Ardlie K - Search Results

1

Characterization of single-nucleotide polymorphisms in coding regions of human genes.

Cargill M, Altshuler D, Ireland J, Sklar P, Ardlie K, Patil N, Shaw N, Lane CR, Lim EP, Kalyanaraman N, Nemesh J, Ziaugra L, Friedland L, Rolfe A, Warrington J, Lipshutz R, Daley GQ, Lander ES. Cargill M, et al. Among authors: ardlie k. Nat Genet. 1999 Jul;22(3):231-8. doi: 10.1038/10290. Nat Genet. 1999. PMID: 10391209

2

Impact of migration and fitness on the stability of lethal t-haplotype polymorphism in Mus musculus: a computer study.

Durand D, Ardlie K, Buttel L, Levin SA, Silver LM. Durand D, et al. Among authors: ardlie k. Genetics. 1997 Apr;145(4):1093-108. doi: 10.1093/genetics/145.4.1093. Genetics. 1997. PMID: 9093861 Free PMC article. Review.

3

Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse.

Lindblad-Toh K, Winchester E, Daly MJ, Wang DG, Hirschhorn JN, Laviolette JP, Ardlie K, Reich DE, Robinson E, Sklar P, Shah N, Thomas D, Fan JB, Gingeras T, Warrington J, Patil N, Hudson TJ, Lander ES. Lindblad-Toh K, et al. Among authors: ardlie k. Nat Genet. 2000 Apr;24(4):381-6. doi: 10.1038/74215. Nat Genet. 2000. PMID: 10742102

4

Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion.

Ardlie K, Liu-Cordero SN, Eberle MA, Daly M, Barrett J, Winchester E, Lander ES, Kruglyak L. Ardlie K, et al. Am J Hum Genet. 2001 Sep;69(3):582-9. doi: 10.1086/323251. Epub 2001 Jul 25. Am J Hum Genet. 2001. PMID: 11473344 Free PMC article.

5

The discovery of single-nucleotide polymorphisms--and inferences about human demographic history.

Wakeley J, Nielsen R, Liu-Cordero SN, Ardlie K. Wakeley J, et al. Among authors: ardlie k. Am J Hum Genet. 2001 Dec;69(6):1332-47. doi: 10.1086/324521. Epub 2001 Nov 6. Am J Hum Genet. 2001. PMID: 11704929 Free PMC article.

6

Patterns of linkage disequilibrium in the human genome.

Ardlie KG, Kruglyak L, Seielstad M. Ardlie KG, et al. Nat Rev Genet. 2002 Apr;3(4):299-309. doi: 10.1038/nrg777. Nat Rev Genet. 2002. PMID: 11967554 Review.

7

Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people.

Winckler W, Graham RR, de Bakker PI, Sun M, Almgren P, Tuomi T, Gaudet D, Hudson TJ, Ardlie KG, Daly MJ, Hirschhorn JN, Groop L, Altshuler D. Winckler W, et al. Diabetes. 2005 Mar;54(3):886-92. doi: 10.2337/diabetes.54.3.886. Diabetes. 2005. PMID: 15734869

8

Demonstrating stratification in a European American population.

Campbell CD, Ogburn EL, Lunetta KL, Lyon HN, Freedman ML, Groop LC, Altshuler D, Ardlie KG, Hirschhorn JN. Campbell CD, et al. Nat Genet. 2005 Aug;37(8):868-72. doi: 10.1038/ng1607. Epub 2005 Jul 24. Nat Genet. 2005. PMID: 16041375

9

Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes.

Winckler W, Burtt NP, Holmkvist J, Cervin C, de Bakker PI, Sun M, Almgren P, Tuomi T, Gaudet D, Hudson TJ, Ardlie KG, Daly MJ, Hirschhorn JN, Altshuler D, Groop L. Winckler W, et al. Diabetes. 2005 Aug;54(8):2336-42. doi: 10.2337/diabetes.54.8.2336. Diabetes. 2005. PMID: 16046299

10

Comprehensive association testing of common mitochondrial DNA variation in metabolic disease.

Saxena R, de Bakker PI, Singer K, Mootha V, Burtt N, Hirschhorn JN, Gaudet D, Isomaa B, Daly MJ, Groop L, Ardlie KG, Altshuler D. Saxena R, et al. Among authors: ardlie kg. Am J Hum Genet. 2006 Jul;79(1):54-61. doi: 10.1086/504926. Epub 2006 May 24. Am J Hum Genet. 2006. PMID: 16773565 Free PMC article.

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