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...

by Roy-Gagnon, Marie-Hélène, Mathias, Rasika A, Wilson, Alexander F
Published 2005

Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment

by Mandal, Diptasri M, Sorant, Alexa JM, Atwood, Larry D, Wilson, Alexander F, Bailey-Wilson, Joan E
Published 2006

Critical values and variation in type I error along chromosomes in the COGA dataset using the applied pseudo-trait method

by Papanicolaou, George J, Justice, Cristina M, Kovac, Illija M, Sorant, Alexa JM, Wilson, Alexander F
Published 2005

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

by Schwantes-An, Tae-Hwi, Sung, Heejong, Sabourin, Jeremy A., Justice, Cristina M., Sorant, Alexa J. M., Wilson, Alexander F.
Published 2016

Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data

by Mathias, Rasika A, Roy-Gagnon, Marie-Hélène, Justice, Cristina M, Papanicolaou, George J, Fan, Yu Ti, Pugh, Elizabeth W, Wilson, Alexander F
Published 2003

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

by Simpson, Claire L, Justice, Cristina M, Krishnan, Mera, Wojciechowski, Robert, Sung, Heejong, Cai, Jerry, Green, Tiffany, Lewis, Deyana, Behneman, Dana, Wilson, Alexander F, Bailey-Wilson, Joan E
Published 2011

Performance of random forests and logic regression methods using mini-exome sequence data

by Kim, Yoonhee, Li, Qing, Cropp, Cheryl D, Sung, Heejong, Cai, Juanliang, Simpson, Claire L, Perry, Brian, Dasgupta, Abhijit, Malley, James D, Wilson, Alexander F, Bailey-Wilson, Joan E
Published 2011

Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression

by Sung, Heejong, Kim, Yoonhee, Cai, Juanliang, Cropp, Cheryl D, Simpson, Claire L, Li, Qing, Perry, Brian C, Sorant, Alexa JM, Bailey-Wilson, Joan E, Wilson, Alexander F
Published 2011

Targeted Deep Resequencing Identifies Coding Variants in the PEAR1 Gene That Play a Role in Platelet Aggregation

by Kim, Yoonhee, Suktitipat, Bhoom, Yanek, Lisa R., Faraday, Nauder, Wilson, Alexander F., Becker, Diane M., Becker, Lewis C., Mathias, Rasika A.
Published 2013

Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis

by Justice, Cristina M., Bishop, Kevin, Carrington, Blake, Mullikin, Jim C., Swindle, Kandice, Marosy, Beth, Sood, Raman, Miller, Nancy H., Wilson, Alexander F.
Published 2016

A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q

by Mathias, Rasika A, Gao, Peisong, Goldstein, Janet L, Wilson, Alexander F, Pugh, Elizabeth W, Furbert-Harris, Paulette, Dunston, Georgia M, Malveaux, Floyd J, Togias, Alkis, Barnes, Kathleen C, Beaty, Terri H, Huang, Shau-Ku
Published 2006

Genetic Modifiers of Neurofibromatosis Type 1-Associated Café-au-Lait Macule Count Identified Using Multi-platform Analysis

by Pemov, Alexander, Sung, Heejong, Hyland, Paula L., Sloan, Jennifer L., Ruppert, Sarah L., Baldwin, Andrea M., Boland, Joseph F., Bass, Sara E., Lee, Hyo Jung, Jones, Kristine M., Zhang, Xijun, Mullikin, James C., Widemann, Brigitte C., Wilson, Alexander F., Stewart, Douglas R.
Published 2014