| Year |
Citation |
Score |
| 2023 |
Wang S, Chiu CY, Wilson AF, Bailey-Wilson JE, Agron E, Chew EY, Ahn J, Xiong M, Fan R. Gene-level association analysis of bivariate ordinal traits with functional regressions. Genetic Epidemiology. PMID 37101379 DOI: 10.1002/gepi.22524 |
0.31 |
|
| 2022 |
Chiu CY, Wang S, Zhang B, Luo Y, Simpson C, Zhang W, Wilson AF, Bailey-Wilson JE, Agron E, Chew EY, Zhang J, Xiong M, Fan R. Gene-level association analysis of ordinal traits with functional ordinal logistic regressions. Genetic Epidemiology. PMID 35438198 DOI: 10.1002/gepi.22451 |
0.314 |
|
| 2021 |
Jiang Y, Chiu CY, Yan Q, Chen W, Gorin MB, Conley YP, Lakhal-Chaieb ML, Cook RJ, Amos CI, Wilson AF, Bailey-Wilson JE, McMahon FJ, Vazquez AI, Yuan A, Zhong X, et al. Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration. Journal of the American Statistical Association. 116: 531-545. PMID 34321704 DOI: 10.1080/01621459.2020.1799809 |
0.345 |
|
| 2020 |
Justice CM, Cuellar A, Bala K, Sabourin JA, Cunningham ML, Crawford K, Phipps JM, Zhou Y, Cilliers D, Byren JC, Johnson D, Wall SA, Morton JEV, Noons P, Sweeney E, ... ... Wilson AF, et al. A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis. Human Genetics. PMID 32266521 DOI: 10.1007/S00439-020-02157-Z |
0.35 |
|
| 2020 |
Jiang Y, Chiu C, Yan Q, Chen W, Gorin MB, Conley YP, Lakhal-Chaieb ML, Cook RJ, Amos CI, Wilson AF, Bailey-Wilson JE, McMahon FJ, Vazquez AI, Yuan A, Zhong X, et al. Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration Journal of the American Statistical Association. 1-15. DOI: 10.1080/01621459.2020.1799809 |
0.373 |
|
| 2019 |
Chiu CY, Zhang B, Wang S, Shao J, Lakhal-Chaieb ML, Cook RJ, Wilson AF, Bailey-Wilson JE, Xiong M, Fan R. Gene-based association analysis of survival traits via functional regression-based mixed effect cox models for related samples. Genetic Epidemiology. PMID 31502722 DOI: 10.1002/Gepi.22254 |
0.436 |
|
| 2018 |
Chiu CY, Yuan F, Zhang BS, Yuan A, Li X, Fang HB, Lange K, Weeks DE, Wilson AF, Bailey-Wilson JE, Musolf AM, Stambolian D, Lakhal-Chaieb ML, Cook RJ, McMahon FJ, et al. Linear mixed models for association analysis of quantitative traits with next-generation sequencing data. Genetic Epidemiology. PMID 30537345 DOI: 10.1002/Gepi.22177 |
0.417 |
|
| 2018 |
Shane B, Pangilinan F, Mills JL, Fan R, Gong T, Cropp CD, Kim Y, Ueland PM, Bailey-Wilson JE, Wilson AF, Brody LC, Molloy AM. The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population. The American Journal of Clinical Nutrition. PMID 30339177 DOI: 10.1093/Ajcn/Nqy209 |
0.347 |
|
| 2018 |
Sabourin JA, Cropp CD, Sung H, Brody LC, Bailey-Wilson JE, Wilson AF. ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available. Genetic Epidemiology. PMID 30334581 DOI: 10.1002/Gepi.22168 |
0.396 |
|
| 2018 |
Szekely E, Schwantes-An TL, Justice CM, Sabourin JA, Jansen PR, Muetzel RL, Sharp W, Tiemeier H, Sung H, White TJ, Wilson AF, Shaw P. Genetic associations with childhood brain growth, defined in two longitudinal cohorts. Genetic Epidemiology. PMID 29682794 DOI: 10.1002/Gepi.22122 |
0.334 |
|
| 2017 |
Justice CM, Kim J, Kim SD, Kim K, Yagnik G, Cuellar A, Carrington B, Lu CL, Sood R, Boyadjiev SA, Wilson AF. A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non-coding element. American Journal of Medical Genetics. Part A. PMID 28985029 DOI: 10.1002/Ajmg.A.38392 |
0.358 |
|
| 2016 |
Schwantes-An TH, Sung H, Sabourin JA, Justice CM, Sorant AJ, Wilson AF. Type I error rates of rare single nucleotide variants are inflated in tests of association with non-normally distributed traits using simple linear regression methods. Bmc Proceedings. 10: 385-388. PMID 27980666 DOI: 10.1186/S12919-016-0060-7 |
0.361 |
|
| 2016 |
Chiu CY, Jung J, Wang Y, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Mills JL, Boehnke M, Xiong M, Fan R. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing. Genetic Epidemiology. PMID 27917525 DOI: 10.1002/Gepi.22014 |
0.436 |
|
| 2016 |
Fan R, Chiu CY, Jung J, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Chen Z, Mills JL, Xiong M. A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits. Genetic Epidemiology. PMID 27374056 DOI: 10.1002/Gepi.21984 |
0.39 |
|
| 2016 |
Justice CM, Bishop K, Carrington B, Mullikin JC, Swindle K, Marosy B, Sood R, Miller NH, Wilson AF. Evaluation of IRX Genes and Conserved Non-coding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis. G3 (Bethesda, Md.). PMID 27172222 DOI: 10.1534/G3.116.029975 |
0.42 |
|
| 2016 |
Molloy AM, Pangilinan F, Mills JL, Shane B, O'Neill MB, McGaughey DM, Velkova A, Abaan HO, Ueland PM, McNulty H, Ward M, Strain JJ, Cunningham C, Casey M, Cropp CD, ... ... Wilson AF, et al. A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin. American Journal of Human Genetics. PMID 27132595 DOI: 10.1016/J.Ajhg.2016.03.005 |
0.346 |
|
| 2015 |
Wang Y, Liu A, Mills JL, Boehnke M, Wilson AF, Bailey-Wilson JE, Xiong M, Wu CO, Fan R. Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models. Genetic Epidemiology. 39: 259-75. PMID 25809955 DOI: 10.1002/Gepi.21895 |
0.396 |
|
| 2014 |
Pemov A, Sung H, Hyland PL, Sloan JL, Ruppert SL, Baldwin AM, Boland JF, Bass SE, Lee HJ, Jones KM, Zhang X, Mullikin JC, Widemann BC, Wilson AF, et al. Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis. Plos Genetics. 10: e1004575. PMID 25329635 DOI: 10.1371/Journal.Pgen.1004575 |
0.359 |
|
| 2014 |
Fan R, Wang Y, Mills JL, Carter TC, Lobach I, Wilson AF, Bailey-Wilson JE, Weeks DE, Xiong M. Generalized functional linear models for gene-based case-control association studies. Genetic Epidemiology. 38: 622-37. PMID 25203683 DOI: 10.1002/Gepi.21840 |
0.404 |
|
| 2013 |
Fan R, Wang Y, Mills JL, Wilson AF, Bailey-Wilson JE, Xiong M. Functional linear models for association analysis of quantitative traits. Genetic Epidemiology. 37: 726-42. PMID 24130119 DOI: 10.1002/Gepi.21757 |
0.434 |
|
| 2013 |
Tilley MK, Justice CM, Swindle K, Marosy B, Wilson AF, Miller NH. CHD7 gene polymorphisms and familial idiopathic scoliosis. Spine. 38: E1432-6. PMID 23883829 DOI: 10.1097/Brs.0B013E3182A51781 |
0.39 |
|
| 2013 |
Kim Y, Suktitipat B, Yanek LR, Faraday N, Wilson AF, Becker DM, Becker LC, Mathias RA. Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation. Plos One. 8: e64179. PMID 23704978 DOI: 10.1371/Journal.Pone.0064179 |
0.349 |
|
| 2013 |
Kirino Y, Zhou Q, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Özyazgan Y, Ugurlu S, Erer B, Abaci N, Ustek D, Meguro A, Ueda A, Takeno M, Inoko H, ... ... Wilson AF, et al. Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease. Proceedings of the National Academy of Sciences of the United States of America. 110: 8134-9. PMID 23633568 DOI: 10.1073/Pnas.1306352110 |
0.362 |
|
| 2013 |
Desch KC, Ozel AB, Siemieniak D, Kalish Y, Shavit JA, Thornburg CD, Sharathkumar AA, McHugh CP, Laurie CC, Crenshaw A, Mirel DB, Kim Y, Cropp CD, Molloy AM, Kirke PN, ... ... Wilson AF, et al. Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association. Proceedings of the National Academy of Sciences of the United States of America. 110: 588-93. PMID 23267103 DOI: 10.1073/Pnas.1219885110 |
0.42 |
|
| 2012 |
Justice CM, Yagnik G, Kim Y, Peter I, Jabs EW, Erazo M, Ye X, Ainehsazan E, Shi L, Cunningham ML, Kimonis V, Roscioli T, Wall SA, Wilkie AO, Stoler J, ... ... Wilson AF, et al. A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9. Nature Genetics. 44: 1360-4. PMID 23160099 DOI: 10.1038/Ng.2463 |
0.326 |
|
| 2012 |
Miller NH, Justice CM, Marosy B, Swindle K, Kim Y, Roy-Gagnon MH, Sung H, Behneman D, Doheny KF, Pugh E, Wilson AF. Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2. Human Heredity. 74: 36-44. PMID 23154503 DOI: 10.1159/000343751 |
0.658 |
|
| 2012 |
Suktitipat B, Mathias RA, Vaidya D, Yanek LR, Young JH, Becker LC, Becker DM, Wilson AF, Fallin MD. The robustness of generalized estimating equations for association tests in extended family data. Human Heredity. 74: 17-26. PMID 23038411 DOI: 10.1159/000341636 |
0.421 |
|
| 2011 |
Sung H, Kim Y, Cai J, Cropp CD, Simpson CL, Li Q, Perry BC, Sorant AJ, Bailey-Wilson JE, Wilson AF. Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression. Bmc Proceedings. 5: S15. PMID 22373501 DOI: 10.1186/1753-6561-5-S9-S15 |
0.462 |
|
| 2011 |
Kim Y, Li Q, Cropp CD, Sung H, Cai J, Simpson CL, Perry B, Dasgupta A, Malley JD, Wilson AF, Bailey-Wilson JE. Performance of random forests and logic regression methods using mini-exome sequence data. Bmc Proceedings. 5: S104. PMID 22373484 DOI: 10.1186/1753-6561-5-S9-S104 |
0.361 |
|
| 2011 |
Simpson CL, Justice CM, Krishnan M, Wojciechowski R, Sung H, Cai J, Green T, Lewis D, Behneman D, Wilson AF, Bailey-Wilson JE. Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data. Bmc Proceedings. 5: S83. PMID 22373393 DOI: 10.1186/1753-6561-5-S9-S83 |
0.473 |
|
| 2011 |
Bailey-Wilson JE, Wilson AF. Linkage analysis in the next-generation sequencing era. Human Heredity. 72: 228-36. PMID 22189465 DOI: 10.1159/000334381 |
0.415 |
|
| 2011 |
Hemmelmann C, Daw EW, Wilson AF. Quality control issues and the identification of rare functional variants with next-generation sequencing data. Genetic Epidemiology. 35: S22-8. PMID 22128054 DOI: 10.1002/Gepi.20645 |
0.413 |
|
| 2011 |
Wilson AF, Ziegler A. Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis. Genetic Epidemiology. 35: S107-14. PMID 22128050 DOI: 10.1002/Gepi.20659 |
0.441 |
|
| 2010 |
Assimes TL, Hólm H, Kathiresan S, Reilly MP, Thorleifsson G, Voight BF, Erdmann J, Willenborg C, Vaidya D, Xie C, Patterson CC, Morgan TM, Burnett MS, Li M, Hlatky MA, ... ... Wilson AF, et al. Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. Journal of the American College of Cardiology. 56: 1552-63. PMID 20933357 DOI: 10.1016/J.Jacc.2010.06.022 |
0.323 |
|
| 2010 |
Mathias RA, Kim Y, Sung H, Yanek LR, Mantese VJ, Hererra-Galeano JE, Ruczinski I, Wilson AF, Faraday N, Becker LC, Becker DM. A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease. Bmc Medical Genomics. 3: 22. PMID 20529293 DOI: 10.1186/1755-8794-3-22 |
0.342 |
|
| 2010 |
Marosy B, Justice CM, Vu C, Zorn A, Nzegwu N, Wilson AF, Miller NH. Identification of susceptibility loci for scoliosis in FIS families with triple curves. American Journal of Medical Genetics. Part A. 152: 846-55. PMID 20358593 DOI: 10.1002/Ajmg.A.33222 |
0.429 |
|
| 2010 |
Cheng CY, Lee KE, Duggal P, Moore EL, Wilson AF, Klein R, Bailey-Wilson JE, Klein BE. Genome-wide linkage analysis of multiple metabolic factors: evidence of genetic heterogeneity. Obesity (Silver Spring, Md.). 18: 146-52. PMID 19444228 DOI: 10.1038/Oby.2009.142 |
0.375 |
|
| 2009 |
Biesecker LG, Mullikin JC, Facio FM, Turner C, Cherukuri PF, Blakesley RW, Bouffard GG, Chines PS, Cruz P, Hansen NF, Teer JK, Maskeri B, Young AC, Manolio TA, ... Wilson AF, et al. The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine. Genome Research. 19: 1665-74. PMID 19602640 DOI: 10.1101/Gr.092841.109 |
0.526 |
|
| 2009 |
Mathias RA, Deepa M, Deepa R, Wilson AF, Mohan V. Heritability of quantitative traits associated with type 2 diabetes mellitus in large multiplex families from South India. Metabolism: Clinical and Experimental. 58: 1439-45. PMID 19570552 DOI: 10.1016/J.Metabol.2009.04.041 |
0.359 |
|
| 2008 |
Roy-Gagnon MH, Mathias RA, Fallin MD, Jee SH, Broman KW, Wilson AF. An extension of the regression of offspring on mid-parent to test for association and estimate locus-specific heritability: the revised ROMP method. Annals of Human Genetics. 72: 115-25. PMID 18042270 DOI: 10.1111/J.1469-1809.2007.00401.X |
0.682 |
|
| 2007 |
Paddock S, Laje G, Charney D, Rush AJ, Wilson AF, Sorant AJ, Lipsky R, Wisniewski SR, Manji H, McMahon FJ. Association of GRIK4 with outcome of antidepressant treatment in the STAR*D cohort. The American Journal of Psychiatry. 164: 1181-8. PMID 17671280 DOI: 10.1176/Appi.Ajp.2007.06111790 |
0.315 |
|
| 2006 |
Mathias RA, Hening W, Washburn M, Allen RP, Lesage S, Wilson AF, Earley CJ. Segregation analysis of restless legs syndrome: possible evidence for a major gene in a family study using blinded diagnoses. Human Heredity. 62: 157-64. PMID 17063029 DOI: 10.1159/000096443 |
0.398 |
|
| 2006 |
Alden KJ, Marosy B, Nzegwu N, Justice CM, Wilson AF, Miller NH. Idiopathic scoliosis: identification of candidate regions on chromosome 19p13. Spine. 31: 1815-9. PMID 16845357 DOI: 10.1097/01.Brs.0000227264.23603.Dc |
0.374 |
|
| 2006 |
Mathias RA, Gao P, Goldstein JL, Wilson AF, Pugh EW, Furbert-Harris P, Dunston GM, Malveaux FJ, Togias A, Barnes KC, Beaty TH, Huang SK. A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q. Bmc Genetics. 7: 38. PMID 16774684 DOI: 10.1186/1471-2156-7-38 |
0.397 |
|
| 2006 |
Marosy B, Justice CM, Nzegwu N, Kumar G, Wilson AF, Miller NH. Lack of association between the aggrecan gene and familial idiopathic scoliosis. Spine. 31: 1420-5. PMID 16741449 DOI: 10.1097/01.Brs.0000219944.18223.52 |
0.362 |
|
| 2006 |
McMahon FJ, Buervenich S, Charney D, Lipsky R, Rush AJ, Wilson AF, Sorant AJ, Papanicolaou GJ, Laje G, Fava M, Trivedi MH, Wisniewski SR, Manji H. Variation in the gene encoding the serotonin 2A receptor is associated with outcome of antidepressant treatment. American Journal of Human Genetics. 78: 804-14. PMID 16642436 DOI: 10.1086/503820 |
0.339 |
|
| 2006 |
Mandal DM, Sorant AJ, Atwood LD, Wilson AF, Bailey-Wilson JE. Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment. Bmc Genetics. 7: 21. PMID 16618369 DOI: 10.1186/1471-2156-7-21 |
0.387 |
|
| 2006 |
Miller NH, Marosy B, Justice CM, Novak SM, Tang EY, Boyce P, Pettengil J, Doheny KF, Pugh EW, Wilson AF. Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32. American Journal of Medical Genetics. Part A. 140: 1059-68. PMID 16596674 DOI: 10.1002/Ajmg.A.31211 |
0.385 |
|
| 2006 |
Choh AC, Czerwinski SA, Lee M, Demerath EW, Cole SA, Wilson AF, Towne B, Siervogel RM. Quantitative genetic analysis of blood pressure reactivity to orthostatic tilt using principal components analysis. Journal of Human Hypertension. 20: 281-9. PMID 16437129 DOI: 10.1038/Sj.Jhh.1001975 |
0.341 |
|
| 2005 |
Roy-Gagnon MH, Mathias RA, Wilson AF. Application of the regression of offspring on mid-parent method to detect associations between single-nucleotide polymorphisms and the beta 2 electroencephalogram phenotype in the COGA data. Bmc Genetics. 6: S56. PMID 16451668 DOI: 10.1186/1471-2156-6-S1-S56 |
0.663 |
|
| 2005 |
Papanicolaou GJ, Justice CM, Kovac IM, Sorant AJ, Wilson AF. Critical values and variation in type I error along chromosomes in the COGA dataset using the applied pseudo-trait method. Bmc Genetics. 6: S54. PMID 16451666 DOI: 10.1186/1471-2156-6-S1-S54 |
0.377 |
|
| 2005 |
Choh AC, Czerwinski SA, Lee M, Demerath EW, Wilson AF, Towne B, Siervogel RM. Quantitative genetic analysis of blood pressure response during the cold pressor test. American Journal of Hypertension. 18: 1211-7. PMID 16182112 DOI: 10.1016/J.Amjhyper.2004.11.041 |
0.343 |
|
| 2005 |
Miller NH, Justice CM, Marosy B, Doheny KF, Pugh E, Zhang J, Dietz HC, Wilson AF. Identification of candidate regions for familial idiopathic scoliosis. Spine. 30: 1181-7. PMID 15897833 DOI: 10.1097/01.Brs.0000162282.46160.0A |
0.368 |
|
| 2004 |
Manolio TA, Boerwinkle E, O'Donnell CJ, Wilson AF. Genetics of ultrasonographic carotid atherosclerosis. Arteriosclerosis, Thrombosis, and Vascular Biology. 24: 1567-77. PMID 15256397 DOI: 10.1161/01.Atv.0000138789.11433.C1 |
0.543 |
|
| 2003 |
Mathias RA, Roy-Gagnon MH, Justice CM, Papanicolaou GJ, Fan YT, Pugh EW, Wilson AF. Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data. Bmc Genetics. 4: S36. PMID 14975104 DOI: 10.1186/1471-2156-4-S1-S36 |
0.631 |
|
| 2003 |
Manolio TA, Barnes KC, Beaty TH, Levett PN, Naidu RP, Wilson AF. Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods. Human Genetics. 113: 437-46. PMID 12928863 DOI: 10.1007/S00439-003-1005-6 |
0.556 |
|
| 2003 |
Platte P, Papanicolaou GJ, Johnston J, Klein CM, Doheny KF, Pugh EW, Roy-Gagnon MH, Stunkard AJ, Francomano CA, Wilson AF. A study of linkage and association of body mass index in the Old Order Amish. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 121: 71-80. PMID 12888987 DOI: 10.1002/Ajmg.C.20005 |
0.656 |
|
| 2003 |
Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, Kakol J, Buyske S, Chui B, Cohen P, de Toma C, Ehm M, Glanowski S, He C, Heil J, Markianos K, ... ... Wilson AF, et al. A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set. American Journal of Human Genetics. 73: 271-84. PMID 12844283 DOI: 10.1086/377137 |
0.345 |
|
| 2003 |
Manolio TA, Barnes KC, Naidu RP, Levett PN, Beaty TH, Wilson AF. Correlates of sensitization to Blomia tropicalis and Dermatophagoides pteronyssinus in asthma in Barbados. International Archives of Allergy and Immunology. 131: 119-26. PMID 12811020 DOI: 10.1159/000070927 |
0.411 |
|
| 2003 |
Boyadjiev SA, Justice CM, Eyaid W, McKusick VA, Lachman RS, Chowdry AB, Jabak M, Zwaan J, Wilson AF, Jabs EW. A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21. Human Genetics. 113: 1-9. PMID 12677423 DOI: 10.1007/S00439-003-0932-6 |
0.365 |
|
| 2003 |
Justice CM, Miller NH, Marosy B, Zhang J, Wilson AF. Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus. Spine. 28: 589-94. PMID 12642767 DOI: 10.1097/01.Brs.0000049940.39801.E6 |
0.379 |
|
| 2002 |
Shugart YY, O'Connell JR, Wilson AF. An evaluation of the variance components approach: type I error, power and size of the estimated effect. European Journal of Human Genetics : Ejhg. 10: 133-6. PMID 11938444 DOI: 10.1038/Sj.Ejhg.5200772 |
0.326 |
|
| 2001 |
Pugh EW, Papanicolaou GJ, Justice CM, Roy-Gagnon MH, Sorant AJ, Kingman A, Wilson AF. Comparison of variance components, ANOVA and regression of offspring on midparent (ROMP) methods for SNP markers. Genetic Epidemiology. 21: S794-9. PMID 11793780 DOI: 10.1002/Gepi.2001.21.S1.S794 |
0.69 |
|
| 2001 |
Mandal DM, Wilson AF, Bailey-Wilson JE. Effects of misspecification of allele frequencies on the power of Haseman-Elston sib-pair linkage method for quantitative traits American Journal of Medical Genetics. 103: 308-313. PMID 11746011 DOI: 10.1002/Ajmg.1566 |
0.421 |
|
| 2000 |
Schaid DJ, Elston RC, Tran L, Wilson AF. Model-free sib-pair linkage analysis: Combining full-sib and half-sib pairs Genetic Epidemiology. 19: 30-51. PMID 10861895 DOI: 10.1002/1098-2272(200007)19:1<30::Aid-Gepi3>3.0.Co;2-X |
0.406 |
|
| 2000 |
Mandal DM, Wilson AF, Elston RC, Weissbecker K, Keats BJ, Bailey-Wilson JE. Effects of misspecification of allele frequencies on the type I error rate of model-free linkage analysis Human Heredity. 50: 126-132. PMID 10799971 DOI: 10.1159/000022900 |
0.383 |
|
| 2000 |
Wilson AF, Sorant AJM. Equivalence of single- and multilocus markers: Power to detect linkage with composite markers derived from biallelic loci American Journal of Human Genetics. 66: 1610-1615. PMID 10762546 DOI: 10.1086/302889 |
0.387 |
|
| 1999 |
Mandal DM, Sorant AJM, Pugh EW, Marcus SE, Klein AP, Mathias RA, O'Neill J, Temiyakarn LF, Wilson AF, Bailey-Wilson JE. Environmental covariates: Effects on the power of sib-pair linkage methods Genetic Epidemiology. 17. PMID 10597507 DOI: 10.1002/Gepi.13701707105 |
0.32 |
|
| 1999 |
Juo SHH, Pugh EW, Baffoe-Bonnie A, Kingman A, Sorant AJM, Klein AP, O'Neill J, Mathias RA, Wilson AF, Bailey-Wilson JE. Possible linkage of alcoholism, monoamine oxidase activity and P300 amplitude to markers on chromosome 12q24 Genetic Epidemiology. 17. PMID 10597435 DOI: 10.1002/Gepi.1370170733 |
0.307 |
|
| 1999 |
Goldin LR, Chase GA, Wilson AF. Regional inference with averaged P values increases the power to detect linkage Genetic Epidemiology. 17: 157-164. PMID 10446463 DOI: 10.1002/(Sici)1098-2272(1999)17:3<157::Aid-Gepi1>3.0.Co;2-P |
0.363 |
|
| 1997 |
Pugh EW, Jaquish CE, Sorant AJM, Doetsch JP, Bailey-Wilson JE, Wilson AF. Comparison of sib-pair and variance-components methods for genomic screening Genetic Epidemiology. 14: 867-872. PMID 9433592 DOI: 10.1002/(Sici)1098-2272(1997)14:6<867::Aid-Gepi51>3.0.Co;2-K |
0.36 |
|
| 1997 |
Sautter FJ, McDermott BE, Cornwell J, Wilson AF, Johnson J, Vasterling JJ. Neuropsychological deficits in probands from multiply-affected schizophrenic families Journal of Psychiatric Research. 31: 497-508. PMID 9368192 DOI: 10.1016/S0022-3956(97)00024-1 |
0.3 |
|
| 1996 |
Svetkey LP, McKeown SP, Wilson AF. Heritability of salt sensitivity in black Americans Hypertension. 28: 854-858. PMID 8901834 DOI: 10.1161/01.Hyp.28.5.854 |
0.318 |
|
| 1995 |
Pugh EW, Mandal DM, Wilson AF. A graphical approach for presenting linkage results from a genomic screen Genetic Epidemiology. 12: 807-812. PMID 8788013 DOI: 10.1002/Gepi.1370120646 |
0.365 |
|
| 1995 |
Nick TG, George V, Elston RC, Wilson AF. Statistical validity for testing associations between genetic markers and quantitative traits in family data Genetic Epidemiology. 12: 145-161. PMID 7607415 DOI: 10.1002/Gepi.1370120204 |
0.45 |
|
| 1993 |
Bailey-Wilson JE, Wilson AF, Bamba V. Linkage analysis in a large pedigree ascertained due to essential familial hypercholesterolemia Genetic Epidemiology. 10: 665-669. PMID 8314078 DOI: 10.1002/Gepi.1370100656 |
0.426 |
|
| 1993 |
Wilson AF, Elston RC. Statistical validity of the Haseman-Elston sib-pair test in small samples Genetic Epidemiology. 10: 593-598. PMID 8314066 DOI: 10.1002/Gepi.1370100644 |
0.349 |
|
| 1993 |
Wilson AF. Methods and applications of genetic analysis in the study of cardiovascular disease: A summary of contributions to GAW8 Genetic Epidemiology. 10: 503-512. PMID 8314051 DOI: 10.1002/Gepi.1370100629 |
0.353 |
|
| 1991 |
Wilson AF, Elston RC, Tran LD, Siervogel RM. Use of the robust sib-pair method to screen for single-locus, multiple-locus, and pleiotropic effects: Application to traits related to hypertension American Journal of Human Genetics. 48: 862-872. PMID 2018038 |
0.303 |
|
| 1990 |
Wilson AF, Elston RC, Sellers TA, Bailey-Wilson JE, Gersting JM, Deen DK, Sorant AJM, Tran LD, Amos CI, Siervogel RM. Stepwise oligogenic segregation and linkage analysis illustrated with dopamine-β-hydroxylase activity American Journal of Medical Genetics. 35: 425-432. PMID 2309793 DOI: 10.1002/Ajmg.1320350321 |
0.381 |
|
| 1990 |
Elston RC, Wilson AF. Genetic linkage and complex diseases I: A comment Genetic Epidemiology. 7: 17-19. DOI: 10.1002/Gepi.1370070104 |
0.326 |
|
| 1989 |
Wilson AF, Tanna VL, Winokur G, Elston RC, Hill EM. Linkage analysis of depression spectrum disease. Biological Psychiatry. 26: 163-75. PMID 2736265 DOI: 10.1016/0006-3223(89)90020-6 |
0.36 |
|
| 1989 |
Tanna VL, Wilson AF, Winokur G, Elston RC. Linkage analysis of pure depressive disease. Journal of Psychiatric Research. 23: 99-107. PMID 2585349 DOI: 10.1016/0022-3956(89)90001-0 |
0.42 |
|
| 1988 |
Hill EM, Wilson AF, Elston RC, Winokur G. Evidence for possible linkage between genetic markers and affective disorders. Biological Psychiatry. 24: 903-17. PMID 3233232 DOI: 10.1016/0006-3223(88)90225-9 |
0.391 |
|
| 1988 |
Tanna VL, Wilson AF, Winokur G, Elston RC. Possible linkage between alcoholism and esterase-D. Journal of Studies On Alcohol. 49: 472-6. PMID 3216652 DOI: 10.15288/Jsa.1988.49.472 |
0.389 |
|
| 1987 |
Crowe RR, Noyes R, Wilson AF, Elston RC, Ward LJ. A Linkage Study of Panic Disorder Archives of General Psychiatry. 44: 933-937. PMID 3675131 DOI: 10.1001/Archpsyc.1987.01800230013003 |
0.372 |
|
| 1987 |
Asamoah A, Wilson AF, Elston RC, Dalferes E, Berenson GS. Segregation and linkage analyses of dopamine-beta-hydroxylase activity in a six-generation pedigree. American Journal of Medical Genetics. 27: 613-21. PMID 3631133 DOI: 10.1002/Ajmg.1320270314 |
0.36 |
|
| 1986 |
Townley RG, Bewtra A, Wilson AF, Hopp RJ, Elston RC, Nair N, Watt GD. Segregation analysis of bronchial response to methacholine inhalation challenge in families with and without asthma The Journal of Allergy and Clinical Immunology. 77: 101-107. PMID 3944368 DOI: 10.1016/0091-6749(86)90330-1 |
0.311 |
|
| 1986 |
Wilson AF, Bailey-Wilson JE, Cleton FJ. Linkage analysis of Dutch families at high risk for breast cancer Genetic Epidemiology. 3: 87-92. PMID 3471674 DOI: 10.1002/Gepi.1370030714 |
0.421 |
|
| 1986 |
Wilson AF. Analysis of human genetic linkage Mathematical Biosciences. 80: 139-140. DOI: 10.1016/0025-5564(86)90071-4 |
0.348 |
|
| 1984 |
Wilson AF, Elston RC, Siervogel RM, Weinshilboum R, Ward LJ. Linkage relationships between a major gene for catechol-O-methyltransferase activity and 25 polymorphic marker systems American Journal of Medical Genetics. 19: 525-532. PMID 6507499 DOI: 10.1002/Ajmg.1320190314 |
0.433 |
|
| Show low-probability matches. |