 |
0.417 |
|
| 2019 |
Leung YY, Amlie-Wolf A, Wang L, Schellenberg GD. P3-122: INFERRING THE NONCODING REGULATORY MECHANISMS UNDERLYING GENETIC SUSCEPTIBILITY CONTRIBUTED BY DIFFERENT CSF ENDOPHENOTYPES IN AD Alzheimer's & Dementia. 15: P977-P977. DOI: 10.1016/J.Jalz.2019.06.3150 |
0.382 |
|
| 2019 |
Wang L, Leung YY, Valladares O, Chou Y, Kuzma AB, Gangadharan P, Cantwell LB, Qu L, Lin H, Malamon JS, Zhao Y, Martin ER, Naj A, Schellenberg GD, Sequencing AD. P2-134: Genome Center For Alzheimer'S Disease Whole Exome (Wes) And Whole Genome Sequencing (Wgs) Data Update Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2541 |
0.364 |
|
| 2019 |
Argenziano M, Manduchi E, Littleton S, Leonard ME, Su C, Lu S, Hodge KM, Pippin JA, Schellenberg GD, Johnson ME, Wells AD, Grant SFA, Chesi A. High-Resolution Genomewide Promoter-Focused Connectome Implicates Microglia Causal Genes For Alzheimer’S Disease Alzheimers & Dementia. 15: 238. DOI: 10.1016/J.Jalz.2019.06.044 |
0.342 |
|
| 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, ... ... Schellenberg GD, 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 |
0.39 |
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| 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 |
0.389 |
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| 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, ... ... Schellenberg GD, 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 |
0.471 |
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| 2018 |
Leung YY, Valladares O, Chou YF, Lin HJ, Kuzma AB, Cantwell L, Qu L, Gangadharan P, Salerno WJ, Schellenberg GD, Wang LS. VCPA: genomic Variant Calling pipeline and data management tool for Alzheimer's Disease Sequencing Project. Bioinformatics (Oxford, England). PMID 30351394 DOI: 10.1093/Bioinformatics/Bty894 |
0.327 |
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| 2018 |
Guerreiro R, Orme T, Naj AC, Kuzma AB, Schellenberg GD, Bras J. Is APOE ε4 required for Alzheimer's disease to develop in TREM2 p.R47H variant carriers? Neuropathology and Applied Neurobiology. PMID 30229991 DOI: 10.1111/Nan.12517 |
0.477 |
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| 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, ... ... Schellenberg GD, 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 |
0.441 |
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| 2018 |
Belitskaya-Lévy I, Dysken M, Guarino P, Sano M, Asthana S, Vertrees JE, Pallaki M, Llorente M, Love S, Schellenberg G. Impact of apolipoprotein E genotypes on vitamin E and memantine treatment outcomes in Alzheimer's disease. Alzheimer's & Dementia (New York, N. Y.). 4: 344-349. PMID 30175228 DOI: 10.1016/J.Trci.2018.06.001 |
0.386 |
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| 2018 |
Amlie-Wolf A, Tang M, Mlynarski EE, Kuksa PP, Valladares O, Katanic Z, Tsuang D, Brown CD, Schellenberg GD, Wang LS. INFERNO: inferring the molecular mechanisms of noncoding genetic variants. Nucleic Acids Research. PMID 30113658 DOI: 10.1093/Nar/Gky686 |
0.339 |
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| 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, ... ... Schellenberg GD, 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 |
0.476 |
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| 2018 |
Sanchez-Contreras MY, Kouri N, Cook CN, Serie DJ, Heckman MG, Finch NA, Caselli RJ, Uitti RJ, Wszolek ZK, Graff-Radford N, Petrucelli L, Wang LS, Schellenberg GD, Dickson DW, Rademakers R, et al. Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci. Molecular Neurodegeneration. 13: 37. PMID 29986742 DOI: 10.1186/S13024-018-0267-3 |
0.4 |
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| 2018 |
Chen P, Guarino PD, Dysken MW, Pallaki M, Asthana S, Llorente MD, Love S, Vertrees JE, Schellenberg GD, Sano M. Neuropsychiatric Symptoms and Caregiver Burden in Individuals With Alzheimer's Disease: The TEAM-AD VA Cooperative Study. Journal of Geriatric Psychiatry and Neurology. 891988718783897. PMID 29966477 DOI: 10.1177/0891988718783897 |
0.399 |
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| 2018 |
Naj AC, Lin H, Vardarajan BN, White S, Lancour D, Ma Y, Schmidt M, Sun F, Butkiewicz M, Bush WS, Kunkle BW, Malamon J, Amin N, Choi SH, Hamilton-Nelson KL, ... ... Schellenberg GD, et al. Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project. Genomics. PMID 29857119 DOI: 10.1016/J.Ygeno.2018.05.004 |
0.361 |
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| 2018 |
Hohman TJ, Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Gifford KA, Bush WS, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, ... ... Schellenberg GD, et al. Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau. Jama Neurology. PMID 29801024 DOI: 10.1001/Jamaneurol.2018.0821 |
0.438 |
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| 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, ... ... Schellenberg G, 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 |
0.444 |
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| 2018 |
Bonham LW, Karch CM, Fan CC, Tan C, Geier EG, Wang Y, Wen N, Broce IJ, Li Y, Barkovich MJ, Ferrari R, Hardy J, Momeni P, Höglinger G, Müller U, ... ... Schellenberg GD, et al. CXCR4 involvement in neurodegenerative diseases. Translational Psychiatry. 8: 73. PMID 29636460 DOI: 10.1038/S41398-017-0049-7 |
0.453 |
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| 2018 |
Karch CM, Wen N, Fan CC, Yokoyama JS, Kouri N, Ross OA, Höglinger G, Müller U, Ferrari R, Hardy J, Schellenberg GD, Sleiman PM, Momeni P, Hess CP, Miller BL, et al. Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum. Jama Neurology. PMID 29630712 DOI: 10.1001/Jamaneurol.2018.0372 |
0.335 |
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| 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, ... ... Schellenberg GD, 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 |
0.487 |
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| 2018 |
Teslovich TM, Kim DS, Yin X, Stancáková A, Jackson AU, Wielscher M, Naj A, Perry JRB, Huyghe JR, Stringham HM, Davis JP, Raulerson CK, Welch RP, Fuchsberger C, Locke AE, ... ... Schellenberg GD, et al. Identification of seven novel loci associated with amino acid levels using single variant and gene-based tests in 8,545 Finnish men from the METSIM study. Human Molecular Genetics. PMID 29481666 DOI: 10.1093/Hmg/Ddy067 |
0.331 |
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| 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, ... ... Schellenberg G, 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 |
0.446 |
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| 2018 |
Broce I, Karch CM, Wen N, Fan CC, Wang Y, Hong Tan C, Kouri N, Ross OA, Höglinger GU, Muller U, Hardy J, Momeni P, Hess CP, Dillon WP, ... ... Schellenberg GD, et al. Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. Plos Medicine. 15: e1002487. PMID 29315334 DOI: 10.1371/Journal.Pmed.1002487 |
0.366 |
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| 2018 |
Khan RR, Altmann A, Napolioni V, Kim Y, Guerreiro R, Bras JT, Carmona S, Pereira M, Santana I, Hardy J, Mead S, Cruchaga C, Fernandez MV, Holstege H, Flier WMVd, ... ... Schellenberg GD, et al. P4-240: Stop-Gain Variant In Microglia-Expressed Gene Gmip Is Associated With Early-Onset Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.07.061 |
0.447 |
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| 2018 |
Rajabli F, Hamilton-Nelson KL, Vance JM, Martin ER, Griswold AJ, Schellenberg GD, Haines JL, Farrer LAA, Wang L, Beecham GW, Pericak-Vance MAA. P2-106: African American Whole Exome Sequencing Suggests Risk Coding Variants In Idh1 Gene Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.792 |
0.306 |
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| 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 |
0.386 |
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| 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, ... ... Schellenberg GD, 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 |
0.429 |
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| 2018 |
Kuzma AB, Faber K, Salerno WJ, Leung YY, Cantwell LB, Gupta N, Fulton R, Valladares O, Vogel B, Appelbaum E, Choi SH, Hamilton-Nelson KL, Zhao Y, Muzny D, Qu L, ... ... Schellenberg G, et al. P1-149: The Alzheimer'S Disease Sequencing Project (Adsp) Data Update 2018 Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.152 |
0.382 |
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| 2018 |
Dumitrescu L, Deming Y, Lu Q, Beecham GW, Kunkle BW, Del-Aguila JL, Fernandez MV, Budde JP, Fagan AM, Jager PLD, Albert MS, Moghekar A, Riemenschneider M, Petersen RC, Barnes LL, ... ... Schellenberg GD, et al. P1-139: The Contribution Of Sex-Specific Associations In Genetic Studies Of Alzheimer'S Disease Pathology Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.142 |
0.459 |
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| 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, ... ... Schellenberg G, et al. The Alzheimer's Disease Sequencing Project: Study design and sample selection. Neurology. Genetics. 3: e194. PMID 29184913 DOI: 10.1212/Nxg.0000000000000194 |
0.458 |
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| 2017 |
Tan CH, Fan CC, Mormino EC, Sugrue LP, Broce IJ, Hess CP, Dillon WP, Bonham LW, Yokoyama JS, Karch CM, Brewer JB, Rabinovici GD, Miller BL, Schellenberg GD, Kauppi K, et al. Polygenic hazard score: an enrichment marker for Alzheimer's associated amyloid and tau deposition. Acta Neuropathologica. PMID 29177679 DOI: 10.1007/S00401-017-1789-4 |
0.379 |
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| 2017 |
Gerstenecker A, Roberson ED, Schellenberg GD, Standaert DG, Shprecher DR, Kluger BM, Litvan I. Genetic influences on cognition in progressive supranuclear palsy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29076559 DOI: 10.1002/Mds.27196 |
0.326 |
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| 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, ... ... Schellenberg GD, 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 |
0.45 |
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| 2017 |
Tan CH, Hyman BT, Tan JJX, Hess CP, Dillon WP, Schellenberg GD, Besser LM, Kukull WA, Kauppi K, McEvoy LK, Andreassen OA, Dale AM, Fan CC, Desikan RS. Polygenic hazard scores in preclinical Alzheimer disease. Annals of Neurology. 82: 484-488. PMID 28940650 DOI: 10.1002/Ana.25029 |
0.409 |
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| 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, ... ... Schellenberg GD, et al. Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport. Jama Neurology. PMID 28738127 DOI: 10.1001/Jamaneurol.2017.1518 |
0.46 |
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| 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, ... ... Schellenberg GD, 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 |
0.457 |
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| 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, ... ... Schellenberg GD, 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 |
0.44 |
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| 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, ... ... Schellenberg GD, 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 |
0.461 |
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| 2017 |
Yokoyama JS, Karch CM, Fan CC, Bonham LW, Kouri N, Ross OA, Rademakers R, Kim J, Wang Y, Höglinger GU, Müller U, Ferrari R, Hardy J, Momeni P, ... ... Schellenberg GD, et al. Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia. Acta Neuropathologica. PMID 28271184 DOI: 10.1007/S00401-017-1693-Y |
0.427 |
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| 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, ... ... Schellenberg G, 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 |
0.37 |
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| 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, ... ... Schellenberg G, 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 |
0.467 |
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| 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 |
0.344 |
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| 2017 |
Naj AC, Schellenberg GD. Genomic variants, genes, and pathways of Alzheimer's disease: An overview. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 174: 5-26. PMID 27943641 DOI: 10.1002/Ajmg.B.32499 |
0.472 |
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| 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 |
0.44 |
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| 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 |
0.432 |
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| 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, ... ... Schellenberg GD, 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 |
0.393 |
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| 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 |
0.35 |
|
| 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, ... ... Schellenberg GD, 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 |
0.405 |
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| 2017 |
Valladares O, Kuzma AB, Greenfest-Allen E, Childress DM, Cweibel R, Gangadharan P, Lin H, Qu L, Leung YY, Naj AC, Stoeckert CJ, Schellenberg GD, Wang L. [P3-097]: NIA GENETICS OF ALZHEIMER's DISEASE DATA STORAGE SITE (NIAGADS): 2017 Alzheimer's & Dementia. 13: P971-P971. DOI: 10.1016/J.Jalz.2017.06.1307 |
0.416 |
|
| 2017 |
Kuzma AB, Faber K, Salerno W, Leung YY, Cantwell LB, Feolo M, Stine A, Gupta N, Fulton R, Valladares O, Cweibel R, Appelbaum E, Choi SH, Hamilton-Nelson KL, Lin H, ... ... Schellenberg GD, et al. [P3-090]: THE ALZHEIMER's DISEASE SEQUENCING PROJECT (ADSP) DATA UPDATE 2017 Alzheimer's & Dementia. 13: P968-P968. DOI: 10.1016/J.Jalz.2017.06.1300 |
0.382 |
|
| 2016 |
Guarino PD, Vertrees JE, Asthana S, Sano M, Llorente MD, Pallaki M, Love S, Schellenberg GD, Dysken MW. Measuring informed consent capacity in an Alzheimer's disease clinical trial. Alzheimer's & Dementia (New York, N. Y.). 2: 258-266. PMID 29067313 DOI: 10.1016/J.Trci.2016.09.001 |
0.393 |
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| 2016 |
Chapuis J, Flaig A, Grenier-Boley B, Eysert F, Pottiez V, Deloison G, Vandeputte A, Ayral AM, Mendes T, Desai S, Goate AM, Kauwe JS, Leroux F, Herledan A, Demiautte F, ... ... Schellenberg GD, et al. Genome-wide, high-content siRNA screening identifies the Alzheimer's genetic risk factor FERMT2 as a major modulator of APP metabolism. Acta Neuropathologica. PMID 27933404 DOI: 10.1007/S00401-016-1652-Z |
0.42 |
|
| 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, ... ... Schellenberg GD, 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 |
0.419 |
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| 2016 |
Jakobsdottir J, van der Lee SJ, Bis JC, Chouraki V, Li-Kroeger D, Yamamoto S, Grove ML, Naj A, Vronskaya M, Salazar JL, DeStefano AL, Brody JA, Smith AV, Amin N, Sims R, ... ... Schellenberg GD, et al. Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease. Plos Genetics. 12: e1006327. PMID 27764101 DOI: 10.1371/Journal.Pgen.1006327 |
0.418 |
|
| 2016 |
Bonham LW, Geier EG, Fan CC, Leong JK, Besser L, Kukull WA, Kornak J, Andreassen OA, Schellenberg GD, Rosen HJ, Dillon WP, Hess CP, Miller BL, Dale AM, Desikan RS, et al. Age-dependent effects of APOE ε4 in preclinical Alzheimer's disease. Annals of Clinical and Translational Neurology. 3: 668-677. PMID 27648456 DOI: 10.1002/Acn3.333 |
0.462 |
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| 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, ... ... Schellenberg GD, 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 |
0.464 |
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| 2016 |
Allen M, Burgess JD, Ballard T, Serie D, Wang X, Younkin CS, Sun Z, Kouri N, Baheti S, Wang C, Carrasquillo MM, Nguyen T, Lincoln S, Malphrus K, Murray M, ... ... Schellenberg GD, et al. Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci. Acta Neuropathologica. PMID 27115769 DOI: 10.1007/S00401-016-1576-7 |
0.343 |
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| 2016 |
Yokoyama JS, Wang Y, Schork AJ, Thompson WK, Karch CM, Cruchaga C, McEvoy LK, Witoelar A, Chen CH, Holland D, Brewer JB, Franke A, Dillon WP, Wilson DM, Mukherjee P, ... ... Schellenberg GD, et al. Association Between Genetic Traits for Immune-Mediated Diseases and Alzheimer Disease. Jama Neurology. PMID 27088644 DOI: 10.1001/Jamaneurol.2016.0150 |
0.463 |
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| 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, 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 |
0.473 |
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| 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 |
0.436 |
|
| 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 |
0.461 |
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| 2016 |
Kuzma A, Valladares O, Cweibel R, Greenfest-Allen E, Childress DM, Malamon J, Gangadharan P, Zhao Y, Qu L, Leung YY, Naj AC, Stoeckert CJ, Schellenberg GD, Wang L. NIAGADS: The NIA Genetics of Alzheimer's Disease Data Storage Site Alzheimer's & Dementia. 12: 1200-1203. DOI: 10.1016/J.Jalz.2016.08.018 |
0.444 |
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| 2016 |
Allen M, Wang X, Burgess JD, Nguyen T, Malphrus KG, Nho K, Serie D, Strickland SL, Lincoln S, Carrasquillo MM, Crook JE, Schellenberg GD, Knopman DS, Saykin AJ, Lowe VJ, et al. Blood Gene Expression Changes Implicated In Alzheimer’S Disease Alzheimers & Dementia. 12: 448. DOI: 10.1016/J.Jalz.2016.06.865 |
0.311 |
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| 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 |
0.44 |
|
| 2016 |
Jian X, Bis JC, Kunkle BW, Hamilton KL, Beecham GW, Bush WS, Salerno W, Lancour D, Ma Y, Chen Y, DeStefano AL, Dupuis J, Boerwinkle E, Schellenberg GD, Seshadri S, et al. Rare Deleterious And Loss-Of-Function Variants In Oprl1 And Gas2L2 Contribute To The Risk Of Late-Onset Alzheimer’S Disease: Alzheimer’S Disease Sequencing Project Case-Control Study Alzheimers & Dementia. 12: 163. DOI: 10.1016/J.Jalz.2016.06.765 |
0.376 |
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| 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, ... ... Schellenberg GD, 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 |
0.432 |
|
| 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 |
0.374 |
|
| 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 |
0.357 |
|
| 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 |
0.421 |
|
| 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, 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 |
0.402 |
|
| 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, ... ... Schellenberg GD, 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 |
0.44 |
|
| 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 |
0.439 |
|
| 2016 |
Gangadharan P, Partch AB, Valladares O, Greenfest-Allen E, Childress DM, Cweibel R, Malamon J, Lin H, Zhao Y, Khaladkar M, Naj AC, Stoeckert CJ, Schellenberg GD, Wang L. P3-093: NIA Genetics of Alzheimer’s Disease Data Storage Site (NIAGADS): 2016 Update Alzheimer's & Dementia. 12: P855-P856. DOI: 10.1016/J.Jalz.2016.06.1752 |
0.352 |
|
| 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 |
0.418 |
|
| 2016 |
Amlie-Wolf A, Tang M, King J, Dombroski BA, Wang L, Schellenberg GD. Computational Identification Of Regulatory Mechanisms Affected By Noncoding Variants Associated With Late-Onset Alzheimer'S Disease Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.1288 |
0.428 |
|
| 2015 |
Escott-Price V, Sims R, Bannister C, Harold D, Vronskaya M, Majounie E, Badarinarayan N, Morgan K, Passmore P, Holmes C, Powell J, Brayne C, Gill M, ... ... Schellenberg GD, et al. Common polygenic variation enhances risk prediction for Alzheimer's disease. Brain : a Journal of Neurology. PMID 26490334 DOI: 10.1093/Brain/Awv268 |
0.444 |
|
| 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 |
0.436 |
|
| 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, ... ... Schellenberg GD, 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 |
0.452 |
|
| 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, ... ... Schellenberg GD, 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 |
0.43 |
|
| 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, ... ... Schellenberg GD, 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 |
0.446 |
|
| 2015 |
Kouri N, Ross OA, Dombroski B, Younkin CS, Serie DJ, Soto-Ortolaza A, Baker M, Finch NC, Yoon H, Kim J, Fujioka S, McLean CA, Ghetti B, Spina S, Cantwell LB, ... ... Schellenberg GD, et al. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Nature Communications. 6: 7247. PMID 26077951 DOI: 10.1038/Ncomms8247 |
0.341 |
|
| 2015 |
Wheeler JM, McMillan PJ, Hawk M, Iba M, Robinson L, Xu GJ, Dombroski BA, Jeong D, Dichter MA, Juul H, Loomis E, Raskind M, Leverenz JB, Trojanowski JQ, Lee VM, ... Schellenberg GD, et al. High copy wildtype human 1N4R tau expression promotes early pathological tauopathy accompanied by cognitive deficits without progressive neurofibrillary degeneration. Acta Neuropathologica Communications. 3: 33. PMID 26041339 DOI: 10.1186/S40478-015-0210-6 |
0.389 |
|
| 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, ... ... Schellenberg GD, 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 |
0.442 |
|
| 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, ... ... Schellenberg GD, et al. A novel Alzheimer disease locus located near the gene encoding tau protein. Molecular Psychiatry. PMID 25778476 DOI: 10.1038/Mp.2015.23 |
0.434 |
|
| 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, ... ... Schellenberg GD, 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 |
0.351 |
|
| 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, et al. PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease. Neurology. 84: 972-80. PMID 25663231 DOI: 10.1212/Wnl.0000000000001332 |
0.349 |
|
| 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, ... ... Schellenberg GD, 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 |
0.453 |
|
| 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, ... ... Schellenberg GD, 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 |
0.383 |
|
| 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 |
0.399 |
|
| 2015 |
Wang W, Lin C, Partch AB, Valladares O, Cantwell L, Naj AC, Wang L, Schellenberg GD. Multiple deletion copy number variants (CNVs) are associated with late-onset Alzheimer's disease: The Alzheimer’s disease genetics consortium Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.07.263 |
0.467 |
|
| 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 |
0.37 |
|
| 2015 |
Allen M, Wang X, Younkin CS, Burgess JD, Ballard T, Serie D, Wang C, Sun Z, Baheti S, Carrasquillo MM, Nguyen T, Malphrus KG, Lincoln S, Zou F, Chai H, ... Schellenberg GD, et al. P2-025: Genetic and epigenetic influences on brain gene expression in psp Alzheimer's & Dementia. 11: P490-P491. DOI: 10.1016/J.Jalz.2015.06.561 |
0.305 |
|
| 2015 |
Partch AB, Laufer D, Valladares O, Iodice J, Greenfest-Allen E, Childress DM, Malamon J, Gangadharan P, Arnold SE, Stoeckert CJ, Schellenberg GD, Wang L. P1-061: Nia genetics of Alzheimer's disease data storage site (NIAGADS): 2015 update Alzheimer's & Dementia. 11: P362-P362. DOI: 10.1016/J.Jalz.2015.06.258 |
0.417 |
|
| 2015 |
Tsuang D, Vardarajan BN, Bird TD, Boeve B, Schaid D, Taner N, Allen M, Barral S, Bennett DA, Cruchaga C, Goate A, Graff-Radford N, Faber K, Farlow MR, Foroud TM, ... ... Schellenberg GD, et al. MAPT haplotypes modify the association between head injury and risk of Alzheimer’s disease Alzheimers & Dementia. 11: 361. DOI: 10.1016/J.Jalz.2015.06.256 |
0.311 |
|
| 2015 |
Allen M, Wang X, Serie D, Strickland SL, Burgess JD, Nguyen T, Malphrus KG, Lincoln S, Carrasquillo MM, Crook J, Schellenberg GD, Knopman DS, Lowe VJ, Jack CR, Younkin SG, et al. Exploiting blood transcriptome for gene and pathway identification in Alzheimer's disease Alzheimers & Dementia. 11: 357. DOI: 10.1016/J.Jalz.2015.06.245 |
0.393 |
|
| 2014 |
Warmus BA, Sekar DR, McCutchen E, Schellenberg GD, Roberts RC, McMahon LL, Roberson ED. Tau-mediated NMDA receptor impairment underlies dysfunction of a selectively vulnerable network in a mouse model of frontotemporal dementia. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 16482-95. PMID 25471585 DOI: 10.1523/Jneurosci.3418-14.2014 |
0.312 |
|
| 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, ... ... Schellenberg GD, 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 |
0.423 |
|
| 2014 |
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, ... ... Schellenberg GD, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/Nature13772 |
0.302 |
|
| 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, ... ... Schellenberg GD, 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 |
0.415 |
|
| 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, ... ... Schellenberg GD, 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 |
0.441 |
|
| 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, ... ... Schellenberg GD, 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 |
0.47 |
|
| 2014 |
Samocha KE, Robinson EB, Sanders SJ, Stevens C, Sabo A, McGrath LM, Kosmicki JA, Rehnström K, Mallick S, Kirby A, Wall DP, MacArthur DG, Gabriel SB, DePristo M, Purcell SM, ... ... Schellenberg GD, et al. A framework for the interpretation of de novo mutation in human disease. Nature Genetics. 46: 944-50. PMID 25086666 DOI: 10.1038/Ng.3050 |
0.335 |
|
| 2014 |
Sud R, Geller ET, Schellenberg GD. Antisense-mediated Exon Skipping Decreases Tau Protein Expression: A Potential Therapy For Tauopathies. Molecular Therapy. Nucleic Acids. 3: e180. PMID 25072694 DOI: 10.1038/Mtna.2014.30 |
0.385 |
|
| 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 |
0.478 |
|
| 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, ... ... Schellenberg GD, 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 |
0.465 |
|
| 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, ... ... Schellenberg GD, 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 |
0.413 |
|
| 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, ... ... Schellenberg GD, 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 |
0.332 |
|
| 2014 |
Carayol J, Schellenberg GD, Dombroski B, Amiet C, Génin B, Fontaine K, Rousseau F, Vazart C, Cohen D, Frazier TW, Hardan AY, Dawson G, Rio Frio T. A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism. Frontiers in Genetics. 5: 33. PMID 24600472 DOI: 10.3389/Fgene.2014.00033 |
0.355 |
|
| 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, ... ... Schellenberg GD, 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 |
0.437 |
|
| 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, ... ... Schellenberg GD, 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 |
0.481 |
|
| 2014 |
Dysken MW, Sano M, Asthana S, Vertrees JE, Pallaki M, Llorente M, Love S, Schellenberg GD, McCarten JR, Malphurs J, Prieto S, Chen P, Loreck DJ, Trapp G, Bakshi RS, et al. Effect of vitamin E and memantine on functional decline in Alzheimer disease: the TEAM-AD VA cooperative randomized trial. Jama. 311: 33-44. PMID 24381967 DOI: 10.1001/Jama.2013.282834 |
0.328 |
|
| 2014 |
McMillan CT, Toledo JB, Avants BB, Cook PA, Wood EM, Suh E, Irwin DJ, Powers J, Olm C, Elman L, McCluskey L, Schellenberg GD, Lee VM, Trojanowski JQ, Van Deerlin VM, et al. Genetic and neuroanatomic associations in sporadic frontotemporal lobar degeneration. Neurobiology of Aging. 35: 1473-82. PMID 24373676 DOI: 10.1016/J.Neurobiolaging.2013.11.029 |
0.381 |
|
| 2014 |
Borenstein AR, Wu Y, Bowen JD, McCormick WC, Uomoto J, McCurry SM, Schellenberg GD, Larson EB. Incidence rates of dementia, Alzheimer disease, and vascular dementia in the Japanese American population in Seattle, WA: the Kame Project. Alzheimer Disease and Associated Disorders. 28: 23-9. PMID 24045327 DOI: 10.1097/Wad.0B013E3182A2E32F |
0.376 |
|
| 2014 |
Toledo JB, Van Deerlin VM, Lee EB, Suh E, Baek Y, Robinson JL, Xie SX, McBride J, Wood EM, Schuck T, Irwin DJ, Gross RG, Hurtig H, McCluskey L, Elman L, ... ... Schellenberg G, et al. A platform for discovery: The University of Pennsylvania Integrated Neurodegenerative Disease Biobank. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 477-84.e1. PMID 23978324 DOI: 10.1016/J.Jalz.2013.06.003 |
0.328 |
|
| 2014 |
Dysken MW, Guarino PD, Vertrees JE, Asthana S, Sano M, Llorente M, Pallaki M, Love S, Schellenberg GD, McCarten JR, Malphurs J, Prieto S, Chen P, Loreck DJ, Carney S, et al. Vitamin E and memantine in Alzheimer's disease: clinical trial methods and baseline data. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 36-44. PMID 23583234 DOI: 10.1016/J.Jalz.2013.01.014 |
0.362 |
|
| 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 |
0.47 |
|
| 2014 |
Reitz C, Cheng R, Kunkle BW, Beecham G, Pericak-Vance MA, Farrer LA, Haines J, Schellenberg GD, Mayeux R. P1-054: LINKAGE ANALYSES OF EXTENDED CARIBBEAN HISPANIC FAMILIES INDICATES NOVEL LOCI ASSOCIATED WITH FAMILIAL LATE-ONSET ALZHEIMER'S DISEASE Alzheimer's & Dementia. 10: P323-P323. DOI: 10.1016/J.Jalz.2014.05.290 |
0.384 |
|
| 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 |
0.433 |
|
| 2014 |
Sud R, Dombroski B, Vrettos N, Schellenberg GD. Zinc-Finger Nuclease-Induced Targeted Deletion Reveals Existence Of An Enhancer Element Within The Microtubule-Associated Protein Tau (Mapt) Gene Alzheimers & Dementia. 10: 788. DOI: 10.1016/J.Jalz.2014.05.1527 |
0.302 |
|
| 2014 |
Wang L, Wang L, Valladares O, Childress DM, Partch A, Laufer D, Iodice J, Lawrence C, Hu T, Malamon J, Tang M, Lin C, Arnold SE, Stoeckert CJ, Schellenberg GD. P3-020: NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITE (NIAGADS): 2014 UPDATE Alzheimer's & Dementia. 10: P634-P635. DOI: 10.1016/J.Jalz.2014.05.1107 |
0.401 |
|
| 2014 |
Holmans P, Bellenguez C, Wang L, Schellenberg GD, Seshadri S, Amouyel P, Williams J, Jones L. O4-04-01: GENE EXPRESSION NETWORK ANALYSIS IMPLICATES THE IMMUNE RESPONSE IN GENETIC SUSCEPTIBILITY TO LATE-ONSET AD Alzheimer's & Dementia. 10: P256-P256. DOI: 10.1016/J.Jalz.2014.04.402 |
0.337 |
|
| 2014 |
Dourlen P, Dermaut B, Grenier-Boley B, Bellenguez C, Dupont C, Abdelfettah F, Schellenberg GD, Lambert J, Williams J, Amouyel P, Seshadri S. Functional Validation Of Novel Alzheimer Genetic Risk Loci Using Drosophila Alzheimers & Dementia. 10: 246. DOI: 10.1016/J.Jalz.2014.04.376 |
0.377 |
|
| 2014 |
Lee SJvd, Naj A, Duijn Cv, Schellenberg GD, Jakobsdottir J, Williams J, Wang L, Vronskaya M, Amouyel P, Sims R, Seshadri S. Exome Chip Meta-Analysis Of Alzheimer'S Disease In The Igap Consortium Alzheimers & Dementia. 10: 245. DOI: 10.1016/J.Jalz.2014.04.374 |
0.427 |
|
| 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, ... Schellenberg GD, 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 |
0.438 |
|
| 2013 |
Stutzbach LD, Xie SX, Naj AC, Albin R, Gilman S, Lee VM, Trojanowski JQ, Devlin B, Schellenberg GD. The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease. Acta Neuropathologica Communications. 1: 31. PMID 24252572 DOI: 10.1186/2051-5960-1-31 |
0.436 |
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| 2013 |
Kalimo H, Lalowski M, Bogdanovic N, Philipson O, Bird TD, Nochlin D, Schellenberg GD, Brundin R, Olofsson T, Soliymani R, Baumann M, Wirths O, Bayer TA, Nilsson LN, Basun H, et al. The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated Aβ. Acta Neuropathologica Communications. 1: 60. PMID 24252272 DOI: 10.1186/2051-5960-1-60 |
0.436 |
|
| 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, ... ... Schellenberg GD, 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 |
0.46 |
|
| 2013 |
He X, Sanders SJ, Liu L, De Rubeis S, Lim ET, Sutcliffe JS, Schellenberg GD, Gibbs RA, Daly MJ, Buxbaum JD, State MW, Devlin B, Roeder K. Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. Plos Genetics. 9: e1003671. PMID 23966865 DOI: 10.1371/Journal.Pgen.1003671 |
0.373 |
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| 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 |
0.438 |
|
| 2013 |
Liu L, Sabo A, Neale BM, Nagaswamy U, Stevens C, Lim E, Bodea CA, Muzny D, Reid JG, Banks E, Coon H, Depristo M, Dinh H, Fennel T, Flannick J, ... ... Schellenberg GD, et al. Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. Plos Genetics. 9: e1003443. PMID 23593035 DOI: 10.1371/Journal.Pgen.1003443 |
0.323 |
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| 2013 |
Dombroski BA, Galasko DR, Mata IF, Zabetian CP, Craig UK, Garruto RM, Oyanagi K, Schellenberg GD. C9orf72 hexanucleotide repeat expansion and Guam amyotrophic lateral sclerosis-Parkinsonism-dementia complex. Jama Neurology. 70: 742-5. PMID 23588498 DOI: 10.1001/Jamaneurol.2013.1817 |
0.302 |
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| 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, ... ... Schellenberg GD, 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 |
0.491 |
|
| 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, ... ... Schellenberg GD, 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 |
0.413 |
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| 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, ... ... Schellenberg GD, 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 |
0.442 |
|
| 2013 |
Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Trojanowski JQ, Weintraub D, Chen-Plotkin AS, ... ... Schellenberg GD, et al. APOE ε4 increases risk for dementia in pure synucleinopathies. Jama Neurology. 70: 223-8. PMID 23407718 DOI: 10.1001/Jamaneurol.2013.600 |
0.418 |
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| 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 |
0.443 |
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| 2013 |
Zhao W, Marchani EE, Cheung CY, Steinbart EJ, Schellenberg GD, Bird TD, Wijsman EM. Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 201-12. PMID 23355194 DOI: 10.1002/Ajmg.B.32133 |
0.433 |
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| 2013 |
Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, MacArthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, ... ... Schellenberg GD, et al. Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron. 77: 235-42. PMID 23352160 DOI: 10.1016/J.Neuron.2012.12.029 |
0.317 |
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| 2013 |
Borenstein A, Wu Y, Mortimer J, Bowen J, McCormick W, McCurry S, Schellenberg G, Larson E. P3-172: The association between diabetes and dementia/Alzheimer's disease is modified by age: The Kame Project Alzheimer's & Dementia. 9: P616-P616. DOI: 10.1016/J.Jalz.2013.05.1244 |
0.383 |
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| 2013 |
Ryvkin P, Leung YY, Dragomir I, Schuck T, Schellenberg G, Arnold S, Chen-Plotkin A, Van Deerlin V, Lee V, Trojanowski J, Gregory B, Wang L. P3-064: Characterizing the Alzheimer's disease prefrontal cortex transcriptome by multiple RNA-sequencing Alzheimer's & Dementia. 9: P574-P574. DOI: 10.1016/J.Jalz.2013.05.1134 |
0.333 |
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| 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 |
0.301 |
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| 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 |
0.438 |
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| 2013 |
Lin C, Valladares O, Childress M, Partch A, Laufer D, Iodice J, Stoeckert C, Schellenberg G, Wang L. P3-018: NIA genetics of Alzheimer's disease data storage site (NIAGADS): 2013 update Alzheimer's & Dementia. 9: P556-P556. DOI: 10.1016/J.Jalz.2013.05.1087 |
0.417 |
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| 2013 |
Mukherjee S, Thornton T, Naj A, Kim S, Kauwe J, Fardo D, Valladares O, Wijsman E, Schellenberg G, Crane P. GWAS of the joint ADGC data set identifies novel common variants associated with late-onset Alzheimer's disease Alzheimers & Dementia. 9: 550. DOI: 10.1016/J.Jalz.2013.05.1071 |
0.428 |
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| 2013 |
Mukherjee S, Walter S, Yang H, Jarvik G, Crosslin D, Lee S, Fardo D, Green R, Sherva R, Walker R, Larson E, Schellenberg G, Glymour M, Crane P. Vascular disease, vascular risk factors and risk of late-onset Alzheimer's disease: Mendelian randomization analyses in the combined ADGC dataset Alzheimers & Dementia. 9: 694. DOI: 10.1016/J.Jalz.2013.04.370 |
0.375 |
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| 2013 |
Beecham G, Hamilton-Nelson K, Naj A, Wang L, Martin E, Mayeux R, Haines J, Farrer L, Schellenberg G, Pericak-Vance M, Montine T. O4-06-04: Late-onset Alzheimer's disease neuropathology genomic screen identifies novel loci for neuritic plaque and other Alzheimer's neuropathology features Alzheimer's & Dementia. 9: P693-P693. DOI: 10.1016/J.Jalz.2013.04.368 |
0.421 |
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| 2013 |
Kohli M, Kunkle B, Naj A, Carney RM, Hamilton-Nelson K, Rolati S, Whitehead PL, Gilbert J, Martin E, Beecham G, Wang L, Mayeux R, Haines J, Farrer L, Schellenberg G, et al. The identification of rare variants in late-onset Alzheimer’s disease using extended families Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.04.239 |
0.378 |
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| 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 |
0.382 |
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| 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, ... ... Schellenberg GD, 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 |
0.336 |
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| 2012 |
Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Kukull W, Nelson PT, Jicha GA, ... ... Schellenberg GD, et al. GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology. Neurology. 79: 1944-50. PMID 23035075 DOI: 10.1212/Wnl.0B013E3182735E9A |
0.441 |
|
| 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 |
0.471 |
|
| 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, ... ... Schellenberg GD, 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 |
0.375 |
|
| 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, ... ... Schellenberg GD, 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, ... ... Schellenberg GD, 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 |
0.459 |
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| 2012 |
Schellenberg GD, Montine TJ. The genetics and neuropathology of Alzheimer's disease. Acta Neuropathologica. 124: 305-23. PMID 22618995 DOI: 10.1007/S00401-012-0996-2 |
0.47 |
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| 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, ... ... Schellenberg GD, 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 |
0.472 |
|
| 2012 |
Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, Polak P, Yoon S, Maguire J, Crawford EL, Campbell NG, ... ... Schellenberg GD, et al. Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature. 485: 242-5. PMID 22495311 DOI: 10.1038/Nature11011 |
0.348 |
|
| 2012 |
Majounie E, Renton AE, Mok K, Dopper EG, Waite A, Rollinson S, Chiò A, Restagno G, Nicolaou N, Simon-Sanchez J, van Swieten JC, Abramzon Y, Johnson JO, Sendtner M, Pamphlett R, ... ... Schellenberg GD, et al. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. The Lancet. Neurology. 11: 323-30. PMID 22406228 DOI: 10.1016/S1474-4422(12)70043-1 |
0.359 |
|
| 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, ... ... Schellenberg GD, 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 |
0.359 |
|
| 2012 |
Igap, Schellenberg GD. International Genomics of Alzheimer's Disease Project (IGAP) genome-wide association study Alzheimers & Dementia. 8: 101. DOI: 10.1016/J.Jalz.2012.05.254 |
0.364 |
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| 2012 |
Reitz C, Manly J, Hall KS, Evans D, Bennett D, Buxbaum J, Ertekin-Taner N, Fallin D, Kamboh I, Foroud T, Goate A, Farrer L, Pericak-Vance M, Haines J, Mayeux R, ... Schellenberg G, et al. CTNNA3, CAPRIN2 and SPG20 are significantly associated with Alzheimer's disease in preliminary analyses of a genome-wide association study in African-Americans Alzheimers & Dementia. 8: 100. DOI: 10.1016/J.Jalz.2012.05.251 |
0.401 |
|
| 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 |
0.464 |
|
| 2012 |
Ertekin-Taner N, Allen M, Murray M, Crook J, Serie D, Zou F, Chai HS, Younkin C, Pankratz V, Carrasquillo M, Rowley C, Nair A, Middha S, Maharjan S, Nguyen T, ... ... Schellenberg G, et al. O5-03-03: Genetic association of progressive supranuclear palsy (PSP) risk loci variants with brain gene expression and neuropathology endophenotypes Alzheimer's & Dementia. 8: P735-P735. DOI: 10.1016/J.Jalz.2012.05.1983 |
0.35 |
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| 2012 |
Wang L, Valladares O, Lin C, Cantwell L, Foroud T, Schellenberg G. P4-116: The NIA Genetics of Alzheimer's Disease Data Storage Site (NIAGADS) Alzheimer's & Dementia. 8: P672-P672. DOI: 10.1016/J.Jalz.2012.05.1819 |
0.416 |
|
| 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 |
0.45 |
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| 2012 |
Lin C, Valladares O, Dombroski B, Wang L, Schellenberg G. Duplications in chr15q11 are associated with late-onset Alzheimer's disease in the Caucasian population Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1796 |
0.416 |
|
| 2012 |
Stutzbach L, Hawk M, Gilman S, Lee V, Trojanowski J, Schellenberg G. ER stress in Alzheimer's disease and PSP: Common disease mechanism? Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1234 |
0.37 |
|
| 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, ... ... Schellenberg G, 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 |
0.447 |
|
| 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 |
0.327 |
|
| 2011 |
Carayol J, Schellenberg GD, Dombroski B, Genin E, Rousseau F, Dawson G. Autism risk assessment in siblings of affected children using sex-specific genetic scores. Molecular Autism. 2: 17. PMID 22017886 DOI: 10.1186/2040-2392-2-17 |
0.306 |
|
| 2011 |
McMillan PJ, Kraemer BC, Robinson L, Leverenz JB, Raskind M, Schellenberg G. Truncation of tau at E391 promotes early pathologic changes in transgenic mice. Journal of Neuropathology and Experimental Neurology. 70: 1006-19. PMID 22002427 DOI: 10.1097/Nen.0B013E31823557Fb |
0.366 |
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| 2011 |
Höglinger GU, Melhem NM, Dickson DW, Sleiman PM, Wang LS, Klei L, Rademakers R, de Silva R, Litvan I, Riley DE, van Swieten JC, Heutink P, Wszolek ZK, Uitti RJ, Vandrovcova J, ... ... Schellenberg GD, et al. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Nature Genetics. 43: 699-705. PMID 21685912 DOI: 10.1038/Ng.859 |
0.434 |
|
| 2011 |
Chen-Plotkin AS, Martinez-Lage M, Sleiman PM, Hu W, Greene R, Wood EM, Bing S, Grossman M, Schellenberg GD, Hatanpaa KJ, Weiner MF, White CL, Brooks WS, Halliday GM, Kril JJ, et al. Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration. Archives of Neurology. 68: 488-97. PMID 21482928 DOI: 10.1001/Archneurol.2011.53 |
0.325 |
|
| 2011 |
Kohen R, Shofer JB, Korvatska O, Petrie EC, Wang LY, Schellenberg GD, Peskind ER, Wilkinson CW. ABCB1 genotype and CSF beta-amyloid in Alzheimer disease. Journal of Geriatric Psychiatry and Neurology. 24: 63-6. PMID 21478475 DOI: 10.1177/0891988711402325 |
0.434 |
|
| 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, ... ... Schellenberg GD, 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 |
0.32 |
|
| 2011 |
Korvatska O, Estes A, Munson J, Dawson G, Bekris LM, Kohen R, Yu CE, Schellenberg GD, Raskind WH. Mutations in the TSGA14 gene in families with autism spectrum disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 303-11. PMID 21438139 DOI: 10.1002/Ajmg.B.31162 |
0.364 |
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| 2011 |
Jayadev S, Nochlin D, Poorkaj P, Steinbart EJ, Mastrianni JA, Montine TJ, Ghetti B, Schellenberg GD, Bird TD, Leverenz JB. Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype. Annals of Neurology. 69: 712-20. PMID 21416485 DOI: 10.1002/Ana.22264 |
0.451 |
|
| 2011 |
Bekris LM, Galloway NM, Millard S, Lockhart D, Li G, Galasko DR, Farlow MR, Clark CM, Quinn JF, Kaye JA, Schellenberg GD, Leverenz JB, Seubert P, Tsuang DW, Peskind ER, et al. Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease. Neurobiology of Aging. 32: 556.e13-23. PMID 21196064 DOI: 10.1016/J.Neurobiolaging.2010.10.020 |
0.435 |
|
| 2011 |
Chapman NH, Estes A, Munson J, Bernier R, Webb SJ, Rothstein JH, Minshew NJ, Dawson G, Schellenberg GD, Wijsman EM. Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16. Human Genetics. 129: 59-70. PMID 20963441 DOI: 10.1007/S00439-010-0899-Z |
0.334 |
|
| 2011 |
Sud R, Geller E, Schellenberg G. Decline in tau levels from antisense oligo treatment: A potential curative mechanism for Alzheimer's disease Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.09.136 |
0.39 |
|
| 2011 |
Wang L, Lin C, Schellenberg G. Distribution of copy number variations in Alzheimer's disease Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.554 |
0.395 |
|
| 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 |
0.405 |
|
| 2011 |
Wang L, Lin C, Schellenberg G. CNV analysis of Alzheimer's disease GWAS results Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.203 |
0.442 |
|
| 2010 |
Han MR, Schellenberg GD, Wang LS. Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study. Bmc Neurology. 10: 90. PMID 20932310 DOI: 10.1186/1471-2377-10-90 |
0.449 |
|
| 2010 |
Kay DM, Stevens CF, Hamza TH, Montimurro JS, Zabetian CP, Factor SA, Samii A, Griffith A, Roberts JW, Molho ES, Higgins DS, Gancher S, Moses L, Zareparsi S, Poorkaj P, ... ... Schellenberg GD, et al. A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2. Neurology. 75: 1189-94. PMID 20876472 DOI: 10.1212/Wnl.0B013E3181F4D832 |
0.323 |
|
| 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, ... ... Schellenberg GD, 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 |
0.418 |
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| 2010 |
Wang K, Bucan M, Grant SF, Schellenberg G, Hakonarson H. Strategies for genetic studies of complex diseases. Cell. 142: 351-3; author reply . PMID 20691891 DOI: 10.1016/J.Cell.2010.07.025 |
0.378 |
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| 2010 |
Carayol J, Schellenberg GD, Tores F, Hager J, Ziegler A, Dawson G. Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk. Molecular Autism. 1: 4. PMID 20678243 DOI: 10.1186/2040-2392-1-4 |
0.368 |
|
| 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, ... ... Schellenberg GD, 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 |
0.378 |
|
| 2010 |
Melrose HL, Dächsel JC, Behrouz B, Lincoln SJ, Yue M, Hinkle KM, Kent CB, Korvatska E, Taylor JP, Witten L, Liang YQ, Beevers JE, Boules M, Dugger BN, Serna VA, ... ... Schellenberg GD, et al. Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice. Neurobiology of Disease. 40: 503-17. PMID 20659558 DOI: 10.1016/J.Nbd.2010.07.010 |
0.305 |
|
| 2010 |
Li G, Shofer JB, Rhew IC, Kukull WA, Peskind ER, McCormick W, Bowen JD, Schellenberg GD, Crane PK, Breitner JC, Larson EB. Age-varying association between statin use and incident Alzheimer's disease. Journal of the American Geriatrics Society. 58: 1311-7. PMID 20533968 DOI: 10.1111/J.1532-5415.2010.02906.X |
0.426 |
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| 2010 |
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... ... Schellenberg GD, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/Nature09146 |
0.332 |
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| 2010 |
Marchani EE, Bird TD, Steinbart EJ, Rosenthal E, Yu CE, Schellenberg GD, Wijsman EM. Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1031-41. PMID 20333730 DOI: 10.1002/Ajmg.B.31072 |
0.401 |
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| 2010 |
Trojanowski JQ, Arnold SE, Karlawish JH, Brunden K, Cary M, Davatzikos C, Detre J, Gaulton G, Grossman M, Hurtig H, Jedrziewski K, McCluskey L, Naylor M, Polsky D, Schellenberg GD, et al. Design of comprehensive Alzheimer's disease centers to address unmet national needs. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 6: 150-5. PMID 20298979 DOI: 10.1016/J.Jalz.2009.11.004 |
0.397 |
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| 2010 |
Khachaturian ZS, Barnes D, Einstein R, Johnson S, Lee V, Roses A, Sager MA, Shankle WR, Snyder PJ, Petersen RC, Schellenberg G, Trojanowski J, Aisen P, Albert MS, Breitner JC, et al. Developing a national strategy to prevent dementia: Leon Thal Symposium 2009. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 6: 89-97. PMID 20298968 DOI: 10.1016/J.Jalz.2010.01.008 |
0.383 |
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| 2010 |
Van Deerlin VM, Sleiman PM, Martinez-Lage M, Chen-Plotkin A, Wang LS, Graff-Radford NR, Dickson DW, Rademakers R, Boeve BF, Grossman M, Arnold SE, Mann DM, Pickering-Brown SM, Seelaar H, Heutink P, ... ... Schellenberg GD, et al. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nature Genetics. 42: 234-9. PMID 20154673 DOI: 10.1038/Ng.536 |
0.415 |
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| 2010 |
Borenstein AR, Mortimer JA, Ding Ding, Schellenberg GD, DeCarli C, Qianhua Zhao, Copenhaver C, Qihao Guo, Shugang Chu, Galasko D, Salmon DP, Qi Dai, Yougui Wu, Petersen R, Zhen Hong. Effects of apolipoprotein E-epsilon4 and -epsilon2 in amnestic mild cognitive impairment and dementia in Shanghai: SCOBHI-P. American Journal of Alzheimer's Disease and Other Dementias. 25: 233-8. PMID 20142627 DOI: 10.1177/1533317509357736 |
0.344 |
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| 2010 |
Yu CE, Bird TD, Bekris LM, Montine TJ, Leverenz JB, Steinbart E, Galloway NM, Feldman H, Woltjer R, Miller CA, Wood EM, Grossman M, McCluskey L, Clark CM, Neumann M, ... ... Schellenberg GD, et al. The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration. Archives of Neurology. 67: 161-70. PMID 20142524 DOI: 10.1001/Archneurol.2009.328 |
0.333 |
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| 2010 |
Payami H, Kay DM, Zabetian CP, Schellenberg GD, Factor SA, McCulloch CC. Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease. Genetic Epidemiology. 34: 92-9. PMID 19582778 DOI: 10.1002/Gepi.20439 |
0.343 |
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| 2010 |
Bekris LM, Galloway NM, Montine TJ, Schellenberg GD, Yu CE. APOE mRNA and protein expression in postmortem brain are modulated by an extended haplotype structure. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 409-17. PMID 19554612 DOI: 10.1002/Ajmg.B.30993 |
0.436 |
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| 2010 |
Maestrini E, Pagnamenta AT, Lamb JA, Bacchelli E, Sykes NH, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri TS, Minopoli F, Reichert J, Cai G, Buxbaum JD, ... ... Schellenberg GD, et al. High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. Molecular Psychiatry. 15: 954-68. PMID 19401682 DOI: 10.1038/Mp.2009.34 |
0.373 |
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| 2010 |
Bekris LM, Galloway N, Li G, Galasko DR, DeCarli C, Farlow MR, Clark CM, Quinn JF, Kaye JA, Schellenberg GD, Leverenz JB, Seubert P, Tsuang DW, Peskind ER, Yu CE. P1-056: Genetic variation within APP processing genes correlates with cerebrospinal fluid APP cleavage product levels in Alzheimer patients and cognitively normal subjects Alzheimer's & Dementia. 6: S189-S190. DOI: 10.1016/J.Jalz.2010.05.604 |
0.346 |
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| 2010 |
Schellenberg GD, Höglinger G, Sleiman P, Rademakers R, Kei L, Silva Rd, Wang L, Yu C, Heutink P, Swieten Jv, Farrer M, Hardy J, Lees A, Devlin B, Hakonarson H, et al. A genome-wide association study of progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.254 |
0.301 |
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| 2009 |
Sieh W, Choi Y, Chapman NH, Craig UK, Steinbart EJ, Rothstein JH, Oyanagi K, Garruto RM, Bird TD, Galasko DR, Schellenberg GD, Wijsman EM. Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates. Human Molecular Genetics. 18: 3725-38. PMID 19567404 DOI: 10.1093/Hmg/Ddp300 |
0.397 |
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| 2009 |
Khachaturian ZS, Camà J, Andrieu S, Avila J, Boada Rovira M, Breteler M, Froelich L, Gauthier S, Gómez-Isla T, Khachaturian AS, Kuller LH, Larson EB, Lopez OL, Martinez-Lage JM, Petersen RC, ... Schellenberg GD, et al. Creating a transatlantic research enterprise for preventing Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 5: 361-6. PMID 19560106 DOI: 10.1016/J.Jalz.2009.05.158 |
0.324 |
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| 2009 |
Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, ... ... Schellenberg GD, et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. Plos Genetics. 5: e1000536. PMID 19557195 DOI: 10.1371/Journal.Pgen.1000536 |
0.382 |
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| 2009 |
Petrie EC, Cross DJ, Galasko D, Schellenberg GD, Raskind MA, Peskind ER, Minoshima S. Preclinical evidence of Alzheimer changes: convergent cerebrospinal fluid biomarker and fluorodeoxyglucose positron emission tomography findings. Archives of Neurology. 66: 632-7. PMID 19433663 DOI: 10.1001/Archneurol.2009.59 |
0.316 |
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| 2009 |
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, ... ... Schellenberg GD, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 459: 569-73. PMID 19404257 DOI: 10.1038/Nature07953 |
0.359 |
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| 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, ... ... Schellenberg GD, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999 |
0.351 |
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| 2009 |
Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards KL, Schellenberg GD, Tsuang DW, Yearout D, et al. LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1034-41. PMID 19343804 DOI: 10.1002/Mds.22514 |
0.351 |
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| 2009 |
Guthrie CR, Schellenberg GD, Kraemer BC. SUT-2 potentiates tau-induced neurotoxicity in Caenorhabditis elegans. Human Molecular Genetics. 18: 1825-38. PMID 19273536 DOI: 10.1093/Hmg/Ddp099 |
0.338 |
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| 2009 |
Little DM, Crooks VC, Petitti DB, Chiu V, Schellenberg GD, Slezak JM, Jacobsen SJ. Mortality, dementia, and apolipoprotein E genotype in elderly white women in the United States. Journal of the American Geriatrics Society. 57: 231-6. PMID 19207139 DOI: 10.1111/J.1532-5415.2008.02113.X |
0.326 |
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| 2008 |
McMillan P, Korvatska E, Poorkaj P, Evstafjeva Z, Robinson L, Greenup L, Leverenz J, Schellenberg GD, D'Souza I. Tau isoform regulation is region- and cell-specific in mouse brain. The Journal of Comparative Neurology. 511: 788-803. PMID 18925637 DOI: 10.1002/Cne.21867 |
0.309 |
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| 2008 |
Winton MJ, Van Deerlin VM, Kwong LK, Yuan W, Wood EM, Yu CE, Schellenberg GD, Rademakers R, Caselli R, Karydas A, Trojanowski JQ, Miller BL, Lee VM. A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro. Febs Letters. 582: 2252-6. PMID 18505686 DOI: 10.1016/J.Febslet.2008.05.024 |
0.354 |
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| 2008 |
Bekris LM, Millard SP, Galloway NM, Vuletic S, Albers JJ, Li G, Galasko DR, DeCarli C, Farlow MR, Clark CM, Quinn JF, Kaye JA, Schellenberg GD, Tsuang D, Peskind ER, et al. Multiple SNPs within and surrounding the apolipoprotein E gene influence cerebrospinal fluid apolipoprotein E protein levels. Journal of Alzheimer's Disease : Jad. 13: 255-66. PMID 18430993 DOI: 10.3233/Jad-2008-13303 |
0.417 |
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| 2008 |
Basun H, Bogdanovic N, Ingelsson M, Almkvist O, Näslund J, Axelman K, Bird TD, Nochlin D, Schellenberg GD, Wahlund LO, Lannfelt L. Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease. Archives of Neurology. 65: 499-505. PMID 18413473 DOI: 10.1001/Archneur.65.4.499 |
0.367 |
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| 2008 |
Van Deerlin VM, Leverenz JB, Bekris LM, Bird TD, Yuan W, Elman LB, Clay D, Wood EM, Chen-Plotkin AS, Martinez-Lage M, Steinbart E, McCluskey L, Grossman M, Neumann M, Wu IL, ... ... Schellenberg GD, et al. TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. The Lancet. Neurology. 7: 409-16. PMID 18396105 DOI: 10.1016/S1474-4422(08)70071-1 |
0.331 |
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| 2008 |
Mata IF, Samii A, Schneer SH, Roberts JW, Griffith A, Leis BC, Schellenberg GD, Sidransky E, Bird TD, Leverenz JB, Tsuang D, Zabetian CP. Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders. Archives of Neurology. 65: 379-82. PMID 18332251 DOI: 10.1001/Archneurol.2007.68 |
0.347 |
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| 2008 |
Jayadev S, Steinbart EJ, Chi YY, Kukull WA, Schellenberg GD, Bird TD. Conjugal Alzheimer disease: risk in children when both parents have Alzheimer disease. Archives of Neurology. 65: 373-8. PMID 18332250 DOI: 10.1001/Archneurol.2007.61 |
0.386 |
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| 2008 |
Crawford DC, Nord AS, Badzioch MD, Ranchalis J, McKinstry LA, Ahearn M, Bertucci C, Shephard C, Wong M, Rieder MJ, Schellenberg GD, Nickerson DA, Heagerty PJ, Wijsman EM, Jarvik GP. A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk. Journal of Lipid Research. 49: 588-96. PMID 18056683 DOI: 10.1194/Jlr.M700409-Jlr200 |
0.365 |
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| 2008 |
Brune CW, Korvatska E, Allen-Brady K, Cook EH, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon H. Heterogeneous association between engrailed-2 and autism in the CPEA network. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 187-93. PMID 17948868 DOI: 10.1002/Ajmg.B.30585 |
0.325 |
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| 2008 |
Borghesani PR, Johnson LC, Shelton AL, Peskind ER, Aylward EH, Schellenberg GD, Cherrier MM. Altered medial temporal lobe responses during visuospatial encoding in healthy APOE*4 carriers. Neurobiology of Aging. 29: 981-91. PMID 17350142 DOI: 10.1016/J.Neurobiolaging.2007.01.012 |
0.358 |
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| 2008 |
Dysken M, Guarino P, Love SB, Asthana S, Sano M, Llorente M, Vertrees J, Vatassery G, Schellenberg G, Tomaska J. P4-363: A randomized clinical trial of vitamin E and memantine in Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.2434 |
0.334 |
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| 2008 |
Wijsman EM, Choi Y, Steinbart EJ, Bird TD, Schellenberg GD. P3-272: Genome scan for age-at-onset loci in the National Institutes of Mental Health Alzheimer's disease sample Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1840 |
0.371 |
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| 2008 |
Raskind MA, Petrie EC, Wilkinson CW, Li G, Chi P, Galasko DR, Quinn JF, Kaye JA, Clark CM, Farlow MR, DeCarli C, Wang LY, Leverenz JB, Schellenberg GD, Peskind ER. P3-090: Cerebrospinal fluid norepinephrine increases with aging, Alzheimers disease and APOE4 genotype Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1654 |
0.4 |
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| 2008 |
Li G, Galasko DR, Quinn JF, Kaye JA, Clark CM, Farlow MR, DeCarli C, Raskind MA, Petrie EC, Leverenz J, Shofer JB, Schellenberg GD, Cottrell B, Peskind ER. P3-085: Age- and APOE-related cerebrospinal fluid Alzheimer's disease biomarker changes in normal controls Alzheimer's & Dementia. 4: T542-T543. DOI: 10.1016/J.Jalz.2008.05.1649 |
0.381 |
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| 2007 |
Brickell KL, Leverenz JB, Steinbart EJ, Rumbaugh M, Schellenberg GD, Nochlin D, Lampe TH, Holm IE, Van Deerlin V, Yuan W, Bird TD. Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 1050-5. PMID 17615170 DOI: 10.1136/Jnnp.2006.113803 |
0.352 |
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| 2007 |
Kraemer BC, Schellenberg GD. SUT-1 enables tau-induced neurotoxicity in C. elegans. Human Molecular Genetics. 16: 1959-71. PMID 17576746 DOI: 10.1093/Hmg/Ddm143 |
0.35 |
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| 2007 |
Galasko D, Salmon D, Gamst A, Olichney J, Thal LJ, Silbert L, Kaye J, Brooks P, Adonay R, Craig UK, Schellenberg G, Borenstein AR. Prevalence of dementia in Chamorros on Guam: relationship to age, gender, education, and APOE. Neurology. 68: 1772-81. PMID 17515539 DOI: 10.1212/01.Wnl.0000262028.16738.64 |
0.346 |
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| 2007 |
Borenstein AR, Mortimer JA, Schofield E, Wu Y, Salmon DP, Gamst A, Olichney J, Thal LJ, Silbert L, Kaye J, Craig UL, Schellenberg GD, Galasko DR. Cycad exposure and risk of dementia, MCI, and PDC in the Chamorro population of Guam. Neurology. 68: 1764-71. PMID 17515538 DOI: 10.1212/01.Wnl.0000262027.31623.B2 |
0.313 |
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| 2007 |
Leverenz JB, Yu CE, Montine TJ, Steinbart E, Bekris LM, Zabetian C, Kwong LK, Lee VM, Schellenberg GD, Bird TD. A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology. Brain : a Journal of Neurology. 130: 1360-74. PMID 17439980 DOI: 10.1093/Brain/Awm069 |
0.373 |
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| 2007 |
Yu CE, Seltman H, Peskind ER, Galloway N, Zhou PX, Rosenthal E, Wijsman EM, Tsuang DW, Devlin B, Schellenberg GD. Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association. Genomics. 89: 655-65. PMID 17434289 DOI: 10.1016/J.Ygeno.2007.02.002 |
0.421 |
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| 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, ... ... Schellenberg GD, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985 |
0.345 |
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| 2007 |
Sieh W, Yu CE, Bird TD, Schellenberg GD, Wijsman EM. Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease. Human Heredity. 63: 26-34. PMID 17215579 DOI: 10.1159/000098459 |
0.337 |
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| 2007 |
Kay DM, Moran D, Moses L, Poorkaj P, Zabetian CP, Nutt J, Factor SA, Yu CE, Montimurro JS, Keefe RG, Schellenberg GD, Payami H. Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients. Annals of Neurology. 61: 47-54. PMID 17187375 DOI: 10.1002/Ana.21039 |
0.322 |
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| 2007 |
Sundar PD, Yu CE, Sieh W, Steinbart E, Garruto RM, Oyanagi K, Craig UK, Bird TD, Wijsman EM, Galasko DR, Schellenberg GD. Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia. Human Molecular Genetics. 16: 295-306. PMID 17185385 DOI: 10.1093/Hmg/Ddl463 |
0.324 |
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| 2007 |
Kraemer B, Schellenberg GD. Using Caenorhabditis elegans models of neurodegenerative disease to identify neuroprotective strategies. International Review of Neurobiology. 77: 219-46. PMID 17178476 DOI: 10.1016/S0074-7742(06)77007-6 |
0.359 |
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| 2007 |
Li GG, Shofer J, Kukull WA, Peskind E, McCormick W, Bowen JD, Schellenberg GD, Crane P, Breitner JC, Larson EB. P-169: Association between statins and risk of AD is age dependent Alzheimer's & Dementia. 3: S152-S152. DOI: 10.1016/J.Jalz.2007.04.132 |
0.363 |
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| 2006 |
Riekse RG, Li G, Petrie EC, Leverenz JB, Vavrek D, Vuletic S, Albers JJ, Montine TJ, Lee VM, Lee M, Seubert P, Galasko D, Schellenberg GD, Hazzard WR, Peskind ER. Effect of statins on Alzheimer's disease biomarkers in cerebrospinal fluid. Journal of Alzheimer's Disease : Jad. 10: 399-406. PMID 17183151 DOI: 10.3233/Jad-2006-10408 |
0.391 |
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| 2006 |
Brickell KL, Steinbart EJ, Rumbaugh M, Payami H, Schellenberg GD, Van Deerlin V, Yuan W, Bird TD. Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer disease. Archives of Neurology. 63: 1307-11. PMID 16966510 DOI: 10.1001/Archneur.63.9.1307 |
0.393 |
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| 2006 |
Schellenberg GD. Early Alzheimer's disease genetics. Journal of Alzheimer's Disease : Jad. 9: 367-72. PMID 16914874 DOI: 10.3233/Jad-2006-9S341 |
0.454 |
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| 2006 |
Tsuang DW, Riekse RG, Purganan KM, David AC, Montine TJ, Schellenberg GD, Steinbart EJ, Petrie EC, Bird TD, Leverenz JB. Lewy body pathology in late-onset familial Alzheimer's disease: a clinicopathological case series. Journal of Alzheimer's Disease : Jad. 9: 235-42. PMID 16914833 DOI: 10.3233/Jad-2006-9302 |
0.417 |
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| 2006 |
Ramos EM, Lin MT, Larson EB, Maezawa I, Tseng LH, Edwards KL, Schellenberg GD, Hansen JA, Kukull WA, Jin LW. Tumor necrosis factor alpha and interleukin 10 promoter region polymorphisms and risk of late-onset Alzheimer disease. Archives of Neurology. 63: 1165-9. PMID 16908746 DOI: 10.1001/Archneur.63.8.1165 |
0.353 |
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| 2006 |
Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, et al. Evidence for multiple loci from a genome scan of autism kindreds. Molecular Psychiatry. 11: 1049-60, 979. PMID 16880825 DOI: 10.1038/Sj.Mp.4001874 |
0.304 |
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| 2006 |
Peskind ER, Li G, Shofer J, Quinn JF, Kaye JA, Clark CM, Farlow MR, DeCarli C, Raskind MA, Schellenberg GD, Lee VM, Galasko DR. Age and apolipoprotein E*4 allele effects on cerebrospinal fluid beta-amyloid 42 in adults with normal cognition. Archives of Neurology. 63: 936-9. PMID 16831961 DOI: 10.1001/Archneur.63.7.936 |
0.306 |
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| 2006 |
Kraemer BC, Burgess JK, Chen JH, Thomas JH, Schellenberg GD. Molecular pathways that influence human tau-induced pathology in Caenorhabditis elegans. Human Molecular Genetics. 15: 1483-96. PMID 16600994 DOI: 10.1093/Hmg/Ddl067 |
0.389 |
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| 2006 |
Leverenz JB, Fishel MA, Peskind ER, Montine TJ, Nochlin D, Steinbart E, Raskind MA, Schellenberg GD, Bird TD, Tsuang D. Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype. Archives of Neurology. 63: 370-6. PMID 16533963 DOI: 10.1001/Archneur.63.3.370 |
0.43 |
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| 2006 |
Malkani R, D'Souza I, Gwinn-Hardy K, Schellenberg GD, Hardy J, Momeni P. A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia. Neurobiology of Disease. 22: 401-3. PMID 16503405 DOI: 10.1016/J.Nbd.2005.12.001 |
0.392 |
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| 2006 |
Carlson CS, Heagerty PJ, Hatsukami TS, Richter RJ, Ranchalis J, Lewis J, Bacus TJ, McKinstry LA, Schellenberg GD, Rieder M, Nickerson D, Furlong CE, Chait A, Jarvik GP. TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular disease. Journal of Lipid Research. 47: 1014-24. PMID 16474172 DOI: 10.1194/Jlr.M500517-Jlr200 |
0.339 |
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| 2006 |
Zabetian CP, Lauricella CJ, Tsuang DW, Leverenz JB, Schellenberg GD, Payami H. Analysis of the LRRK2 G2019S mutation in Alzheimer Disease. Archives of Neurology. 63: 156-7. PMID 16401756 DOI: 10.1001/Archneur.63.1.156 |
0.428 |
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| 2006 |
D'Souza I, Schellenberg GD. Arginine/serine-rich protein interaction domain-dependent modulation of a tau exon 10 splicing enhancer: altered interactions and mechanisms for functionally antagonistic FTDP-17 mutations Delta280K AND N279K. The Journal of Biological Chemistry. 281: 2460-9. PMID 16308321 DOI: 10.1074/Jbc.M505809200 |
0.333 |
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| 2006 |
Li G, Kukull WA, Peskind E, McCormick W, Bowen JD, Teri L, Schellenberg GD, Larson EB. Differential Effect of Statins on Risk of AD by Age, Sex, and APOE Genotype: Findings From a Community-based Prospective Cohort Study Alzheimer Disease & Associated Disorders. 20: S103-S104. DOI: 10.1097/00002093-200607001-00027 |
0.351 |
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| 2006 |
Leung YY, Chou Y, Arnold SE, Trojanowski JQ, Schellenberg GD, Wang L. P2-279: CSF SMALL RNA BIOMARKERS FOR ALZHEIMER'S DISEASE Alzheimer's & Dementia. 14: P785-P786. DOI: 10.1016/J.Jalz.2018.06.968 |
0.357 |
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| 2006 |
Beecham GW, Vardarajan BN, Blue E, Bush WS, Jaworski J, Barral S, Kunkle BW, Martin ER, Reitz C, van Duijn CM, Haines JL, Schellenberg GD, Mayeux R, Wijsman E, Pericak-Vance MA. P2-108: WHOLE-GENOME SEQUENCING IN NON-HISPANIC WHITE FAMILIES IMPLICATES RARE VARIATION IN LATE-ONSET ALZHEIMER'S DISEASE RISK Alzheimer's & Dementia. 14: P710-P710. DOI: 10.1016/J.Jalz.2018.06.794 |
0.422 |
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| 2006 |
Chesi A, Manduchi E, Leonard M, Wang L, Lu S, Hodge K, Schellenberg G, Johnson M, Wells A, Grant S. O3-03-04: A HIGH RESOLUTION CAPTURE-C PROMOTER INTERACTOME IMPLICATES CAUSAL GENES AT ALZHEIMER'S DISEASE GWAS LOCI Alzheimer's & Dementia. 14: P1016-P1016. DOI: 10.1016/J.Jalz.2018.06.2785 |
0.386 |
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| 2006 |
Gangadharan P, Leung YY, Valladares O, Chou Y, Kuzma AB, Cantwell LB, Qu L, Lin H, Zhao Y, Malamon JS, Naj AC, Salerno WJ, Schellenberg GD, Wang L. P4-044: THE GCAD CLOUD-BASED WORKFLOW FOR PROCESSING WHOLE EXOME AND WHOLE GENOME DATA FROM THE ALZHEIMER'S DISEASE SEQUENCING PROJECT Alzheimer's & Dementia. 14: P1450-P1450. DOI: 10.1016/J.Jalz.2018.06.2446 |
0.371 |
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| 2006 |
Vogel B, Kuzma AB, Valladares O, Greenfest-Allen E, Gangadharan P, Zhao Y, Zhong C, Katanic Z, Qu L, Lin H, Leung YY, Naj AC, Stoeckert CJ, Schellenberg G, Wang L. P1-157: NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITE (NIAGADS): UPDATE 2018 Alzheimer's & Dementia. 14: P337-P337. DOI: 10.1016/J.Jalz.2018.06.161 |
0.417 |
|
| 2006 |
Amlie-Wolf A, Tang M, Dombroski BA, Way J, Vrettos N, Chou Y, Mlynarski EE, Brown CD, Schellenberg G, Wang L. P1-145: INFERRING THE MOLECULAR MECHANISMS OF NONCODING AD-ASSOCIATED GENETIC VARIANTS Alzheimer's & Dementia. 14: P331-P332. DOI: 10.1016/J.Jalz.2018.06.148 |
0.39 |
|
| 2006 |
Momeni P, Malkani R, D'Souza I, Gwinn-Hardy K, Schellenberg GD, Hardy J. P3-157: A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia Alzheimer's & Dementia. 2: S420-S420. DOI: 10.1016/J.Jalz.2006.05.1425 |
0.322 |
|
| 2006 |
Galasko D, Salmon D, Olichney J, Thal LJ, Gamst A, Silbert L, Kaye J, Borenstein A, Schellenberg G, Brooks P, Adonay R, Craig U. P3-147: The prevalence of dementia among elderly chamorros on guam and lack of association with the APO e4 allele Alzheimer's & Dementia. 2: S417-S417. DOI: 10.1016/J.Jalz.2006.05.1415 |
0.362 |
|
| 2005 |
Li X, Rowland LP, Mitsumoto H, Przedborski S, Bird TD, Schellenberg GD, Peskind E, Johnson N, Siddique T, Mesulam MM, Weintraub S, Mastrianni JA. Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia. Annals of Neurology. 58: 858-64. PMID 16315279 DOI: 10.1002/Ana.20646 |
0.447 |
|
| 2005 |
Li G, Shofer JB, Kukull WA, Peskind ER, Tsuang DW, Breitner JC, McCormick W, Bowen JD, Teri L, Schellenberg GD, Larson EB. Serum cholesterol and risk of Alzheimer disease: a community-based cohort study. Neurology. 65: 1045-50. PMID 16217057 DOI: 10.1212/01.Wnl.0000178989.87072.11 |
0.397 |
|
| 2005 |
Rademakers R, Melquist S, Cruts M, Theuns J, Del-Favero J, Poorkaj P, Baker M, Sleegers K, Crook R, De Pooter T, Bel Kacem S, Adamson J, Van den Bossche D, Van den Broeck M, Gass J, ... ... Schellenberg GD, et al. High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy. Human Molecular Genetics. 14: 3281-92. PMID 16195395 DOI: 10.1093/Hmg/Ddi361 |
0.338 |
|
| 2005 |
Faraone SV, Skol AD, Tsuang DW, Young KA, Haverstock SL, Prabhudesai S, Mena F, Menon AS, Leong L, Sautter F, Baldwin C, Bingham S, Weiss D, Collins J, Keith T, ... ... Schellenberg GD, et al. Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 139: 91-100. PMID 16152571 DOI: 10.1002/Ajmg.B.30213 |
0.302 |
|
| 2005 |
Devlin B, Cook EH, Coon H, Dawson G, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD. Autism and the serotonin transporter: the long and short of it. Molecular Psychiatry. 10: 1110-6. PMID 16103890 DOI: 10.1038/Sj.Mp.4001724 |
0.329 |
|
| 2005 |
Rozek LS, Hatsukami TS, Richter RJ, Ranchalis J, Nakayama K, McKinstry LA, Gortner DA, Boyko E, Schellenberg GD, Furlong CE, Jarvik GP. The correlation of paraoxonase (PON1) activity with lipid and lipoprotein levels differs with vascular disease status. Journal of Lipid Research. 46: 1888-95. PMID 15995178 DOI: 10.1194/Jlr.M400489-Jlr200 |
0.329 |
|
| 2005 |
Hall DA, Leehey MA, Filley CM, Steinbart E, Montine T, Schellenberg GD, Bosque P, Nixon R, Bird T. PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia. Neurology. 64: 1304-6. PMID 15824374 DOI: 10.1212/01.Wnl.0000156911.70131.06 |
0.38 |
|
| 2005 |
Poorkaj P, Moses L, Montimurro JS, Nutt JG, Schellenberg GD, Payami H. Parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism. Bmc Neurology. 5: 4. PMID 15725358 DOI: 10.1186/1471-2377-5-4 |
0.32 |
|
| 2005 |
Borenstein AR, Wu Y, Mortimer JA, Schellenberg GD, McCormick WC, Bowen JD, McCurry S, Larson EB. Developmental and vascular risk factors for Alzheimer's disease. Neurobiology of Aging. 26: 325-34. PMID 15639310 DOI: 10.1016/J.Neurobiolaging.2004.04.010 |
0.399 |
|
| 2005 |
D'Souza I, Schellenberg GD. Regulation of tau isoform expression and dementia. Biochimica Et Biophysica Acta. 1739: 104-15. PMID 15615630 DOI: 10.1016/J.Bbadis.2004.08.009 |
0.413 |
|
| 2005 |
Sung YJ, Dawson G, Munson J, Estes A, Schellenberg GD, Wijsman EM. Genetic investigation of quantitative traits related to autism: use of multivariate polygenic models with ascertainment adjustment. American Journal of Human Genetics. 76: 68-81. PMID 15547804 DOI: 10.1086/426951 |
0.309 |
|
| 2005 |
Wijsman EM, Daw EW, Yu X, Steinbart EJ, Nochlin D, Bird TD, Schellenberg GD. APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 132: 14-20. PMID 15389756 DOI: 10.1002/Ajmg.B.30087 |
0.421 |
|
| 2004 |
Li G, Higdon R, Kukull WA, Peskind E, Van Valen Moore K, Tsuang D, van Belle G, McCormick W, Bowen JD, Teri L, Schellenberg GD, Larson EB. Statin therapy and risk of dementia in the elderly: a community-based prospective cohort study. Neurology. 63: 1624-8. PMID 15534246 DOI: 10.1212/01.Wnl.0000142963.90204.58 |
0.386 |
|
| 2004 |
Yu CE, Devlin B, Galloway N, Loomis E, Schellenberg GD. ADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR. Genomics. 84: 600-12. PMID 15498468 DOI: 10.1016/J.Ygeno.2004.06.003 |
0.3 |
|
| 2004 |
Wijsman EM, Daw EW, Yu CE, Payami H, Steinbart EJ, Nochlin D, Conlon EM, Bird TD, Schellenberg GD. Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2. American Journal of Human Genetics. 75: 398-409. PMID 15248153 DOI: 10.1086/423393 |
0.375 |
|
| 2004 |
Devlin B, Bennett P, Dawson G, Figlewicz DA, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD. Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 126: 46-50. PMID 15048647 DOI: 10.1002/Ajmg.B.20125 |
0.341 |
|
| 2004 |
McMillan PJ, Leverenz JB, Bird TD, Schellenberg GD, Craft S. P4-285 Insulin degrading enzyme immunostaining is decreased in the hippocampus of familial Alzheimer's disease subjects with presenilin 1 mutations Neurobiology of Aging. 25: S556. DOI: 10.1016/S0197-4580(04)81843-8 |
0.371 |
|
| 2004 |
Kraemer BC, Thomas JH, Schellenberg GD. O1-04-02 Genetic modifiers of pathological TAU in Caenorhabidits elegans Neurobiology of Aging. 25: S16-S17. DOI: 10.1016/S0197-4580(04)80053-8 |
0.309 |
|
| 2004 |
Schellenberg GD. PL-1-2 Genetics of Alzheimer's disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80002-2 |
0.438 |
|
| 2003 |
Schellenberg GD. Alzheimer disease genes: presenilin 2 mutation number 9 and still counting. Archives of Neurology. 60: 1521-2. PMID 14623722 DOI: 10.1001/Archneur.60.11.1521 |
0.409 |
|
| 2003 |
Furukawa K, Wang Y, Yao PJ, Fu W, Mattson MP, Itoyama Y, Onodera H, D'Souza I, Poorkaj PH, Bird TD, Schellenberg GD. Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutation. Journal of Neurochemistry. 87: 427-36. PMID 14511120 DOI: 10.1046/J.1471-4159.2003.02020.X |
0.31 |
|
| 2003 |
Kraemer BC, Zhang B, Leverenz JB, Thomas JH, Trojanowski JQ, Schellenberg GD. Neurodegeneration and defective neurotransmission in a Caenorhabditis elegans model of tauopathy. Proceedings of the National Academy of Sciences of the United States of America. 100: 9980-5. PMID 12872001 DOI: 10.1073/Pnas.1533448100 |
0.39 |
|
| 2003 |
Craft S, Asthana S, Cook DG, Baker LD, Cherrier M, Purganan K, Wait C, Petrova A, Latendresse S, Watson GS, Newcomer JW, Schellenberg GD, Krohn AJ. Insulin dose-response effects on memory and plasma amyloid precursor protein in Alzheimer's disease: interactions with apolipoprotein E genotype. Psychoneuroendocrinology. 28: 809-22. PMID 12812866 DOI: 10.1016/S0306-4530(02)00087-2 |
0.307 |
|
| 2003 |
Jarvik GP, Hatsukami TS, Carlson C, Richter RJ, Jampsa R, Brophy VH, Margolin S, Rieder M, Nickerson D, Schellenberg GD, Heagerty PJ, Furlong CE. Paraoxonase activity, but not haplotype utilizing the linkage disequilibrium structure, predicts vascular disease. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 1465-71. PMID 12805074 DOI: 10.1161/01.Atv.0000081635.96290.D3 |
0.326 |
|
| 2003 |
Skol AD, Young KA, Tsuang DW, Faraone SV, Haverstock SL, Bingham S, Prabhudesai S, Mena F, Menon AS, Yu CE, Rundell P, Pepple J, Sauter F, Baldwin C, Weiss D, ... ... Schellenberg GD, et al. Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large Veterans Affairs Cooperative Study sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 118: 8-15. PMID 12627457 DOI: 10.1002/Ajmg.B.10055 |
0.323 |
|
| 2003 |
Cook DG, Leverenz JB, McMillan PJ, Kulstad JJ, Ericksen S, Roth RA, Schellenberg GD, Jin LW, Kovacina KS, Craft S. Reduced hippocampal insulin-degrading enzyme in late-onset Alzheimer's disease is associated with the apolipoprotein E-epsilon4 allele. The American Journal of Pathology. 162: 313-9. PMID 12507914 DOI: 10.1016/S0002-9440(10)63822-9 |
0.414 |
|
| 2002 |
Kukull WA, Higdon R, Bowen JD, McCormick WC, Teri L, Schellenberg GD, van Belle G, Jolley L, Larson EB. Dementia and Alzheimer disease incidence: a prospective cohort study. Archives of Neurology. 59: 1737-46. PMID 12433261 DOI: 10.1001/Archneur.59.11.1737 |
0.384 |
|
| 2002 |
Poorkaj P, Muma NA, Zhukareva V, Cochran EJ, Shannon KM, Hurtig H, Koller WC, Bird TD, Trojanowski JQ, Lee VM, Schellenberg GD. An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype. Annals of Neurology. 52: 511-6. PMID 12325083 DOI: 10.1002/Ana.10340 |
0.343 |
|
| 2002 |
Sultana R, Yu CE, Yu J, Munson J, Chen D, Hua W, Estes A, Cortes F, de la Barra F, Yu D, Haider ST, Trask BJ, Green ED, Raskind WH, Disteche CM, ... ... Schellenberg GD, et al. Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins. Genomics. 80: 129-34. PMID 12160723 DOI: 10.1006/Geno.2002.6810 |
0.332 |
|
| 2002 |
Yu CE, Dawson G, Munson J, D'Souza I, Osterling J, Estes A, Leutenegger AL, Flodman P, Smith M, Raskind WH, Spence MA, McMahon W, Wijsman EM, Schellenberg GD. Presence of large deletions in kindreds with autism. American Journal of Human Genetics. 71: 100-15. PMID 12058345 DOI: 10.1086/341291 |
0.331 |
|
| 2002 |
D'Souza I, Schellenberg GD. tau Exon 10 expression involves a bipartite intron 10 regulatory sequence and weak 5' and 3' splice sites. The Journal of Biological Chemistry. 277: 26587-99. PMID 12000767 DOI: 10.1074/Jbc.M203794200 |
0.303 |
|
| 2002 |
Zareparsi S, James DM, Kaye JA, Bird TD, Schellenberg GD, Payami H. HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer disease. Neurology. 58: 973-5. PMID 11914421 DOI: 10.1212/Wnl.58.6.973 |
0.319 |
|
| 2002 |
Edland SD, Tobe VO, Rieder MJ, Bowen JD, McCormick W, Teri L, Schellenberg GD, Larson EB, Nickerson DA, Kukull WA. Mitochondrial genetic variants and Alzheimer disease: a case-control study of the T4336C and G5460A variants. Alzheimer Disease and Associated Disorders. 16: 1-7. PMID 11882743 DOI: 10.1097/00002093-200201000-00001 |
0.439 |
|
| 2002 |
Galasko D, Salmon DP, Craig UK, Thal LJ, Schellenberg G, Wiederholt W. Clinical features and changing patterns of neurodegenerative disorders on Guam, 1997-2000. Neurology. 58: 90-7. PMID 11781411 DOI: 10.1212/Wnl.58.1.90 |
0.358 |
|
| 2001 |
Tsuang DW, Skol AD, Faraone SV, Bingham S, Young KA, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Bisset D, Pepple J, Sauter F, Baldwin C, Weiss D, Collins J, ... ... Schellenberg GD, et al. Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample. American Journal of Medical Genetics. 105: 662-8. PMID 11803512 DOI: 10.1002/Ajmg.1550 |
0.303 |
|
| 2001 |
Poorkaj P, Tsuang D, Wijsman E, Steinbart E, Garruto RM, Craig UK, Chapman NH, Anderson L, Bird TD, Plato CC, Perl DP, Weiderholt W, Galasko D, Schellenberg GD. TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of Guam. Archives of Neurology. 58: 1871-8. PMID 11708997 DOI: 10.1001/Archneur.58.11.1871 |
0.318 |
|
| 2001 |
Borenstein Graves A, Mortimer JA, Bowen JD, McCormick WC, McCurry SM, Schellenberg GD, Larson EB. Head circumference and incident Alzheimer's disease: modification by apolipoprotein E. Neurology. 57: 1453-60. PMID 11673588 DOI: 10.1212/Wnl.57.8.1453 |
0.39 |
|
| 2001 |
Poorkaj P, Kas A, D'Souza I, Zhou Y, Pham Q, Stone M, Olson MV, Schellenberg GD. A genomic sequence analysis of the mouse and human microtubule-associated protein tau. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 700-12. PMID 11641718 DOI: 10.1007/S00335-001-2044-8 |
0.424 |
|
| 2001 |
Moceri VM, Kukull WA, Emanual I, van Belle G, Starr JR, Schellenberg GD, McCormick WC, Bowen JD, Teri L, Larson EB. Using census data and birth certificates to reconstruct the early-life socioeconomic environment and the relation to the development of Alzheimer's disease. Epidemiology (Cambridge, Mass.). 12: 383-9. PMID 11416775 DOI: 10.1097/00001648-200107000-00007 |
0.434 |
|
| 2001 |
Peskind ER, Wilkinson CW, Petrie EC, Schellenberg GD, Raskind MA. Increased CSF cortisol in AD is a function of APOE genotype. Neurology. 56: 1094-8. PMID 11320185 DOI: 10.1212/Wnl.56.8.1094 |
0.378 |
|
| 2001 |
Poorkaj P, Grossman M, Steinbart E, Payami H, Sadovnick A, Nochlin D, Tabira T, Trojanowski JQ, Borson S, Galasko D, Reich S, Quinn B, Schellenberg G, Bird TD. Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia. Archives of Neurology. 58: 383-7. PMID 11255441 DOI: 10.1001/Archneur.58.3.383 |
0.391 |
|
| 2001 |
Baskin F, Rosenberg RN, Iyer L, Schellenberg GD, Hynan L, Nee LE. Platelet APP isoform ratios in asymptomatic young adults expressing an AD-related presenilin-1 mutation. Journal of the Neurological Sciences. 183: 85-8. PMID 11166800 DOI: 10.1016/S0022-510X(00)00483-4 |
0.388 |
|
| 2000 |
Schellenberg GD, D'Souza I, Poorkaj P. The genetics of Alzheimer's disease. Current Psychiatry Reports. 2: 158-64. PMID 11122949 DOI: 10.1007/S11920-000-0061-Z |
0.452 |
|
| 2000 |
Jarvik GP, Rozek LS, Brophy VH, Hatsukami TS, Richter RJ, Schellenberg GD, Furlong CE. Paraoxonase (PON1) phenotype is a better predictor of vascular disease than is PON1(192) or PON1(55) genotype. Arteriosclerosis, Thrombosis, and Vascular Biology. 20: 2441-7. PMID 11073850 DOI: 10.1161/01.Atv.20.11.2441 |
0.38 |
|
| 2000 |
Brophy VH, Jarvik GP, Richter RJ, Rozek LS, Schellenberg GD, Furlong CE. Analysis of paraoxonase (PON1) L55M status requires both genotype and phenotype. Pharmacogenetics. 10: 453-60. PMID 10898114 DOI: 10.1097/00008571-200007000-00008 |
0.331 |
|
| 2000 |
Craft S, Asthana S, Schellenberg G, Baker L, Cherrier M, Boyt AA, Martins RN, Raskind M, Peskind E, Plymate S. Insulin effects on glucose metabolism, memory, and plasma amyloid precursor protein in Alzheimer's disease differ according to apolipoprotein-E genotype. Annals of the New York Academy of Sciences. 903: 222-8. PMID 10818510 DOI: 10.1111/J.1749-6632.2000.Tb06371.X |
0.36 |
|
| 2000 |
D'Souza I, Schellenberg GD. Determinants of 4-repeat tau expression. Coordination between enhancing and inhibitory splicing sequences for exon 10 inclusion. The Journal of Biological Chemistry. 275: 17700-9. PMID 10748133 DOI: 10.1074/Jbc.M909470199 |
0.31 |
|
| 2000 |
Furukawa K, D'Souza I, Crudder CH, Onodera H, Itoyama Y, Poorkaj P, Bird TD, Schellenberg GD. Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism. Neuroreport. 11: 57-60. PMID 10683829 DOI: 10.1097/00001756-200001170-00011 |
0.336 |
|
| 2000 |
Daw EW, Payami H, Nemens EJ, Nochlin D, Bird TD, Schellenberg GD, Wijsman EM. The number of trait loci in late-onset Alzheimer disease. American Journal of Human Genetics. 66: 196-204. PMID 10631151 DOI: 10.1086/302710 |
0.435 |
|
| 2000 |
Schellenberg GD, D'Souza I, Poorkaj P, Bird TD. Tau mutations and gene expression Neurobiology of Aging. 21: 284. DOI: 10.1016/S0197-4580(00)83227-3 |
0.31 |
|
| 2000 |
Fishel MA, Tsuang DW, Raskind MA, Nochlin D, Schellenberg G, Bird TD, Leverenz JB. Lewy body pathology in familial (presenilin-2) Alzheimer's disease Neurobiology of Aging. 21: 66. DOI: 10.1016/S0197-4580(00)82516-6 |
0.402 |
|
| 1999 |
Bretsky PM, Buckwalter JG, Seeman TE, Miller CA, Poirier J, Schellenberg GD, Finch CE, Henderson VW. Evidence for an interaction between apolipoprotein E genotype, gender, and Alzheimer disease. Alzheimer Disease and Associated Disorders. 13: 216-21. PMID 10609670 DOI: 10.1097/00002093-199910000-00007 |
0.42 |
|
| 1999 |
Tsuang D, Larson EB, Bowen J, McCormick W, Teri L, Nochlin D, Leverenz JB, Peskind ER, Lim A, Raskind MA, Thompson ML, Mirra SS, Gearing M, Schellenberg GD, Kukull W. The utility of apolipoprotein E genotyping in the diagnosis of Alzheimer disease in a community-based case series. Archives of Neurology. 56: 1489-95. PMID 10593304 DOI: 10.1001/Archneur.56.12.1489 |
0.407 |
|
| 1999 |
Blander G, Kipnis J, Leal JF, Yu CE, Schellenberg GD, Oren M. Physical and functional interaction between p53 and the Werner's syndrome protein. The Journal of Biological Chemistry. 274: 29463-9. PMID 10506209 DOI: 10.1074/Jbc.274.41.29463 |
0.31 |
|
| 1999 |
Craft S, Asthana S, Schellenberg G, Cherrier M, Baker LD, Newcomer J, Plymate S, Latendresse S, Petrova A, Raskind M, Peskind E, Lofgreen C, Grimwood K. Insulin metabolism in Alzheimer's disease differs according to apolipoprotein E genotype and gender. Neuroendocrinology. 70: 146-52. PMID 10461029 DOI: 10.1159/000054469 |
0.308 |
|
| 1999 |
D'Souza I, Poorkaj P, Hong M, Nochlin D, Lee VM, Bird TD, Schellenberg GD. Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements. Proceedings of the National Academy of Sciences of the United States of America. 96: 5598-603. PMID 10318930 DOI: 10.1073/Pnas.96.10.5598 |
0.347 |
|
| 1999 |
Bird TD, Nochlin D, Poorkaj P, Cherrier M, Kaye J, Payami H, Peskind E, Lampe TH, Nemens E, Boyer PJ, Schellenberg GD. A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L) Brain : a Journal of Neurology. 122: 741-56. PMID 10219785 DOI: 10.1093/Brain/122.4.741 |
0.354 |
|
| 1999 |
Iijima M, Tabira T, Poorkaj P, Schellenberg GD, Trojanowski JQ, Lee VM, Schmidt ML, Takahashi K, Nabika T, Matsumoto T, Yamashita Y, Yoshioka S, Ishino H. A distinct familial presenile dementia with a novel missense mutation in the tau gene. Neuroreport. 10: 497-501. PMID 10208578 DOI: 10.1097/00001756-199902250-00010 |
0.355 |
|
| 1999 |
Yasuda M, Maeda K, Hashimoto M, Yamashita H, Ikejiri Y, Bird TD, Tanaka C, Schellenberg GD. A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2. Archives of Neurology. 56: 65-9. PMID 9923762 DOI: 10.1001/Archneur.56.1.65 |
0.432 |
|
| 1998 |
Hong M, Zhukareva V, Vogelsberg-Ragaglia V, Wszolek Z, Reed L, Miller BI, Geschwind DH, Bird TD, McKeel D, Goate A, Morris JC, Wilhelmsen KC, Schellenberg GD, Trojanowski JQ, Lee VM. Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. Science (New York, N.Y.). 282: 1914-7. PMID 9836646 DOI: 10.1126/Science.282.5395.1914 |
0.4 |
|
| 1998 |
Leverenz JB, Yu CE, Schellenberg GD. Aging-associated neuropathology in Werner syndrome. Acta Neuropathologica. 96: 421-4. PMID 9797008 DOI: 10.1007/S004010050914 |
0.341 |
|
| 1998 |
Clark LN, Poorkaj P, Wszolek Z, Geschwind DH, Nasreddine ZS, Miller B, Li D, Payami H, Awert F, Markopoulou K, Andreadis A, D'Souza I, Lee VM, Reed L, Trojanowski JQ, ... ... Schellenberg G, et al. Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. Proceedings of the National Academy of Sciences of the United States of America. 95: 13103-7. PMID 9789048 DOI: 10.1073/Pnas.95.22.13103 |
0.37 |
|
| 1998 |
Carmelli D, Swan GE, Reed T, Miller B, Wolf PA, Jarvik GP, Schellenberg GD. Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twins. Neurology. 50: 1580-5. PMID 9633697 DOI: 10.1212/Wnl.50.6.1580 |
0.306 |
|
| 1998 |
Furukawa K, Guo Q, Schellenberg GD, Mattson MP. Presenilin-1 mutation alters NGF-induced neurite outgrowth, calcium homeostasis, and transcription factor (AP-1) activation in PC12 cells. Journal of Neuroscience Research. 52: 618-24. PMID 9632318 DOI: 10.1002/(Sici)1097-4547(19980601)52:5<618::Aid-Jnr14>3.0.Co;2-Y |
0.32 |
|
| 1998 |
Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, Andreadis A, Wiederholt WC, Raskind M, Schellenberg GD. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Annals of Neurology. 43: 815-25. PMID 9629852 DOI: 10.1002/Ana.410430617 |
0.415 |
|
| 1998 |
Hubble JP, Kurth JH, Glatt SL, Kurth MC, Schellenberg GD, Hassanein RE, Lieberman A, Koller WC. Gene-toxin interaction as a putative risk factor for Parkinson's disease with dementia. Neuroepidemiology. 17: 96-104. PMID 9592786 DOI: 10.1159/000026159 |
0.363 |
|
| 1998 |
Poorkaj P, Sharma V, Anderson L, Nemens E, Alonso ME, Orr H, White J, Heston L, Bird TD, Schellenberg GD. Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene. Human Mutation. 11: 216-21. PMID 9521423 DOI: 10.1002/(Sici)1098-1004(1998)11:3<216::Aid-Humu6>3.0.Co;2-F |
0.353 |
|
| 1998 |
Craft S, Peskind E, Schwartz MW, Schellenberg GD, Raskind M, Porte D. Cerebrospinal fluid and plasma insulin levels in Alzheimer's disease: relationship to severity of dementia and apolipoprotein E genotype. Neurology. 50: 164-8. PMID 9443474 DOI: 10.1212/Wnl.50.1.164 |
0.337 |
|
| 1997 |
Zareparsi S, Kaye J, Camicioli R, Grimslid H, Oken B, Litt M, Nutt J, Bird T, Schellenberg G, Payami H. Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes. Annals of Neurology. 42: 655-8. PMID 9382478 DOI: 10.1002/Ana.410420417 |
0.389 |
|
| 1997 |
O'Meara ES, Kukull WA, Sheppard L, Bowen JD, McCormick WC, Teri L, Pfanschmidt M, Thompson JD, Schellenberg GD, Larson EB. Head injury and risk of Alzheimer's disease by apolipoprotein E genotype. American Journal of Epidemiology. 146: 373-84. PMID 9290497 DOI: 10.1093/Oxfordjournals.Aje.A009290 |
0.381 |
|
| 1997 |
Payami H, Schellenberg GD, Zareparsi S, Kaye J, Sexton GJ, Head MA, Matsuyama SS, Jarvik LF, Miller B, McManus DQ, Bird TD, Katzman R, Heston L, Norman D, Small GW. Evidence for association of HLA-A2 allele with onset age of Alzheimer's disease. Neurology. 49: 512-8. PMID 9270587 DOI: 10.1212/Wnl.49.2.512 |
0.346 |
|
| 1997 |
Jarvik GP, Goode EL, Austin MA, Auwerx J, Deeb S, Schellenberg GD, Reed T. Evidence that the apolipoprotein E-genotype effects on lipid levels can change with age in males: a longitudinal analysis. American Journal of Human Genetics. 61: 171-81. PMID 9245998 DOI: 10.1086/513902 |
0.305 |
|
| 1997 |
Bird TD, Wijsman EM, Nochlin D, Leehey M, Sumi SM, Payami H, Poorkaj P, Nemens E, Rafkind M, Schellenberg GD. Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD. Neurology. 48: 949-54. PMID 9109883 DOI: 10.1212/Wnl.48.4.949 |
0.405 |
|
| 1997 |
O'Meara ES, Kukull WA, Schellenberg GD, Bowen JD, McCormick WC, Teri L, Pfanschmidt M, Thompson JD, Larson EB. Alzheimer's disease and history of blood transfusion by apolipoprotein-E genotype. Neuroepidemiology. 16: 86-93. PMID 9057170 DOI: 10.1159/000109675 |
0.412 |
|
| 1997 |
Tsuang D, Raskind MA, Leverenz J, Peskind ER, Schellenberg G, Bird TD. The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tangles. Biological Psychiatry. 41: 191-5. PMID 9018389 DOI: 10.1016/S0006-3223(96)00119-9 |
0.441 |
|
| 1997 |
Richter R, Rosenberg R, Taubman K, Risser R, Farmer I, Ebalo E, Dreadfulwater J, Weiner M, Schaefer F, Schellenberg G, Svetlik D, Cullum M. 5-12-18 Apolipoprotein E genotype and Alzheimer's disease in the Cherokee Indians of Oklahoma Journal of the Neurological Sciences. 150. DOI: 10.1016/S0022-510X(97)86328-9 |
0.422 |
|
| 1996 |
Bird TD, Levy-Lahad E, Poorkaj P, Sharma V, Nemens E, Lahad A, Lampe TH, Schellenberg GD. Wide range in age of onset for chromosome 1--related familial Alzheimer's disease. Annals of Neurology. 40: 932-6. PMID 9007102 DOI: 10.1002/Ana.410400619 |
0.357 |
|
| 1996 |
Ikeda M, Sharma V, Sumi SM, Rogaeva EA, Poorkaj P, Sherrington R, Nee L, Tsuda T, Oda N, Watanabe M, Aoki M, Shoji M, Abe K, Itoyama Y, Hirai S, ... Schellenberg GD, et al. The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients. Annals of Neurology. 40: 912-7. PMID 9007097 DOI: 10.1002/Ana.410400614 |
0.403 |
|
| 1996 |
McMillan PJ, Leverenz JB, Poorkaj P, Schellenberg GD, Dorsa DM. Neuronal expression of STM2 mRNA in human brain is reduced in Alzheimer's disease. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 44: 1215-22. PMID 8918895 DOI: 10.1177/44.11.8918895 |
0.389 |
|
| 1996 |
Rosenberg RN, Richter RW, Risser RC, Taubman K, Prado-Farmer I, Ebalo E, Posey J, Kingfisher D, Dean D, Weiner MF, Svetlik D, Adams P, Honig LS, Cullum CM, Schaefer FV, ... Schellenberg GD, et al. Genetic factors for the development of Alzheimer disease in the Cherokee Indian. Archives of Neurology. 53: 997-1000. PMID 8859062 |
0.314 |
|
| 1996 |
Kukull WA, Schellenberg GD, Bowen JD, McCormick WC, Yu CE, Teri L, Thompson JD, O'Meara ES, Larson EB. Apolipoprotein E in Alzheimer's disease risk and case detection: a case-control study. Journal of Clinical Epidemiology. 49: 1143-8. PMID 8826994 DOI: 10.1016/0895-4356(96)00195-3 |
0.417 |
|
| 1996 |
Yu CE, Oshima J, Hisama FM, Matthews S, Trask BJ, Schellenberg GD. A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21. Genomics. 35: 431-40. PMID 8812476 DOI: 10.1006/Geno.1996.0382 |
0.315 |
|
| 1996 |
Anouti A, Schmidt K, Lyons KE, Hubble JP, Schellenberg G, Golbe LI, Lang AE, Galvez-Jimenez N, Hershey L, Koller WC. Normal distribution of apolipoprotein E alleles in progressive supranuclear palsy. Neurology. 46: 1156-7. PMID 8780111 DOI: 10.1212/Wnl.46.4.1156 |
0.376 |
|
| 1996 |
Scheuner D, Eckman C, Jensen M, Song X, Citron M, Suzuki N, Bird TD, Hardy J, Hutton M, Kukull W, Larson E, Levy-Lahad E, Viitanen M, Peskind E, Poorkaj P, ... Schellenberg G, et al. Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease. Nature Medicine. 2: 864-70. PMID 8705854 DOI: 10.1038/Nm0896-864 |
0.324 |
|
| 1996 |
Levy-Lahad E, Poorkaj P, Wang K, Fu YH, Oshima J, Mulligan J, Schellenberg GD. Genomic structure and expression of STM2, the chromosome 1 familial Alzheimer disease gene. Genomics. 34: 198-204. PMID 8661049 DOI: 10.1006/Geno.1996.0266 |
0.392 |
|
| 1996 |
Payami H, Zareparsi S, Montee KR, Sexton GJ, Kaye JA, Bird TD, Yu CE, Wijsman EM, Heston LL, Litt M, Schellenberg GD. Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women. American Journal of Human Genetics. 58: 803-11. PMID 8644745 |
0.307 |
|
| 1996 |
Tsuang D, Kukull W, Sheppard L, Barnhart RL, Peskind E, Edland SD, Schellenberg G, Raskind M, Larson EB. Impact of sample selection on APOE epsilon 4 allele frequency: a comparison of two Alzheimer's disease samples. Journal of the American Geriatrics Society. 44: 704-7. PMID 8642164 DOI: 10.1111/J.1532-5415.1996.Tb01836.X |
0.371 |
|
| 1996 |
Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Positional cloning of the Werner's syndrome gene. Science (New York, N.Y.). 272: 258-62. PMID 8602509 DOI: 10.1126/Science.272.5259.258 |
0.324 |
|
| 1996 |
Hisama FM, Schellenberg GD. Progress in Molecular Genetics of Alzheimer's Disease: The Neuroscientist. 2: 3-6. DOI: 10.1177/107385849600200106 |
0.465 |
|
| 1996 |
Richter R, Farmer I, Taubman K, VanWinkle N, Persson D, Weiner M, Dean D, Ebalo E, Musick B, Kingfisher D, Schaefer F, Schellenberg G, Rosenbere R. 223 A study of dementia within the Cherokee nation of Oklahoma Neurobiology of Aging. 17. DOI: 10.1016/S0197-4580(96)80225-9 |
0.32 |
|
| 1995 |
Jarvik GP, Wijsman EM, Kukull WA, Schellenberg GD, Yu C, Larson EB. Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case-control study. Neurology. 45: 1092-6. PMID 7783869 DOI: 10.1212/Wnl.45.6.1092 |
0.416 |
|
| 1995 |
Schellenberg GD. Molecular genetics of familial Alzheimer's disease. Arzneimittel-Forschung. 45: 418-24. PMID 7763337 |
0.305 |
|
| 1995 |
Levy-Lahad E, Wijsman EM, Nemens E, Anderson L, Goddard KA, Weber JL, Bird TD, Schellenberg GD. A familial Alzheimer's disease locus on chromosome 1. Science (New York, N.Y.). 269: 970-3. PMID 7638621 DOI: 10.1126/Science.7638621 |
0.435 |
|
| 1995 |
Schellenberg GD. Progress in Alzheimer's disease genetics. Current Opinion in Neurology. 8: 262-7. PMID 7582040 DOI: 10.1097/00019052-199508000-00003 |
0.461 |
|
| 1995 |
Levy-Lahad E, Lahad A, Wijsman EM, Bird TD, Schellenberg GD. Apolipoprotein E genotypes and age of onset in early-onset familial Alzheimer's disease. Annals of Neurology. 38: 678-80. PMID 7574468 DOI: 10.1002/Ana.410380420 |
0.444 |
|
| 1995 |
Schellenberg GD. Genetic dissection of Alzheimer disease, a heterogeneous disorder. Proceedings of the National Academy of Sciences of the United States of America. 92: 8552-9. PMID 7567974 DOI: 10.1073/Pnas.92.19.8552 |
0.464 |
|
| 1995 |
Payami H, Montee KR, Kaye JA, Wijsman EM, Bird T, Yu CE, Heston LL, Schellenberg GD. The Apolipoprotein E E4 Allele and Sex-Specific Risk of Alzheimer's Disease Jama. 273: 373-374. DOI: 10.1001/Jama.1995.03520290025014 |
0.333 |
|
| 1994 |
Hinds TR, Kukull WA, Van Belle G, Schellenberg GD, Villacres EC, Larson EB. Relationship between serum alpha 1-antichymotrypsin and Alzheimer's disease. Neurobiology of Aging. 15: 21-7. PMID 8159260 DOI: 10.1016/0197-4580(94)90141-4 |
0.407 |
|
| 1994 |
Payami H, Montee KR, Kaye JA, Bird TD, Yu CE, Wijsman EM, Schellenberg GD. Alzheimer's disease, apolipoprotein E4, and gender. Jama. 271: 1316-7. PMID 8158809 DOI: 10.1001/Jama.1994.03510410028015 |
0.398 |
|
| 1994 |
Nakura J, Wijsman EM, Miki T, Kamino K, Yu CE, Oshima J, Fukuchi Ki, Weber JL, Piussan C, Melaragno MI, Epstein CJ, Scappaticci S, Fraccaro M, Matsumura T, Murano S, ... ... Schellenberg GD, et al. Homozygosity Mapping of the Werner Syndrome Locus (WRN) Genomics. 23: 600-608. PMID 7851888 DOI: 10.1006/Geno.1994.1548 |
0.363 |
|
| 1994 |
Schellenberg GD. Alzheimer's disease: implications of genetic studies. Neurobiology of Aging. 15: S141-4. PMID 7700439 DOI: 10.1016/0197-4580(94)90192-9 |
0.443 |
|
| 1993 |
Nakura J, Miki T, Nagano K, Kihara K, Ye L, Kamino K, Fujiwara Y, Yoshida S, Murano S, Fukuchi K, Wijsman EM, Martin GM, Schellenberg GD, Ogihara T. Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8. Gerontology. 39: 11-15. PMID 8365666 DOI: 10.1159/000213560 |
0.303 |
|
| 1993 |
Wijsman EM, Bird TD, Martin GM, Schellenberg GD. The Seattle Alzheimer's disease data set. Genetic Epidemiology. 10: 365-9. PMID 8314028 DOI: 10.1002/Gepi.1370100606 |
0.356 |
|
| 1993 |
Payami H, Kaye J, Heston LL, Bird TD, Schellenberg GD. Apolipoprotein E genotype and Alzheimer's disease. Lancet. 342: 738. PMID 8103834 DOI: 10.1016/0140-6736(93)91728-5 |
0.423 |
|
| 1992 |
Kukull WA, Hinds TR, Schellenberg GD, van Belle G, Larson EB. Increased platelet membrane fluidity as a diagnostic marker for Alzheimer's disease: a test in population-based cases and controls. Neurology. 42: 607-14. PMID 1549223 DOI: 10.1212/Wnl.42.3.607 |
0.329 |
|
| 1992 |
Schellenberg GD, Bird TD, Wijsman EM, Orr HT, Anderson L, Nemens E, White JA, Bonnycastle L, Weber JL, Alonso ME. Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14. Science (New York, N.Y.). 258: 668-71. PMID 1411576 DOI: 10.1126/Science.1411576 |
0.392 |
|
| 1992 |
Schellenberg GD, Boehnke M, Wijsman EM, Moore DK, Martin GM, Bird TD. Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's disease. Annals of Neurology. 31: 223-7. PMID 1349467 DOI: 10.1002/Ana.410310214 |
0.43 |
|
| 1991 |
Hsiao KK, Cass C, Schellenberg GD, Bird T, Devine-Gage E, Wisniewski H, Prusiner SB. A prion protein variant in a family with the telencephalic form of Gerstmann-Sträussler-Scheinker syndrome. Neurology. 41: 681-4. PMID 1674116 DOI: 10.1212/Wnl.41.5.681 |
0.326 |
|
| 1990 |
Eto K, Sumi SM, Bird TD, McEvoy-Bush T, Boehnke M, Schellenberg G. Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family? Archives of Neurology. 47: 968-74. PMID 2396938 DOI: 10.1001/Archneur.1990.00530090038011 |
0.331 |
|
| 1990 |
Martin GM, Schellenberg GD, Wijsman EM, Bird TD. Alzheimer's disease. Dominant susceptibility genes. Nature. 347: 124. PMID 2395467 DOI: 10.1038/347124A0 |
0.437 |
|
| 1989 |
Bird TD, Sumi SM, Nemens EJ, Nochlin D, Schellenberg G, Lampe TH, Sadovnick A, Chui H, Miner GW, Tinklenberg J. Phenotypic heterogeneity in familial Alzheimer's disease: a study of 24 kindreds. Annals of Neurology. 25: 12-25. PMID 2913924 DOI: 10.1002/Ana.410250104 |
0.384 |
|
| 1989 |
Bird TD, Schellenberg GD, Wijsman EM, Martin GM. Evidence for etiologic heterogeneity in Alzheimer's disease. Neurobiology of Aging. 10: 432-4; discussion 44. PMID 2812202 DOI: 10.1016/0197-4580(89)90085-7 |
0.462 |
|
| 1989 |
Bird TD, Lampe TH, Nemens EJ, Sumi SM, Nochlin D, Schellenberg GD, Wijsman EM. Characteristics of familial Alzheimer's disease in nine kindreds of Volga German ancestry. Progress in Clinical and Biological Research. 317: 229-34. PMID 2602419 DOI: 10.1097/00002093-198802030-00135 |
0.462 |
|
| 1989 |
Schellenberg GD, Bird TD, Wijsman EM, Moore DK, Martin GM. The genetics of Alzheimer's disease. Biomedicine & Pharmacotherapy = Biomã©Decine & Pharmacothã©Rapie. 43: 463-8. PMID 2531010 DOI: 10.1016/0753-3322(89)90106-6 |
0.482 |
|
| 1988 |
Schellenberg GD, Bird TD, Wijsman EM, Moore DK, Boehnke M, Bryant EM, Lampe TH, Nochlin D, Sumi SM, Deeb SS. Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease. Science (New York, N.Y.). 241: 1507-10. PMID 3420406 DOI: 10.1126/Science.3420406 |
0.427 |
|
| 1988 |
Bird TD, Lampe TH, Nemens EJ, Miner GW, Sumi SM, Schellenberg GD. Familial Alzheimer's disease in American descendants of the Volga Germans: probable genetic founder effect. Annals of Neurology. 23: 25-31. PMID 3345066 DOI: 10.1002/Ana.410230106 |
0.421 |
|
| 1987 |
Bird TD, Boehnke M, Anderson J, Lampe TH, Schellenberg G, Larson EB. The frequency of C4B variants of complement in familial and sporadic Alzheimer disease. Alzheimer Disease and Associated Disorders. 1: 251-5. PMID 3502596 DOI: 10.1097/00002093-198701040-00004 |
0.417 |
|
| 1987 |
Schellenberg GD, Deeb SS, Boehnke M, Bryant EM, Martin GM, Lampe TH, Bird TD. Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type. Journal of Neurogenetics. 4: 97-108. PMID 2885403 DOI: 10.3109/01677068709102337 |
0.379 |
|
| 1987 |
Bird TD, Boehnke M, Schellenberg GD, Deeb SS, Lipe HP. The use of apolipoprotein CII as a genetic marker for myotonic dystrophy. Archives of Neurology. 44: 273-5. PMID 2881531 DOI: 10.1001/Archneur.1987.00520150029015 |
0.329 |
|
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