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Variation is the spice of life.
Kruglyak L, Nickerson DA. Kruglyak L, et al. Nat Genet. 2001 Mar;27(3):234-6. doi: 10.1038/85776. Nat Genet. 2001. PMID: 11242096 No abstract available.
A reference panel of 64,976 haplotypes for genotype imputation.
McCarthy S, Das S, Kretzschmar W, Delaneau O, Wood AR, Teumer A, Kang HM, Fuchsberger C, Danecek P, Sharp K, Luo Y, Sidore C, Kwong A, Timpson N, Koskinen S, Vrieze S, Scott LJ, Zhang H, Mahajan A, Veldink J, Peters U, Pato C, van Duijn CM, Gillies CE, Gandin I, Mezzavilla M, Gilly A, Cocca M, Traglia M, Angius A, Barrett JC, Boomsma D, Branham K, Breen G, Brummett CM, Busonero F, Campbell H, Chan A, Chen S, Chew E, Collins FS, Corbin LJ, Smith GD, Dedoussis G, Dorr M, Farmaki AE, Ferrucci L, Forer L, Fraser RM, Gabriel S, Levy S, Groop L, Harrison T, Hattersley A, Holmen OL, Hveem K, Kretzler M, Lee JC, McGue M, Meitinger T, Melzer D, Min JL, Mohlke KL, Vincent JB, Nauck M, Nickerson D, Palotie A, Pato M, Pirastu N, McInnis M, Richards JB, Sala C, Salomaa V, Schlessinger D, Schoenherr S, Slagboom PE, Small K, Spector T, Stambolian D, Tuke M, Tuomilehto J, Van den Berg LH, Van Rheenen W, Volker U, Wijmenga C, Toniolo D, Zeggini E, Gasparini P, Sampson MG, Wilson JF, Frayling T, de Bakker PI, Swertz MA, McCarroll S, Kooperberg C, Dekker A, Altshuler D, Willer C, Iacono W, Ripatti S, Soranzo N, Walter K, Swaroop A, Cucca F, Anderson CA, Myers RM, Boehnke M, McCarthy MI, Durbin R; Haplotype Reference Consortium. McCarthy S, et al. Nat Genet. 2016 Oct;48(10):1279-83. doi: 10.1038/ng.3643. Epub 2016 Aug 22. Nat Genet. 2016. PMID: 27548312 Free PMC article.
Sequence variation and linkage disequilibrium in the human T-cell receptor beta (TCRB) locus.
Subrahmanyan L, Eberle MA, Clark AG, Kruglyak L, Nickerson DA. Subrahmanyan L, et al. Am J Hum Genet. 2001 Aug;69(2):381-95. doi: 10.1086/321297. Epub 2001 Jun 29. Am J Hum Genet. 2001. PMID: 11438886 Free PMC article.
Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.
Fullerton SM, Clark AG, Weiss KM, Nickerson DA, Taylor SL, Stengârd JH, Salomaa V, Vartiainen E, Perola M, Boerwinkle E, Sing CF. Fullerton SM, et al. Am J Hum Genet. 2000 Oct;67(4):881-900. doi: 10.1086/303070. Epub 2000 Sep 13. Am J Hum Genet. 2000. PMID: 10986041 Free PMC article.
Sequence variation in the human angiotensin converting enzyme.
Rieder MJ, Taylor SL, Clark AG, Nickerson DA. Rieder MJ, et al. Nat Genet. 1999 May;22(1):59-62. doi: 10.1038/8760. Nat Genet. 1999. PMID: 10319862
DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.
Nickerson DA, Taylor SL, Weiss KM, Clark AG, Hutchinson RG, Stengård J, Salomaa V, Vartiainen E, Boerwinkle E, Sing CF. Nickerson DA, et al. Nat Genet. 1998 Jul;19(3):233-40. doi: 10.1038/907. Nat Genet. 1998. PMID: 9662394
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.
Emond MJ, Louie T, Emerson J, Zhao W, Mathias RA, Knowles MR, Wright FA, Rieder MJ, Tabor HK, Nickerson DA, Barnes KC; National Heart, Lung, and Blood Institute (NHLBI) GO Exome Sequencing Project; Lung GO, Gibson RL, Bamshad MJ. Emond MJ, et al. Nat Genet. 2012 Jul 8;44(8):886-9. doi: 10.1038/ng.2344. Nat Genet. 2012. PMID: 22772370 Free PMC article.
Mutational and selective effects on copy-number variants in the human genome.
Cooper GM, Nickerson DA, Eichler EE. Cooper GM, et al. Nat Genet. 2007 Jul;39(7 Suppl):S22-9. doi: 10.1038/ng2054. Nat Genet. 2007. PMID: 17597777 Review.
Mapping complex disease loci in whole-genome association studies.
Carlson CS, Eberle MA, Kruglyak L, Nickerson DA. Carlson CS, et al. Nature. 2004 May 27;429(6990):446-52. doi: 10.1038/nature02623. Nature. 2004. PMID: 15164069 Review.
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