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Items: 1 to 20 of 31

1.

Quality control procedures for genome-wide association studies.

Turner S, Armstrong LL, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes G, Jarvik G, Jiang L, Kullo IJ, Li R, Ling H, Manolio TA, Matsumoto M, McCarty CA, McDavid AN, Mirel DB, Paschall JE, Pugh EW, Rasmussen LV, Wilke RA, Zuvich RL, Ritchie MD.

Curr Protoc Hum Genet. 2011 Jan;Chapter 1:Unit1.19. doi: 10.1002/0471142905.hg0119s68.

2.

Genetic cardiovascular risk prediction: will we get there?

Thanassoulis G, Vasan RS.

Circulation. 2010 Nov 30;122(22):2323-34. doi: 10.1161/CIRCULATIONAHA.109.909309. Review. No abstract available.

3.

A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses.

Ripatti S, Tikkanen E, Orho-Melander M, Havulinna AS, Silander K, Sharma A, Guiducci C, Perola M, Jula A, Sinisalo J, Lokki ML, Nieminen MS, Melander O, Salomaa V, Peltonen L, Kathiresan S.

Lancet. 2010 Oct 23;376(9750):1393-400. doi: 10.1016/S0140-6736(10)61267-6.

4.

A genome-wide association study of red blood cell traits using the electronic medical record.

Kullo IJ, Ding K, Jouni H, Smith CY, Chute CG.

PLoS One. 2010 Sep 28;5(9). pii: e13011. doi: 10.1371/journal.pone.0013011.

5.

Leveraging informatics for genetic studies: use of the electronic medical record to enable a genome-wide association study of peripheral arterial disease.

Kullo IJ, Fan J, Pathak J, Savova GK, Ali Z, Chute CG.

J Am Med Inform Assoc. 2010 Sep-Oct;17(5):568-74. doi: 10.1136/jamia.2010.004366.

6.

Early identification of cardiovascular risk using genomics and proteomics.

Kullo IJ, Cooper LT.

Nat Rev Cardiol. 2010 Jun;7(6):309-17. doi: 10.1038/nrcardio.2010.53. Review.

7.

Performance of common genetic variants in breast-cancer risk models.

Wacholder S, Hartge P, Prentice R, Garcia-Closas M, Feigelson HS, Diver WR, Thun MJ, Cox DG, Hankinson SE, Kraft P, Rosner B, Berg CD, Brinton LA, Lissowska J, Sherman ME, Chlebowski R, Kooperberg C, Jackson RD, Buckman DW, Hui P, Pfeiffer R, Jacobs KB, Thomas GD, Hoover RN, Gail MH, Chanock SJ, Hunter DJ.

N Engl J Med. 2010 Mar 18;362(11):986-93. doi: 10.1056/NEJMoa0907727. Erratum in: N Engl J Med. 2010 Dec 2;363(23):2272.

8.

Association between a literature-based genetic risk score and cardiovascular events in women.

Paynter NP, Chasman DI, Paré G, Buring JE, Cook NR, Miletich JP, Ridker PM.

JAMA. 2010 Feb 17;303(7):631-7. doi: 10.1001/jama.2010.119.

9.

Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study.

Brautbar A, Ballantyne CM, Lawson K, Nambi V, Chambless L, Folsom AR, Willerson JT, Boerwinkle E.

Circ Cardiovasc Genet. 2009 Jun;2(3):279-85. doi: 10.1161/CIRCGENETICS.108.817338.

10.

Using lifetime risk estimates in personal genomic profiles: estimation of uncertainty.

Yang Q, Flanders WD, Moonesinghe R, Ioannidis JP, Guessous I, Khoury MJ.

Am J Hum Genet. 2009 Dec;85(6):786-800. doi: 10.1016/j.ajhg.2009.10.017.

11.

Genome-wide association studies for atherosclerotic vascular disease and its risk factors.

Ding K, Kullo IJ.

Circ Cardiovasc Genet. 2009 Feb;2(1):63-72. doi: 10.1161/CIRCGENETICS.108.816751. Review. No abstract available.

12.

Genotype imputation.

Li Y, Willer C, Sanna S, Abecasis G.

Annu Rev Genomics Hum Genet. 2009;10:387-406. doi: 10.1146/annurev.genom.9.081307.164242. Review.

13.

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.

Khoury MJ, McBride CM, Schully SD, Ioannidis JP, Feero WG, Janssens AC, Gwinn M, Simons-Morton DG, Bernhardt JM, Cargill M, Chanock SJ, Church GM, Coates RJ, Collins FS, Croyle RT, Davis BR, Downing GJ, Duross A, Friedman S, Gail MH, Ginsburg GS, Green RC, Greene MH, Greenland P, Gulcher JR, Hsu A, Hudson KL, Kardia SL, Kimmel PL, Lauer MS, Miller AM, Offit K, Ransohoff DF, Roberts JS, Rasooly RS, Stefansson K, Terry SF, Teutsch SM, Trepanier A, Wanke KL, Witte JS, Xu J; Centers for Disease Control and Prevention..

Genet Med. 2009 Aug;11(8):559-67. doi: 10.1097/GIM.0b013e3181b13a6c.

14.

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

Erdmann J, Grosshennig A, Braund PS, König IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Trégouët DA, Cambien F, Bruse P, Aherrahrou Z, Wagner AK, Stark K, Schwartz SM, Salomaa V, Elosua R, Melander O, Voight BF, O'Donnell CJ, Peltonen L, Siscovick DS, Altshuler D, Merlini PA, Peyvandi F, Bernardinelli L, Ardissino D, Schillert A, Blankenberg S, Zeller T, Wild P, Schwarz DF, Tiret L, Perret C, Schreiber S, El Mokhtari NE, Schäfer A, März W, Renner W, Bugert P, Klüter H, Schrezenmeir J, Rubin D, Ball SG, Balmforth AJ, Wichmann HE, Meitinger T, Fischer M, Meisinger C, Baumert J, Peters A, Ouwehand WH; Italian Atherosclerosis, Thrombosis, and Vascular Biology Working Group.; Myocardial Infarction Genetics Consortium.; Wellcome Trust Case Control Consortium.; Cardiogenics Consortium., Deloukas P, Thompson JR, Ziegler A, Samani NJ, Schunkert H.

Nat Genet. 2009 Mar;41(3):280-2. doi: 10.1038/ng.307.

15.

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.

Gudbjartsson DF, Bjornsdottir US, Halapi E, Helgadottir A, Sulem P, Jonsdottir GM, Thorleifsson G, Helgadottir H, Steinthorsdottir V, Stefansson H, Williams C, Hui J, Beilby J, Warrington NM, James A, Palmer LJ, Koppelman GH, Heinzmann A, Krueger M, Boezen HM, Wheatley A, Altmuller J, Shin HD, Uh ST, Cheong HS, Jonsdottir B, Gislason D, Park CS, Rasmussen LM, Porsbjerg C, Hansen JW, Backer V, Werge T, Janson C, Jönsson UB, Ng MC, Chan J, So WY, Ma R, Shah SH, Granger CB, Quyyumi AA, Levey AI, Vaccarino V, Reilly MP, Rader DJ, Williams MJ, van Rij AM, Jones GT, Trabetti E, Malerba G, Pignatti PF, Boner A, Pescollderungg L, Girelli D, Olivieri O, Martinelli N, Ludviksson BR, Ludviksdottir D, Eyjolfsson GI, Arnar D, Thorgeirsson G, Deichmann K, Thompson PJ, Wjst M, Hall IP, Postma DS, Gislason T, Gulcher J, Kong A, Jonsdottir I, Thorsteinsdottir U, Stefansson K.

Nat Genet. 2009 Mar;41(3):342-7. doi: 10.1038/ng.323.

PMID:
19198610
16.

Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers.

Jakobsdottir J, Gorin MB, Conley YP, Ferrell RE, Weeks DE.

PLoS Genet. 2009 Feb;5(2):e1000337. doi: 10.1371/journal.pgen.1000337.

17.

Large scale association analysis of novel genetic loci for coronary artery disease.

Coronary Artery Disease Consortium., Samani NJ, Deloukas P, Erdmann J, Hengstenberg C, Kuulasmaa K, McGinnis R, Schunkert H, Soranzo N, Thompson J, Tiret L, Ziegler A.

Arterioscler Thromb Vasc Biol. 2009 May;29(5):774-80. doi: 10.1161/ATVBAHA.108.181388.

18.

Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3.

Paynter NP, Chasman DI, Buring JE, Shiffman D, Cook NR, Ridker PM.

Ann Intern Med. 2009 Jan 20;150(2):65-72.

19.

Risk prediction of prevalent diabetes in a Swiss population using a weighted genetic score--the CoLaus Study.

Lin X, Song K, Lim N, Yuan X, Johnson T, Abderrahmani A, Vollenweider P, Stirnadel H, Sundseth SS, Lai E, Burns DK, Middleton LT, Roses AD, Matthews PM, Waeber G, Cardon L, Waterworth DM, Mooser V.

Diabetologia. 2009 Apr;52(4):600-8. doi: 10.1007/s00125-008-1254-y.

PMID:
19139842
20.

Common variants at 30 loci contribute to polygenic dyslipidemia.

Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, Kaplan L, Bennett D, Li Y, Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, Guiducci C, Burtt NP, Parish S, Clarke R, Zelenika D, Kubalanza KA, Morken MA, Scott LJ, Stringham HM, Galan P, Swift AJ, Kuusisto J, Bergman RN, Sundvall J, Laakso M, Ferrucci L, Scheet P, Sanna S, Uda M, Yang Q, Lunetta KL, Dupuis J, de Bakker PI, O'Donnell CJ, Chambers JC, Kooner JS, Hercberg S, Meneton P, Lakatta EG, Scuteri A, Schlessinger D, Tuomilehto J, Collins FS, Groop L, Altshuler D, Collins R, Lathrop GM, Melander O, Salomaa V, Peltonen L, Orho-Melander M, Ordovas JM, Boehnke M, Abecasis GR, Mohlke KL, Cupples LA.

Nat Genet. 2009 Jan;41(1):56-65. doi: 10.1038/ng.291.

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