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Eden R. Martin - Publications

Affiliations: 
Human Genetics and Genomes University of Miami, Coral Gables, FL 
Area:
Genetics, Biostatistics Biology, Epidemiology, Bioinformatics Biology
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250 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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, ... ... Martin E, 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  0.324
2022 Heath L, Earls JC, Magis AT, Kornilov SA, Lovejoy JC, Funk CC, Rappaport N, Logsdon BA, Mangravite LM, Kunkle BW, Martin ER, Naj AC, Ertekin-Taner N, Golde TE, Hood L, et al. Manifestations of Alzheimer's disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90. Scientific Reports. 12: 6117. PMID 35413975 DOI: 10.1038/s41598-022-09825-2  0.355
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, ... Martin ER, 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  0.331
2020 Griswold AJ, Sivasankaran SK, Van Booven D, Gardner OK, Rajabli F, Whitehead PL, Hamilton-Nelson KL, Adams LD, Scott AM, Hofmann NK, Vance JM, Cuccaro ML, Bush WS, Martin ER, Byrd GS, et al. Immune and Inflammatory Pathways Implicated by Whole Blood Transcriptomic Analysis in a Diverse Ancestry Alzheimer's Disease Cohort. Journal of Alzheimer's Disease : Jad. PMID 32597797 DOI: 10.3233/Jad-190855  0.386
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, ... ... Martin ER, 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  0.412
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, 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  0.451
2019 Gardner OK, Wang L, Van Booven D, Whitehead PL, Hamilton-Nelson KL, Adams LD, Starks TD, Hofmann NK, Vance JM, Cuccaro ML, Martin ER, Byrd GS, Haines JL, Bush WS, Beecham GW, et al. RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways. Human Molecular Genetics. PMID 31162550 DOI: 10.1093/Hmg/Ddz110  0.315
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, 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  0.329
2019 Martin ER, Gao XR, Haines JL, Pericak-Vance MA, Li Y. P1-139: TESTS OF DISEASE RISK VERSUS AGE AT ONSET: A POWER COMPARISON Alzheimer's & Dementia. 15: P290-P290. DOI: 10.1016/J.Jalz.2019.06.694  0.322
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  0.365
2019 Gardner OK, Wang L, Booven DV, Whitehead PL, Hamilton-Nelson KL, Adams LD, Starks TD, Hofmann NK, Vance JM, Cuccaro ML, Martin ER, Byrd GS, Haines JL, Bush WS, Beecham GW, et al. O3-13-04: Genetic Variants In Alzheimer'S Disease-Associated Regions Have Different Effects On Rna Editing Rates In African-American And Non-Hispanic White Populations Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4699  0.352
2019 Jaworski J, Kunkle BW, Rajabli F, Adams LD, Starks TD, Goate AM, Cuccaro ML, Vance JM, Martin ER, Foroud TM, Mayeux R, Reitz C, Byrd GS, Beecham GW, Pericak-Vance MA. O3-13-02: Genome-Wide Linkage Analysis Of African-American Alzheimer Disease Families Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4697  0.373
2019 Griswold AJ, Gardner OK, Booven DV, Jean-Francois M, Hamilton-Nelson KL, Whitehead PL, Adams LD, Starks TD, Hofmann NK, Cuccaro ML, Martin ER, Vance JM, Byrd GS, Haines JL, Bush WS, et al. P4-114: Eqtl Analysis Identifies Ancestry Specific Regulatory Effects Of Alzheimer Disease Associated Variants Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3775  0.425
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  0.41
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, ... ... Martin ER, 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  0.405
2019 Li Y, Slifer SH, Schmidt MA, Naj A, Gao XR, Martin ER. P3-123: Identification Of Genes Modifying Age-At-Onset Of Alzheimer'S Disease In The Alzheimer'S Disease Genetics Consortium (Adgc) Cohorts Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3151  0.405
2019 Jean-Francois M, Johnson FS, Baez P, Martinez I, Adams LD, Vance JM, Martin ER, Ayodele T, Pericak-Vance MA, Cuccaro ML, Beecham GW, Reitz C. P2-150: Degree Of Inbreeding In Multiplex Caribbean Hispanic Families Loaded For Early-Onset Alzheimer'S Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2557  0.361
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  0.353
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, 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  0.42
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, ... ... Martin ER, 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  0.383
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, ... ... Martin ER, 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  0.473
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, ... ... Martin ER, 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  0.395
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, 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  0.428
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, ... ... Martin E, 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  0.406
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  0.334
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, 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  0.428
2018 Kunkle BW, Jaworski J, Rajabli F, Adams LD, Cuccaro ML, Vance JM, Goate AM, Martin ER, Foroud TM, Reitz C, Beecham GW, Mayeux R, Pericak-Vance MA. P1-154: Genome-Wide Linkage Analyses Of African American Families Supports Evidence Of Linkage To Chromosome 12 Alzheimers & Dementia. 14: 336. DOI: 10.1016/J.Jalz.2018.06.158  0.35
2018 Griswold AJ, Sivasankaran SK, Gardner OK, Rajabli F, Hamilton-Nelson KL, Rolati S, Hofmann NK, Whitehead PL, Adams LD, Byrd GS, Martin ER, Cuccaro ML, Bush WS, Haines JL, Vance JM, et al. P1-144: Transcriptomic Analysis Of Whole Blood In African American And Non-Hispanic White Alzheimer Disease Cases And Controls Alzheimers & Dementia. 14: 331. DOI: 10.1016/J.Jalz.2018.06.147  0.314
2017 Martin ER, Tunc I, Liu Z, Slifer SH, Beecham AH, Beecham GW. Properties of global- and local-ancestry adjustments in genetic association tests in admixed populations. Genetic Epidemiology. PMID 29288582 DOI: 10.1002/Gepi.22103  0.338
2017 Sanders AR, Beecham GW, Guo S, Dawood K, Rieger G, Badner JA, Gershon ES, Krishnappa RS, Kolundzija AB, Duan J, Gejman PV, Bailey JM, Martin ER. Genome-Wide Association Study of Male Sexual Orientation. Scientific Reports. 7: 16950. PMID 29217827 DOI: 10.1038/S41598-017-15736-4  0.379
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, et al. The Alzheimer's Disease Sequencing Project: Study design and sample selection. Neurology. Genetics. 3: e194. PMID 29184913 DOI: 10.1212/Nxg.0000000000000194  0.405
2017 Chung RH, Kinnamon DD, Martin ER. Single Marker Family-Based Association Analysis Conditional on Parental Information. Methods in Molecular Biology (Clifton, N.J.). 1666: 391-407. PMID 28980256 DOI: 10.1007/978-1-4939-7274-6_19  0.698
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, ... Martin ER, et al. Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport. Jama Neurology. PMID 28738127 DOI: 10.1001/Jamaneurol.2017.1518  0.391
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, 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  0.46
2017 Kunkle BW, Carney RM, Kohli MA, Naj AC, Hamilton-Nelson KL, Whitehead PL, Wang L, Lang R, Cuccaro ML, Vance JM, Byrd GS, Beecham GW, Gilbert JR, Martin ER, Haines JL, et al. Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease. Neuroscience Letters. PMID 28400126 DOI: 10.1016/J.Neulet.2017.04.014  0.442
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, ... ... Martin ER, 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  0.403
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  0.423
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, 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  0.425
2017 Reitz C, Tang M, Reyes-Dumeyer D, Kunkle BW, Hamilton-Nelson KL, Lantigua R, Medrano M, Martin ER, Jimenez-Velazquez IZ, Pericak-Vance MA, Mayeux R, Beecham GW. [P2-105]: COLLECTION OF MULTIPLEX FAMILIES WITH UNEXPLAINED EARLY-ONSET ALZHEIMER's DISEASE FOR GENOMIC RESEARCH Alzheimer's & Dementia. 13: P647-P647. DOI: 10.1016/J.Jalz.2017.06.755  0.389
2016 Page J, Constantino JN, Zambrana K, Martin E, Tunc I, Zhang Y, Abbacchi A, Messinger D. Quantitative autistic trait measurements index background genetic risk for ASD in Hispanic families. Molecular Autism. 7: 39. PMID 27606047 DOI: 10.1186/S13229-016-0100-1  0.34
2016 Hussman JP, Beecham AH, Schmidt M, Martin ER, McCauley JL, Vance JM, Haines JL, Pericak-Vance MA. GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis. Genes and Immunity. PMID 27278126 DOI: 10.1038/Gene.2016.23  0.329
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, ... ... Martin ER, 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  0.39
2016 Xiong N, Li N, Martin E, Yu J, Li J, Liu J, Lee DY, Isacson O, Vance J, Qing H, Wang T, Lin Z. hVMAT2: A Target of Individualized Medication for Parkinson's Disease. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. PMID 27137201 DOI: 10.1007/S13311-016-0435-5  0.38
2016 Wang L, Maldonado L, Beecham GW, Martin ER, Evatt ML, Ritchie JC, Haines JL, Zabetian CP, Payami H, Pericak-Vance MA, Vance JM, Scott WK. DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient. Neurology. Genetics. 2: e72. PMID 27123490 DOI: 10.1212/Nxg.0000000000000072  0.32
2016 Nuytemans K, Maldonado L, Ali A, John-Williams K, Beecham GW, Martin E, Scott WK, Vance JM. Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants. Neurology. Genetics. 2: e44. PMID 27066581 DOI: 10.1212/Nxg.0000000000000044  0.41
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  0.411
2016 Wang X, Li N, Xiong N, You Q, Li J, Yu J, Qing H, Wang T, Cordell HJ, Isacson O, Vance JM, Martin ER, Zhao Y, Cohen BM, Buttner EA, et al. Genetic Variants of Microtubule Actin Cross-linking Factor 1 (MACF1) Confer Risk for Parkinson's Disease. Molecular Neurobiology. PMID 27021023 DOI: 10.1007/S12035-016-9861-Y  0.358
2016 Gangi DN, Messinger DS, Martin ER, Cuccaro ML. Dopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention. Autism Research : Official Journal of the International Society For Autism Research. PMID 26990357 DOI: 10.1002/Aur.1623  0.329
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  0.45
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  0.385
2016 Cukier HN, Kunkle BW, Rolati S, Whitehead PL, Vance JM, Cuccaro ML, Carney RM, Gilbert JR, Martin ER, Beecham GW, Haines JL, Pericak-Vance MA, Hamilton-Nelson KL. O1-09-02: Whole Exome Sequencing of Late Onset Multiplex Families Identifies Rare Coding Variants in Known and Novel Alzheimer’s Disease Genes Alzheimer's & Dementia. 12: P196-P197. DOI: 10.1016/J.Jalz.2016.06.342  0.384
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  0.416
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  0.385
2015 Kennedy JL, Xiong N, Yu J, Zai CC, Pouget JG, Li J, Liu K, Qing H, Wang T, Martin E, Levy DL, Lin Z. Increased Nigral SLC6A3 Activity in Schizophrenia Patients: Findings From the Toronto-McLean Cohorts. Schizophrenia Bulletin. PMID 26707863 DOI: 10.1093/Schbul/Sbv191  0.361
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, 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  0.425
2015 Griswold AJ, Dueker ND, Van Booven D, Rantus JA, Jaworski JM, Slifer SH, Schmidt MA, Hulme W, Konidari I, Whitehead PL, Cuccaro ML, Martin ER, Haines JL, Gilbert JR, Hussman JP, et al. Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Molecular Autism. 6: 43. PMID 26185613 DOI: 10.1186/S13229-015-0034-Z  0.399
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, ... ... Martin ER, 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  0.405
2015 Kozol RA, Cukier HN, Zou B, Mayo V, De Rubeis S, Cai G, Griswold AJ, Whitehead PL, Haines JL, Gilbert JR, Cuccaro ML, Martin ER, Baker JD, Buxbaum JD, Pericak-Vance MA, et al. Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis. Human Molecular Genetics. 24: 4006-23. PMID 25882707 DOI: 10.1093/Hmg/Ddv138  0.305
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, ... ... Martin ER, 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 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  0.378
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, ... ... Martin ER, 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  0.382
2015 Sanders AR, Martin ER, Beecham GW, Guo S, Dawood K, Rieger G, Badner JA, Gershon ES, Krishnappa RS, Kolundzija AB, Duan J, Gejman PV, Bailey JM. Genome-wide scan demonstrates significant linkage for male sexual orientation. Psychological Medicine. 45: 1379-88. PMID 25399360 DOI: 10.1017/S0033291714002451  0.307
2015 Humphries CE, Kohli MA, Nathanson L, Whitehead P, Beecham G, Martin E, Mash DC, Pericak-Vance MA, Gilbert J. Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 44: 977-87. PMID 25380588 DOI: 10.3233/Jad-141989  0.302
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, 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  0.401
2015 Beecham GW, Kunkle BW, Vardarajan B, Whitehead PL, Rolati S, Martin ER, Gilbert JR, Mayeux R, Haines JL, Pericak-Vance MA. O3-13-02: Whole-exome sequencing in early-onset Alzheimer disease cases identifies novel candidate genes Alzheimer's & Dementia. 11: P251-P251. DOI: 10.1016/J.Jalz.2015.07.310  0.37
2015 Cukier HN, Kunkle BW, Rolati S, Hamilton-Nelson KL, Kohli MA, Dombroski BA, Vardarajan BN, Whitehead PL, Booven DJV, Martin ER, Beecham GW, Farrer LA, Cuccaro ML, Vance JM, Mayeux R, et al. ABCA7 deletion associated with Alzheimer's disease in african americans Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.06.549  0.361
2014 Chung RH, Tsai WY, Martin ER. Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data. Plos One. 9: e107800. PMID 25244564 DOI: 10.1371/Journal.Pone.0107800  0.437
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, ... ... Martin ER, 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  0.409
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, 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  0.383
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, ... ... Martin ER, 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  0.453
2014 Kinnamon DD, Martin ER. Valid Monte Carlo permutation tests for genetic case-control studies with missing genotypes. Genetic Epidemiology. 38: 325-44. PMID 24723341 DOI: 10.1002/Gepi.21805  0.696
2014 Huang A, Martin ER, Vance JM, Cai X. Detecting genetic interactions in pathway-based genome-wide association studies. Genetic Epidemiology. 38: 300-9. PMID 24719383 DOI: 10.1002/Gepi.21803  0.364
2014 Nuytemans K, Inchausti V, Beecham GW, Wang L, Dickson DW, Trojanowski JQ, Lee VM, Mash DC, Frosch MP, Foroud TM, Honig LS, Montine TJ, Dawson TM, Martin ER, Scott WK, et al. Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 827-30. PMID 24573903 DOI: 10.1002/Mds.25838  0.333
2014 Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, et al. Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders. Molecular Autism. 5: 1. PMID 24410847 DOI: 10.1186/2040-2392-5-1  0.428
2014 Pericak-Vance M, Reitz C, Kunkle BW, Vardarajan BN, Kohli MA, Naj AC, Whitehead PL, Perry W, Martin E, Beecham G, Gilbert J, Farrer LA, Haines J, Schellenberg GD, Mayeux R. P2-131: WHOLE-EXOME SEQUENCING OF HISPANIC EARLY-ONSET ALZHEIMER DISEASE FAMILIES IDENTIFIES RARE VARIANTS IN MULTIPLE ALZHEIMER'S-RELATED GENES Alzheimer's & Dementia. 10: P518-P519. DOI: 10.1016/J.Jalz.2014.05.806  0.441
2014 Carney R, Kohli MA, Kunkle BW, Martin ER, Beecham GW, Gilbert JR, Pericak-Vance MA. P1-036: CLINICAL CHARACTERISTICS OF LATE ONSET ALZHEIMER DISEASE IN AN EXTENDED FAMILY WITH A MISSENSE VARIANT IN TTC3 Alzheimer's & Dementia. 10: P316-P316. DOI: 10.1016/J.Jalz.2014.05.271  0.389
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, 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  0.428
2013 Moreno-Estrada A, Gravel S, Zakharia F, McCauley JL, Byrnes JK, Gignoux CR, Ortiz-Tello PA, Martínez RJ, Hedges DJ, Morris RW, Eng C, Sandoval K, Acevedo-Acevedo S, Norman PJ, Layrisse Z, ... ... Martin ER, et al. Reconstructing the population genetic history of the Caribbean. Plos Genetics. 9: e1003925. PMID 24244192 DOI: 10.1371/Journal.Pgen.1003925  0.312
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, ... ... Martin ER, 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  0.462
2013 Park YS, Schmidt M, Martin ER, Pericak-Vance MA, Chung RH. Pathway-PDT: a flexible pathway analysis tool for nuclear families. Bmc Bioinformatics. 14: 267. PMID 24006871 DOI: 10.1186/1471-2105-14-267  0.358
2013 Nuytemans K, Bademci G, Kohli MM, Beecham GW, Wang L, Young JI, Nahab F, Martin ER, Gilbert JR, Benatar M, Haines JL, Scott WK, Züchner S, Pericak-Vance MA, Vance JM. C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Annals of Human Genetics. 77: 351-63. PMID 23845100 DOI: 10.1111/Ahg.12033  0.343
2013 Wang L, Nuytemans K, Bademci G, Jauregui C, Martin ER, Scott WK, Vance JM, Zuchner S. High-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2. Human Mutation. 34: 1071-4. PMID 23616242 DOI: 10.1002/Humu.22344  0.41
2013 Norton N, Li D, Rampersaud E, Morales A, Martin ER, Zuchner S, Guo S, Gonzalez M, Hedges DJ, Robertson PD, Krumm N, Nickerson DA, Hershberger RE. Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy. Circulation. Cardiovascular Genetics. 6: 144-53. PMID 23418287 DOI: 10.1161/Circgenetics.111.000062  0.456
2013 Nuytemans K, Bademci G, Inchausti V, Dressen A, Kinnamon DD, Mehta A, Wang L, Züchner S, Beecham GW, Martin ER, Scott WK, Vance JM. Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease. Neurology. 80: 982-9. PMID 23408866 DOI: 10.1212/Wnl.0B013E31828727D4  0.713
2013 Kohli MA, John-Williams K, Rajbhandary R, Naj A, Whitehead P, Hamilton K, Carney RM, Wright C, Crocco E, Gwirtzman HE, Lang R, Beecham G, Martin ER, Gilbert J, Benatar M, et al. Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians. Neurobiology of Aging. 34: 1519.e5-12. PMID 23107433 DOI: 10.1016/J.Neurobiolaging.2012.10.003  0.391
2013 Pericak-Vance M, Kunkle B, Kholi M, Naj A, Perry W, Hamilton K, Whitehead PL, Levin B, Carney R, Crocco E, Wright C, Beecham G, Martin E, Wang L, Gilbert J, et al. P3-021: Variant-domain mapping in confirmed late-onset Alzheimer disease (LOAD) loci identifies multiple genomic regions with potentially functional variants Alzheimer's & Dementia. 9: P557-P557. DOI: 10.1016/J.Jalz.2013.05.1090  0.393
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  0.421
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  0.353
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  0.397
2012 Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, Jaworski JM, Salyakina D, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Martin ER, et al. Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human Molecular Genetics. 21: 3513-23. PMID 22543975 DOI: 10.1093/Hmg/Dds164  0.388
2012 Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, et al. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Annals of Neurology. 71: 370-84. PMID 22451204 DOI: 10.1002/Ana.22687  0.4
2012 Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, ... ... Martin ER, et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. Plos Genetics. 8: e1002548. PMID 22438815 DOI: 10.1371/Journal.Pgen.1002548  0.44
2012 Kinnamon DD, Hershberger RE, Martin ER. Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants. Plos One. 7: e30238. PMID 22363423 DOI: 10.1371/Journal.Pone.0030238  0.725
2012 Norton N, Robertson PD, Rieder MJ, Züchner S, Rampersaud E, Martin E, Li D, Nickerson DA, Hershberger RE. Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era Circulation: Cardiovascular Genetics. 5: 167-174. PMID 22337857 DOI: 10.1161/Circgenetics.111.961805  0.337
2012 Chung RH, Martin ER. Single-marker family-based association analysis conditional on parental information. Methods in Molecular Biology (Clifton, N.J.). 850: 359-70. PMID 22307708 DOI: 10.1007/978-1-61779-555-8_19  0.393
2012 Wang L, Hara K, Van Baaren JM, Price JC, Beecham GW, Gallins PJ, Whitehead PL, Wang G, Lu C, Slifer MA, Züchner S, Martin ER, Mash D, Haines JL, Pericak-Vance MA, et al. Vitamin D receptor and Alzheimer's disease: a genetic and functional study. Neurobiology of Aging. 33: 1844.e1-9. PMID 22306846 DOI: 10.1016/J.Neurobiolaging.2011.12.038  0.385
2012 Panagiotou OA, Ioannidis JPA, Hirschhorn JN, Abecasis GR, Frayling TM, McCarthy MI, Lindgren CM, Beaty TH, Eriksson N, Polychronakos C, Kathirensan S, Plenge RM, Spritz R, Payami H, Martin ER, et al. What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations International Journal of Epidemiology. 41: 273-286. PMID 22253303 DOI: 10.1093/Ije/Dyr178  0.38
2012 Thomas V, Liu Z, Srinivasan SK, Chung R, Martin E, Levine EA, Freimanis RI, Hu JJ. Abstract 2613: Racial/Ethnic specific polygenic models of breast cancer risk Cancer Research. 72: 2613-2613. DOI: 10.1158/1538-7445.Am2012-2613  0.304
2012 Pericak-Vance M, Zuchner S, Kohli M, John-Williams K, Naj A, Rajbhandary R, Whitehead PL, Hamilton-Nelson K, Carney R, Wright C, Crocco E, Gwirtzman H, Lang R, Beecham G, Martin E, et al. Large repeat expansions in the C9ORF72 gene contribute to a spectrum of neurodegenerative disorders including Alzheimer's disease in Caucasians, but not African-Americans Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2013.08.277  0.366
2012 Haines J, Naj A, Kohli M, Hamilton-Nelson K, Rajbhandary R, Whitehead PL, Carney R, Crocco E, Wright C, Beecham G, Martin E, Gilbert J, Zuchner S, Pericak-Vance M, Levin B. O5-03-01: Deep resequencing of 9 confirmed late-onset Alzheimer's disease (LOAD) loci identifies multiple genomic regions with potentially functional variants Alzheimer's & Dementia. 8: P734-P735. DOI: 10.1016/J.Jalz.2012.05.1981  0.38
2012 Thornton-Wells T, Brown-Gentry K, Baker A, Torstenson E, Dudek S, Jiang L, Ritchie M, Martin E, Pericak-Vance M, Haines J. Biological knowledge-driven approach to gene-gene interaction analysis in the Alzheimer's Disease Genetics Consortium Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1843  0.38
2012 Zuchner S, Kohli M, Naj A, Hamilton K, Rajbhandary R, Plitnik T, John-Williams K, Whitehead PL, Gilbert J, Martin E, Beecham G, Haines J, Pericak-Vance M. Exome sequencing of extended late-onset Alzheimer's disease families identifies a variant in the TTC3 gene Alzheimers & Dementia. 8: 679. DOI: 10.1016/J.Jalz.2012.05.1839  0.438
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  0.381
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, ... Martin ER, 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  0.394
2011 Martins M, Rosa A, Guedes LC, Fonseca BV, Gotovac K, Violante S, Mestre T, Coelho M, Rosa MM, Martin ER, Vance JM, Outeiro TF, Wang L, Borovecki F, Ferreira JJ, et al. Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's disease. Plos One. 6: e25443. PMID 22003392 DOI: 10.1371/Journal.Pone.0025443  0.321
2011 Chung RH, Schmidt MA, Martin ER. CAPL: an efficient association software package using family and case-control data and accounting for population stratification. Bmc Bioinformatics. 12: 201. PMID 21612626 DOI: 10.1186/1471-2105-12-201  0.334
2011 Hedges DJ, Guettouche T, Yang S, Bademci G, Diaz A, Andersen A, Hulme WF, Linker S, Mehta A, Edwards YJ, Beecham GW, Martin ER, Pericak-Vance MA, Zuchner S, Vance JM, et al. Comparison of three targeted enrichment strategies on the SOLiD sequencing platform. Plos One. 6: e18595. PMID 21559511 DOI: 10.1371/Journal.Pone.0018595  0.314
2011 Rampersaud E, Siegfried JD, Norton N, Li D, Martin E, Hershberger RE. Rare variant mutations identified in pediatric patients with dilated cardiomyopathy. Progress in Pediatric Cardiology. 31: 39-47. PMID 21483645 DOI: 10.1016/J.Ppedcard.2010.11.008  0.315
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, ... ... Martin ER, 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  0.329
2011 Edwards YJ, Beecham GW, Scott WK, Khuri S, Bademci G, Tekin D, Martin ER, Jiang Z, Mash DC, ffrench-Mullen J, Pericak-Vance MA, Tsinoremas N, Vance JM. Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach. Plos One. 6: e16917. PMID 21364952 DOI: 10.1371/Journal.Pone.0016917  0.384
2011 Norton N, Li D, Rieder MJ, Siegfried JD, Rampersaud E, Züchner S, Mangos S, Gonzalez-Quintana J, Wang L, McGee S, Reiser J, Martin E, Nickerson DA, Hershberger RE. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy American Journal of Human Genetics. 88: 273-282. PMID 21353195 DOI: 10.1016/J.Ajhg.2011.01.016  0.415
2011 Butler MW, Burt A, Edwards TL, Zuchner S, Scott WK, Martin ER, Vance JM, Wang L. Vitamin D receptor gene as a candidate gene for Parkinson disease. Annals of Human Genetics. 75: 201-10. PMID 21309754 DOI: 10.1111/J.1469-1809.2010.00631.X  0.423
2011 Martin ER, Rampersaud E. Family-based genetic association tests. Cold Spring Harbor Protocols. 2011: pdb.top96. PMID 21285276 DOI: 10.1101/Pdb.Top96  0.387
2011 Hussman JP, Chung RH, Griswold AJ, Jaworski JM, Salyakina D, Ma D, Konidari I, Whitehead PL, Vance JM, Martin ER, Cuccaro ML, Gilbert JR, Haines JL, Pericak-Vance MA. A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism. Molecular Autism. 2: 1. PMID 21247446 DOI: 10.1186/2040-2392-2-1  0.372
2011 Thornton-Wells T, Torstenson E, Dudek S, Ritchie M, Martin E, Pericak-Vance M, Haines J. Discovery and Replication of Gene-Gene Interactions in Multiple Independent Datasets from the Alzheimer Disease Genetics Consortium Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.548  0.395
2011 Martin E, Naj A, Park YS, Gallins P, Hamilton K, Rajbhandary R, Haines J, Pericak-Vance M. Genome-Wide Association Analysis Identifies Novel Loci Associated with the Onset Age Among Cases with Late-Onset Alzheimer’s Disease Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.526  0.402
2010 Naj AC, Beecham GW, Martin ER, Gallins PJ, Powell EH, Konidari I, Whitehead PL, Cai G, Haroutunian V, Scott WK, Vance JM, Slifer MA, Gwirtsman HE, Gilbert JR, Haines JL, et al. Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. Plos Genetics. 6: e1001130. PMID 20885792 DOI: 10.1371/Journal.Pgen.1001130  0.428
2010 Chung RH, Schmidt MA, Morris RW, Martin ER. CAPL: a novel association test using case-control and family data and accounting for population stratification. Genetic Epidemiology. 34: 747-55. PMID 20878716 DOI: 10.1002/Gepi.20539  0.36
2010 Martin ER, Kinnamon DD, Schmidt MA, Powell EH, Zuchner S, Morris RW. SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies. Bioinformatics (Oxford, England). 26: 2803-10. PMID 20861027 DOI: 10.1093/Bioinformatics/Btq526  0.696
2010 Bademci G, Edwards TL, Torres AL, Scott WK, Züchner S, Martin ER, Vance JM, Wang L. A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease. Human Mutation. 31: E1767-71. PMID 20809526 DOI: 10.1002/Humu.21351  0.381
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, ... ... Martin ER, 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  0.387
2010 Beecham GW, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. APOE is not associated with Alzheimer disease: a cautionary tale of genotype imputation. Annals of Human Genetics. 74: 189-94. PMID 20529013 DOI: 10.1111/J.1469-1809.2010.00573.X  0.451
2010 Rampersaud E, Kinnamon DD, Hamilton K, Khuri S, Hershberger RE, Martin ER. Common susceptibility variants examined for association with dilated cardiomyopathy. Annals of Human Genetics. 74: 110-6. PMID 20201937 DOI: 10.1111/J.1469-1809.2010.00566.X  0.736
2010 Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, Beecham GW, Wang L, Züchner S, Konidari I, Wang G, Singer C, Nahab F, Scott B, Stajich JM, Pericak-Vance M, ... ... Martin ER, et al. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Annals of Human Genetics. 74: 97-109. PMID 20070850 DOI: 10.1111/J.1469-1809.2009.00560.X  0.431
2010 Cukier HN, Rabionet R, Konidari I, Rayner-Evans MY, Baltos ML, Wright HH, Abramson RK, Martin ER, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Novel variants identified in methyl-CpG-binding domain genes in autistic individuals. Neurogenetics. 11: 291-303. PMID 19921286 DOI: 10.1007/S10048-009-0228-7  0.342
2010 Edwards TL, Torstensen E, Dudek S, Martin ER, Ritchie MD. A cross-validation procedure for general pedigrees and matched odds ratio fitness metric implemented for the multifactor dimensionality reduction pedigree disequilibrium test. Genetic Epidemiology. 34: 194-9. PMID 19697353 DOI: 10.1002/Gepi.20447  0.371
2010 Ma DQ, Rabionet R, Konidari I, Jaworski J, Cukier HN, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA, Martin ER. Association and gene-gene interaction of SLC6A4 and ITGB3 in autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 477-83. PMID 19588468 DOI: 10.1002/Ajmg.B.31003  0.436
2010 Beecham GW, Schnetz-Boutaud N, Bartlett J, Naj A, Gilbert J, Martin ER, Buxbaum J, Haines JL, Pericak-Vance MA. Copy number polymorphism at chromosome 19 locus associated with late-onset Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.349  0.4
2009 Hedges DJ, Hedges D, Burges D, Powell E, Almonte C, Huang J, Young S, Boese B, Schmidt M, Pericak-Vance MA, Martin E, Zhang X, Harkins TT, Züchner S. Exome sequencing of a multigenerational human pedigree. Plos One. 4: e8232. PMID 20011588 DOI: 10.1371/Journal.Pone.0008232  0.399
2009 Gao X, Martin ER. Using allele sharing distance for detecting human population stratification. Human Heredity. 68: 182-91. PMID 19521100 DOI: 10.1159/000224638  0.338
2009 Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, ... Martin ER, et al. A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Annals of Human Genetics. 73: 263-73. PMID 19456320 DOI: 10.1111/J.1469-1809.2009.00523.X  0.445
2009 Slifer MA, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. Resolving the relationship between ApolipoproteinE and depression. Neuroscience Letters. 455: 116-9. PMID 19368858 DOI: 10.1016/J.Neulet.2009.03.007  0.308
2009 Zhang L, Martin ER, Morris RW, Li YJ. Association test for X-linked QTL in family-based designs. American Journal of Human Genetics. 84: 431-44. PMID 19344875 DOI: 10.1016/J.Ajhg.2009.02.010  0.405
2009 Gao X, Martin ER, Liu Y, Mayhew G, Vance JM, Scott WK. Genome-wide linkage screen in familial Parkinson disease identifies loci on chromosomes 3 and 18. American Journal of Human Genetics. 84: 499-504. PMID 19327735 DOI: 10.1016/J.Ajhg.2009.03.005  0.433
2009 Liang X, Slifer M, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Gilbert JR, Pericak-Vance MA, Haines JL. Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10. Human Mutation. 30: 463-71. PMID 19241460 DOI: 10.1002/Humu.20953  0.475
2009 Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, Haines JL, Pericak-Vance MA. Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. American Journal of Human Genetics. 84: 35-43. PMID 19118814 DOI: 10.1016/J.Ajhg.2008.12.008  0.439
2009 Edwards TL, Pericak-Vance M, Gilbert JR, Haines JL, Martin ER, Ritchie MD. An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 721-35. PMID 19105203 DOI: 10.1002/Ajmg.B.30899  0.446
2009 Wang L, Edwards T, Daffu G, Burt A, Konidari I, Scott W, Zuchner S, Martin E, Vance J. P3.149 Rare deletion in the tyrosine hydroxylase gene contributes to Parkinson disease risk Parkinsonism & Related Disorders. 15: S186. DOI: 10.1016/S1353-8020(09)70713-8  0.373
2009 Butler M, Vance J, Burt A, Zuchner S, Scott W, Martin E, Wang L. P3.148 Common genetic variants at the 5′ end of vitamin D receptor (VDR) gene are associated with Parkinson disease (PD) susceptibility Parkinsonism & Related Disorders. 15: S186. DOI: 10.1016/S1353-8020(09)70712-6  0.378
2009 Edwards T, Scott W, Almonte C, Burt A, Powell E, Beecham G, Wang L, Zuchner S, Konidari I, Wang G, Pericak-Vance M, Haines J, Vance J, Martin E. P3.116 Genome-wide signiflcant conflrmation of SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease Parkinsonism & Related Disorders. 15: S178. DOI: 10.1016/S1353-8020(09)70680-7  0.394
2009 Chung R, Edwards T, Scott W, Almonte C, Burt A, Powell E, Beecham G, Konidari I, Pericak-Vance M, Haines J, Zuchner S, Wang G, Wang L, Vance J, Martin E. P1.126 Developing a risk model for Parkinson disease Parkinsonism & Related Disorders. 15: S61. DOI: 10.1016/S1353-8020(09)70248-2  0.322
2009 Naj AC, Beecham GW, Slifer MA, Martin ER, Gallins PJ, Konidari I, Whitehead PL, Cai G, Kajiwara Y, Haroutunian V, Gwirtsman HE, Gilbert JR, Haines JL, Buxbaum JD, Pericak-Vance MA. Genome-wide association study validates associations in APOE, VDR, SORL1, WWC1, and ELAVL4 and identifies novel candidate genes for late-onset Alzheimer's disease Alzheimers & Dementia. 5. DOI: 10.1016/J.Jalz.2009.05.519  0.44
2009 Beecham GW, Naj AC, Cai G, Kajiwara Y, Haroutunian V, Konidari I, Gallins P, Whitehead P, Gilbert JR, Slifer MA, Gwirstman H, Martin ER, Buxbaum J, Haines JL, Pericak-Vance MA. GRB-associated binding protein 2 (GAB2) interacts with APOE to alter risk of late-onset Alzheimer's disease Alzheimers & Dementia. 5: 111. DOI: 10.1016/J.Jalz.2009.05.348  0.347
2009 Slifer MA, Naj A, Beecham G, Martin E, Konidari I, Whitehead P, Gallins P, Cai G, Kajiwara Y, Haroutunian V, Vance J, Haines J, Buxbaum J, Pericak-Vance M. ELAVL4 locus confirmed in depression of Alzheimer's disease Alzheimers & Dementia. 5: 468. DOI: 10.1016/J.Jalz.2009.04.793  0.3
2008 Züchner S, Gilbert JR, Martin ER, Leon-Guerrero CR, Xu PT, Browning C, Bronson PG, Whitehead P, Schmechel DE, Haines JL, Pericak-Vance MA. Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3. Annals of Human Genetics. 72: 725-31. PMID 18761660 DOI: 10.1111/J.1469-1809.2008.00474.X  0.457
2008 Hancock DB, Martin ER, Vance JM, Scott WK. Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease. Neurogenetics. 9: 249-62. PMID 18663495 DOI: 10.1007/S10048-008-0137-1  0.384
2008 Ewens WJ, Spielman RS, Kaplan NL, Gao X, Morris RW, Martin ER. Disease associations and family-based tests. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 1.12. PMID 18633973 DOI: 10.1002/0471142905.Hg0112S58  0.459
2008 Chung RH, Schmidt S, Martin ER, Hauser ER. Ordered-subset analysis (OSA) for family-based association mapping of complex traits. Genetic Epidemiology. 32: 627-37. PMID 18473393 DOI: 10.1002/Gepi.20340  0.433
2008 Martin ER, Schmidt MA. The future is now - Will the real disease gene please stand up? Human Heredity. 66: 127-135. PMID 18382092 DOI: 10.1159/000119112  0.468
2008 Hancock DB, Martin ER, Mayhew GM, Stajich JM, Jewett R, Stacy MA, Scott BL, Vance JM, Scott WK. Pesticide exposure and risk of Parkinson's disease: a family-based case-control study. Bmc Neurology. 8: 6. PMID 18373838 DOI: 10.1186/1471-2377-8-6  0.345
2008 Li YW, Martin ER, Li YJ. EMK: A novel program for family-based allelic and genotypic association tests on quantitative traits Annals of Human Genetics. 72: 388-396. PMID 18307576 DOI: 10.1111/J.1469-1809.2008.00432.X  0.416
2008 Zhang L, Martin ER, Chung RH, Li YJ, Morris RW. X-LRT: a likelihood approach to estimate genetic risks and test association with X-linked markers using a case-parents design. Genetic Epidemiology. 32: 370-80. PMID 18278816 DOI: 10.1002/Gepi.20311  0.419
2008 Gao X, Starmer J, Martin ER. A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms. Genetic Epidemiology. 32: 361-9. PMID 18271029 DOI: 10.1002/Gepi.20310  0.399
2008 Wang G, van der Walt JM, Mayhew G, Li YJ, Züchner S, Scott WK, Martin ER, Vance JM. Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein. American Journal of Human Genetics. 82: 283-9. PMID 18252210 DOI: 10.1016/J.Ajhg.2007.09.021  0.408
2008 Gao X, Scott WK, Wang G, Mayhew G, Li YJ, Vance JM, Martin ER. Gene-Gene interaction between FGF20 and MAOB in parkinson disease Annals of Human Genetics. 72: 157-162. PMID 18205889 DOI: 10.1111/J.1469-1809.2007.00418.X  0.378
2008 Thornton-Wells TA, Moore JH, Martin ER, Pericak-Vance MA, Haines JL. Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis. Genetic Epidemiology. 32: 187-203. PMID 18076107 DOI: 10.1002/Gepi.20294  0.42
2008 Schmidt S, Schmidt MA, Qin X, Martin ER, Hauser ER. Increased efficiency of case-control association analysis by using allele-sharing and covariate information. Human Heredity. 65: 154-65. PMID 17934318 DOI: 10.1159/000109732  0.426
2008 Slifer MA, Beecham GW, Martin ER, Wang G, Gilbert JR, Haines JL, Vance J, Pericak-Vance MA. O2-06-02: A genetic susceptibility locus for depression of Alzheimer's disease and Parkinson's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.350  0.354
2008 Martin ER, Turner SD, Beecham GW, Gilbert JR, Haines JL, Pericak-Vance MA, Ritchie MD. P3-240: Genome-wide analysis of gene-gene interaction in Alzheimer's disease Alzheimer's & Dementia. 4: T591-T591. DOI: 10.1016/J.Jalz.2008.05.1807  0.392
2008 Hara K, Gilbert J, Gallins P, Whitehead P, Beecham G, Slifer M, Martin E, Haines J, Pericak-Vance M. P3-228: Genetic association of vitamin D receptor gene on chromosome 12q with late-onset Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1795  0.371
2008 Gilbert JR, Beecham G, Gallins P, Slifer M, Martin ER, Haines J, Pericak-Vance MA. P3-223: Genome-wide association analysis of the age-at-onset for individuals with Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1790  0.395
2008 Beecham GW, Slifer MA, Martin ER, Li Y, Carney RM, Gilbert JR, Haines JL, Pericak-Vance MA. P3-200: Genomic convergence of late-onset Alzheimer's disease candidate genes Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1766  0.403
2008 Lin PI, Vance JM, Pericak-Vance MA, Martin ER. Response to Zaykin and Shibata American Journal of Human Genetics. 82: 796-797. DOI: 10.1016/J.Ajhg.2008.02.004  0.392
2007 Schmidt M, Qin X, Martin ER, Hauser ER, Schmidt S. Two-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategies. Bmc Proceedings. 1: S138. PMID 18466481 DOI: 10.1186/1753-6561-1-S1-S138  0.439
2007 Qin X, Schmidt S, Martin E, Hauser ER. Visualizing genotype x phenotype relationships in the GAW15 simulated data. Bmc Proceedings. 1: S132. PMID 18466475 DOI: 10.1186/1753-6561-1-S1-S132  0.377
2007 Mei H, Cuccaro ML, Martin ER. Multifactor dimensionality reduction-phenomics: A novel method to capture genetic heterogeneity with use of phenotypic variables American Journal of Human Genetics. 81: 1251-1261. PMID 17999363 DOI: 10.1086/522307  0.423
2007 Ashley-Koch AE, Jaworski J, Ma de Q, Mei H, Ritchie MD, Skaar DA, Robert Delong G, Worley G, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA. Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk. Psychiatric Genetics. 17: 221-6. PMID 17621165 DOI: 10.1097/Ypg.0B013E32809C2F75  0.448
2007 Liang X, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease. Human Mutation. 28: 1065-73. PMID 17573676 DOI: 10.1002/Humu.20567  0.48
2007 Hancock DB, Martin ER, Li YJ, Scott WK. Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations. Genetic Epidemiology. 31: 883-93. PMID 17565751 DOI: 10.1002/Gepi.20249  0.382
2007 Schmidt S, Qin X, Schmidt MA, Martin ER, Hauser ER. Interpreting analyses of continuous covariates in affected sibling pair linkage studies. Genetic Epidemiology. 31: 541-52. PMID 17410529 DOI: 10.1002/Gepi.20227  0.432
2007 Lin PI, Vance JM, Pericak-Vance MA, Martin ER. No gene is an island: the flip-flop phenomenon. American Journal of Human Genetics. 80: 531-8. PMID 17273975 DOI: 10.1086/512133  0.414
2007 Chung RH, Morris RW, Zhang L, Li YJ, Martin ER. X-APL: an improved family-based test of association in the presence of linkage for the X chromosome. American Journal of Human Genetics. 80: 59-68. PMID 17160894 DOI: 10.1086/510630  0.388
2007 Chung RH, Hauser ER, Martin ER. Interpretation of simultaneous linkage and family-based association tests in genome screens. Genetic Epidemiology. 31: 134-42. PMID 17123303 DOI: 10.1002/Gepi.20196  0.416
2007 Rampersaud E, Morris RW, Weinberg CR, Speer MC, Martin ER. Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent-of-origin (POO) effects in the presence of missing parental genotypes when unaffected siblings are available. Genetic Epidemiology. 31: 18-30. PMID 17096358 DOI: 10.1002/Gepi.20189  0.397
2006 North BV, Sham PC, Knight J, Martin ER, Curtis D. Investigation of the ability of haplotype association and logistic regression to identify associated susceptibility loci. Annals of Human Genetics. 70: 893-906. PMID 17044864 DOI: 10.1111/J.1469-1809.2006.00301.X  0.4
2006 Kang SJ, Scott WK, Li YJ, Hauser MA, van der Walt JM, Fujiwara K, Mayhew GM, West SG, Vance JM, Martin ER. Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 2175-80. PMID 17044053 DOI: 10.1002/Mds.21151  0.424
2006 Chung RH, Hauser ER, Martin ER. The APL test: extension to general nuclear families and haplotypes and examination of its robustness. Human Heredity. 61: 189-99. PMID 16877866 DOI: 10.1159/000094774  0.369
2006 Lin PI, Martin ER, Bronson PG, Browning-Large C, Small GW, Schmechel DE, Welsh-Bohmer KA, Haines JL, Gilbert JR, Pericak-Vance MA. Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease. Neurology. 67: 64-8. PMID 16832079 DOI: 10.1212/01.Wnl.0000223438.90113.4E  0.445
2006 Collins AL, Ma D, Whitehead PL, Martin ER, Wright HH, Abramson RK, Hussman JP, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Investigation of autism and GABA receptor subunit genes in multiple ethnic groups. Neurogenetics. 7: 167-74. PMID 16770606 DOI: 10.1007/S10048-006-0045-1  0.387
2006 Lin PI, Martin ER, Browning-Large CA, Schmechel DE, Welsh-Bohmer KA, Doraiswamy PM, Gilbert JR, Haines JL, Pericak-Vance MA. Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis. Neurogenetics. 7: 157-65. PMID 16770605 DOI: 10.1007/S10048-006-0047-Z  0.416
2006 Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA. An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder. Annals of Human Genetics. 70: 281-92. PMID 16674551 DOI: 10.1111/J.1469-1809.2006.00253.X  0.419
2006 Schmidt S, Schmidt MA, Qin X, Martin ER, Hauser ER. Linkage analysis with gene-environment interaction: model illustration and performance of ordered subset analysis. Genetic Epidemiology. 30: 409-22. PMID 16671105 DOI: 10.1002/Gepi.20152  0.393
2006 Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Lack of association between autism and SLC25A12. The American Journal of Psychiatry. 163: 929-31. PMID 16648338 DOI: 10.1176/Ajp.2006.163.5.929  0.447
2006 Slifer MA, Martin ER, Bronson PG, Browning-Large C, Doraiswamy PM, Welsh-Bohmer KA, Gilbert JR, Haines JL, Pericak-Vance MA. Lack of association between UBQLN1 and Alzheimer disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 208-13. PMID 16526030 DOI: 10.1002/Ajmg.B.30298  0.403
2006 Allen AS, Martin ER, Qin X, Li YJ. Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring. Genetic Epidemiology. 30: 248-58. PMID 16496310 DOI: 10.1002/Gepi.20141  0.36
2006 Martin ER, Ritchie MD, Hahn L, Kang S, Moore JH. A novel method to identify gene-gene effects in nuclear families: The MDR-PDT Genetic Epidemiology. 30: 111-123. PMID 16374833 DOI: 10.1002/Gepi.20128  0.435
2006 Liang X, Schnetz-Boutaud N, Kenealy SJ, Jiang L, Bartlett J, Lynch B, Gaskell PC, Gwirtsman H, McFarland L, Bembe ML, Bronson P, Gilbert JR, Martin ER, Pericak-Vance MA, Haines JL. Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus. Molecular Psychiatry. 11: 280-5. PMID 16222332 DOI: 10.1038/Sj.Mp.4001766  0.397
2006 Li YJ, Scott WK, Zhang L, Lin PI, Oliveira SA, Skelly T, Doraiswamy MP, Welsh-Bohmer KA, Martin ER, Haines JL, Pericak-Vance MA, Vance JM. Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases. Neurobiology of Aging. 27: 1087-93. PMID 15985314 DOI: 10.1016/J.Neurobiolaging.2005.05.013  0.42
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  0.41
2006 Zuchner S, Xu P, Browning C, Bronson PG, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. P1-362: Genetic evaluation of the Alzheimer’s disease locus on chromosome 9p21.3 Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.740  0.34
2006 Martin E, Thornton-Wells T, Edwards T, Hahn L, Bronson P, Gilbert J, Haines J, Pericak-Vance M, Ritchie M. P1-355: Joint analysis of candidate genes in AD through data reduction Alzheimer's & Dementia. 2: S201-S202. DOI: 10.1016/J.Jalz.2006.05.733  0.322
2006 Bronson PG, Wall NN, Haines JL, Schmechel DE, Gilbert JR, Pericak-Vance MA, Martin ER. P1-345: Evidence for association between late-onset Alzheimer's disease and MTHFR on chromosome 1 Alzheimer's & Dementia. 2: S198-S198. DOI: 10.1016/J.Jalz.2006.05.723  0.373
2006 Schnetz-Boutaud N, Liang X, Martin ER, Anderson BM, Zuchner S, Gilbert JR, Pericak-Vance MA, Haines JL. P1-313: Examination of the effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.691  0.33
2005 Schmidt M, Hauser ER, Martin ER, Schmidt S. Extension of the SIMLA package for generating pedigrees with complex inheritance patterns: environmental covariates, gene-gene and gene-environment interaction. Statistical Applications in Genetics and Molecular Biology. 4: Article15. PMID 16646832 DOI: 10.2202/1544-6115.1133  0.404
2005 Li YJ, Martin ER, Zhang L, Allen AS. Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study. Bmc Genetics. 6: S53. PMID 16451665 DOI: 10.1186/1471-2156-6-S1-S53  0.401
2005 Mei H, Ma D, Ashley-Koch A, Martin ER. Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data. Bmc Genetics. 6: S145. PMID 16451605 DOI: 10.1186/1471-2156-6-S1-S145  0.382
2005 Martin ER, Bronson PG, Li YJ, Wall N, Chung RH, Schmechel DE, Small G, Xu PT, Bartlett J, Schnetz-Boutaud N, Haines JL, Gilbert JR, Pericak-Vance MA. Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease. Journal of Medical Genetics. 42: 787-92. PMID 16199552 DOI: 10.1136/Jmg.2004.029553  0.484
2005 Boyles AL, Scott WK, Martin ER, Schmidt S, Li YJ, Ashley-Koch A, Bass MP, Schmidt M, Pericak-Vance MA, Speer MC, Hauser ER. Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing. Human Heredity. 59: 220-7. PMID 16093727 DOI: 10.1159/000087122  0.32
2005 Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA. Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism. American Journal of Human Genetics. 77: 377-88. PMID 16080114 DOI: 10.1086/433195  0.436
2005 van der Walt JM, Scott WK, Slifer S, Gaskell PC, Martin ER, Welsh-Bohmer K, Creason M, Crunk A, Fuzzell D, McFarland L, Kroner CC, Jackson CE, Haines JL, Pericak-Vance MA. Maternal lineages and Alzheimer disease risk in the Old Order Amish. Human Genetics. 118: 115-22. PMID 16078048 DOI: 10.1007/S00439-005-0032-X  0.372
2005 Slifer MA, Martin ER, Haines JL, Pericak-Vance MA. The ubiquilin 1 gene and Alzheimer's disease. The New England Journal of Medicine. 352: 2752-3; author reply. PMID 15987928 DOI: 10.1056/Nejm200506303522618  0.366
2005 Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA. Analysis of the RELN gene as a genetic risk factor for autism. Molecular Psychiatry. 10: 563-71. PMID 15558079 DOI: 10.1038/Sj.Mp.4001614  0.472
2004 Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes. Neuroscience Letters. 372: 209-14. PMID 15542242 DOI: 10.1016/J.Neulet.2004.09.037  0.42
2004 Oliveira SA, Scott WK, Zhang F, Stajich JM, Fujiwara K, Hauser M, Scott BL, Pericak-Vance MA, Vance JM, Martin ER. Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype. Neurogenetics. 5: 147-55. PMID 15459824 DOI: 10.1007/S10048-004-0180-5  0.405
2004 Nicodemus KK, Stenger JE, Schmechel DE, Welsh-Bohmer KA, Saunders AM, Roses AD, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA, Martin ER. Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease. Neurogenetics. 5: 201-8. PMID 15455263 DOI: 10.1007/S10048-004-0189-9  0.436
2004 van der Walt JM, Dementieva YA, Martin ER, Scott WK, Nicodemus KK, Kroner CC, Welsh-Bohmer KA, Saunders AM, Roses AD, Small GW, Schmechel DE, Murali Doraiswamy P, Gilbert JR, Haines JL, Vance JM, et al. Analysis of European mitochondrial haplogroups with Alzheimer disease risk. Neuroscience Letters. 365: 28-32. PMID 15234467 DOI: 10.1016/J.Neulet.2004.04.051  0.388
2004 Li YJ, Hauser MA, Scott WK, Martin ER, Booze MW, Qin XJ, Walter JW, Nance MA, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Goetz CG, et al. Apolipoprotein E controls the risk and age at onset of Parkinson disease. Neurology. 62: 2005-9. PMID 15184605 DOI: 10.1212/01.Wnl.0000128089.53030.Ac  0.39
2004 North BV, Curtis D, Martin ER, Lai EH, Roses AD, Sham PC. Further investigation of linkage disequilibrium SNPs and their ability to identify associated susceptibility loci. Annals of Human Genetics. 68: 240-8. PMID 15180704 DOI: 10.1046/J.1529-8817.2004.00086.X  0.443
2004 van der Walt JM, Noureddine MA, Kittappa R, Hauser MA, Scott WK, McKay R, Zhang F, Stajich JM, Fujiwara K, Scott BL, Pericak-Vance MA, Vance JM, Martin ER. Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease. American Journal of Human Genetics. 74: 1121-7. PMID 15122513 DOI: 10.1086/421052  0.392
2004 Raiford KL, Shao Y, Allen IC, Martin ER, Menold MM, Wright HH, Abramson RK, Worley G, DeLong GR, Vance JM, Cuccaro ML, Gilbert JR, Pericak-Vance MA. No association between the APOE gene and autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 57-60. PMID 14755445 DOI: 10.1002/Ajmg.B.20104  0.357
2004 Martin E, Bronson P, Jiang L, Welsh-Bohmer K, Schmechel D, Small G, Haines J, Gilbert J, Pericak-Vance M, Moore J. P4-134 A multilocus association analysis of APOE, LRP1 and A2M in Alzheimer disease Neurobiology of Aging. 25: S513. DOI: 10.1016/S0197-4580(04)81692-0  0.386
2004 Pericak-Vance MA, Bronson P, Martin ER, Browning C, Rayner M, Xu P, Small GW, Roses AD, Schmechel DE, Doraiswamy PM, Welsh-Bohmer KA, Haines JL, Gilbert JR. P4-080 Genetic studies of Alzheimer disease on chromosome 9P Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81638-5  0.358
2003 Ewens WJ, Spielman RS, Kaplan NL, Martin ER. Disease associations and family-based tests. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 1.12. PMID 18428340 DOI: 10.1002/0471142905.Hg0112S38  0.459
2003 Rampersaud E, Allen A, Li YJ, Shao Y, Bass M, Haynes C, Ashley-Koch A, Martin ER, Schmidt S, Hauser ER. Adjusting for covariates on a slippery slope: linkage analysis of change over time. Bmc Genetics. 4: S50. PMID 14975118 DOI: 10.1186/1471-2156-4-S1-S50  0.308
2003 Li YJ, Oliveira SA, Xu P, Martin ER, Stenger JE, Scherzer CR, Hauser MA, Scott WK, Small GW, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, et al. Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease. Human Molecular Genetics. 12: 3259-67. PMID 14570706 DOI: 10.1093/Hmg/Ddg357  0.417
2003 Martin ER, Bass MP, Gilbert JR, Pericak-Vance MA, Hauser ER. Genotype-based association test for general pedigrees: the genotype-PDT. Genetic Epidemiology. 25: 203-13. PMID 14557988 DOI: 10.1002/Gepi.10258  0.46
2003 Martin ER, Bass MP, Hauser ER, Kaplan NL. Accounting for linkage in family-based tests of association with missing parental genotypes. American Journal of Human Genetics. 73: 1016-26. PMID 14551902 DOI: 10.1086/378779  0.411
2003 Oliveira SA, Martin ER, Scott WK, Nicodemus KK, Small GW, Schmechel DE, Doraiswamy PM, Roses AD, Saunders AM, Gilbert JR, Haines JL, Vance JM, Pericak-Vance MA. The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease. Neuroscience Letters. 347: 143-6. PMID 12875906 DOI: 10.1016/S0304-3940(03)00670-0  0.429
2003 Oliveira SA, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons KE, Pahwa R, Stern MB, Hiner BC, Jankovic J, Ondo WG, Allen FH, Scott BL, Goetz CG, ... ... Martin ER, et al. Association study of Parkin gene polymorphisms with idiopathic Parkinson disease. Archives of Neurology. 60: 975-80. PMID 12873854 DOI: 10.1001/Archneur.60.7.975  0.409
2003 Oliveira SA, Scott WK, Martin ER, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Ondo WG, Allen FH, Scott BL, Goetz CG, Small GW, et al. Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. Annals of Neurology. 53: 624-9. PMID 12730996 DOI: 10.1002/Ana.10524  0.338
2003 van der Walt JM, Martin ER, Scott WK, Zhang F, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, et al. Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease. Neurology. 60: 1189-91. PMID 12682333 DOI: 10.1212/01.Wnl.0000055929.84668.9A  0.418
2003 Hauser MA, Li YJ, Takeuchi S, Walters R, Noureddine M, Maready M, Darden T, Hulette C, Martin E, Hauser E, Xu H, Schmechel D, Stenger JE, Dietrich F, Vance J. Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage. Human Molecular Genetics. 12: 671-7. PMID 12620972 DOI: 10.1093/Hmg/Ddg070  0.401
2003 van der Walt JM, Nicodemus KK, Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, et al. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. American Journal of Human Genetics. 72: 804-11. PMID 12618962 DOI: 10.1086/373937  0.344
2003 Barcellos LF, Oksenberg JR, Begovich AB, Martin ER, Schmidt S, Vittinghoff E, Goodin DS, Pelletier D, Lincoln RR, Bucher P, Swerdlin A, Pericak-Vance MA, Haines JL, Hauser SL. HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course. American Journal of Human Genetics. 72: 710-6. PMID 12557126 DOI: 10.1086/367781  0.307
2003 Crawford N, Uthoff S, Eichenberger M, Cobbs G, Petras R, Martin E, Galandiuk S. Characterization of genotype-phenotype correlations show that the IBD2 susceptibility locus is associated with colonic Crohn's disease and ulcerative colitis Gastroenterology. 124: A48. DOI: 10.1016/S0016-5085(03)80237-8  0.38
2002 Uthoff SM, Crawford NP, Eichenberger MR, Hamilton CJ, Petras RE, Martin ER, Galandiuk S. Association of ulcerative colitis with the inflammatory bowel disease susceptibility locus IBD2 in non-Jewish Caucasians and evidence of genetic heterogeneity among racial and ethnic populations with Crohn disease. American Journal of Medical Genetics. 113: 242-9. PMID 12439891 DOI: 10.1002/Ajmg.10762  0.423
2002 Haines JL, Bradford Y, Garcia ME, Reed AD, Neumeister E, Pericak-Vance MA, Rimmler JB, Menold MM, Martin ER, Oksenberg JR, Barcellos LF, Lincoln R, Hauser SL. Multiple susceptibility loci for multiple sclerosis. Human Molecular Genetics. 11: 2251-6. PMID 12217953 DOI: 10.1093/Hmg/11.19.2251  0.349
2002 Schmidt S, Barcellos LF, DeSombre K, Rimmler JB, Lincoln RR, Bucher P, Saunders AM, Lai E, Martin ER, Vance JM, Oksenberg JR, Hauser SL, Pericak-Vance MA, Haines JL. Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis. American Journal of Human Genetics. 70: 708-17. PMID 11836653 DOI: 10.1086/339269  0.436
2001 Menold MM, Shao Y, Wolpert CM, Donnelly SL, Raiford KL, Martin ER, Ravan SA, Abramson RK, Wright HH, Delong GR, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder. Journal of Neurogenetics. 15: 245-59. PMID 12092907 DOI: 10.3109/01677060109167380  0.392
2001 Kaplan NL, Martin ER. Power calculations for a general class of tests of linkage and association that use nuclear families with affected and unaffected sibs Theoretical Population Biology. 60: 193-201. PMID 11855953 DOI: 10.1006/Tpbi.2001.1541  0.363
2001 Schmidt S, Shao Y, Hauser ER, Slifer SH, Martin ER, Scott WK, Speer MC, Pericak-Vance MA. Life after the screen: making sense of many P-values. Genetic Epidemiology. 21: S546-51. PMID 11793734 DOI: 10.1002/Gepi.2001.21.S1.S546  0.311
2001 Hardy SW, Weir BS, Kaplan NL, Martin ER. Analysis of single nucleotide polymorphisms in candidate genes using the pedigree disequilibrium test. Genetic Epidemiology. 21: S441-6. PMID 11793716 DOI: 10.1002/Gepi.2001.21.S1.S441  0.441
2001 Pericak-Vance MA, Rimmler JB, Martin ER, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Goodkin DE, Hauser SL. Linkage and association analysis of chromosome 19q13 in multiple sclerosis. Neurogenetics. 3: 195-201. PMID 11714099 DOI: 10.1007/S100480100119  0.38
2001 Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH, Goetz CG, et al. Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease. Jama. 286: 2245-50. PMID 11710889 DOI: 10.1001/Jama.286.18.2245  0.449
2001 de Silva R, Weiler M, Morris HR, Martin ER, Wood NW, Lees AJ. Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy. Neuroscience Letters. 311: 145-8. PMID 11578815 DOI: 10.1016/S0304-3940(01)02109-7  0.404
2001 Martin ER, Bass MP, Kaplan NL. Correcting for a potential bias in the pedigree disequilibrium test American Journal of Human Genetics. 68: 1065-1067. PMID 11254459 DOI: 10.1086/319525  0.413
2000 Martin ER, Lai EH, Gilbert JR, Rogala AR, Afshari AJ, Riley J, Finch KL, Stevens JF, Livak KJ, Slotterbeck BD, Slifer SH, Warren LL, Conneally PM, Schmechel DE, Purvis I, et al. SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease. American Journal of Human Genetics. 67: 383-94. PMID 10869235 DOI: 10.1086/303003  0.466
2000 McItyre LM, Martin ER, Simonsen KL, Kaplan NL. Circumventing multiple testing: A multilocus Monte Carlo approach to testing for association Genetic Epidemiology. 19: 18-29. PMID 10861894 DOI: 10.1002/1098-2272(200007)19:1<18::Aid-Gepi2>3.0.Co;2-Y  0.374
2000 Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL, Ravan SA, Zimmerman A, Gilbert JR, Vance JM, Maddox LO, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. American Journal of Medical Genetics. 96: 43-8. PMID 10686550 DOI: 10.1002/(Sici)1096-8628(20000207)96:1<43::Aid-Ajmg9>3.0.Co;2-3  0.356
2000 Martin ER, Gilbert JR, Lai EH, Riley J, Rogala AR, Slotterbeck BD, Sipe CA, Grubber JM, Warren LL, Conneally PM, Saunders AM, Schmechel DE, Purvis I, Pericak-Vance MA, Roses AD, et al. Analysis of association at single nucleotide polymorphisms in the APOE region. Genomics. 63: 7-12. PMID 10662539 DOI: 10.1006/Geno.1999.6057  0.415
2000 Martin ER, Kaplan NL. A Monte Carlo procedure for two-stage tests with correlated data Genetic Epidemiology. 18: 48-62. PMID 10603458 DOI: 10.1002/(Sici)1098-2272(200001)18:1<48::Aid-Gepi4>3.0.Co;2-S  0.349
2000 Kaplan NL, Monks SA, Martin ER. A test for linkage and association in general pedigrees Genescreen. 1: 65-67. DOI: 10.1046/J.1466-9218.2000.00023.X  0.359
1999 Monks SA, Martin ER, Umbach DM, Kaplan NL. Two tests of association for a susceptibility locus for families of variable size: An example using two sampling strategies Genetic Epidemiology. 17: S655-S660. PMID 10597509 DOI: 10.1002/Gepi.13701707107  0.383
1999 Anderson JL, Hauser ER, Martin ER, Scott WK, Ashley-Koch A, Kim KJ, Monks SA, Haynes CS, Speer MC, Pericak-Vance MA. Complete genomic screen for disease susceptibility loci in nuclear families. Genetic Epidemiology. 17: S473-8. PMID 10597478 DOI: 10.1002/Gepi.1370170776  0.435
1999 Grubber JM, Saunders AM, Crane-Gatherum AR, Scott WK, Martin ER, Haynes CS, Conneally PM, Small GW, Roses AD, Haines JL, Pericak-Vance MA. Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K). Neuroscience Letters. 269: 115-9. PMID 10430518 DOI: 10.1016/S0304-3940(99)00426-7  0.342
1999 Allison DB, Heo M, Kaplan N, Martin ER. Sibling-based tests of linkage and association for quantitative traits American Journal of Human Genetics. 64: 1754-1764. PMID 10330363 DOI: 10.1086/302404  0.366
1999 Rogaeva EA, Premkumar S, Grubber J, Serneels L, Scott WK, Kawarai T, Song Y, Hill DL, Abou-Donia SM, Martin ER, Vance JJ, Yu G, Orlacchio A, Pei Y, Nishimura M, et al. An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease. Nature Genetics. 22: 19-22. PMID 10319855 DOI: 10.1038/8729  0.418
1998 Haines JL, Terwedow HA, Burgess K, Pericak-Vance MA, Rimmler JB, Martin ER, Oksenberg JR, Lincoln R, Zhang DY, Banatao DR, Gatto N, Goodkin DE, Hauser SL. Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group. Human Molecular Genetics. 7: 1229-34. PMID 9668163 DOI: 10.1093/Hmg/7.8.1229  0.402
1997 Simonsen KL, Kaplan NL, Martin ER. A monte carlo permutation approach to choosing an affection status model for bipolar affective disorder Genetic Epidemiology. 14: 681-686. PMID 9433563 DOI: 10.1002/(Sici)1098-2272(1997)14:6<681::Aid-Gepi22>3.0.Co;2-L  0.331
1997 Martin ER, Kaplan NL, Weir BS. Tests for linkage and association in nuclear families. American Journal of Human Genetics. 61: 439-48. PMID 9311750 DOI: 10.1086/514860  0.416
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