Alexander F. Wilson - Publications

Johns Hopkins University, Baltimore, MD 
Public Health, Statistics, Genetics

86 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
2015 Sung H, Sorant AJM, Sabourin JA, Schwantes-An TH, Justice CM, Bailey-Wilson JE, Wilson AF. Tiled regression reduces type i error rates in tests of association of rare single nucleotide variants with non-normally distributed traits, compared with simple linear regression Proceedings - 2015 Ieee International Conference On Bioinformatics and Biomedicine, Bibm 2015. 1336-1340. DOI: 10.1109/BIBM.2015.7359872  0.44
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  0.44
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  0.44
2014 Ziegler A, Wilson AF, Gagnon F. Informatics and genetic epidemiology. Methods of Information in Medicine. 53: 1-2. PMID 24407729  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
2012 Liang J, Wang D, Renaud G, Wolfsberg TG, Wilson AF, Burgess SM. The stat3/socs3a pathway is a key regulator of hair cell regeneration in zebrafish. [corrected]. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 10662-73. PMID 22855815 DOI: 10.1523/JNEUROSCI.5785-10.2012  0.44
2012 David SP, Hamidovic A, Chen GK, Bergen AW, Wessel J, Kasberger JL, Brown WM, Petruzella S, Thacker EL, Kim Y, Nalls MA, Tranah GJ, Sung YJ, Ambrosone CB, Arnett D, ... ... Wilson AF, et al. Genome-wide meta-analyses of smoking behaviors in African Americans. Translational Psychiatry. 2: e119. PMID 22832964 DOI: 10.1038/tp.2012.41  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
2008 Herrera-Galeano JE, Becker DM, Wilson AF, Yanek LR, Bray P, Vaidya D, Faraday N, Becker LC. A novel variant in the platelet endothelial aggregation receptor-1 gene is associated with increased platelet aggregability. Arteriosclerosis, Thrombosis, and Vascular Biology. 28: 1484-90. PMID 18511696 DOI: 10.1161/ATVBAHA.108.168971  0.44
2008 Lekman M, Laje G, Charney D, Rush AJ, Wilson AF, Sorant AJ, Lipsky R, Wisniewski SR, Manji H, McMahon FJ, Paddock S. The FKBP5-gene in depression and treatment response--an association study in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) Cohort. Biological Psychiatry. 63: 1103-10. PMID 18191112 DOI: 10.1016/j.biopsych.2007.10.026  0.44
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  0.44
2007 Laje G, Paddock S, Manji H, Rush AJ, Wilson AF, Charney D, McMahon FJ. Genetic markers of suicidal ideation emerging during citalopram treatment of major depression. The American Journal of Psychiatry. 164: 1530-8. PMID 17898344 DOI: 10.1176/appi.ajp.2007.06122018  0.44
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  0.44
2007 Bray PF, Mathias RA, Faraday N, Yanek LR, Fallin MD, Herrera-Galeano JE, Wilson AF, Becker LC, Becker DM. Heritability of platelet function in families with premature coronary artery disease. Journal of Thrombosis and Haemostasis : Jth. 5: 1617-23. PMID 17663734 DOI: 10.1111/j.1538-7836.2007.02618.x  0.44
2007 Hu XZ, Rush AJ, Charney D, Wilson AF, Sorant AJ, Papanicolaou GJ, Fava M, Trivedi MH, Wisniewski SR, Laje G, Paddock S, McMahon FJ, Manji H, Lipsky RH. Association between a functional serotonin transporter promoter polymorphism and citalopram treatment in adult outpatients with major depression. Archives of General Psychiatry. 64: 783-92. PMID 17606812 DOI: 10.1001/archpsyc.64.7.783  0.44
2007 Faraday N, Yanek LR, Mathias R, Herrera-Galeano JE, Vaidya D, Moy TF, Fallin MD, Wilson AF, Bray PF, Becker LC, Becker DM. Heritability of platelet responsiveness to aspirin in activation pathways directly and indirectly related to cyclooxygenase-1. Circulation. 115: 2490-6. PMID 17470694 DOI: 10.1161/CIRCULATIONAHA.106.667584  0.44
2007 Kovac IP, Havlik RJ, Foley D, Peila R, Hernandez D, Wavrant-De Vrièze F, Singleton A, Egan J, Taub D, Rodriguez B, Masaki K, Curb JD, Fujimoto WY, Wilson AF. Linkage and association analyses of type 2 diabetes/impaired glucose metabolism and adiponectin serum levels in Japanese Americans from Hawaii. Diabetes. 56: 537-40. PMID 17259404 DOI: 10.2337/db06-0443  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
2003 Mathias RA, Wilson AF, Beaty TH, Liang KY. Model comparison and the likelihood ratio test in segregation analysis. Genetic Epidemiology. 25: 382-3. PMID 14639708 DOI: 10.1002/gepi.10273  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
1997 Svetkey LP, Chen YT, McKeown SP, Preis L, Wilson AF. Preliminary evidence of linkage of salt sensitivity in black Americans at the β2-adrenergic receptor locus Hypertension. 29: 918-922. PMID 9095077  0.44
1996 Svetkey LP, McKeown SP, Wilson AF. Heritability of salt sensitivity in black Americans Hypertension. 28: 854-858. PMID 8901834  0.44
1996 Cambrien F, Tirei L, Cheung B, Lindpaintner K, Larson MG, Wilson AF. Absence of association or genetic linkage between the angiotensin- converting-enzyme gene and left ventricular mass [4] New England Journal of Medicine. 335: 1070-1071. PMID 8801454 DOI: 10.1056/NEJM199610033351417  0.44
1996 Lindpaintner K, Lee M, Larson MG, Rao VS, Pfeffer MA, Ordovas JM, Schaefer EJ, Wilson AF, Wilson PW, Vasan RS, Myers RH, Levy D. Absence of association or genetic linkage between the angiotensin-converting-enzyme gene and left ventricular mass. The New England Journal of Medicine. 334: 1023-8. PMID 8598840 DOI: 10.1056/NEJM199604183341604  0.44
1996 Atwood LD, Wilson AF, Bailey-Wilson JE, Carruth JN, Elston RC. On the distribution of the likelihood ratio test statistic for a mixture of two normal distributions Communications in Statistics Part B: Simulation and Computation. 25: 733-740.  0.44
1995 Sautter FJ, McDermott BE, Cornwell J, Johnson J, Borges A, Wilson AF, Vasterling JJ, Foundas AL. A preliminary study of the neuropsychological heterogeneity of familial schizophrenia. Schizophrenia Research. 18: 1-7. PMID 8929755 DOI: 10.1016/0920-9964(95)00015-1  0.44
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  0.44
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  0.44
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  0.44
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  0.44
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  0.44
1992 Atwood LD, Wilson AF, Elston RC, Bailey-Wilson JE. Computational aspects of fitting a mixture of two normal distributions using maximum likelihood Communications in Statistics - Simulation and Computation. 21: 769-781. DOI: 10.1080/03610919208813049  0.44
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  0.44
1991 Elston RC, Wilson AF. Genometric analysis of mental diseases Psychiatric Genetics. 1: 1-4.  0.44
1990 Sellers TA, Bailey-Wilson JE, Elston RC, Wilson AF, Elston GZ, Ooi WL, Rothschild H. Evidence for mendelian inheritance in the pathogenesis of lung cancer. Journal of the National Cancer Institute. 82: 1272-9. PMID 2374177 DOI: 10.1093/jnci/82.15.1272  0.44
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  0.44
1990 Elston RC, Wilson AF. Genetic linkage and complex diseases I: A comment Genetic Epidemiology. 7: 17-19. DOI: 10.1002/gepi.1370070104  0.44
1989 Amos CI, Elston RC, Wilson AF, Bailey-Wilson JE. A more powerful robust sib-pair test of linkage for quantitative traits Genetic Epidemiology. 6: 435-449. PMID 2753353  0.44
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  0.44
1989 Bailey-Wilson JE, Elston RC, Wilson AF, Amos CI. A comparison of some sib-pair linkage methods and multiple locus extensions Progress in Clinical and Biological Research. 329: 129-134. PMID 2622941  0.44
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  0.44
1989 Wilson AF. Software survey section Thrombosis Research. 56. DOI: 10.1016/0049-3848(89)90245-4  0.44
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