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Items: 8

1.

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.

Schunkert H, Götz A, Braund P, McGinnis R, Tregouet DA, Mangino M, Linsel-Nitschke P, Cambien F, Hengstenberg C, Stark K, Blankenberg S, Tiret L, Ducimetiere P, Keniry A, Ghori MJ, Schreiber S, El Mokhtari NE, Hall AS, Dixon RJ, Goodall AH, Liptau H, Pollard H, Schwarz DF, Hothorn LA, Wichmann HE, König IR, Fischer M, Meisinger C, Ouwehand W, Deloukas P, Thompson JR, Erdmann J, Ziegler A, Samani NJ; Cardiogenics Consortium..

Circulation. 2008 Apr 1;117(13):1675-84. doi: 10.1161/CIRCULATIONAHA.107.730614.

2.

Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans.

Saleheen D, Alexander M, Rasheed A, Wormser D, Soranzo N, Hammond N, Butterworth A, Zaidi M, Haycock P, Bumpstead S, Potter S, Blackburn H, Gray E, Di Angelantonio E, Kaptoge S, Shah N, Samuel M, Janjua A, Sheikh N, Haider SR, Murtaza M, Ahmad U, Hakeem A, Memon MA, Mallick NH, Azhar M, Samad A, Rasheed SZ, Gardezi AR, Memon NA, Ghaffar A, Memon FU, Zaman KS, Kundi A, Yaqoob Z, Cheema LA, Qamar N, Faruqui A, Jooma R, Niazi JH, Hussain M, Kumar K, Saleem A, Kumar K, Daood MS, Memon F, Gul AA, Abbas S, Zafar J, Shahid F, Memon Z, Bhatti SM, Kayani W, Ali SS, Fahim M, Ishaq M, Frossard P, Deloukas P, Danesh J.

Arterioscler Thromb Vasc Biol. 2010 Jul;30(7):1467-73. doi: 10.1161/ATVBAHA.109.197210. Review.

3.

Type 2 diabetes and polymorphisms on chromosome 9p21: a meta-analysis.

Cugino D, Gianfagna F, Santimone I, de Gaetano G, Donati MB, Iacoviello L, Di Castelnuovo A.

Nutr Metab Cardiovasc Dis. 2012 Aug;22(8):619-25. doi: 10.1016/j.numecd.2010.11.010. Review.

PMID:
21315566
4.

9p21 and the genetic revolution for coronary artery disease.

Roberts R, Stewart AF.

Clin Chem. 2012 Jan;58(1):104-12. doi: 10.1373/clinchem.2011.172759. Review.

5.

Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.

Dichgans M, Malik R, König IR, Rosand J, Clarke R, Gretarsdottir S, Thorleifsson G, Mitchell BD, Assimes TL, Levi C, O'Donnell CJ, Fornage M, Thorsteinsdottir U, Psaty BM, Hengstenberg C, Seshadri S, Erdmann J, Bis JC, Peters A, Boncoraglio GB, März W, Meschia JF, Kathiresan S, Ikram MA, McPherson R, Stefansson K, Sudlow C, Reilly MP, Thompson JR, Sharma P, Hopewell JC, Chambers JC, Watkins H, Rothwell PM, Roberts R, Markus HS, Samani NJ, Farrall M, Schunkert H; METASTROKE Consortium.; CARDIoGRAM Consortium.; C4D Consortium.; International Stroke Genetics Consortium..

Stroke. 2014 Jan;45(1):24-36. doi: 10.1161/STROKEAHA.113.002707. Review.

6.

Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus.

Cunnington MS, Keavney B.

Curr Atheroscler Rep. 2011 Jun;13(3):193-201. doi: 10.1007/s11883-011-0178-z. Review.

PMID:
21487702
7.

Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis.

Patel RS, Asselbergs FW, Quyyumi AA, Palmer TM, Finan CI, Tragante V, Deanfield J, Hemingway H, Hingorani AD, Holmes MV.

J Am Coll Cardiol. 2014 Jun 3;63(21):2234-45. doi: 10.1016/j.jacc.2014.01.065. Review.

8.

Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals.

Alg VS, Sofat R, Houlden H, Werring DJ.

Neurology. 2013 Jun 4;80(23):2154-65. doi: 10.1212/WNL.0b013e318295d751. Review.

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