Purcell S - Search Results

1

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.

Korn JM, Kuruvilla FG, McCarroll SA, Wysoker A, Nemesh J, Cawley S, Hubbell E, Veitch J, Collins PJ, Darvishi K, Lee C, Nizzari MM, Gabriel SB, Purcell S, Daly MJ, Altshuler D. Korn JM, et al. Among authors: purcell s. Nat Genet. 2008 Oct;40(10):1253-60. doi: 10.1038/ng.237. Epub 2008 Sep 7. Nat Genet. 2008. PMID: 18776909 Free PMC article.

2

Parental phenotypes in family-based association analysis.

Purcell S, Sham P, Daly MJ. Purcell S, et al. Am J Hum Genet. 2005 Feb;76(2):249-59. doi: 10.1086/427886. Epub 2004 Dec 21. Am J Hum Genet. 2005. PMID: 15614722 Free PMC article. Review.

3

Two quantitative trait loci for prepulse inhibition of startle identified on mouse chromosome 16 using chromosome substitution strains.

Petryshen TL, Kirby A, Hammer RP Jr, Purcell S, O'Leary SB, Singer JB, Hill AE, Nadeau JH, Daly MJ, Sklar P. Petryshen TL, et al. Among authors: purcell s. Genetics. 2005 Dec;171(4):1895-904. doi: 10.1534/genetics.105.045658. Epub 2005 Jul 5. Genetics. 2005. PMID: 15998716 Free PMC article.

4

Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4.

Plenge RM, Padyukov L, Remmers EF, Purcell S, Lee AT, Karlson EW, Wolfe F, Kastner DL, Alfredsson L, Altshuler D, Gregersen PK, Klareskog L, Rioux JD. Plenge RM, et al. Among authors: purcell s. Am J Hum Genet. 2005 Dec;77(6):1044-60. doi: 10.1086/498651. Epub 2005 Nov 1. Am J Hum Genet. 2005. PMID: 16380915 Free PMC article.

5

Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.

Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG. Fisher SA, et al. Among authors: purcell s. Hum Mutat. 2006 Aug;27(8):778-85. doi: 10.1002/humu.20358. Hum Mutat. 2006. PMID: 16835882

6

Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration.

Maller J, George S, Purcell S, Fagerness J, Altshuler D, Daly MJ, Seddon JM. Maller J, et al. Among authors: purcell s. Nat Genet. 2006 Sep;38(9):1055-9. doi: 10.1038/ng1873. Epub 2006 Aug 27. Nat Genet. 2006. PMID: 16936732

7

WHAP: haplotype-based association analysis.

Purcell S, Daly MJ, Sham PC. Purcell S, et al. Bioinformatics. 2007 Jan 15;23(2):255-6. doi: 10.1093/bioinformatics/btl580. Epub 2006 Nov 21. Bioinformatics. 2007. PMID: 17118959

AVAILABILITY: WHAP is a C/C++ program, freely available from the author's website: http://pngu.mgh.harvard.edu/purcell/whap/...

AVAILABILITY: WHAP is a C/C++ program, freely available from the author's website: http://pngu.mgh.harvard.edu/purcell/whap/.. …

8

Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome.

Weiss LA, Purcell S, Waggoner S, Lawrence K, Spektor D, Daly MJ, Sklar P, Skuse D. Weiss LA, et al. Among authors: purcell s. Hum Mol Genet. 2007 Jan 1;16(1):107-13. doi: 10.1093/hmg/ddl445. Epub 2006 Dec 12. Hum Mol Genet. 2007. PMID: 17164267

9

Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes.

Winckler W, Weedon MN, Graham RR, McCarroll SA, Purcell S, Almgren P, Tuomi T, Gaudet D, Boström KB, Walker M, Hitman G, Hattersley AT, McCarthy MI, Ardlie KG, Hirschhorn JN, Daly MJ, Frayling TM, Groop L, Altshuler D. Winckler W, et al. Among authors: purcell s. Diabetes. 2007 Mar;56(3):685-93. doi: 10.2337/db06-0202. Diabetes. 2007. PMID: 17327436

10

Ascertainment through family history of disease often decreases the power of family-based association studies.

Ferreira MA, Sham P, Daly MJ, Purcell S. Ferreira MA, et al. Among authors: purcell s. Behav Genet. 2007 Jul;37(4):631-6. doi: 10.1007/s10519-007-9149-0. Epub 2007 Mar 20. Behav Genet. 2007. PMID: 17372818

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