Eden R. Martin - Publications

Affiliations: 
Human Genetics and Genomes University of Miami, Coral Gables, FL 
Area:
Genetics, Biostatistics Biology, Epidemiology, Bioinformatics Biology

136 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
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2015 Galor A, Covington D, Levitt AE, McManus KT, Seiden B, Felix ER, Kalangara J, Feuer W, Patin DJ, Martin ER, Sarantopoulos KD, Levitt RC. Neuropathic ocular pain due to dry eye is associated with multiple comorbid chronic pain syndromes. The Journal of Pain : Official Journal of the American Pain Society. PMID 26606863 DOI: 10.1016/j.jpain.2015.10.019  0.8
2015 Galor A, Batawi H, Felix ER, Margolis TP, Sarantopoulos KD, Martin ER, Levitt RC. Incomplete response to artificial tears is associated with features of neuropathic ocular pain. The British Journal of Ophthalmology. PMID 26377416 DOI: 10.1136/bjophthalmol-2015-307094  0.8
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  0.8
2015 Levitt AE, Galor A, Weiss JS, Felix ER, Martin ER, Patin DJ, Sarantopoulos KD, Levitt RC. Chronic dry eye symptoms after LASIK: parallels and lessons to be learned from other persistent post-operative pain disorders. Molecular Pain. 11: 21. PMID 25896684 DOI: 10.1186/s12990-015-0020-7  0.8
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  0.8
2015 Galor A, Felix ER, Feuer W, Shalabi N, Martin ER, Margolis TP, Sarantopoulos CD, Levitt RC. Dry eye symptoms align more closely to non-ocular conditions than to tear film parameters. The British Journal of Ophthalmology. 99: 1126-9. PMID 25710726 DOI: 10.1136/bjophthalmol-2014-306481  0.8
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  0.8
2015 Galor A, Levitt RC, Felix ER, Martin ER, Sarantopoulos CD. Neuropathic ocular pain: an important yet underevaluated feature of dry eye. Eye (London, England). 29: 301-12. PMID 25376119 DOI: 10.1038/eye.2014.263  0.8
2015 Galor A, Zlotcavitch L, Walter SD, Felix ER, Feuer W, Martin ER, Margolis TP, Sarantopoulos KD, Levitt RC. Dry eye symptom severity and persistence are associated with symptoms of neuropathic pain. The British Journal of Ophthalmology. 99: 665-8. PMID 25336572 DOI: 10.1136/bjophthalmol-2014-306057  0.8
2015 Griswold AJ, Dueker ND, 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. DOI: 10.1186/s13229-015-0034-z  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2013 Hadjixenofontos A, Schmidt MA, Whitehead PL, Konidari I, Hedges DJ, Wright HH, Abramson RK, Menon R, Williams SM, Cuccaro ML, Haines JL, Gilbert JR, Pericak-Vance MA, Martin ER, McCauley JL. Evaluating mitochondrial DNA variation in autism spectrum disorders. Annals of Human Genetics. 77: 9-21. PMID 23130936 DOI: 10.1111/j.1469-1809.2012.00736.x  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2011 Martin ER, Rampersaud E. Family-based genetic association tests Cold Spring Harbor Protocols. 6. DOI: 10.1101/pdb.top96  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2010 Edwards TL, Turner SD, Torstenson ES, Dudek SM, Martin ER, Ritchie MD. A general framework for formal tests of interaction after exhaustive search methods with applications to MDR and MDR-PDT. Plos One. 5: e9363. PMID 20186329 DOI: 10.1371/journal.pone.0009363  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2010 Tapanes-Castillo A, Weaver EJ, Smith RP, Kamei Y, Caspary T, Hamilton-Nelson KL, Slifer SH, Martin ER, Bixby JL, Lemmon VP. A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice. Neurogenetics. 11: 53-71. PMID 19565280 DOI: 10.1007/s10048-009-0203-3  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2008 Chung RH, Morris RW, Martin ER. Response to Ding and Lin American Journal of Human Genetics. 82: 530-531. DOI: 10.1016/j.ajhg.2008.01.001  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2007 Hancock DB, Martin ER, Stajich JM, Jewett R, Stacy MA, Scott BL, Vance JM, Scott WK. Smoking, caffeine, and nonsteroidal anti-inflammatory drugs in families with Parkinson disease. Archives of Neurology. 64: 576-80. PMID 17420321 DOI: 10.1001/archneur.64.4.576  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2006 Hancock DB, Martin ER, Fujiwara K, Stacy MA, Scott BL, Stajich JM, Jewett R, Li YJ, Hauser MA, Vance JM, Scott WK. NOS2A and the modulating effect of cigarette smoking in Parkinson's disease. Annals of Neurology. 60: 366-73. PMID 16823855 DOI: 10.1002/ana.20915  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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/appi.ajp.163.5.929  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2005 Martin ER. Linkage Disequilibrium and Association Analysis Genetic Analysis of Complex Diseases: Second Edition. 329-353. DOI: 10.1002/9780471781141.ch12  0.8
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  0.8
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  0.8
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  0.8
2004 Kraus VB, Li YJ, Martin ER, Jordan JM, Renner JB, Doherty M, Wilson AG, Moskowitz R, Hochberg M, Loeser R, Hooper M, Sundseth S. Articular hypermobility is a protective factor for hand osteoarthritis. Arthritis and Rheumatism. 50: 2178-83. PMID 15248215 DOI: 10.1002/art.20354  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2004 Bass MP, Martin ER, Hauser ER. Pedigree generation for analysis of genetic linkage and association Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 93-103. PMID 14992495  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
2003 Klein C, Hedrich K, Wellenbrock C, Kann M, Harris J, Marder K, Lang AE, Schwinger E, Ozelius LJ, Vieregge P, Pramstaller PP, Kramer PL. Frequency of parkin mutations in late-onset Parkinson's disease. Annals of Neurology. 54: 415-6; author reply . PMID 12953277 DOI: 10.1002/ana.10737  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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  0.8
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