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Items: 1 to 20 of 43

1.

Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium.

Pasaniuc B, Zaitlen N, Lettre G, Chen GK, Tandon A, Kao WH, Ruczinski I, Fornage M, Siscovick DS, Zhu X, Larkin E, Lange LA, Cupples LA, Yang Q, Akylbekova EL, Musani SK, Divers J, Mychaleckyj J, Li M, Papanicolaou GJ, Millikan RC, Ambrosone CB, John EM, Bernstein L, Zheng W, Hu JJ, Ziegler RG, Nyante SJ, Bandera EV, Ingles SA, Press MF, Chanock SJ, Deming SL, Rodriguez-Gil JL, Palmer CD, Buxbaum S, Ekunwe L, Hirschhorn JN, Henderson BE, Myers S, Haiman CA, Reich D, Patterson N, Wilson JG, Price AL.

PLoS Genet. 2011 Apr;7(4):e1001371. doi: 10.1371/journal.pgen.1001371. Epub 2011 Apr 21.

2.

Dating the age of admixture via wavelet transform analysis of genome-wide data.

Pugach I, Matveyev R, Wollstein A, Kayser M, Stoneking M.

Genome Biol. 2011;12(2):R19. doi: 10.1186/gb-2011-12-2-r19. Epub 2011 Feb 25.

3.

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

Lettre G, Palmer CD, Young T, Ejebe KG, Allayee H, Benjamin EJ, Bennett F, Bowden DW, Chakravarti A, Dreisbach A, Farlow DN, Folsom AR, Fornage M, Forrester T, Fox E, Haiman CA, Hartiala J, Harris TB, Hazen SL, Heckbert SR, Henderson BE, Hirschhorn JN, Keating BJ, Kritchevsky SB, Larkin E, Li M, Rudock ME, McKenzie CA, Meigs JB, Meng YA, Mosley TH, Newman AB, Newton-Cheh CH, Paltoo DN, Papanicolaou GJ, Patterson N, Post WS, Psaty BM, Qasim AN, Qu L, Rader DJ, Redline S, Reilly MP, Reiner AP, Rich SS, Rotter JI, Liu Y, Shrader P, Siscovick DS, Tang WH, Taylor HA, Tracy RP, Vasan RS, Waters KM, Wilks R, Wilson JG, Fabsitz RR, Gabriel SB, Kathiresan S, Boerwinkle E.

PLoS Genet. 2011 Feb 10;7(2):e1001300. doi: 10.1371/journal.pgen.1001300.

4.

Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia.

Yang JJ, Cheng C, Devidas M, Cao X, Fan Y, Campana D, Yang W, Neale G, Cox NJ, Scheet P, Borowitz MJ, Winick NJ, Martin PL, Willman CL, Bowman WP, Camitta BM, Carroll A, Reaman GH, Carroll WL, Loh M, Hunger SP, Pui CH, Evans WE, Relling MV.

Nat Genet. 2011 Mar;43(3):237-41. doi: 10.1038/ng.763. Epub 2011 Feb 6.

5.

Ancestry informative marker panels for African Americans based on subsets of commercially available SNP arrays.

Tandon A, Patterson N, Reich D.

Genet Epidemiol. 2011 Jan;35(1):80-3. doi: 10.1002/gepi.20550.

6.

Adjustment for local ancestry in genetic association analysis of admixed populations.

Wang X, Zhu X, Qin H, Cooper RS, Ewens WJ, Li C, Li M.

Bioinformatics. 2011 Mar 1;27(5):670-7. doi: 10.1093/bioinformatics/btq709. Epub 2010 Dec 17.

7.

Joint testing of genotype and ancestry association in admixed families.

Tang H, Siegmund DO, Johnson NA, Romieu I, London SJ.

Genet Epidemiol. 2010 Dec;34(8):783-91. doi: 10.1002/gepi.20520.

8.

Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups.

Waters KM, Stram DO, Hassanein MT, Le Marchand L, Wilkens LR, Maskarinec G, Monroe KR, Kolonel LN, Altshuler D, Henderson BE, Haiman CA.

PLoS Genet. 2010 Aug 26;6(8). pii: e1001078. doi: 10.1371/journal.pgen.1001078.

9.

Biological, clinical and population relevance of 95 loci for blood lipids.

Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S, Chasman DI, Willer CJ, Johansen CT, Fouchier SW, Isaacs A, Peloso GM, Barbalic M, Ricketts SL, Bis JC, Aulchenko YS, Thorleifsson G, Feitosa MF, Chambers J, Orho-Melander M, Melander O, Johnson T, Li X, Guo X, Li M, Shin Cho Y, Jin Go M, Jin Kim Y, Lee JY, Park T, Kim K, Sim X, Twee-Hee Ong R, Croteau-Chonka DC, Lange LA, Smith JD, Song K, Hua Zhao J, Yuan X, Luan J, Lamina C, Ziegler A, Zhang W, Zee RY, Wright AF, Witteman JC, Wilson JF, Willemsen G, Wichmann HE, Whitfield JB, Waterworth DM, Wareham NJ, Waeber G, Vollenweider P, Voight BF, Vitart V, Uitterlinden AG, Uda M, Tuomilehto J, Thompson JR, Tanaka T, Surakka I, Stringham HM, Spector TD, Soranzo N, Smit JH, Sinisalo J, Silander K, Sijbrands EJ, Scuteri A, Scott J, Schlessinger D, Sanna S, Salomaa V, Saharinen J, Sabatti C, Ruokonen A, Rudan I, Rose LM, Roberts R, Rieder M, Psaty BM, Pramstaller PP, Pichler I, Perola M, Penninx BW, Pedersen NL, Pattaro C, Parker AN, Pare G, Oostra BA, O'Donnell CJ, Nieminen MS, Nickerson DA, Montgomery GW, Meitinger T, McPherson R, McCarthy MI, McArdle W, Masson D, Martin NG, Marroni F, Mangino M, Magnusson PK, Lucas G, Luben R, Loos RJ, Lokki ML, Lettre G, Langenberg C, Launer LJ, Lakatta EG, Laaksonen R, Kyvik KO, Kronenberg F, König IR, Khaw KT, Kaprio J, Kaplan LM, Johansson A, Jarvelin MR, Janssens AC, Ingelsson E, Igl W, Kees Hovingh G, Hottenga JJ, Hofman A, Hicks AA, Hengstenberg C, Heid IM, Hayward C, Havulinna AS, Hastie ND, Harris TB, Haritunians T, Hall AS, Gyllensten U, Guiducci C, Groop LC, Gonzalez E, Gieger C, Freimer NB, Ferrucci L, Erdmann J, Elliott P, Ejebe KG, Döring A, Dominiczak AF, Demissie S, Deloukas P, de Geus EJ, de Faire U, Crawford G, Collins FS, Chen YD, Caulfield MJ, Campbell H, Burtt NP, Bonnycastle LL, Boomsma DI, Boekholdt SM, Bergman RN, Barroso I, Bandinelli S, Ballantyne CM, Assimes TL, Quertermous T, Altshuler D, Seielstad M, Wong TY, Tai ES, Feranil AB, Kuzawa CW, Adair LS, Taylor HA Jr, Borecki IB, Gabriel SB, Wilson JG, Holm H, Thorsteinsdottir U, Gudnason V, Krauss RM, Mohlke KL, Ordovas JM, Munroe PB, Kooner JS, Tall AR, Hegele RA, Kastelein JJ, Schadt EE, Rotter JI, Boerwinkle E, Strachan DP, Mooser V, Stefansson K, Reilly MP, Samani NJ, Schunkert H, Cupples LA, Sandhu MS, Ridker PM, Rader DJ, van Duijn CM, Peltonen L, Abecasis GR, Boehnke M, Kathiresan S.

Nature. 2010 Aug 5;466(7307):707-13. doi: 10.1038/nature09270.

10.

New approaches to population stratification in genome-wide association studies.

Price AL, Zaitlen NA, Reich D, Patterson N.

Nat Rev Genet. 2010 Jul;11(7):459-63. doi: 10.1038/nrg2813. Review.

11.

Genotype imputation for genome-wide association studies.

Marchini J, Howie B.

Nat Rev Genet. 2010 Jul;11(7):499-511. doi: 10.1038/nrg2796. Review.

PMID:
20517342
12.

Genome-wide analysis of the structure of the South African Coloured Population in the Western Cape.

de Wit E, Delport W, Rugamika CE, Meintjes A, Möller M, van Helden PD, Seoighe C, Hoal EG.

Hum Genet. 2010 Aug;128(2):145-53. doi: 10.1007/s00439-010-0836-1. Epub 2010 May 20.

PMID:
20490549
13.

Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations.

Bryc K, Velez C, Karafet T, Moreno-Estrada A, Reynolds A, Auton A, Hammer M, Bustamante CD, Ostrer H.

Proc Natl Acad Sci U S A. 2010 May 11;107 Suppl 2:8954-61. doi: 10.1073/pnas.0914618107. Epub 2010 May 5.

14.

Genome-wide association studies in diverse populations.

Rosenberg NA, Huang L, Jewett EM, Szpiech ZA, Jankovic I, Boehnke M.

Nat Rev Genet. 2010 May;11(5):356-66. doi: 10.1038/nrg2760. Review.

15.

Mexican-American admixture mapping analyses for diabetic nephropathy in type 2 diabetes mellitus.

Adler S, Pahl M, Abboud H, Nicholas S, Ipp E, Seldin M.

Semin Nephrol. 2010 Mar;30(2):141-9. doi: 10.1016/j.semnephrol.2010.01.005.

16.

Leveraging genetic variability across populations for the identification of causal variants.

Zaitlen N, Paşaniuc B, Gur T, Ziv E, Halperin E.

Am J Hum Genet. 2010 Jan;86(1):23-33. doi: 10.1016/j.ajhg.2009.11.016.

17.

A composite of multiple signals distinguishes causal variants in regions of positive selection.

Grossman SR, Shlyakhter I, Karlsson EK, Byrne EH, Morales S, Frieden G, Hostetter E, Angelino E, Garber M, Zuk O, Lander ES, Schaffner SF, Sabeti PC.

Science. 2010 Feb 12;327(5967):883-6. doi: 10.1126/science.1183863. Epub 2010 Jan 7. Erratum in: Science. 2012 Feb17;335(6070):796. Shylakhter, Ilya [corrected to Shlyakhter, Ilya]..

18.

Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children.

Hancock DB, Romieu I, Shi M, Sienra-Monge JJ, Wu H, Chiu GY, Li H, del Rio-Navarro BE, Willis-Owen SA, Weiss ST, Raby BA, Gao H, Eng C, Chapela R, Burchard EG, Tang H, Sullivan PF, London SJ.

PLoS Genet. 2009 Aug;5(8):e1000623. doi: 10.1371/journal.pgen.1000623. Epub 2009 Aug 28. Erratum in: PLoS Genet. 2009 Dec;5(12). doi: 10.1371/annotation/dde89c4c-03f7-4747-8426-180c4ecee5d5. Willis-Owens, Saffron A G [corrected to Willis-Owen, Saffron A G].

19.

A genome-wide association study of hypertension and blood pressure in African Americans.

Adeyemo A, Gerry N, Chen G, Herbert A, Doumatey A, Huang H, Zhou J, Lashley K, Chen Y, Christman M, Rotimi C.

PLoS Genet. 2009 Jul;5(7):e1000564. doi: 10.1371/journal.pgen.1000564. Epub 2009 Jul 17.

20.

Sensitive detection of chromosomal segments of distinct ancestry in admixed populations.

Price AL, Tandon A, Patterson N, Barnes KC, Rafaels N, Ruczinski I, Beaty TH, Mathias R, Reich D, Myers S.

PLoS Genet. 2009 Jun;5(6):e1000519. doi: 10.1371/journal.pgen.1000519. Epub 2009 Jun 19.

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