Winston K. Scott, Ph.D. - Publications

Affiliations: 
2012 Anthropology State University of New York, Albany, Albany, NY, United States 
Area:
Latin American Studies, Industrial and Labor Relations, Latin American History

227 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
2021 Myers HF, Fair AM, Villalta F, Walz K, Beech BM, Scott WK, Haas DW. Transdisciplinary Perspectives on Precision Medicine. Health Equity. 5: 288-298. PMID 34036211 DOI: 10.1089/heq.2020.0131  0.01
2021 Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, ... Scott WK, et al. Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology. PMID 33938021 DOI: 10.1002/ana.26094  1
2021 Griswold AJ, Celis K, Bussies PL, Rajabli F, Whitehead PL, Hamilton-Nelson KL, Beecham GW, Dykxhoorn DM, Nuytemans K, Wang L, Gardner OK, Dorfsman DA, Bigio EH, Mesulam MM, Weintraub S, ... Scott WK, et al. Increased APOE ε4 expression is associated with the difference in Alzheimer's disease risk from diverse ancestral backgrounds. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 33522086 DOI: 10.1002/alz.12287  1
2021 Stein CM, Benchek P, Bartlett J, Igo RP, Sobota RS, Chervenak K, Mayanja-Kizza H, von Reyn CF, Lahey T, Bush WS, Boom WH, Scott WK, Marsit C, Sirugo G, Williams SM. Methylome-wide analysis reveals epigenetic marks associated with resistance to tuberculosis in HIV-infected individuals from East Africa. The Journal of Infectious Diseases. PMID 33400784 DOI: 10.1093/infdis/jiaa785  0.01
2020 Ramos J, Chowdhury AR, Caywood LJ, Prough M, Denise Fuzzell M, Fuzzell S, Miskimen K, Whitehead PL, Adams LD, Laux R, Song Y, Ogrocki P, Lerner AJ, Vance JM, Haines JL, Scott WK, et al. Lower Levels of Education Are Associated with Cognitive Impairment in the Old Order Amish. Journal of Alzheimer's Disease : Jad. PMID 33285633 DOI: 10.3233/JAD-200909  1
2020 Nuytemans K, Rajabli F, Bussies PL, Celis K, Scott WK, Singer C, Luca CC, Vinuela A, Pericak-Vance MA, Vance JM. Novel Variants in and Identified in Latino Parkinson Disease Cohort Enriched for Caribbean Origin. Frontiers in Neurology. 11: 573733. PMID 33281709 DOI: 10.3389/fneur.2020.573733  1
2020 Thanikachalam S, Hodapp E, Chang TC, Swols DM, Cengiz FB, Guo S, Zafeer MF, Seyhan S, Bademci G, Scott WK, Grajewski A, Tekin M. Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida. Genes. 11. PMID 32224865 DOI: 10.3390/genes11040350  0.01
2019 Fan BJ, Bailey JC, Igo RP, Kang JH, Boumenna T, Brilliant MH, Budenz DL, Fingert JH, Gaasterland T, Gaasterland D, Hauser MA, Kraft P, Lee RK, Lichter PR, Liu Y, ... Scott WK, et al. Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis. Jama Ophthalmology. PMID 31436842 DOI: 10.1001/Jamaophthalmol.2019.3109  1
2019 Young JI, Sivasankaran SK, Wang L, Ali A, Mehta A, Davis DA, Dykxhoorn DM, Petito CK, Beecham GW, Martin ER, Mash DC, Pericak-Vance M, Scott WK, Montine TJ, Vance JM. Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease. Neurology. Genetics. 5: e342. PMID 31403079 DOI: 10.1212/Nxg.0000000000000342  1
2019 Nuytemans K, Manrique CP, Uhlenberg A, Scott WK, Cuccaro ML, Luca CC, Singer C, Vance JM. Motivations for Participation in Parkinson Disease Genetic Research Among Hispanics versus Non-Hispanics. Frontiers in Genetics. 10: 658. PMID 31379924 DOI: 10.3389/fgene.2019.00658  1
2019 Waksmunski AR, Igo RP, Song YE, Cooke Bailey JN, Laux R, Fuzzell D, Fuzzell S, Adams LD, Caywood L, Prough M, Stambolian D, Scott WK, Pericak-Vance MA, Haines JL. Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish. Human Genetics. PMID 31367973 DOI: 10.1007/S00439-019-02050-4  1
2019 Ramos J, Caywood LJ, Prough M, Fuzzell MD, Fuzzell S, Miskimen K, Whitehead PL, Adams LD, Laux R, Song Y, Ogrocki P, Lerner AJ, Vance JM, Scott WK, Pericak-Vance MA, et al. P3-140: Protective Effect Of Education On Cognitive Function In The Old Order Amish Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3168  1
2018 Mitchell SL, Uppal K, Williamson SM, Liu K, Burgess LG, Tran V, Umfress AC, Jarrell KL, Cooke Bailey JN, Agarwal A, Pericak-Vance M, Haines JL, Scott WK, Jones DP, Brantley MA. The Carnitine Shuttle Pathway is Altered in Patients With Neovascular Age-Related Macular Degeneration. Investigative Ophthalmology & Visual Science. 59: 4978-4985. PMID 30326066 DOI: 10.1167/Iovs.18-25137  1
2018 Scott WK, Medie FM, Ruffin F, Sharma-Kuinkel BK, Cyr DD, Guo S, Dykxhoorn DM, Skov RL, Bruun NE, Dahl A, Lerche CJ, Petersen A, Larsen AR, Lauridsen TK, Johansen HK, et al. Human genetic variation in GLS2 is associated with development of complicated Staphylococcus aureus bacteremia. Plos Genetics. 14: e1007667. PMID 30289878 DOI: 10.1371/Journal.Pgen.1007667  0.01
2018 Nittala MG, Song YE, Sardell R, Adams LD, Pan S, Velaga SB, Horst V, Dana D, Caywood L, Laux R, Fuzzell D, Fuzzell S, Scott WK, Cooke Bailey JN, Igo RP, et al. AMISH EYE STUDY: Baseline Spectral Domain Optical Coherence Tomography Characteristics of Age-Related Macular Degeneration. Retina (Philadelphia, Pa.). PMID 29746403 DOI: 10.1097/Iae.0000000000002210  0.01
2018 Hou L, Kember RL, Roach JC, O'Connell JR, Craig DW, Bucan M, Scott WK, Pericak-Vance M, Haines JL, Crawford MH, Shuldiner AR, McMahon FJ. Author Correction: A population-specific reference panel empowers genetic studies of Anabaptist populations. Scientific Reports. 8: 6771. PMID 29691419 DOI: 10.1038/S41598-018-24604-8  1
2018 Bailey JNC, Gharahkhani P, Kang JH, Butkiewicz M, Sullivan DA, Weinreb RN, Aschard H, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert JH, ... Scott WK, et al. Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets. Investigative Ophthalmology & Visual Science. 59: 629-636. PMID 29392307 DOI: 10.1167/Iovs.17-22708  1
2018 Hui KY, Fernandez-Hernandez H, Hu J, Schaffner A, Pankratz N, Hsu NY, Chuang LS, Carmi S, Villaverde N, Li X, Rivas M, Levine AP, Bao X, Labrias PR, Haritunians T, ... Scott WK, et al. Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Science Translational Medicine. 10. PMID 29321258 DOI: 10.1126/Scitranslmed.Aai7795  1
2017 Stein CM, Sausville L, Wejse C, Sobota RS, Zetola NM, Hill PC, Boom WH, Scott WK, Sirugo G, Williams SM. Genomics of human pulmonary tuberculosis: from genes to pathways. Current Genetic Medicine Reports. 5: 149-166. PMID 29805915 DOI: 10.1007/S40142-017-0130-9  0.01
2017 Aschard H, Kang JH, Iglesias AI, Hysi P, Cooke Bailey JN, Khawaja AP, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert JH, Budenz DL, ... Scott WK, et al. Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis. European Journal of Human Genetics : Ejhg. PMID 28853718 DOI: 10.1038/Ejhg.2017.136  0.01
2017 Persad PJ, Heid IM, Weeks DE, Baird PN, de Jong EK, Haines JL, Pericak-Vance MA, Scott WK. Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Investigative Ophthalmology & Visual Science. 58: 4027-4038. PMID 28813576 DOI: 10.1167/Iovs.17-21734  1
2017 Hou L, Kember RL, Roach JC, O'Connell JR, Craig DW, Bucan M, Scott WK, Pericak-Vance M, Haines JL, Crawford MH, Shuldiner AR, McMahon FJ. A population-specific reference panel empowers genetic studies of Anabaptist populations. Scientific Reports. 7: 6079. PMID 28729679 DOI: 10.1038/S41598-017-05445-3  1
2017 Sobota RS, Stein CM, Kodaman N, Maro I, Wieland-Alter W, Igo RP, Magohe A, Malone LL, Chervenak K, Hall NB, Matee M, Mayanja-Kizza H, Joloba M, Moore JH, Scott WK, et al. A chromosome 5q31.1 locus associates with tuberculin skin test reactivity in HIV-positive individuals from tuberculosis hyper-endemic regions in east Africa. Plos Genetics. 13: e1006710. PMID 28628665 DOI: 10.1371/Journal.Pgen.1006710  0.01
2017 Yan Q, Ahn SH, Medie FM, Sharma-Kuinkel BK, Park LP, Scott WK, Deshmukh H, Tsalik EL, Cyr DD, Woods CW, Yu CA, Adams C, Qi R, Hansen B, Fowler VG. Candidate genes on murine chromosome 8 are associated with susceptibility to Staphylococcus aureus infection in mice and are involved with Staphylococcus aureus septicemia in humans. Plos One. 12: e0179033. PMID 28594911 DOI: 10.1371/Journal.Pone.0179033  0.01
2016 Sardell RJ, Persad PJ, Pan SS, Whitehead P, Adams LD, Laux RA, Fortun JA, Brantley MA, Kovach JL, Schwartz SG, Agarwal A, Haines JL, Scott WK, Pericak-Vance MA. Progression Rate From Intermediate to Advanced Age-Related Macular Degeneration Is Correlated With the Number of Risk Alleles at the CFH Locus. Investigative Ophthalmology & Visual Science. 57: 6107-6115. PMID 27832277 DOI: 10.1167/Iovs.16-19519  1
2016 Belle K, Shabazz FS, Nuytemans K, Davis DA, Ali A, Young JL, Scott WK, Mash DC, Vance JM, Dykxhoorn DM. Generation of disease-specific autopsy-confirmed iPSCs lines from postmortem isolated Peripheral Blood Mononuclear Cells. Neuroscience Letters. PMID 27826014 DOI: 10.1016/J.Neulet.2016.10.065  1
2016 Sardell RJ, Nittala MG, Adams LD, Laux RA, Cooke Bailey JN, Fuzzell D, Fuzzell S, Reinhart-Mercer L, Caywood LJ, Horst V, Mackay T, Dana D, Sadda SR, Scott WK, Stambolian D, et al. Heritability of Choroidal Thickness in the Amish. Ophthalmology. PMID 27771146 DOI: 10.1016/J.Ophtha.2016.09.001  1
2016 Pasquale LR, Aschard H, Kang JH, Bailey JN, Lindström S, Chasman DI, Christen WG, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert J, ... Scott WK, et al. Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample. Menopause (New York, N.Y.). PMID 27760082 DOI: 10.1097/Gme.0000000000000741  1
2016 Khawaja AP, Cooke Bailey JN, Kang JH, Allingham RR, Hauser MA, Brilliant M, Budenz DL, Christen WG, Fingert J, Gaasterland D, Gaasterland T, Kraft P, Lee RK, Lichter PR, Liu Y, ... Scott WK, et al. Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses. Investigative Ophthalmology & Visual Science. 57: 5046-5052. PMID 27661856 DOI: 10.1167/Iovs.16-20017  1
2016 Liu Y, Bailey JC, Helwa I, Dismuke WM, Cai J, Drewry M, Brilliant MH, Budenz DL, Christen WG, Chasman DI, Fingert JH, Gaasterland D, Gaasterland T, Gordon MO, Igo RP, ... Scott WK, et al. A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium. Investigative Ophthalmology & Visual Science. 57: 3974-3981. PMID 27537254 DOI: 10.1167/Iovs.16-19688  1
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  1
2016 Hoffman JD, van Grinsven MJ, Li C, Brantley M, McGrath J, Agarwal A, Scott WK, Schwartz SG, Kovach J, Pericak-Vance M, Sanchez CI, Haines JL. Genetic Association Analysis of Drusen Progression. Investigative Ophthalmology & Visual Science. 57: 2225-2231. PMID 27116550 DOI: 10.1167/Iovs.15-18571  1
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  1
2016 Cooke Bailey JN, Hoffman JD, Sardell RJ, Scott WK, Pericak-Vance MA, Haines JL. The Application of Genetic Risk Scores in Age-Related Macular Degeneration: A Review. Journal of Clinical Medicine. 5. PMID 26959068 DOI: 10.3390/Jcm5030031  1
2016 Sobota RS, Stein CM, Kodaman N, Scheinfeldt LB, Maro I, Wieland-Alter W, Igo RP, Magohe A, Malone LL, Chervenak K, Hall NB, Modongo C, Zetola N, Matee M, Joloba M, ... ... Scott WK, et al. A Locus at 5q33.3 Confers Resistance to Tuberculosis in Highly Susceptible Individuals. American Journal of Human Genetics. 98: 514-524. PMID 26942285 DOI: 10.1016/J.Ajhg.2016.01.015  1
2016 Hicks JE, Konidari I, Scott BL, Stajich JM, Ashley-Koch AE, Gilbert JR, Scott WK. Linkage of familial essential tremor to chromosome 5q35. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 26918299 DOI: 10.1002/Mds.26582  1
2016 Bailey JN, Loomis SJ, Kang JH, Allingham RR, Gharahkhani P, Khor CC, Burdon KP, Aschard H, Chasman DI, Igo RP, Hysi PG, Glastonbury CA, Ashley-Koch A, Brilliant M, Brown AA, ... ... Scott WK, et al. Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nature Genetics. PMID 26752265 DOI: 10.1038/Ng.3482  1
2016 Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, ... ... Scott WK, et al. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics. 48: 134-43. PMID 26691988 DOI: 10.1038/Ng.3448  1
2015 Kovach JL, Schwartz SG, Agarwal A, Brantley MA, Pan SS, Haines JL, Scott WK, Pericak-Vance MA. The Relationship Between Reticular Pseudodrusen and Severity of AMD. Ophthalmology. PMID 26681389 DOI: 10.1016/J.Ophtha.2015.10.036  1
2015 Hall JB, Cooke Bailey JN, Hoffman JD, Pericak-Vance MA, Scott WK, Kovach JL, Schwartz SG, Agarwal A, Brantley MA, Haines JL, Bush WS. Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models. Bmc Bioinformatics. 16: 329. PMID 26467978 DOI: 10.1186/S12859-015-0760-4  1
2015 DeLorenze GN, Nelson CL, Scott WK, Allen AS, Ray GT, Tsai AL, Quesenberry CP, Fowler VG. Polymorphisms In HLA Class II Genes Are Associated With Susceptibility To Staphylococcus aureus Infection In A Caucasian Population. The Journal of Infectious Diseases. PMID 26450422 DOI: 10.1093/infdis/jiv483  1
2015 D'Aoust LN, Cummings AC, Laux R, Fuzzell D, Caywood L, Reinhart-Mercer L, Scott WK, Pericak-Vance MA, Haines JL. Examination of candidate exonic variants for association to Alzheimer disease in the Amish. Plos One. 10: e0118043. PMID 25668194 DOI: 10.1371/Journal.Pone.0118043  1
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  1
2015 Wang L, Evatt ML, Maldonado LG, Perry WR, Ritchie JC, Beecham GW, Martin ER, Haines JL, Pericak-Vance MA, Vance JM, Scott WK. Vitamin D from different sources is inversely associated with Parkinson disease. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 560-6. PMID 25545356 DOI: 10.1002/Mds.26117  1
2015 Sharp ME, Caccappolo E, Mejia-Santana H, Tang MX, Rosado L, Orbe Reilly M, Ruiz D, Louis ED, Comella C, Nance M, Bressman S, Scott WK, Tanner C, Waters C, Fahn S, et al. The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 278-83. PMID 25393808 DOI: 10.1002/Mds.26065  1
2015 Hall JB, Cooke Bailey JN, Hoffman JD, Pericak-Vance MA, Scott WK, Kovach JL, Schwartz SG, Agarwal A, Brantley MA, Haines JL, Bush WS. Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models Bmc Bioinformatics. 16. DOI: 10.1186/s12859-015-0760-4  1
2014 Liu Y, Garrett ME, Yaspan BL, Bailey JC, Loomis SJ, Brilliant M, Budenz DL, Christen WG, Fingert JH, Gaasterland D, Gaasterland T, Kang JH, Lee RK, Lichter P, Moroi SE, ... ... Scott WK, et al. DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma. Investigative Ophthalmology & Visual Science. 55: 8251-8. PMID 25414181 DOI: 10.1167/Iovs.14-15712  1
2014 Hamza TH, Hill-Burns EM, Scott WK, Vance JM, Factor SA, Zabetian CP, Payami H. Glutamate receptor gene GRIN2A, coffee, and Parkinson disease. Plos Genetics. 10: e1004774. PMID 25411979 DOI: 10.1371/Journal.Pgen.1004774  1
2014 Crawford DC, Dumitrescu L, Goodloe R, Brown-Gentry K, Boston J, McClellan B, Sutcliffe C, Wiseman R, Baker P, Pericak-Vance MA, Scott WK, Allen M, Mayo P, Schnetz-Boutaud N, Dilks HH, et al. Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study. Circulation. Cardiovascular Genetics. 7: 848-53. PMID 25363704 DOI: 10.1161/Circgenetics.113.000369  1
2014 Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, ... ... Scott WK, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics. 46: 989-93. PMID 25064009 DOI: 10.1038/Ng.3043  1
2014 Bailey JN, Yaspan BL, Pasquale LR, Hauser MA, Kang JH, Loomis SJ, Brilliant M, Budenz DL, Christen WG, Fingert J, Gaasterland D, Gaasterland T, Kraft P, Lee RK, Lichter PR, ... ... Scott WK, et al. Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma. Human Genetics. 133: 1319-30. PMID 25037249 DOI: 10.1007/S00439-014-1468-7  1
2014 Courtenay MD, Cade W, Schwartz SG, Kovach JL, Agarwal A, Wang G, Haines JL, Pericak-Vance MA, Scott WK. Set-based joint test of interaction between SNPs in the VEGF pathway and exogenous estrogen finds association with age-related macular degeneration. Investigative Ophthalmology & Visual Science. PMID 25015356 DOI: 10.1167/Iovs.14-14494  1
2014 Hoffman JD, Cooke Bailey JN, D'Aoust L, Cade W, Ayala-Haedo J, Fuzzell D, Laux R, Adams LD, Reinhart-Mercer L, Caywood L, Whitehead-Gay P, Agarwal A, Wang G, Scott WK, Pericak-Vance MA, et al. Rare complement factor H variant associated with age-related macular degeneration in the Amish. Investigative Ophthalmology & Visual Science. 55: 4455-60. PMID 24906858 DOI: 10.1167/Iovs.13-13684  1
2014 Yan Q, Sharma-Kuinkel BK, Deshmukh H, Tsalik EL, Cyr DD, Lucas J, Woods CW, Scott WK, Sempowski GD, Thaden JT, Thaden J, Rude TH, Ahn SH, Fowler VG. Dusp3 and Psme3 are associated with murine susceptibility to Staphylococcus aureus infection and human sepsis. Plos Pathogens. 10: e1004149. PMID 24901344 DOI: 10.1371/Journal.Ppat.1004149  1
2014 White MJ, Tacconelli A, Chen JS, Wejse C, Hill PC, Gomes VF, Velez-Edwards DR, Østergaard LJ, Hu T, Moore JH, Novelli G, Scott WK, Williams SM, Sirugo G. Epiregulin (EREG) and human V-ATPase (TCIRG1): genetic variation, ethnicity and pulmonary tuberculosis susceptibility in Guinea-Bissau and The Gambia. Genes and Immunity. 15: 370-7. PMID 24898387 DOI: 10.1038/Gene.2014.28  1
2014 Carnes MU, Liu YP, Allingham RR, Whigham BT, Havens S, Garrett ME, Qiao C, Katsanis N, Wiggs JL, Pasquale LR, Ashley-Koch A, Oh EC, Hauser MA. Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. Plos Genetics. 10: e1004372. PMID 24875647 DOI: 10.1371/Journal.Pgen.1004372  1
2014 Rosentul DC, Plantinga TS, Farcas M, Oosting M, Hamza OJ, Scott WK, Alexander BD, Yang JC, Laird GM, Joosten LA, van der Meer JW, Perfect JR, Kullberg BJ, van der Ven AJ, Johnson MD, et al. Role of autophagy genetic variants for the risk of Candida infections. Medical Mycology. 52: 333-41. PMID 24713404 DOI: 10.1093/Mmy/Myt035  1
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  1
2014 Nelson CL, Pelak K, Podgoreanu MV, Ahn SH, Scott WK, Allen AS, Cowell LG, Rude TH, Zhang Y, Tong A, Ruffin F, Sharma-Kuinkel BK, Fowler VG. A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting. Bmc Infectious Diseases. 14: 83. PMID 24524581 DOI: 10.1186/1471-2334-14-83  1
2014 Smeekens SP, Malireddi RK, Plantinga TS, Buffen K, Oosting M, Joosten LA, Kullberg BJ, Perfect JR, Scott WK, van de Veerdonk FL, Xavier RJ, van de Vosse E, Kanneganti TD, Johnson MD, Netea MG. Autophagy is redundant for the host defense against systemic Candida albicans infections. European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology. 33: 711-22. PMID 24202731 DOI: 10.1007/s10096-013-2002-x  1
2014 Alcalay RN, Caccappolo E, Mejia-Santana H, Tang MX, Rosado L, Orbe Reilly M, Ruiz D, Louis ED, Comella CL, Nance MA, Bressman SB, Scott WK, Tanner CM, Mickel SF, Waters CH, et al. Cognitive and motor function in long-duration PARKIN-associated Parkinson disease. Jama Neurology. 71: 62-7. PMID 24190026 DOI: 10.1001/Jamaneurol.2013.4498  1
2013 Pasquale LR, Loomis SJ, Weinreb RN, Kang JH, Yaspan BL, Bailey JC, Gaasterland D, Gaasterland T, Lee RK, Scott WK, Lichter PR, Budenz DL, Liu Y, Realini T, Friedman DS, et al. Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States. Molecular Vision. 19: 1471-81. PMID 23869166  1
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  1
2013 Davis MF, Cummings AC, D'Aoust LN, Jiang L, Velez Edwards DR, Laux R, Reinhart-Mercer L, Fuzzell D, Scott WK, Pericak-Vance MA, Lee SL, Haines JL. Parkinson disease loci in the mid-western Amish. Human Genetics. 132: 1213-21. PMID 23793441 DOI: 10.1007/S00439-013-1316-1  1
2013 Cummings AC, Torstenson E, Davis MF, D'Aoust LN, Scott WK, Pericak-Vance MA, Bush WS, Haines JL. Evaluating power and type 1 error in large pedigree analyses of binary traits. Plos One. 8: e62615. PMID 23658753 DOI: 10.1371/Journal.Pone.0062615  1
2013 Wang G, Dubovy SR, Kovach JL, Schwartz SG, Agarwal A, Scott WK, Haines JL, Pericak-Vance MA. Variants at chromosome 10q26 locus and the expression of HTRA1 in the retina. Experimental Eye Research. 112: 102-5. PMID 23644223 DOI: 10.1016/J.Exer.2013.04.019  1
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  1
2013 Naj AC, Scott WK, Courtenay MD, Cade WH, Schwartz SG, Kovach JL, Agarwal A, Wang G, Haines JL, Pericak-Vance MA. Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis. Annals of Human Genetics. 77: 215-31. PMID 23577725 DOI: 10.1111/Ahg.12011  1
2013 Wang G, Scott WK, Agarwal A, Haines JL, Pericak-Vance MA. Coding variants in ARMS2 and the risk of age-related macular degeneration. Jama Ophthalmology. 131: 804-5. PMID 23572227 DOI: 10.1001/Jamaophthalmol.2013.589  1
2013 Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GH, Sim X, Weeks DE, Guymer RH, ... ... Scott WK, et al. Seven new loci associated with age-related macular degeneration. Nature Genetics. 45: 433-9, 439e1-2. PMID 23455636 DOI: 10.1038/Ng.2578  1
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  1
2013 Smeekens SP, Ng A, Kumar V, Johnson MD, Plantinga TS, van Diemen C, Arts P, Verwiel ET, Gresnigt MS, Fransen K, van Sommeren S, Oosting M, Cheng SC, Joosten LA, Hoischen A, ... ... Scott WK, et al. Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans. Nature Communications. 4: 1342. PMID 23299892 DOI: 10.1038/Ncomms2343  1
2013 Edwards DR, Gilbert JR, Hicks JE, Myers JL, Jiang L, Cummings AC, Guo S, Gallins PJ, Konidari I, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Laux R, Jackson CE, ... ... Scott WK, et al. Linkage and association of successful aging to the 6q25 region in large Amish kindreds. Age (Dordrecht, Netherlands). 35: 1467-77. PMID 22773346 DOI: 10.1007/S11357-012-9447-1  1
2012 Cummings AC, Jiang L, Velez Edwards DR, McCauley JL, Laux R, McFarland LL, Fuzzell D, Knebusch C, Caywood L, Reinhart-Mercer L, Nations L, Gilbert JR, Konidari I, Tramontana M, Cuccaro ML, ... Scott WK, et al. Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. Annals of Human Genetics. 76: 342-51. PMID 22881374 DOI: 10.1111/J.1469-1809.2012.00721.X  1
2012 Hancock DB, Scott WK. Population-based case-control association studies Current Protocols in Human Genetics. PMID 22786610 DOI: 10.1002/0471142905.hg0117s74  1
2012 Piña Y, Houston SK, Murray TG, Koru-Sengul T, Decatur C, Scott WK, Nathanson L, Clarke J, Lampidis TJ. Retinoblastoma treatment: impact of the glycolytic inhibitor 2-deoxy-d-glucose on molecular genomics expression in LH(BETA)T(AG) retinal tumors. Clinical Ophthalmology (Auckland, N.Z.). 6: 817-30. PMID 22701083 DOI: 10.2147/Opth.S29688  1
2012 Johnson NV, Ahn SH, Deshmukh H, Levin MK, Nelson CL, Scott WK, Allen A, Fowler VG, Cowell LG. Haplotype Association Mapping Identifies a Candidate Gene Region in Mice Infected With Staphylococcus aureus. G3 (Bethesda, Md.). 2: 693-700. PMID 22690378 DOI: 10.1534/g3.112.002501  1
2012 Plantinga TS, Johnson MD, Scott WK, Joosten LA, van der Meer JW, Perfect JR, Kullberg BJ, Netea MG. Human genetic susceptibility to Candida infections. Medical Mycology. 50: 785-94. PMID 22662758 DOI: 10.3109/13693786.2012.690902  1
2012 Yeang CH, Ma GC, Shih JC, Yang YS, Chen CP, Chang SP, Wu SH, Liu CS, Kuo SJ, Chou HC, Hwu WL, Cameron AD, Ginsberg NA, Lin YS, Chen M. Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax. Plos One. 7: e34901. PMID 22529953 DOI: 10.1371/journal.pone.0034901  1
2012 Schwartz SG, Agarwal A, Kovach JL, Gallins PJ, Cade W, Postel EA, Wang G, Ayala-Haedo J, Spencer KM, Haines JL, Pericak-Vance MA, Scott WK. The ARMS2 A69S variant and bilateral advanced age-related macular degeneration. Retina (Philadelphia, Pa.). 32: 1486-91. PMID 22481475 DOI: 10.1097/Iae.0B013E318240A540  1
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, ... ... Scott WK, 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  1
2012 Alcalay RN, Caccappolo E, Mejia-Santana H, Tang M-, Rosado L, Orbe Reilly M, Ruiz D, Ross B, Verbitsky M, Kisselev S, Louis E, Comella C, Colcher A, Jennings D, Nance M, ... ... Scott WK, et al. Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study. Neurology. 78: 1434-40. PMID 22442429 DOI: 10.1212/Wnl.0B013E318253D54B  1
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, ... ... Scott WK, 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  1
2012 Velez Edwards DR, Tacconelli A, Wejse C, Hill PC, Morris GA, Edwards TL, Gilbert JR, Myers JL, Park YS, Stryjewski ME, Abbate E, Estevan R, Rabna P, Novelli G, Hamilton CD, ... ... Scott WK, et al. MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. Plos One. 7: e32275. PMID 22384203 DOI: 10.1371/Journal.Pone.0032275  1
2012 Plantinga TS, Johnson MD, Scott WK, van de Vosse E, Velez Edwards DR, Smith PB, Alexander BD, Yang JC, Kremer D, Laird GM, Oosting M, Joosten LA, van der Meer JW, van Dissel JT, Walsh TJ, et al. Toll-like receptor 1 polymorphisms increase susceptibility to candidemia. The Journal of Infectious Diseases. 205: 934-43. PMID 22301633 DOI: 10.1093/Infdis/Jir867  1
2012 Johnson MD, Plantinga TS, van de Vosse E, Velez Edwards DR, Smith PB, Alexander BD, Yang JC, Kremer D, Laird GM, Oosting M, Joosten LA, van der Meer JW, van Dissel JT, Walsh TJ, Perfect JR, ... ... Scott WK, et al. Cytokine gene polymorphisms and the outcome of invasive candidiasis: a prospective cohort study. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 54: 502-10. PMID 22144535 DOI: 10.1093/Cid/Cir827  1
2012 Wang G, Scott WK, Whitehead P, Court BL, Kovach JL, Schwartz SG, Agarwal A, Dubovy S, Haines JL, Pericak-Vance MA. A novel ARMS2 splice variant is identified in human retina. Experimental Eye Research. 94: 187-91. PMID 22138417 DOI: 10.1016/J.Exer.2011.11.005  1
2012 Courtenay MD, Gilbert JR, Jiang L, Cummings AC, Gallins PJ, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Laux R, McCauley JL, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK. Mitochondrial haplogroup X is associated with successful aging in the Amish. Human Genetics. 131: 201-8. PMID 21750925 DOI: 10.1007/S00439-011-1060-3  1
2012 Rosentul DC, Plantinga TS, Scott WK, Alexander BD, van de Geer NM, Perfect JR, Kullberg BJ, Johnson MD, Netea MG. The impact of caspase-12 on susceptibility to candidemia. European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology. 31: 277-80. PMID 21706251 DOI: 10.1007/s10096-011-1307-x  1
2011 Rosentul DC, Plantinga TS, Oosting M, Scott WK, Velez Edwards DR, Smith PB, Alexander BD, Yang JC, Laird GM, Joosten LA, van der Meer JW, Perfect JR, Kullberg BJ, Netea MG, Johnson MD. Genetic variation in the dectin-1/CARD9 recognition pathway and susceptibility to candidemia. The Journal of Infectious Diseases. 204: 1138-45. PMID 21881131 DOI: 10.1093/Infdis/Jir458  1
2011 Hamza TH, Chen H, Hill-Burns EM, Rhodes SL, Montimurro J, Kay DM, Tenesa A, Kusel VI, Sheehan P, Eaaswarkhanth M, Yearout D, Samii A, Roberts JW, Agarwal P, Bordelon Y, ... ... Scott WK, et al. Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee. Plos Genetics. 7: e1002237. PMID 21876681 DOI: 10.1371/Journal.Pgen.1002237  1
2011 Srivastava A, Tang MX, Mejia-Santana H, Rosado L, Louis ED, Caccappolo E, Comella C, Colcher A, Siderowf A, Jennings D, Nance M, Bressman S, Scott WK, Tanner C, Mickel S, et al. The relation between depression and parkin genotype: the CORE-PD study. Parkinsonism & Related Disorders. 17: 740-4. PMID 21856206 DOI: 10.1016/J.Parkreldis.2011.07.008  1
2011 Edwards DR, Gilbert JR, Jiang L, Gallins PJ, Caywood L, Creason M, Fuzzell D, Knebusch C, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK. Successful aging shows linkage to chromosomes 6, 7, and 14 in the Amish. Annals of Human Genetics. 75: 516-28. PMID 21668908 DOI: 10.1111/J.1469-1809.2011.00658.X  1
2011 Houston SK, Pina Y, Clarke J, Koru-Sengul T, Scott WK, Nathanson L, Schefler AC, Murray TG. Regional and temporal differences in gene expression of LH(BETA)T(AG) retinoblastoma tumors. Investigative Ophthalmology & Visual Science. 52: 5359-68. PMID 21571674 DOI: 10.1167/Iovs.10-6321  1
2011 Cummings AC, Lee SL, McCauley JL, Jiang L, Crunk A, McFarland LL, Gallins PJ, Fuzzell D, Knebusch C, Jackson CE, Scott WK, Pericak-Vance MA, Haines JL. A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6. Annals of Human Genetics. 75: 351-8. PMID 21488853 DOI: 10.1111/J.1469-1809.2011.00643.X  1
2011 Spencer KL, Olson LM, Schnetz-Boutaud N, Gallins P, Agarwal A, Iannaccone A, Kritchevsky SB, Garcia M, Nalls MA, Newman AB, Scott WK, Pericak-Vance MA, Haines JL. Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration. Plos One. 6: e17784. PMID 21455292 DOI: 10.1371/Journal.Pone.0017784  1
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  1
2011 Morris GA, Edwards DR, Hill PC, Wejse C, Bisseye C, Olesen R, Edwards TL, Gilbert JR, Myers JL, Stryjewski ME, Abbate E, Estevan R, Hamilton CD, Tacconelli A, Novelli G, ... ... Scott WK, et al. Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and Argentina. Plos One. 6: e16656. PMID 21339808 DOI: 10.1371/Journal.Pone.0016656  1
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  1
2011 Alcalay RN, Siderowf A, Ottman R, Caccappolo E, Mejia-Santana H, Tang MX, Rosado L, Louis E, Ruiz D, Waters C, Fahn S, Cote L, Frucht S, Ford B, Orbe-Reilly M, ... ... Scott WK, et al. Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD study. Neurology. 76: 319-26. PMID 21205674 DOI: 10.1212/Wnl.0B013E31820882Aa  1
2011 Spencer KL, Olson LM, Schnetz-Boutaud N, Gallins P, Wang G, Scott WK, Agarwal A, Jakobsdottir J, Conley Y, Weeks DE, Gorin MB, Pericak-Vance MA, Haines JL. Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility. Investigative Ophthalmology & Visual Science. 52: 1748-54. PMID 21169531 DOI: 10.1167/Iovs.09-5112  1
2011 Caccappolo E, Alcalay RN, Mejia-Santana H, Tang MX, Rakitin B, Rosado L, Louis ED, Comella CL, Colcher A, Jennings D, Nance MA, Bressman S, Scott WK, Tanner CM, Mickel SF, et al. Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study. Journal of the International Neuropsychological Society : Jins. 17: 91-100. PMID 21092386 DOI: 10.1017/S1355617710001190  1
2011 Hennig BJ, Velez-Edwards DR, Schim van der Loeff MF, Bisseye C, Edwards TL, Tacconelli A, Novelli G, Aaby P, Kaye S, Scott WK, Jaye A, Whittle HC, Williams SM, Hill AV, Sirugo G. CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guinea-Bissau, West Africa. Journal of Acquired Immune Deficiency Syndromes (1999). 56: 1-8. PMID 20924289 DOI: 10.1097/Qai.0B013E3181F638Ed  1
2010 Wang G, Scott WK, Haines JL, Pericak-Vance MA. Genotype at polymorphism rs11200638 and HTRA1 expression level. Archives of Ophthalmology (Chicago, Ill. : 1960). 128: 1491-3. PMID 21060055 DOI: 10.1001/Archophthalmol.2010.256  1
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  1
2010 Alcalay RN, Caccappolo E, Mejia-Santana H, Tang MX, Rosado L, Ross BM, Verbitsky M, Kisselev S, Louis ED, Comella C, Colcher A, Jennings D, Nance MA, Bressman SB, Scott WK, et al. Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study. Archives of Neurology. 67: 1116-22. PMID 20837857 DOI: 10.1001/Archneurol.2010.194  1
2010 Ahn SH, Deshmukh H, Johnson N, Cowell LG, Rude TH, Scott WK, Nelson CL, Zaas AK, Marchuk DA, Keum S, Lamlertthon S, Sharma-Kuinkel BK, Sempowski GD, Fowler VG. Two genes on A/J chromosome 18 are associated with susceptibility to Staphylococcus aureus infection by combined microarray and QTL analyses. Plos Pathogens. 6: e1001088. PMID 20824097 DOI: 10.1371/Journal.Ppat.1001088  1
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  1
2010 Hamza TH, Zabetian CP, Tenesa A, Laederach A, Montimurro J, Yearout D, Kay DM, Doheny KF, Paschall J, Pugh E, Kusel VI, Collura R, Roberts J, Griffith A, Samii A, ... Scott WK, et al. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Nature Genetics. 42: 781-5. PMID 20711177 DOI: 10.1038/Ng.642  1
2010 Gbadegesin R, Lavin P, Janssens L, Bartkowiak B, Homstad A, Wu G, Bowling B, Eckel J, Potocky C, Abbott D, Conlon P, Scott WK, Howell D, Hauser E, Winn MP. A new locus for familial FSGS on chromosome 2p. Journal of the American Society of Nephrology : Jasn. 21: 1390-7. PMID 20616172 DOI: 10.1681/Asn.2009101046  1
2010 Marder KS, Tang MX, Mejia-Santana H, Rosado L, Louis ED, Comella CL, Colcher A, Siderowf AD, Jennings D, Nance MA, Bressman S, Scott WK, Tanner CM, Mickel SF, Andrews HF, et al. Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study. Archives of Neurology. 67: 731-8. PMID 20558392 DOI: 10.1001/Archneurol.2010.95  1
2010 Chen W, Stambolian D, Edwards AO, Branham KE, Othman M, Jakobsdottir J, Tosakulwong N, Pericak-Vance MA, Campochiaro PA, Klein ML, Tan PL, Conley YP, Kanda A, Kopplin L, Li Y, ... ... Scott WK, et al. Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 107: 7401-6. PMID 20385819 DOI: 10.1073/Pnas.0912702107  1
2010 Ayala-Haedo JA, Gallins PJ, Whitehead PL, Schwartz SG, Kovach JL, Postel EA, Agarwal A, Wang G, Haines JL, Pericak-Vance MA, Scott WK. Analysis of single nucleotide polymorphisms in the NOS2A gene and interaction with smoking in age-related macular degeneration. Annals of Human Genetics. 74: 195-201. PMID 20374233 DOI: 10.1111/J.1469-1809.2010.00570.X  1
2010 Alcalay RN, Mejia-Santana H, Tang MX, Rakitin B, Rosado L, Ross B, Verbitsky M, Kisselev S, Louis ED, Comella CL, Colcher A, Jennings D, Nance MA, Bressman S, Scott WK, et al. Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease. Journal of Clinical and Experimental Neuropsychology. 32: 775-9. PMID 20182943 DOI: 10.1080/13803390903521018  1
2010 Wang G, Spencer KL, Scott WK, Whitehead P, Court BL, Ayala-Haedo J, Mayo P, Schwartz SG, Kovach JL, Gallins P, Polk M, Agarwal A, Postel EA, Haines JL, Pericak-Vance MA. Analysis of the indel at the ARMS2 3'UTR in age-related macular degeneration. Human Genetics. 127: 595-602. PMID 20182747 DOI: 10.1007/S00439-010-0805-8  1
2010 Montgomery MP, Kamel F, Pericak-Vance MA, Haines JL, Postel EA, Agarwal A, Richards M, Scott WK, Schmidt S. Overall diet quality and age-related macular degeneration. Ophthalmic Epidemiology. 17: 58-65. PMID 20100101 DOI: 10.3109/09286580903450353  1
2010 Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, Beecham GW, Wang L, Züchner S, Konidari I, Wang G, Singer C, Nahab F, Scott B, Stajich JM, Pericak-Vance M, et al. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Annals of Human Genetics. 74: 97-109. PMID 20070850 DOI: 10.1111/J.1469-1809.2009.00560.X  1
2010 Edwards DR, Gallins P, Polk M, Ayala-Haedo J, Schwartz SG, Kovach JL, Spencer K, Wang G, Agarwal A, Postel EA, Haines JL, Pericak-Vance M, Scott WK. Inverse association of female hormone replacement therapy with age-related macular degeneration and interactions with ARMS2 polymorphisms. Investigative Ophthalmology & Visual Science. 51: 1873-9. PMID 19933179 DOI: 10.1167/Iovs.09-4000  1
2010 Velez DR, Wejse C, Stryjewski ME, Abbate E, Hulme WF, Myers JL, Estevan R, Patillo SG, Olesen R, Tacconelli A, Sirugo G, Gilbert JR, Hamilton CD, Scott WK. Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans. Human Genetics. 127: 65-73. PMID 19771452 DOI: 10.1007/S00439-009-0741-7  1
2010 Cummings AC, Jiang L, Edwards DV, Laux R, McFarland LL, Gallins PJ, Caywood L, Creason M, Fuzzell D, Knebusch C, Tramontana MG, Slifer MA, Jackson CE, Scott WK, Pericak-Vance MA, et al. Genome-wide linkage study in the Amish shows evidence for a chromosome 3 locus in late-onset Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.220  1
2009 Alcalay RN, Mejia-Santana H, Tang MX, Rosado L, Verbitsky M, Kisselev S, Ross BM, Louis ED, Comella CL, Colcher A, Jennings D, Nance MA, Bressman S, Scott WK, Tanner C, et al. Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease. Archives of Neurology. 66: 1517-22. PMID 20008657 DOI: 10.1001/Archneurol.2009.267  1
2009 Velez DR, Hulme WF, Myers JL, Stryjewski ME, Abbate E, Estevan R, Patillo SG, Gilbert JR, Hamilton CD, Scott WK. Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and Caucasians. The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease. 13: 1068-76. PMID 19723394  1
2009 Shapshak P, Somboonwit C, Drumright LN, Frost SD, Commins D, Tellinghuisen TL, Scott WK, Duncan R, McCoy C, Page JB, Giunta B, Fernandez F, Singer E, Levine A, Minagar A, et al. Molecular and contextual markers of hepatitis C virus and drug abuse. Molecular Diagnosis & Therapy. 13: 153-79. PMID 19650670 DOI: 10.2165/01250444-200913030-00002  1
2009 Velez DR, Hulme WF, Myers JL, Weinberg JB, Levesque MC, Stryjewski ME, Abbate E, Estevan R, Patillo SG, Gilbert JR, Hamilton CD, Scott WK. NOS2A, TLR4, and IFNGR1 interactions influence pulmonary tuberculosis susceptibility in African-Americans. Human Genetics. 126: 643-53. PMID 19575238 DOI: 10.1007/S00439-009-0713-Y  1
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  1
2009 Wang G, Spencer KL, Court BL, Olson LM, Scott WK, Haines JL, Pericak-Vance MA. Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria. Investigative Ophthalmology & Visual Science. 50: 3084-90. PMID 19255159 DOI: 10.1167/Iovs.08-3240  1
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  1
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  1
2008 Carney RM, Slifer MA, Lin PI, Gaskell PC, Scott WK, Potocky CF, Hulette CM, Welsh-Bohmer KA, Schmechel DE, Vance JM, Pericak-Vance MA. Longitudinal follow-up of late-onset Alzheimer disease families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 571-8. PMID 18361431 DOI: 10.1002/Ajmg.B.30590  1
2008 Spencer KL, Olson LM, Anderson BM, Schnetz-Boutaud N, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. C3 R102G polymorphism increases risk of age-related macular degeneration. Human Molecular Genetics. 17: 1821-4. PMID 18325906 DOI: 10.1093/Hmg/Ddn075  1
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  1
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  1
2008 Spencer KL, Hauser MA, Olson LM, Schmidt S, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration. Human Molecular Genetics. 17: 971-7. PMID 18084039 DOI: 10.1093/Hmg/Ddm369  1
2008 Shuler RK, Schmidt S, Gallins P, Hauser MA, Scott WK, Caldwell J, Agarwal A, Haines JL, Pericak-Vance MA, Postel EA. Peripheral reticular pigmentary change is associated with complement factor H polymorphism (Y402H) in age-related macular degeneration. Ophthalmology. 115: 520-4. PMID 18067970 DOI: 10.1016/J.Ophtha.2007.06.021  1
2008 Shuler RK, Schmidt S, Gallins P, Hauser MA, Scott WK, Caldwell J, Agarwal A, Haines JL, Pericak-Vance MA, Postel EA. Phenotype analysis of patients with the risk variant LOC387715 (A69S) in age-related macular degeneration. American Journal of Ophthalmology. 145: 303-307. PMID 18061132 DOI: 10.1016/J.Ajo.2007.09.027  1
2008 Dodson R, Fomalont EB, Wiik K, Horiuchi S, Hirabayashi H, Edwards PG, Murata Y, Asaki Y, Moellenbrock GA, Scott WK, Taylor AR, Gurvits LI, Paragi Z, Frey S, Shen ZQ, et al. The VSOP 5 GHz active galactic nucleus survey. V. Imaging results for the remaining 140 sources Astrophysical Journal, Supplement Series. 175: 314-355. DOI: 10.1086/525025  1
2007 Hancock DB, Scott WK. Population-based case-control association studies. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 1.17. PMID 18428402 DOI: 10.1002/0471142905.hg0117s52  0.01
2007 Spencer KL, Hauser MA, Olson LM, Schnetz-Boutaud N, Scott WK, Schmidt S, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration. Investigative Ophthalmology & Visual Science. 48: 4277-83. PMID 17724217 DOI: 10.1167/Iovs.06-1427  1
2007 Spencer KL, Hauser MA, Olson LM, Schmidt S, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL. Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration. Human Molecular Genetics. 16: 1986-92. PMID 17576744 DOI: 10.1093/Hmg/Ddm146  1
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  1
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  1
2007 Clark LN, Haamer E, Mejia-Santana H, Harris J, Lesage S, Durr A, Bs SJ, Hedrich K, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, ... Scott W, et al. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 932-7. PMID 17415800 DOI: 10.1002/Mds.21419  1
2007 Scott WK, Schmidt S, Hauser MA, Gallins P, Schnetz-Boutaud N, Spencer KL, Gilbert JR, Agarwal A, Postel EA, Haines JL, Pericak-Vance MA. Independent effects of complement factor H Y402H polymorphism and cigarette smoking on risk of age-related macular degeneration. Ophthalmology. 114: 1151-6. PMID 17241667 DOI: 10.1016/J.Ophtha.2006.08.054  1
2007 Shuler RK, Hauser MA, Caldwell J, Gallins P, Schmidt S, Scott WK, Agarwal A, Haines JL, Pericak-Vance MA, Postel EA. Neovascular age-related macular degeneration and its association with LOC387715 and complement factor H polymorphism. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 63-7. PMID 17210853 DOI: 10.1001/Archopht.125.1.63  1
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  1
2006 Postel EA, Agarwal A, Caldwell J, Gallins P, Toth C, Schmidt S, Scott WK, Hauser MA, Haines JL, Pericak-Vance MA. Complement factor H increases risk for atrophic age-related macular degeneration. Ophthalmology. 113: 1504-7. PMID 16828512 DOI: 10.1016/J.Ophtha.2006.02.049  1
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  1
2006 Schmidt S, Hauser MA, Scott WK, Postel EA, Agarwal A, Gallins P, Wong F, Chen YS, Spencer K, Schnetz-Boutaud N, Haines JL, Pericak-Vance MA. Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration. American Journal of Human Genetics. 78: 852-64. PMID 16642439 DOI: 10.1086/503822  1
2006 McCauley JL, Hahs DW, Jiang L, Scott WK, Welsh-Bohmer KA, Jackson CE, Vance JM, Pericak-Vance MA, Haines JL. Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish. Bmc Medical Genetics. 7: 19. PMID 16515697 DOI: 10.1186/1471-2350-7-19  1
2006 Hahs DW, McCauley JL, Crunk AE, McFarland LL, Gaskell PC, Jiang L, Slifer SH, Vance JM, Scott WK, Welsh-Bohmer KA, Johnson SR, Jackson CE, Pericak-Vance MA, Haines JL. A genome-wide linkage analysis of dementia in the Amish. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 160-6. PMID 16389594 DOI: 10.1002/Ajmg.B.30257  1
2006 Haines JL, Schnetz-Boutaud N, Schmidt S, Scott WK, Agarwal A, Postel EA, Olson L, Kenealy SJ, Hauser M, Gilbert JR, Pericak-Vance MA. Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6. Investigative Ophthalmology & Visual Science. 47: 329-35. PMID 16384981 DOI: 10.1167/Iovs.05-0116  1
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  1
2005 Shah SH, Schmidt MA, Mei H, Scott WK, Hauser ER, Schmidt S. Searching for epistatic interactions in nuclear families using conditional linkage analysis. Bmc Genetics. 6: S148. PMID 16451608 DOI: 10.1186/1471-2156-6-S1-S148  1
2005 Rampersaud E, Scott WK, Hauser ER, Speer MC. Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs. Journal of Medical Genetics. 42: e68. PMID 16326825 DOI: 10.1136/Jmg.2005.032029  1
2005 Schmidt S, Haines JL, Postel EA, Agarwal A, Kwan SY, Gilbert JR, Pericak-Vance MA, Scott WK. Joint effects of smoking history and APOE genotypes in age-related macular degeneration. Molecular Vision. 11: 941-9. PMID 16288198  1
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  1
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  1
2005 Postel EA, Agarwal A, Schmidt S, Fan YT, Scott WK, Gilbert JR, Haines JL, Pericak-Vance MA. Comparing age-related macular degeneration phenotype in probands from singleton and multiplex families. American Journal of Ophthalmology. 139: 820-5. PMID 15860286 DOI: 10.1016/J.Ajo.2004.12.029  1
2005 Ashley-Koch AE, Shao Y, Rimmler JB, Gaskell PC, Welsh-Bohmer KA, Jackson CE, Scott WK, Haines JL, Pericak-Vance MA. An autosomal genomic screen for dementia in an extended Amish family. Neuroscience Letters. 379: 199-204. PMID 15843063 DOI: 10.1016/J.Neulet.2004.12.065  1
2005 Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA. Complement factor H variant increases the risk of age-related macular degeneration. Science (New York, N.Y.). 308: 419-21. PMID 15761120 DOI: 10.1126/Science.1110359  1
2005 Scott WK, Zhang F, Stajich JM, Scott BL, Stacy MA, Vance JM. Family-based case-control study of cigarette smoking and Parkinson disease Neurology. 64: 442-447. PMID 15699372 DOI: 10.1212/01.Wnl.0000150905.93241.B2  1
2005 Mathias RA, Beaty TH, Bailey-Wilson JE, Bickel C, Stockton ML, Barnes KC, Becker T, Knapp M, Vieland VJ, Wu X, Naiman DQ, Bergemann TL, Clarkson DB, Boyles AL, Scott WK, et al. Contents Vol. 59, 2005 Human Heredity. 59: 241-241. DOI: 10.1159/000087469  1
2005 Mathias RA, Beaty TH, Bailey-Wilson JE, Bickel C, Stockton ML, Barnes KC, Becker T, Knapp M, Vieland VJ, Wu X, Naiman DQ, Bergemann TL, Clarkson DB, Boyles AL, Scott WK, et al. Subject Index Vol. 59, 2005 Human Heredity. 59: 240-240. DOI: 10.1159/000087468  1
2005 Scott WK, Schildkraut JM. Complex Genetic Interactions Genetic Analysis of Complex Diseases: Second Edition. 397-421. DOI: 10.1002/9780471781141.ch14  1
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  1
2004 Schmidt S, Scott WK, Postel EA, Agarwal A, Hauser ER, De La Paz MA, Gilbert JR, Weeks DE, Gorin MB, Haines JL, Pericak-Vance MA. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12. Bmc Genetics. 5: 18. PMID 15238159 DOI: 10.1186/1471-2156-5-18  1
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  1
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  1
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  1
2004 Lovell JEJ, Moellenbrock GA, Horiuchi S, Fomalont EB, Scott WK, Hirabayashi H, Dodson RG, Dougherty SM, Edwards PG, Frey S, Gurvits LI, Lister ML, Murphy DW, Paragi Z, Piner BG, et al. The VSOP 5 GHz active galactic nucleus survey. II. Data calibration and imaging Astrophysical Journal, Supplement Series. 155: 27-31. DOI: 10.1086/424820  1
2004 Scott WK, Fomalont EB, Horiuchi S, Lovell JEJ, Moellenbrock GA, Dodson RG, Edwards PG, Coldwell GV, Fodor S, Frey S, Gurvits LI, Hirabayashi H, Lister ML, Mosoni L, Murata Y, et al. The VSOP 5 GHz active galactic nucleus survey. III. Imaging results for the first 102 sources Astrophysical Journal, Supplement Series. 155: 33-72. DOI: 10.1086/424819  1
2004 Horiuchi S, Fomalont EB, Scott WK, Taylor AR, Lovell JEJ, Moellenbrock GA, Dodson R, Murata Y, Hirabayashi H, Edwards PG, Gurvits LI, Shen ZQ. THE VSOP 5 GHz active galactic nucleus survey. IV. The angular size/brightness temperature distribution Astrophysical Journal. 616: 110-122. DOI: 10.1086/424811  1
2004 Paredes JM, Marti J, Scott WK, Zamanov RK. The extragalactic nature of GT 2318+620 Astronomy and Astrophysics. 421: 229-233. DOI: 10.1051/0004-6361:20034446  1
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  1
2003 Scott WK, Hauser ER, Schmechel DE, Welsh-Bohmer KA, Small GW, Roses AD, Saunders AM, Gilbert JR, Vance JM, Haines JL, Pericak-Vance MA. Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22. American Journal of Human Genetics. 73: 1041-51. PMID 14564669 DOI: 10.1086/379083  1
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  1
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  1
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, 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  1
2003 Schmidt S, Postel EA, Agarwal A, Allen IC, Walters SN, De la Paz MA, Scott WK, Haines JL, Pericak-Vance MA, Gilbert JR. Detailed analysis of allelic variation in the ABCA4 gene in age-related maculopathy. Investigative Ophthalmology & Visual Science. 44: 2868-75. PMID 12824224 DOI: 10.1167/Iovs.02-0957  1
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  1
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  1
2003 Hauser ER, Mooser V, Crossman DC, Haines JL, Jones CH, Winkelmann BR, Schmidt S, Scott WK, Roses AD, Pericak-Vance MA, Granger CB, Kraus WE. Design of the Genetics of Early Onset Cardiovascular Disease (GENECARD) study. American Heart Journal. 145: 602-13. PMID 12679755 DOI: 10.1067/Mhj.2003.13  1
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  1
2002 Scott WK, Vance JM, Haines JL, Pericak-Vance MA. Linkage of Parkinsonism and Alzheimer's disease with Lewy body pathology to chromosome 12. Annals of Neurology. 52: 524; author reply 52. PMID 12325086 DOI: 10.1002/Ana.10330  1
2002 Neary JJ, Conlon PJ, Croke D, Dorman A, Keogan M, Zhang FY, Vance JM, Pericak-Vance MA, Scott WK, Winn MP. Linkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1. Journal of the American Society of Nephrology : Jasn. 13: 2052-7. PMID 12138136 DOI: 10.1097/01.Asn.0000022006.49966.F8  1
2002 Li YJ, Scott WK, Hedges DJ, Zhang F, Gaskell PC, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Allen FA, Goetz CG, et al. Age at onset in two common neurodegenerative diseases is genetically controlled. American Journal of Human Genetics. 70: 985-93. PMID 11875758 DOI: 10.1086/339815  1
2002 Farrer M, Hardy J, Hutton M, Maraganore D, Tsuboi Y, Wszolek ZK. Identifying genetic factors in Parkinson disease. Jama. 287: 715-6. PMID 11851532  1
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  1
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  1
2001 Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH, Goetz CG, Small GW, et al. Complete genomic screen in Parkinson disease: evidence for multiple genes. Jama. 286: 2239-44. PMID 11710888 DOI: 10.1001/Jama.286.18.2239  1
2001 Ashley-Koch A, Bonner ER, Gaskell PC, West SG, Tim R, Wolpert CM, Jones R, Farrell CD, Nance M, Svenson IK, Marchuk DA, Boustany RM, Vance JM, Scott WK, Pericak-Vance MA. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia. Neurogenetics. 3: 91-7. PMID 11354831 DOI: 10.1007/S100480000098  1
2001 Oliveira SA, Scott WK, Pericak-Vance MA, Vance JM. Dissecting a complex disease using modern techniques of molecular biology Laboratory Medicine. 32: 594-598. DOI: 10.1309/Uj8W-H1Ht-4B21-Bjxh  1
2001 Peracaula M, Paredes JM, Taylor AR, Dougherty SM, Scott WK. VSOP observations of the X-ray binary LS I +61°303 Astrophysics and Space Science. 276: 123-124.  1
2000 Schmidt S, Saunders AM, De La Paz MA, Postel EA, Heinis RM, Agarwal A, Scott WK, Gilbert JR, McDowell JG, Bazyk A, Gass JD, Haines JL, Pericak-Vance MA. Association of the apolipoprotein E gene with age-related macular degeneration: possible effect modification by family history, age, and gender. Molecular Vision. 6: 287-93. PMID 11141572  1
2000 Pericak-Vance MA, Grubber J, Bailey LR, Hedges D, West S, Santoro L, Kemmerer B, Hall JL, Saunders AM, Roses AD, Small GW, Scott WK, Conneally PM, Vance JM, Haines JL. Identification of novel genes in late-onset Alzheimer's disease. Experimental Gerontology. 35: 1343-52. PMID 11113612 DOI: 10.1016/S0531-5565(00)00196-0  1
2000 Liao HX, Montefiori DC, Patel DD, Lee DM, Scott WK, Pericak-Vance M, Haynes BF. Linkage of the CCR5Δ32 mutation with a functional polymorphism of CD45RA Journal of Immunology. 165: 148-157. PMID 10861047 DOI: 10.4049/Jimmunol.165.1.148  1
2000 Scott WK, Grubber JM, Conneally PM, Small GW, Hulette CM, Rosenberg CK, Saunders AM, Roses AD, Haines JL, Pericak-Vance MA. Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity. American Journal of Human Genetics. 66: 922-32. PMID 10712207 DOI: 10.1086/302828  1
2000 Hirabayashi H, Fomalont EB, Horiuchi S, Lovell JEJ, Moellenbrock GA, Inoue M, Burke BF, Dewdney PE, Gurvits LI, Kobayashi H, Jauncey DL, Murata Y, McCulloch P, Preston RA, Avruch IM, ... ... Scott WK, et al. The VSOP 5 GHz AGN survey I. Compilation and observations Publications of the Astronomical Society of Japan. 52: 997-1014. DOI: 10.1093/Pasj/52.6.997  1
2000 Fomalont EB, Frey S, Paragi Z, Gurvits LI, Scott WK, Taylor AR, Edwards PG, Hirabayashi H. The VSOP 5 GHz continuum survey: The prelaunch VLBA observations Astrophysical Journal, Supplement Series. 131: 95-183. DOI: 10.1086/317368  1
2000 Frey S, Gurvits LI, Paragi Z, Scott WK. Milliarcsecond scale compactness of extragalactic radio sources at cosmological distances Advances in Space Research. 26: 723-726.  1
2000 Grubber JM, Saunders AM, Yamaoka LH, Scott WK, Martin ER, Hill DM, Standen CL, Michael Conneally P, Small GW, Lai EH, Gilbert JR, Roses AD, Haines JL, Pericak-Vance MA. Analysis of chromosome 12 candidate genes in late-onset Alzheimer disease Alzheimer's Reports. 3: 221-226.  1
2000 Dougherty SM, Dewdney PE, Carlson B, Taylor AR, Scott WK, Del Rizzo DA, Petrachenko WT, Burgess T, Cannon WH, Feil G, Feir B, Newby PS, Novikov A. The contribution of Canada to the VSOP mission Advances in Space Research. 26: 649-652.  1
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  1
1999 Scott WK, Yamaoka LH, Stajich JM, Scott BL, Vance JM, Roses AD, Pericak-Vance MA, Watts RL, Nance M, Hubble J, Koller W, Stern MB, Colcher A, Allen FH, Hiner BC, et al. The alpha-synuclein gene is not a major risk factor in familial Parkinson disease. Neurogenetics. 2: 191-2. PMID 10541595 DOI: 10.1007/S100480050083  1
1999 Small GW, Scott WK, Komo S, Yamaoka LH, Farrer LA, Auerbach SH, Saunders AM, Roses AD, Haines JL, Pericak-Vance MA. No association between the HLA-A2 allele and Alzheimer disease. Neurogenetics. 2: 177-82. PMID 10541592 DOI: 10.1007/S100480050080  1
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  1
1999 Small GW, Chen ST, Komo S, Ercoli L, Bookheimer S, Miller K, Lavretsky H, Saxena S, Kaplan A, Dorsey D, Scott WK, Saunders AM, Haines JL, Roses AD, Pericak-Vance MA. Memory self-appraisal in middle-aged and older adults with the apolipoprotein E-4 allele. The American Journal of Psychiatry. 156: 1035-8. PMID 10401448 DOI: 10.1176/Ajp.156.7.1035  1
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  1
1999 Scott WK, Grubber JM, Abou-Donia SM, Church TD, Saunders AM, Roses AD, Pericak-Vance MA, Conneally PM, Small GW, Haines JL. Further evidence linking late-onset Alzheimer disease with chromosome 12. Jama. 281: 513-4. PMID 10022104 DOI: 10.1001/Jama.281.6.513  1
1998 Siddique T, Pericak-Vance MA, Caliendo J, Hong ST, Hung WY, Kaplan J, McKenna-Yasek D, Rimmler JB, Sapp P, Saunders AM, Scott WK, Siddique N, Haines JL, Brown RH. Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis. Neurogenetics. 1: 213-6. PMID 10737125 DOI: 10.1007/S100480050031  1
1998 Scott WK, Yamaoka LH, Bass MP, Gaskell PC, Conneally PM, Small GW, Farrer LA, Auerbach SA, Saunders AM, Roses AD, Haines JL, Pericak-Vance MA. No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease. Neurogenetics. 1: 179-83. PMID 10737120 DOI: 10.1007/S100480050026  1
1998 Lavedan C, Buchholtz S, Auburger G, Albin RL, Athanassiadou A, Blancato J, Burguera JA, Ferrell RE, Kostic V, Leroy E, Leube B, Mota-Vieira L, Papapetropoulos T, Pericak-Vance MA, Pinkus J, ... Scott WK, et al. Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. 5: 401-2. PMID 10048491 DOI: 10.1093/Dnares/5.6.401  1
1998 Farrer LA, Abraham CR, Haines JL, Rogaeva EA, Song Y, McGraw WT, Brindle N, Premkumar S, Scott WK, Yamaoka LH, Saunders AM, Roses AD, Auerbach SA, Sorbi S, Duara R, et al. Association between bleomycin hydrolase and Alzheimer's disease in caucasians. Annals of Neurology. 44: 808-11. PMID 9818937 DOI: 10.1002/Ana.410440515  1
1998 Bass MP, Yamaoka LH, Scott WK, Gaskell PC, Welsh-Bohmer KA, Roses AD, Saunders AM, Haines JL, Pericak-Vance MA. No association of alpha1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients. Neuroscience Letters. 250: 79-82. PMID 9697923 DOI: 10.1016/S0304-3940(98)00398-X  1
1998 Speer MC, Gilchrist JM, Stajich JM, Gaskell PC, Westbrook CA, Horrigan SK, Bartoloni L, Yamaoka LH, Scott WK, Pericak-Vance MA. Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy. Journal of Medical Genetics. 35: 305-8. PMID 9598725 DOI: 10.1136/Jmg.35.4.305  1
1998 Pericak-Vance MA, Bass ML, Yamaoka LH, Gaskell PC, Scott WK, Terwedow HA, Menold MM, Conneally PM, Small GW, Saunders AM, Roses AD, Haines JL. Complete genomic screen in late-onset familial Alzheimer's disease. Neurobiology of Aging. 19: S39-42. PMID 9562466 DOI: 10.1016/S0197-4580(98)00037-2  1
1997 Scott WK, Gaskell PC, Lennon F, Wolpert CM, Menold MM, Aylsworth AS, Warner C, Farrell CD, Boustany RM, Albright SG, Boyd E, Kingston HM, Cumming WJ, Vance JM, Pericak-Vance MA. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia. Neurogenetics. 1: 95-102. PMID 10732810 DOI: 10.1007/S100480050014  1
1997 Scott WK, Staijich JM, Yamaoka LH, Speer MC, Vance JM, Roses AD, Pericak-Vance MA. Genetic complexity and Parkinson's disease. Deane Laboratory Parkinson Disease Research Group. Science (New York, N.Y.). 277: 387-8; author reply . PMID 9518366 DOI: 10.1126/science.277.5324.387  1
1997 Scott WK, Speer MC, Leal SM, Brzustowicz LM, Haynes CS, Pericak-Vance MA. False positive rates in a genomic screen for complex quantitative traits. Genetic Epidemiology. 14: 891-6. PMID 9433596 DOI: 10.1002/(Sici)1098-2272(1997)14:6<891::Aid-Gepi55>3.0.Co;2-H  1
1997 Pericak-Vance MA, Bass MP, Yamaoka LH, Gaskell PC, Scott WK, Terwedow HA, Menold MM, Conneally PM, Small GW, Vance JM, Saunders AM, Roses AD, Haines JL. Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12. Jama. 278: 1237-41. PMID 9333264 DOI: 10.1001/Jama.1997.03550150041033  1
1997 Scott WK, Saunders AM, Gaskell PC, Locke PA, Growdon JH, Farrer LA, Auerbach SA, Roses AD, Haines JL, Pericak-Vance MA. Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease. Annals of Neurology. 42: 376-8. PMID 9307262 DOI: 10.1002/Ana.410420317  1
1997 Scott WK, Yamaoka LH, Locke PA, Rosi BL, Gaskell PC, Saunders AM, Conneally PM, Small GW, Farrer LA, Growdon JH, Roses AD, Pericak-Vance MA, Haines JL. No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease. Genetic Epidemiology. 14: 307-15. PMID 9181359 DOI: 10.1002/(Sici)1098-2272(1997)14:3<307::Aid-Gepi8>3.0.Co;2-1  1
1997 Zheng D, Macera CA, Croft JB, Giles WH, Davis D, Scott WK. Major depression and all-cause mortality among white adults in the United States Annals of Epidemiology. 7: 213-218. PMID 9141645 DOI: 10.1016/S1047-2797(97)00014-8  1
1997 Scott WK, Macera CA, Cornman CB, Sharpe PA. Functional health status as a predictor of mortality in men and women over 65 Journal of Clinical Epidemiology. 50: 291-296. PMID 9120528 DOI: 10.1016/S0895-4356(96)00365-4  1
1997 Kamboh MI, Aston CE, Ferrell RE, Dekosky ST, Haines JL, Scott WK, Pericak-Vance MA. Re: Genetic effect of α1-antichymotrypsin on the risk of Alzheimer disease Genomics. 40: 382-385. PMID 9119413 DOI: 10.1006/Geno.1996.4601  1
1997 Scott WK, Edwards KB, Davis DR, Cornman CB, Macera CA. Risk of institutionalization among community long-term care clients with dementia Gerontologist. 37: 46-51. PMID 9046705 DOI: 10.1093/GERONT/37.1.46  1
1996 Frank EM, McDade HL, Scott WK. Naming in dementia secondary to Parkinson's, Huntington's, and Alzheimer's diseases. Journal of Communication Disorders. 29: 183-97. PMID 8799853 DOI: 10.1016/0021-9924(95)00021-6  1
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