| Year |
Citation |
Score |
| 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, ... ... Wijsman EM, 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 |
0.348 |
|
| 2023 |
Horimoto ARVR, Boyken LA, Blue EE, Grinde KE, Nafikov RA, Sohi HK, Nato AQ, Bis JC, Brusco LI, Morelli L, Ramirez A, Dalmasso MC, Temple S, Satizabal C, Browning SR, ... ... Wijsman EM, et al. Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations. Hgg Advances. 4: 100207. PMID 37333771 DOI: 10.1016/j.xhgg.2023.100207 |
0.312 |
|
| 2019 |
Braggin JE, Bucks SA, Course MM, Smith CL, Sopher B, Osnis L, Shuey KD, Domoto-Reilly K, Caso C, Kinoshita C, Scherpelz KP, Cross C, Grabowski T, Nik SHM, Newman M, ... ... Wijsman EM, et al. Alternative splicing in a presenilin 2 variant associated with Alzheimer disease. Annals of Clinical and Translational Neurology. 6: 762-777. PMID 31020001 DOI: 10.1002/Acn3.755 |
0.378 |
|
| 2019 |
Saad M, Wijsman EM. Association score testing for rare variants and binary traits in family data with shared controls. Briefings in Bioinformatics. 20: 245-253. PMID 28968627 DOI: 10.1093/Bib/Bbx107 |
0.41 |
|
| 2018 |
Beecham GW, Vardarajan B, Blue E, Bush W, Jaworski J, Barral S, DeStefano A, Hamilton-Nelson K, Kunkle B, Martin ER, Naj A, Rajabli F, Reitz C, Thornton T, van Duijn C, ... ... Wijsman E, et al. Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease. Neurology. Genetics. 4: e286. PMID 30569016 DOI: 10.1212/Nxg.0000000000000286 |
0.307 |
|
| 2018 |
Ullah E, Mall R, Abbas MM, Kunji K, Nato AQ, Bensmail H, Wijsman EM, Saad M. Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees. Genome Research. PMID 30514702 DOI: 10.1101/Gr.236315.118 |
0.402 |
|
| 2018 |
Chapman NH, Bernier RA, Webb SJ, Munson J, Blue EM, Chen DH, Heigham E, Raskind WH, Wijsman EM. Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder. Human Genetics. PMID 30276537 DOI: 10.1007/S00439-018-1939-3 |
0.424 |
|
| 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, ... ... Wijsman E, 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 |
0.427 |
|
| 2018 |
Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Wijsman E, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757 |
0.32 |
|
| 2018 |
Nafikov RA, Nato AQ, Sohi H, Wang B, Brown L, Horimoto AR, Vardarajan BN, Barral SM, Tosto G, Mayeux RP, Thornton TA, Blue E, Wijsman EM. Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP. Genetic Epidemiology. PMID 29862559 DOI: 10.1002/Gepi.22133 |
0.459 |
|
| 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, ... ... Wijsman EM, 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 |
0.373 |
|
| 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, ... ... Wijsman E, 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 |
0.407 |
|
| 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, ... ... Wijsman EM, 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 |
0.354 |
|
| 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, ... ... Wijsman E, 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 |
0.39 |
|
| 2017 |
Kunji K, Ullah E, Nato AQ, Wijsman EM, Saad M. GIGI-Quick: A Fast Approach to Impute Missing Genotypes in Genome-Wide Association Family Data. Bioinformatics (Oxford, England). PMID 29267877 DOI: 10.1093/Bioinformatics/Btx782 |
0.403 |
|
| 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, ... Wijsman E, et al. The Alzheimer's Disease Sequencing Project: Study design and sample selection. Neurology. Genetics. 3: e194. PMID 29184913 DOI: 10.1212/Nxg.0000000000000194 |
0.384 |
|
| 2017 |
Blue EE, Yu CE, Thornton TA, Chapman NH, Kernfeld E, Jiang N, Shively KM, Buckingham KJ, Marvin CT, Bamshad MJ, Bird TD, Wijsman EM. Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease. Genes, Brain, and Behavior. PMID 29045054 DOI: 10.1111/Gbb.12429 |
0.417 |
|
| 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 |
0.4 |
|
| 2016 |
Blue EM, Brown LA, Conomos MP, Kirk JL, Nato AQ, Popejoy AB, Raffa J, Ranola J, Wijsman EM, Thornton T. Estimating relationships between phenotypes and subjects drawn from admixed families. Bmc Proceedings. 10: 357-362. PMID 27980662 DOI: 10.1186/S12919-016-0056-3 |
0.383 |
|
| 2016 |
Saad M, Nato AQ, Grimson FL, Lewis SM, Brown LA, Blue EM, Thornton TA, Thompson EA, Wijsman EM. Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data. Bmc Proceedings. 10: 295-301. PMID 27980652 DOI: 10.1186/S12919-016-0046-5 |
0.392 |
|
| 2016 |
Engelman CD, Greenwood CM, Bailey JN, Cantor RM, Kent JW, König IR, Bermejo JL, Melton PE, Santorico SA, Schillert A, Wijsman EM, MacCluer JW, Almasy L. Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals. Bmc Proceedings. 10: 67-70. PMID 27980613 DOI: 10.1186/S12919-016-0007-Z |
0.412 |
|
| 2016 |
Rubinstein M, Patowary A, Stanaway IB, McCord E, Nesbitt RR, Archer M, Scheuer T, Nickerson D, Raskind WH, Wijsman EM, Bernier R, Catterall WA, Brkanac Z. Association of rare missense variants in the second intracellular loop of Na1.7 sodium channels with familial autism. Molecular Psychiatry. 23: 231-239. PMID 27956748 DOI: 10.1038/Mp.2016.222 |
0.375 |
|
| 2016 |
Truong DT, Shriberg LD, Smith SD, Chapman KL, Scheer-Cohen AR, DeMille MM, Adams AK, Nato AQ, Wijsman EM, Eicher JD, Gruen JR. Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders. Human Genetics. PMID 27535846 DOI: 10.1007/S00439-016-1717-Z |
0.403 |
|
| 2016 |
Peter B, Wijsman EM, Nato AQ, Matsushita MM, Chapman KL, Stanaway IB, Wolff J, Oda K, Gabo VB, Raskind WH. Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. Plos One. 11: e0153864. PMID 27120335 DOI: 10.1371/Journal.Pone.0153864 |
0.457 |
|
| 2016 |
Wijsman EM. Family-based approaches: design, imputation, analysis, and beyond. Bmc Genetics. 17: 9-9. PMID 26866700 DOI: 10.1186/S12863-015-0318-5 |
0.439 |
|
| 2016 |
Wijsman E. Alzheimer'S Disease Sequencing Project: Family-Based Analyses Alzheimers & Dementia. 12: 322. DOI: 10.1016/J.Jalz.2016.06.585 |
0.342 |
|
| 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 |
0.324 |
|
| 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 |
0.374 |
|
| 2016 |
Ahmad S, Amin N, Blue E, Lee SJvd, Nato AQ, Sohi H, Wang B, Boerwinkle E, DeStefano AL, Wijsman E, Duijn CMv. Genomewide Linkage Analysis Identifies Novel Candidate Genes For Alzheimer’S Disease Alzheimers & Dementia. 12: 196. DOI: 10.1016/J.Jalz.2016.06.341 |
0.364 |
|
| 2015 |
Saad M, Brkanac Z, Wijsman EM. Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data. Genes, Brain and Behavior. 14: 607-617. PMID 26394601 DOI: 10.1111/Gbb.12250 |
0.429 |
|
| 2015 |
Nato AQ, Chapman NH, Sohi HK, Nguyen HD, Brkanac Z, Wijsman EM. PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers. Bioinformatics (Oxford, England). PMID 26231429 DOI: 10.1093/Bioinformatics/Btv444 |
0.403 |
|
| 2015 |
Chapman NH, Nato AQ, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM. Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics. 134: 1055-68. PMID 26204995 DOI: 10.1007/S00439-015-1585-Y |
0.447 |
|
| 2014 |
Blue EM, Cheung CY, Glazner CG, Conomos MP, Lewis SM, Sverdlov S, Thornton T, Wijsman EM. Identity-by-descent graphs offer a flexible framework for imputation and both linkage and association analyses. Bmc Proceedings. 8: S19. PMID 25519371 DOI: 10.1186/1753-6561-8-S1-S19 |
0.365 |
|
| 2014 |
Thornton T, Conomos MP, Sverdlov S, Blue EM, Cheung CY, Glazner CG, Lewis SM, Wijsman EM. Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing. Bmc Proceedings. 8: S5. PMID 25519330 DOI: 10.1186/1753-6561-8-S1-S5 |
0.352 |
|
| 2014 |
Saad M, Wijsman EM. Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees. Genetic Epidemiology. 38: 579-90. PMID 25132070 DOI: 10.1002/Gepi.21844 |
0.425 |
|
| 2014 |
Blue EM, Sun L, Tintle NL, Wijsman EM. Value of Mendelian laws of segregation in families: data quality control, imputation, and beyond. Genetic Epidemiology. 38: S21-8. PMID 25112184 DOI: 10.1002/Gepi.21821 |
0.399 |
|
| 2014 |
Rubenstein KB, Raskind WH, Berninger VW, Matsushita MM, Wijsman EM. Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 345-56. PMID 24807833 DOI: 10.1002/Ajmg.B.32237 |
0.407 |
|
| 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, ... ... Wijsman EM, 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 |
0.349 |
|
| 2014 |
Cheung CY, Thompson EA, Wijsman EM. Detection of Mendelian consistent genotyping errors in pedigrees. Genetic Epidemiology. 38: 291-9. PMID 24718985 DOI: 10.1002/Gepi.21806 |
0.326 |
|
| 2014 |
Cheung CY, Marchani Blue E, Wijsman EM. A statistical framework to guide sequencing choices in pedigrees. American Journal of Human Genetics. 94: 257-67. PMID 24507777 DOI: 10.1016/J.Ajhg.2014.01.005 |
0.364 |
|
| 2014 |
Saad M, Wijsman EM. Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes. Genetic Epidemiology. 38: 1-9. PMID 24243664 DOI: 10.1002/Gepi.21776 |
0.387 |
|
| 2013 |
Rosenthal EA, Ranchalis J, Crosslin DR, Burt A, Brunzell JD, Motulsky AG, Nickerson DA, Wijsman EM, Jarvik GP. Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia. American Journal of Human Genetics. 93: 1035-45. PMID 24268658 DOI: 10.1016/J.Ajhg.2013.10.019 |
0.468 |
|
| 2013 |
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Wijsman EM, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.3 |
|
| 2013 |
Cheung CY, Thompson EA, Wijsman EM. GIGI: an approach to effective imputation of dense genotypes on large pedigrees. American Journal of Human Genetics. 92: 504-16. PMID 23561844 DOI: 10.1016/J.Ajhg.2013.02.011 |
0.382 |
|
| 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 |
0.456 |
|
| 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 |
0.359 |
|
| 2012 |
Marchani EE, Chapman NH, Cheung CY, Ankenman K, Stanaway IB, Coon HH, Nickerson D, Bernier R, Brkanac Z, Wijsman EM. Identification of rare variants from exome sequence in a large pedigree with autism. Human Heredity. 74: 153-64. PMID 23594493 DOI: 10.1159/000346560 |
0.435 |
|
| 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, ... ... Wijsman EM, 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 |
0.405 |
|
| 2012 |
Wijsman EM. The role of large pedigrees in an era of high-throughput sequencing Human Genetics. 131: 1555-1563. PMID 22714655 DOI: 10.1007/S00439-012-1190-2 |
0.402 |
|
| 2012 |
Kim S, Millard SP, Yu CE, Leong L, Radant A, Dobie D, Tsuang DW, Wijsman EM. Inheritance model introduces differential bias in CNV calls between parents and offspring. Genetic Epidemiology. 36: 488-98. PMID 22628073 DOI: 10.1002/Gepi.21643 |
0.387 |
|
| 2012 |
Chen YZ, Matsushita M, Girirajan S, Lisowski M, Sun E, Sul Y, Bernier R, Estes A, Dawson G, Minshew N, Shellenberg GD, Eichler EE, Rieder MJ, Nickerson DA, Tsuang DW, ... ... Wijsman EM, et al. Evidence for involvement of GNB1L in autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 61-71. PMID 22095694 DOI: 10.1002/Ajmg.B.32002 |
0.384 |
|
| 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, ... ... Wijsman EM, 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 |
0.424 |
|
| 2011 |
Marchani EE, Wijsman EM. Estimation and visualization of identity-by-descent within pedigrees simplifies interpretation of complex trait analysis. Human Heredity. 72: 289-297. PMID 22189471 DOI: 10.1159/000334083 |
0.447 |
|
| 2011 |
Choi Y, Marchani EE, Bird TD, Steinbart EJ, Blacker D, Wijsman EM. Genome scan of age-at-onset in the NIMH Alzheimer disease sample uncovers multiple loci, along with evidence of both genetic and sample heterogeneity. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 785-98. PMID 21812099 DOI: 10.1002/Ajmg.B.31220 |
0.457 |
|
| 2011 |
Rosenthal EA, Ronald J, Rothstein J, Rajagopalan R, Ranchalis J, Wolfbauer G, Albers JJ, Brunzell JD, Motulsky AG, Rieder MJ, Nickerson DA, Wijsman EM, Jarvik GP. Linkage and association of phospholipid transfer protein activity to LASS4. Journal of Lipid Research. 52: 1837-46. PMID 21757428 DOI: 10.1194/Jlr.P016576 |
0.464 |
|
| 2011 |
Liu XQ, Georgiades S, Duku E, Thompson A, Devlin B, Cook EH, Wijsman EM, Paterson AD, Szatmari P. Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders. Journal of the American Academy of Child and Adolescent Psychiatry. 50: 687-696.e13. PMID 21703496 DOI: 10.1016/J.Jaac.2011.05.002 |
0.387 |
|
| 2011 |
Peter B, Raskind WH, Matsushita M, Lisowski M, Vu T, Berninger VW, Wijsman EM, Brkanac Z. Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. Journal of Neurodevelopmental Disorders. 3: 39-49. PMID 21484596 DOI: 10.1007/S11689-010-9065-0 |
0.34 |
|
| 2011 |
Wijsman EM, Pankratz ND, Choi Y, Rothstein JH, Faber KM, Cheng R, Lee JH, Bird TD, Bennett DA, Diaz-Arrastia R, Goate AM, Farlow M, Ghetti B, Sweet RA, Foroud TM, et al. Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. Plos Genetics. 7: e1001308. PMID 21379329 DOI: 10.1371/Journal.Pgen.1001308 |
0.429 |
|
| 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 |
0.422 |
|
| 2011 |
Rubenstein K, Matsushita M, Berninger VW, Raskind WH, Wijsman EM. Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization. Behavior Genetics. 41: 31-42. PMID 20852926 DOI: 10.1007/S10519-010-9390-9 |
0.431 |
|
| 2011 |
Lee J, Cheng R, Pankratz N, Wijsman E, Bird T, Foroud T, Mayeux R. A Genome-Wide Study of Familial Alzheimer’s Disease Supports Additional Candidate Genes: The NIA-LOAD/NCRAD Family Study Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.524 |
0.384 |
|
| 2010 |
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Wijsman EM, 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 |
0.407 |
|
| 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, ... ... Wijsman EM, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/Nature09146 |
0.379 |
|
| 2010 |
Yu CE, Marchani E, Nikisch G, Müller U, Nolte D, Hertel A, Wijsman EM, Bird TD. The N141I mutation in PSEN2: implications for the quintessential case of Alzheimer disease. Archives of Neurology. 67: 631-3. PMID 20457965 DOI: 10.1001/Archneurol.2010.87 |
0.348 |
|
| 2010 |
Wijsman EM, Rothstein JH, Igo RP, Brunzell JD, Motulsky AG, Jarvik GP. Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families. Human Genetics. 127: 705-19. PMID 20383777 DOI: 10.1007/S00439-010-0819-2 |
0.469 |
|
| 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 |
0.454 |
|
| 2010 |
Rosenthal EA, Wijsman EM. Joint linkage and segregation analysis under multiallelic trait inheritance: simplifying interpretations for complex traits. Genetic Epidemiology. 34: 344-353. PMID 20091797 DOI: 10.1002/Gepi.20490 |
0.411 |
|
| 2010 |
Jarvik GP, Rajagopalan R, Rosenthal EA, Wolfbauer G, McKinstry L, Vaze A, Brunzell J, Motulsky AG, Nickerson DA, Heagerty PJ, Wijsman EM, Albers JJ. Genetic and nongenetic sources of variation in phospholipid transfer protein activity. Journal of Lipid Research. 51: 983-90. PMID 19965587 DOI: 10.1194/Jlr.M000125 |
0.34 |
|
| 2010 |
Wijsman EM. Family-based approaches to analysis of GWAS data Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.197 |
0.358 |
|
| 2009 |
Marchani EE, Di Y, Choi Y, Cheung C, Su M, Boehm F, Thompson EA, Wijsman EM. Contrasting identity-by-descent estimators, association studies, and linkage analyses using the Framingham Heart Study data. Bmc Proceedings. 3: S102. PMID 20017966 DOI: 10.1186/1753-6561-3-S7-S102 |
0.391 |
|
| 2009 |
Marchani EE, Callegaro A, Daw EW, Wijsman EM. Combining information from linkage and association methods. Genetic Epidemiology. 33. PMID 19924706 DOI: 10.1002/Gepi.20477 |
0.353 |
|
| 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 |
0.443 |
|
| 2009 |
Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, ... ... Wijsman EM, et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry. 14: 774-85. PMID 19349958 DOI: 10.1038/Mp.2008.135 |
0.421 |
|
| 2009 |
Choi Y, Wijsman EM, Weir BS. Case-control association testing in the presence of unknown relationships. Genetic Epidemiology. 33: 668-78. PMID 19333967 DOI: 10.1002/Gepi.20418 |
0.337 |
|
| 2008 |
Brkanac Z, Chapman NH, Igo RP, Matsushita MM, Nielsen K, Berninger VW, Wijsman EM, Raskind WH. Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci. Behavior Genetics. 38: 462-75. PMID 18607713 DOI: 10.1007/S10519-008-9215-2 |
0.426 |
|
| 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 |
0.372 |
|
| 2008 |
Igo RP, Wijsman EM. Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis. Genetic Epidemiology. 32: 119-131. PMID 17849492 DOI: 10.1002/Gepi.20267 |
0.395 |
|
| 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 |
0.309 |
|
| 2007 |
Sung YJ, Di Y, Fu AQ, Rothstein JH, Sieh W, Tong L, Thompson EA, Wijsman EM. Comparison of multipoint linkage analyses for quantitative traits in the CEPH data: parametric LOD scores, variance components LOD scores, and Bayes factors. Bmc Proceedings. 1: S93. PMID 18466597 DOI: 10.1186/1753-6561-1-S1-S93 |
0.379 |
|
| 2007 |
Wijsman EM, Sung YJ, Buil A, Atkinson E, Bastone L, Christensen GB, Diao G, Feng T, Franceschini N, Huang S, Kan D, Kerner B, Lantieri F, Lee E, Papachristou C, et al. Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data. Genetic Epidemiology. 31: S75-85. PMID 18046772 DOI: 10.1002/Gepi.20283 |
0.414 |
|
| 2007 |
Chanock SJ, Manolio T, Boehnke M, Boerwinkle E, Hunter DJ, Thomas G, Hirschhorn JN, Abecasis G, Altshuler D, Bailey-Wilson JE, Brooks LD, Cardon LR, Daly M, Donnelly P, ... ... Wijsman EM, et al. Replicating genotype-phenotype associations. Nature. 447: 655-60. PMID 17554299 DOI: 10.1038/447655A |
0.301 |
|
| 2007 |
Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH. Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 556-60. PMID 17450541 DOI: 10.1002/Ajmg.B.30471 |
0.469 |
|
| 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 |
0.392 |
|
| 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, ... ... Wijsman EM, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985 |
0.459 |
|
| 2007 |
Sung YJ, Wijsman EM. Accounting for epistasis in linkage analysis of general pedigrees. Human Heredity. 63: 144-52. PMID 17283443 DOI: 10.1159/000099186 |
0.417 |
|
| 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 |
0.402 |
|
| 2007 |
Sung YJ, Thompson EA, Wijsman EM. MCMC-based linkage analysis for complex traits on general pedigrees: multipoint analysis with a two-locus model and a polygenic component. Genetic Epidemiology. 31: 103-14. PMID 17123301 DOI: 10.1002/Gepi.20194 |
0.401 |
|
| 2006 |
Wijsman EM, Rothstein JH, Thompson EA. Multipoint Linkage Analysis with Many Multiallelic or Dense Diallelic Markers: Markov Chain–Monte Carlo Provides Practical Approaches for Genome Scans on General Pedigrees American Journal of Human Genetics. 79: 846-858. PMID 17033961 DOI: 10.1086/508472 |
0.387 |
|
| 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, ... ... Wijsman EM, 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 |
0.402 |
|
| 2006 |
Igo RP, Chapman NH, Wijsman EM. Segregation analysis of a complex quantitative trait: Approaches for identifying influential data points Human Heredity. 61: 80-86. PMID 16679774 DOI: 10.1159/000093085 |
0.379 |
|
| 2006 |
Igo RP, Chapman NH, Berninger VW, Matsushita M, Brkanac Z, Rothstein JH, Holzman T, Nielsen K, Raskind WH, Wijsman EM. Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 15-27. PMID 16331673 DOI: 10.1002/Ajmg.B.30245 |
0.406 |
|
| 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, ... ... Wijsman EM, et al. Evidence for genetic linkage of autism to chromosomes 7 and 4 Molecular Psychiatry. 11: 979. DOI: 10.1038/Sj.Mp.4001918 |
0.381 |
|
| 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 |
0.364 |
|
| 2005 |
Sieh W, Basu S, Fu AQ, Rothstein JH, Scheet PA, Stewart WC, Sung YJ, Thompson EA, Wijsman EM. Comparison of marker types and map assumptions using Markov chain Monte Carlo-based linkage analysis of COGA data. Bmc Genetics. 6: S11. PMID 16451566 DOI: 10.1186/1471-2156-6-S1-S11 |
0.418 |
|
| 2005 |
Wilcox MA, Pugh EW, Zhang H, Zhong X, Levinson DF, Kennedy GC, Wijsman EM. Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3. Genetic Epidemiology. 29: S7-28. PMID 16342186 DOI: 10.1002/Gepi.20106 |
0.393 |
|
| 2005 |
Gagnon F, Jarvik GP, Badzioch MD, Motulsky AG, Brunzell JD, Wijsman EM. Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia. Human Genetics. 117: 494-505. PMID 15959807 DOI: 10.1007/S00439-005-1338-4 |
0.43 |
|
| 2005 |
George AW, Wijsman EM, Thompson EA. MCMC multilocus lod scores: application of a new approach. Human Heredity. 59: 98-108. PMID 15838179 DOI: 10.1159/000085224 |
0.365 |
|
| 2005 |
Raskind WH, Igo RP, Chapman NH, Berninger VW, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Brown M, Wijsman EM. A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency. Molecular Psychiatry. 10: 699-711. PMID 15753956 DOI: 10.1038/Sj.Mp.4001657 |
0.422 |
|
| 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 |
0.419 |
|
| 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 |
0.43 |
|
| 2004 |
Wijsman EM, Yu D. Joint Oligogenic Segregation and Linkage Analysis Using Bayesian Markov Chain Monte Carlo Methods Molecular Biotechnology. 28: 205-226. PMID 15542922 DOI: 10.1385/Mb:28:3:205 |
0.418 |
|
| 2004 |
Chapman NH, Igo RP, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Berninger VW, Wijsman EM, Raskind WH. Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 131: 67-75. PMID 15389770 DOI: 10.1002/Ajmg.B.30018 |
0.45 |
|
| 2004 |
Badzioch MD, Igo RP, Gagnon F, Brunzell JD, Krauss RM, Motulsky AG, Wijsman EM, Jarvik GP. Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan. Arteriosclerosis, Thrombosis, and Vascular Biology. 24: 1942-50. PMID 15331429 DOI: 10.1161/01.Atv.0000143499.09575.93 |
0.434 |
|
| 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 |
0.472 |
|
| 2004 |
Wijsman EM, Robinson NM, Ainsworth KH, Rosenthal EA, Holzman T, Raskind WH. Familial aggregation patterns in mathematical ability. Behavior Genetics. 34: 51-62. PMID 14739696 DOI: 10.1023/B:Bege.0000009476.33020.B9 |
0.365 |
|
| 2003 |
George AW, Basu S, Li N, Rothstein JH, Sieberts SK, Stewart W, Wijsman EM, Thompson EA. Approaches to mapping genetically correlated complex traits. Bmc Genetics. 4: S71. PMID 14975139 DOI: 10.1186/1471-2156-4-S1-S71 |
0.437 |
|
| 2003 |
Wijsman EM. Summary of Group 8: Development and extension of linkage methods. Genetic Epidemiology. 25. PMID 14635171 DOI: 10.1002/Gepi.10286 |
0.378 |
|
| 2003 |
Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JA, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM. A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis. Nature Genetics. 35: 349-56. PMID 14608357 DOI: 10.1038/Ng1268 |
0.392 |
|
| 2003 |
Gagnon F, Jarvik GP, Motulsky AG, Deeb SS, Brunzell JD, Wijsman EM. Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment. Human Genetics. 113: 522-33. PMID 14569462 DOI: 10.1007/S00439-003-1006-5 |
0.4 |
|
| 2003 |
Chapman NH, Raskind WH, Thomson JB, Berninger VW, Wijsman EM. Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 121: 60-70. PMID 12898577 DOI: 10.1002/Ajmg.B.20068 |
0.448 |
|
| 2003 |
Wijsman EM, Rosenthal EA, Hall D, Blundell ML, Sobin C, Heath SC, Williams R, Brownstein MJ, Gogos JA, Karayiorgou M. Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q. Molecular Psychiatry. 8: 695-705, 643. PMID 12874606 DOI: 10.1038/Sj.Mp.4001356 |
0.417 |
|
| 2003 |
Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, Kakol J, Buyske S, Chui B, Cohen P, de Toma C, Ehm M, Glanowski S, He C, Heil J, Markianos K, et al. A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. American Journal of Human Genetics. 73: 271-84. PMID 12844283 DOI: 10.1086/377137 |
0.355 |
|
| 2003 |
Conlon EM, Goode EL, Gibbs M, Stanford JL, Badzioch M, Janer M, Kolb S, Hood L, Ostrander EA, Jarvik GP, Wijsman EM. Oligogenic segregation analysis of hereditary prostate cancer pedigrees: Evidence for multiple loci affecting age at onset International Journal of Cancer. 105: 630-635. PMID 12740911 DOI: 10.1002/Ijc.11128 |
0.348 |
|
| 2003 |
Daw EW, Wijsman EM, Thompson EA. A score for Bayesian genome screening. Genetic Epidemiology. 24: 181-190. PMID 12652522 DOI: 10.1002/Gepi.10230 |
0.437 |
|
| 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, ... Wijsman E, 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 |
0.388 |
|
| 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 |
0.432 |
|
| 2002 |
Hall D, Wijsman EM, Roos JL, Gogos JA, Karayiorgou M. Extended intermarker linkage disequilibrium in the Afrikaners. Genome Research. 12: 956-61. PMID 12045148 DOI: 10.1101/Gr.136202 |
0.413 |
|
| 2002 |
Hsu L, Wijsman EM, Berninger VW, Thomson JB, Raskind WH. Familial aggregation of dyslexia phenotypes. II: paired correlated measures. American Journal of Medical Genetics. 114: 471-8. PMID 11992573 DOI: 10.1002/Ajmg.10523 |
0.376 |
|
| 2002 |
Goddard KA, Wijsman EM. Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers. Genetic Epidemiology. 22: 205-20. PMID 11921081 DOI: 10.1002/Gepi.0177 |
0.337 |
|
| 2002 |
Liu H, Heath SC, Sobin C, Roos JL, Galke BL, Blundell ML, Lenane M, Robertson B, Wijsman EM, Rapoport JL, Gogos JA, Karayiorgou M. Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 99: 3717-22. PMID 11891283 DOI: 10.1073/Pnas.042700699 |
0.351 |
|
| 2002 |
Sieberts SK, Wijsman EM, Thompson EA. Relationship Inference from Trios of Individuals, in the Presence of Typing Error American Journal of Human Genetics. 70: 170-180. PMID 11727198 DOI: 10.1086/338444 |
0.32 |
|
| 2001 |
Chapman NH, Leutenegger AL, Badzioch MD, Bogdan M, Conlon EM, Daw EW, Gagnon F, Li N, Maia JM, Wijsman EM, Thompson EA. The importance of connections: joining components of the Hutterite pedigree. Genetic Epidemiology. 21: S230-5. PMID 11793674 DOI: 10.1002/Gepi.2001.21.S1.S230 |
0.362 |
|
| 2001 |
Wijsman EM, Nur N. On estimating the proportion of variance in a phenotypic trait attributable to a measured locus. Human Heredity. 51: 145-149. PMID 11173965 DOI: 10.1159/000053335 |
0.32 |
|
| 2000 |
Raskind WH, Hsu L, Berninger VW, Thomson JB, Wijsman EM. Familial aggregation of dyslexia phenotypes. Behavior Genetics. 30: 385-96. PMID 11235984 DOI: 10.1023/A:1002700605187 |
0.389 |
|
| 2000 |
Daw EW, Thompson EA, Wijsman EM. Bias in multipoint linkage analysis arising from map misspecification. Genetic Epidemiology. 19: 366-380. PMID 11108646 DOI: 10.1002/1098-2272(200012)19:4<366::Aid-Gepi8>3.0.Co;2-F |
0.341 |
|
| 2000 |
Saavedra-Matiz CA, Chapman NH, Wijsman EM, Horowitz SH, Rosen DR. Linkage of hereditary distal myopathy with desmin accumulation to 2q Human Heredity. 50: 166-170. PMID 10686494 DOI: 10.1159/000022908 |
0.415 |
|
| 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 |
0.383 |
|
| 2000 |
Wijsman EM. Monte Carlo Markov chain methods and model selection in genetic epidemiology Computational Statistics & Data Analysis. 32: 349-360. DOI: 10.1016/S0167-9473(99)00088-2 |
0.329 |
|
| 1999 |
Daw EW, Kumm J, Snow GL, Thompson EA, Wijsman EM. Monte Carlo Markov chain methods for genome screening. Genetic Epidemiology. 17. PMID 10597425 DOI: 10.1002/Gepi.1370170723 |
0.354 |
|
| 1999 |
Daw EW, Heath SC, Wijsman EM. Multipoint Oligogenic Analysis of Age-at-Onset Data with Applications to Alzheimer Disease Pedigrees American Journal of Human Genetics. 64: 839-851. PMID 10053019 DOI: 10.1086/302276 |
0.445 |
|
| 1999 |
Hokanson JE, Brunzell JD, Jarvik GP, Wijsman EM, Austin MA. Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency. American Journal of Human Genetics. 64: 608-618. PMID 9973300 DOI: 10.1086/302234 |
0.355 |
|
| 1999 |
Austin MA, Stephens K, Walden CE, Wijsman E. Linkage analysis of candidate genes and the small, dense low-density lipoprotein phenotype. Atherosclerosis. 142: 79-87. PMID 9920508 DOI: 10.1016/S0021-9150(98)00193-2 |
0.441 |
|
| 1998 |
Chapman NH, Wijsman EM. Genome screens using linkage disequilibrium tests: Optimal marker characteristics and feasibility American Journal of Human Genetics. 63: 1872-1885. PMID 9837839 DOI: 10.1086/302139 |
0.395 |
|
| 1998 |
Snow GL, Wijsman EM. Pedigree analysis package (PAP) vs. MORGAN: Model selection and hypothesis testing on a large pedigree Genetic Epidemiology. 15: 355-369. PMID 9671986 DOI: 10.1002/(Sici)1098-2272(1998)15:4<355::Aid-Gepi3>3.0.Co;2-1 |
0.373 |
|
| 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 |
0.417 |
|
| 1998 |
Li H, Thompson EA, Wijsman EM. Semiparametric estimation of major gene effects for age of onset. Genetic Epidemiology. 15: 279-298. PMID 9593114 DOI: 10.1002/(Sici)1098-2272(1998)15:3<279::Aid-Gepi6>3.0.Co;2-# |
0.369 |
|
| 1998 |
Raskind WH, Conrad EU, Matsushita M, Wijsman EM, Wells DE, Chapman N, Sandell LJ, Wagner M, Houck J. Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses. Human Mutation. 11: 231-9. PMID 9521425 DOI: 10.1002/(Sici)1098-1004(1998)11:3<231::Aid-Humu8>3.0.Co;2-K |
0.396 |
|
| 1998 |
Wijsman EM, Brunzell JD, Jarvik GP, Austin MA, Motulsky AG, Deeb SS. Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex. Arteriosclerosis, Thrombosis, and Vascular Biology. 18: 215-26. PMID 9484986 DOI: 10.1161/01.Atv.18.2.215 |
0.455 |
|
| 1997 |
Heath SC, Snow GL, Thompson EA, Tseng C, Wijsman EM. MCMC segregation and linkage analysis. Genetic Epidemiology. 14: 1011-1016. PMID 9433616 DOI: 10.1002/(Sici)1098-2272(1997)14:6<1011::Aid-Gepi75>3.0.Co;2-L |
0.437 |
|
| 1997 |
Graham J, Chapman NH, Goddard KAB, Goode EL, Wijsman EM, Jarvik GP. Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigrees Genetic Epidemiology. 14: 999-1004. PMID 9433614 DOI: 10.1002/(Sici)1098-2272(1997)14:6<999::Aid-Gepi73>3.0.Co;2-F |
0.431 |
|
| 1997 |
Wijsman EM, Amos CI. Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions. Genetic Epidemiology. 14: 719-735. PMID 9433569 DOI: 10.1002/(Sici)1098-2272(1997)14:6<719::Aid-Gepi28>3.0.Co;2-S |
0.389 |
|
| 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 |
0.431 |
|
| 1996 |
Nakura J, Miki T, Ye L, Mitsuda N, Zhao Y, Kihara K, Yu CE, Oshima J, Fukuchi KI, Wijsman EM, Schellenberg GD, Martin GM, Murano Si, Hashimoto K, Fujiwara Y, et al. Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis. Genomics. 36: 130-41. PMID 8812424 DOI: 10.1006/Geno.1996.0433 |
0.367 |
|
| 1996 |
Edland SD, Silverman JM, Peskind ER, Tsuang D, Wijsman E, Morris JC. Increased risk of dementia in mothers of Alzheimer's disease cases: Evidence for maternal inheritance Neurology. 47: 254-256. PMID 8710088 DOI: 10.1212/Wnl.47.1.254 |
0.337 |
|
| 1996 |
Olshen AB, Wijsman EM. Pedigree analysis package vs. MIXD: fitting the mixed model on a large pedigree. Genetic Epidemiology. 13: 91-106. PMID 8647381 DOI: 10.1002/(Sici)1098-2272(1996)13:1<91::Aid-Gepi8>3.0.Co;2-9 |
0.315 |
|
| 1996 |
Schellenberg GD, Bird TD, Levy-Lahad E, Wijsman EM. 600 Genetic analysis of familial Alzheimer's disease Neurobiology of Aging. 17. DOI: 10.1016/S0197-4580(96)80602-6 |
0.419 |
|
| 1995 |
Goddard KAB, Jarvik GP, Graham J, McNeney B, Hsu L, Siegmund K, Grosser S, Olson J, Wijsman EM. Analysis of quantitative risk factors for a common oligogenic disease. Genetic Epidemiology. 12: 759-764. PMID 8788005 DOI: 10.1002/Gepi.1370120638 |
0.364 |
|
| 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 |
0.343 |
|
| 1995 |
Querfurth HW, Wijsman EM, St George-Hyslop PH, Selkoe DJ. Beta APP mRNA transcription is increased in cultured fibroblasts from the familial Alzheimer's disease-1 family. Brain Research. Molecular Brain Research. 28: 319-37. PMID 7723630 DOI: 10.1016/0169-328X(94)00224-3 |
0.335 |
|
| 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 |
0.45 |
|
| 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 |
0.39 |
|
| 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 |
0.345 |
|
| 1994 |
Palmer SE, Dale DC, Livingston RJ, Wijsman EM, Stephens K. Autosomal dominant cyclic hematopoiesis: exclusion of linkage to the major hematopoietic regulatory gene cluster on chromosome 5. Human Genetics. 93: 195-7. PMID 8112745 DOI: 10.1007/Bf00210609 |
0.389 |
|
| 1994 |
Commenges D, Olson J, Wijsman E. The weighted rank pairwise correlation statistic for linkage analysis: simulation study and application to Alzheimer's disease. Genetic Epidemiology. 11: 201-212. PMID 8013899 DOI: 10.1002/Gepi.1370110209 |
0.398 |
|
| 1994 |
Jarvik GP, Brunzell JD, Austin MA, Krauss RM, Motulsky AG, Wijsman E. Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype. Arteriosclerosis and Thrombosis : a Journal of Vascular Biology / American Heart Association. 14: 1687-94. PMID 7947591 DOI: 10.1161/01.Atv.14.11.1687 |
0.436 |
|
| 1994 |
Jarvik GP, Wijsman EM. Alzheimer's disease and the family effect. Nature Genetics. 8: 115-115. PMID 7842007 DOI: 10.1038/Ng1094-115A |
0.349 |
|
| 1993 |
Lin S, Thompson E, Wijsman E. Achieving irreducibility of the Markov chain Monte Carlo method applied to pedigree data Mathematical Medicine and Biology-a Journal of the Ima. 10: 1-17. PMID 8409623 DOI: 10.1093/Imammb/10.1.1 |
0.3 |
|
| 1993 |
Olson JM, Wijsman EM. Linkage between quantitative trait and marker loci : methods using all relative pairs Genetic Epidemiology. 10: 87-102. PMID 8339928 DOI: 10.1002/Gepi.1370100202 |
0.357 |
|
| 1993 |
Thompson EA, Lin S, Olshen AB, Wijsman EM. Monte Carlo analysis on a large pedigree. Genetic Epidemiology. 10: 677-682. PMID 8314080 DOI: 10.1002/Gepi.1370100658 |
0.333 |
|
| 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 |
0.459 |
|
| 1993 |
Wijsman EM. Genetic analysis of Alzheimer's disease: A summary of contributions to GAW8 Genetic Epidemiology. 10: 349-360. PMID 8314026 DOI: 10.1002/Gepi.1370100604 |
0.42 |
|
| 1993 |
Bonnycastle LL, Yu CE, Wijsman EM, Orr HT, Patterson D, Clancy KP, Goddard KA, Alonso ME, Nemens E, White JA. The c-fos gene and early-onset familial Alzheimer's disease. Neuroscience Letters. 160: 33-6. PMID 8247328 DOI: 10.1016/0304-3940(93)90910-D |
0.426 |
|
| 1993 |
Stephens K, Sybert VP, Wijsman EM, Ehrlich P, Spencer A. A keratin 14 mutational hot spot for epidermolysis bullosa simplex, Dowling-Meara: implications for diagnosis. The Journal of Investigative Dermatology. 101: 240-3. PMID 7688405 DOI: 10.1111/1523-1747.Ep12365079 |
0.35 |
|
| 1992 |
Austin MA, Horowitz H, Wijsman E, Krauss RM, Brunzell J. Bimodality of plasma apolipoprotein B levels in familial combined hyperlipidemia. Atherosclerosis. 92: 67-77. PMID 1575822 DOI: 10.1016/0021-9150(92)90011-5 |
0.326 |
|
| 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 |
0.464 |
|
| 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 |
0.453 |
|
| 1992 |
Deeb SS, Failor RA, Brown BG, Brunzell JD, Albers JJ, Motulsky AG, Wijsman E. Association of apolipoprotein B gene variants with plasma apoB and low density lipoprotein (LDL) cholesterol levels. Human Genetics. 88: 463-70. PMID 1346774 DOI: 10.1007/Bf00215683 |
0.307 |
|
| 1991 |
Austin MA, Wijsman E, Guo S, Krauss RM, Brunzell JD, Deeb S, Vogler GP. Lack of evidence for linkage between low‐density lipoprotein subclass phenotypes and the apolipoprotein B locus in familial combined hyperlipidemia Genetic Epidemiology. 8: 287-297. PMID 1761202 DOI: 10.1002/Gepi.1370080502 |
0.426 |
|
| 1990 |
Martin GM, Schellenberg GD, Wijsman EM, Bird TD. Alzheimer's disease. Dominant susceptibility genes. Nature. 347: 124. PMID 2395467 DOI: 10.1038/347124A0 |
0.32 |
|
| 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 |
0.373 |
|
| 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 |
0.389 |
|
| 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 |
0.442 |
|
| 1988 |
Bowcock AM, Hebert JM, Wijsman E, Gadi I, Cavalli-Sforza LL, Boyd CD. High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q Proceedings of the National Academy of Sciences of the United States of America. 85: 2701-2705. PMID 2895928 DOI: 10.1073/Pnas.85.8.2701 |
0.366 |
|
| 1987 |
Bowcock AM, Hebert JM, Christiano AM, Wijsman E, Cavalli-Sforza LL, Boyd CD. The pro alpha 1 (Iv) collagen gene is linked to the d13s3 locus at the distal end of human chromosome 13q Cytogenetic and Genome Research. 45: 234-236. PMID 2891465 DOI: 10.1159/000132460 |
0.302 |
|
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