Wilson AF - Search Results

1

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

Mathias RA, Roy-Gagnon MH, Justice CM, Papanicolaou GJ, Fan YT, Pugh EW, Wilson AF; Framingham Heart Study. Mathias RA, et al. Among authors: wilson af. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S36. doi: 10.1186/1471-2156-4-S1-S36. BMC Genet. 2003. PMID: 14975104 Free PMC article.

2

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

Papanicolaou GJ, Justice CM, Kovac IM, Sorant AJ, Wilson AF. Papanicolaou GJ, et al. Among authors: wilson af. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S54. doi: 10.1186/1471-2156-6-S1-S54. BMC Genet. 2005. PMID: 16451666 Free PMC article.

3

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.

Roy-Gagnon MH, Mathias RA, Wilson AF. Roy-Gagnon MH, et al. Among authors: wilson af. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S56. doi: 10.1186/1471-2156-6-S1-S56. BMC Genet. 2005. PMID: 16451668 Free PMC article.

4

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

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. Mathias RA, et al. Among authors: wilson af. BMC Genet. 2006 Jun 14;7:38. doi: 10.1186/1471-2156-7-38. BMC Genet. 2006. PMID: 16774684 Free PMC article.

5

Heritability of quantitative traits associated with type 2 diabetes mellitus in large multiplex families from South India.

Mathias RA, Deepa M, Deepa R, Wilson AF, Mohan V. Mathias RA, et al. Among authors: wilson af. Metabolism. 2009 Oct;58(10):1439-45. doi: 10.1016/j.metabol.2009.04.041. Epub 2009 Jul 1. Metabolism. 2009. PMID: 19570552 Free PMC article.

6

Comparison of variance components, ANOVA and regression of offspring on midparent (ROMP) methods for SNP markers.

Pugh EW, Papanicolaou GJ, Justice CM, Roy-Gagnon MH, Sorant AJ, Kingman A, Wilson AF. Pugh EW, et al. Among authors: wilson af. Genet Epidemiol. 2001;21 Suppl 1:S794-9. doi: 10.1002/gepi.2001.21.s1.s794. Genet Epidemiol. 2001. PMID: 11793780

7

An extension of the regression of offspring on mid-parent to test for association and estimate locus-specific heritability: the revised ROMP method.

Roy-Gagnon MH, Mathias RA, Fallin MD, Jee SH, Broman KW, Wilson AF. Roy-Gagnon MH, et al. Among authors: wilson af. Ann Hum Genet. 2008 Jan;72(Pt 1):115-25. doi: 10.1111/j.1469-1809.2007.00401.x. Epub 2007 Nov 27. Ann Hum Genet. 2008. PMID: 18042270

8

Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus.

Justice CM, Miller NH, Marosy B, Zhang J, Wilson AF. Justice CM, et al. Among authors: wilson af. Spine (Phila Pa 1976). 2003 Mar 15;28(6):589-94. doi: 10.1097/01.BRS.0000049940.39801.E6. Spine (Phila Pa 1976). 2003. PMID: 12642767

9

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.

Simpson CL, Justice CM, Krishnan M, Wojciechowski R, Sung H, Cai J, Green T, Lewis D, Behneman D, Wilson AF, Bailey-Wilson JE. Simpson CL, et al. Among authors: wilson af. BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S83. doi: 10.1186/1753-6561-5-S9-S83. BMC Proc. 2011. PMID: 22373393 Free PMC article.

10

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.

Schwantes-An TH, Sung H, Sabourin JA, Justice CM, Sorant AJM, Wilson AF. Schwantes-An TH, et al. Among authors: wilson af. BMC Proc. 2016 Oct 18;10(Suppl 7):385-388. doi: 10.1186/s12919-016-0060-7. eCollection 2016. BMC Proc. 2016. PMID: 27980666 Free PMC article.

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