Thomas A - Search Results

1

Accelerated gene counting for haplotype frequency estimation.

Thomas A. Thomas A. Ann Hum Genet. 2003 Nov;67(Pt 6):608-12. doi: 10.1046/j.1529-8817.2003.00054.x. Ann Hum Genet. 2003. PMID: 14641248

2

GCHap: fast MLEs for haplotype frequencies by gene counting.

Thomas A. Thomas A. Bioinformatics. 2003 Oct 12;19(15):2002-3. doi: 10.1093/bioinformatics/btg254. Bioinformatics. 2003. PMID: 14555636

3

Graphical modeling of the joint distribution of alleles at associated loci.

Thomas A, Camp NJ. Thomas A, et al. Am J Hum Genet. 2004 Jun;74(6):1088-101. doi: 10.1086/421249. Epub 2004 Apr 26. Am J Hum Genet. 2004. PMID: 15114533 Free PMC article.

4

Characterizing allelic associations from unphased diploid data by graphical modeling.

Thomas A. Thomas A. Genet Epidemiol. 2005 Jul;29(1):23-35. doi: 10.1002/gepi.20076. Genet Epidemiol. 2005. PMID: 15838847

5

Maximum likelihood estimates of allele frequencies and error rates from samples of related individuals by gene counting.

Thomas A, Camp NJ. Thomas A, et al. Bioinformatics. 2006 Mar 15;22(6):771-2. doi: 10.1093/bioinformatics/btk049. Epub 2006 Jan 12. Bioinformatics. 2006. PMID: 16410318

6

Identification of regions of positive selection using Shared Genomic Segment analysis.

Cai Z, Camp NJ, Cannon-Albright L, Thomas A. Cai Z, et al. Among authors: thomas a. Eur J Hum Genet. 2011 Jun;19(6):667-71. doi: 10.1038/ejhg.2010.257. Epub 2011 Feb 9. Eur J Hum Genet. 2011. PMID: 21304558 Free PMC article.

7

A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.

Teerlink C, Farnham J, Allen-Brady K, Camp NJ, Thomas A, Leachman S, Cannon-Albright L. Teerlink C, et al. Among authors: thomas a. Hum Genet. 2012 Jan;131(1):77-85. doi: 10.1007/s00439-011-1048-z. Epub 2011 Jun 26. Hum Genet. 2012. PMID: 21706340

8

Shared genomic segment analysis: the power to find rare disease variants.

Knight S, Abo RP, Abel HJ, Neklason DW, Tuohy TM, Burt RW, Thomas A, Camp NJ. Knight S, et al. Among authors: thomas a. Ann Hum Genet. 2012 Nov;76(6):500-9. doi: 10.1111/j.1469-1809.2012.00728.x. Epub 2012 Sep 19. Ann Hum Genet. 2012. PMID: 22989048 Free PMC article.

9

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.

Teerlink CC, Leongamornlert D, Dadaev T, Thomas A, Farnham J, Stephenson RA, Riska S, McDonnell SK, Schaid DJ, Catalona WJ, Zheng SL, Cooney KA, Ray AM, Zuhlke KA, Lange EM, Giles GG, Southey MC, Fitzgerald LM, Rinckleb A, Luedeke M, Maier C, Stanford JL, Ostrander EA, Kaikkonen EM, Sipeky C, Tammela T, Schleutker J, Wiley KE, Isaacs SD, Walsh PC, Isaacs WB, Xu J, Cancel-Tassin G, Cussenot O, Mandal D, Laurie C, Laurie C; PRACTICAL consortium; International Consortium for Prostate Cancer Genetics; Thibodeau SN, Eeles RA, Kote-Jarai Z, Cannon-Albright L. Teerlink CC, et al. Among authors: thomas a. Hum Genet. 2016 Aug;135(8):923-38. doi: 10.1007/s00439-016-1690-6. Epub 2016 Jun 4. Hum Genet. 2016. PMID: 27262462 Free PMC article.

10

Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: ELAC2 and familial early-onset prostate cancer.

Camp NJ, Swensen J, Horne BD, Farnham JM, Thomas A, Cannon-Albright LA, Tavtigian SV. Camp NJ, et al. Among authors: thomas a. Genet Epidemiol. 2005 Apr;28(3):232-43. doi: 10.1002/gepi.20054. Genet Epidemiol. 2005. PMID: 15593091

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