Chromosome 9p21 and Cardiovascular Disease The Story Unfolds

被引：37

作者：

Samani, Nilesh J. ^{[1
]}

Schunkert, Heribert ^{[2
]}

机构：

[1] Univ Leicester, Dept Cardiovasc Sci, Clin Sci Wing, Glenfield Hosp, Leicester LE3 9QP, Leics, England

[2] Med Univ Lubeck, Med Klin 2, D-23538 Lubeck, Germany

来源：

CIRCULATION-CARDIOVASCULAR GENETICS | 2008年 / 1卷 / 02期

关键词：

coronary disease; genetics; myocardial infarction;

D O I：

10.1161/CIRCGENETICS.108.832527

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：81 / 84

页数：4

共 20 条

[1] Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest) [J].

Abdullah, K. G. ;

Li, L. ;

Shen, G. -Q. ;

Hu, Y. ;

Yang, Y. ;

MacKinlay, K. G. ;

Topol, E. J. ;

Wang, Q. K. .

ANNALS OF HUMAN GENETICS, 2008, 72 :654-657

[2] Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study [J].

Assimes, Themistocles L. ;

Knowles, Joshua W. ;

Basu, Analabha ;

Iribarren, Carlos ;

Southwick, Audrey ;

Tang, Hua ;

Absher, Devin ;

Li, Jun ;

Fair, Joan M. ;

Rubin, Geoffrey D. ;

Sidney, Stephen ;

Fortmann, Stephen P. ;

Go, Alan S. ;

Hlatky, Mark A. ;

Myers, Richard M. ;

Risch, Neil ;

Quertermous, Thomas .

HUMAN MOLECULAR GENETICS, 2008, 17 (15) :2320-2328

[3] Association Between the Coronary Artery Disease Risk Locus on Chromosome 9p21.3 and Abdominal Aortic Aneurysm [J].

Bown, Matthew J. ;

Braund, Peter S. ;

Thompson, John ;

London, Nicholas J. M. ;

Samani, Nilesh J. ;

Sayers, Robert D. .

CIRCULATION-CARDIOVASCULAR GENETICS, 2008, 1 (01) :39-42

[4] Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p [J].

Broadbent, Helen M. ;

Peden, John F. ;

Lorkowski, Stefan ;

Goel, Anuj ;

Ongen, Halit ;

Green, Fiona ;

Clarke, Robert ;

Collins, Rory ;

Franzosi, Maria Grazia ;

Tognoni, Gianni ;

Seedorf, Udo ;

Rust, Stephan ;

Eriksson, Per ;

Hamsten, Anders ;

Farrall, Martin ;

Watkins, Hugh .

HUMAN MOLECULAR GENETICS, 2008, 17 (06) :806-814

[5] Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls [J].

Burton, Paul R. ;

Clayton, David G. ;

Cardon, Lon R. ;

Craddock, Nick ;

Deloukas, Panos ;

Duncanson, Audrey ;

Kwiatkowski, Dominic P. ;

McCarthy, Mark I. ;

Ouwehand, Willem H. ;

Samani, Nilesh J. ;

Todd, John A. ;

Donnelly, Peter ;

Barrett, Jeffrey C. ;

Davison, Dan ;

Easton, Doug ;

Evans, David ;

Leung, Hin-Tak ;

Marchini, Jonathan L. ;

Morris, Andrew P. ;

Spencer, Chris C. A. ;

Tobin, Martin D. ;

Attwood, Antony P. ;

Boorman, James P. ;

Cant, Barbara ;

Everson, Ursula ;

Hussey, Judith M. ;

Jolley, Jennifer D. ;

Knight, Alexandra S. ;

Koch, Kerstin ;

Meech, Elizabeth ;

Nutland, Sarah ;

Prowse, Christopher V. ;

Stevens, Helen E. ;

Taylor, Niall C. ;

Walters, Graham R. ;

Walker, Neil M. ;

Watkins, Nicholas A. ;

Winzer, Thilo ;

Jones, Richard W. ;

McArdle, Wendy L. ;

Ring, Susan M. ;

Strachan, David P. ;

Pembrey, Marcus ;

Breen, Gerome ;

St Clair, David ;

Caesar, Sian ;

Gordon-Smith, Katherine ;

Jones, Lisa ;

Fraser, Christine ;

Green, Elain K. .

NATURE, 2007, 447 (7145) :661-678

[6] P15(INK4B) IS A POTENTIAL EFFECTOR OF TGF-BETA-INDUCED CELL-CYCLE ARREST [J].

HANNON, GJ ;

BEACH, D .

NATURE, 1994, 371 (6494) :257-261

[7] Genetics of melanoma predisposition [J].

Hayward, NK .

ONCOGENE, 2003, 22 (20) :3053-3062

[8] The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm [J].

Helgadottir, Anna ;

Thorleifsson, Gudmar ;

Magnusson, Kristinn P. ;

Gretarsdottir, Solveig ;

Steinthorsdottir, Valgerdur ;

Manolescu, Andrei ;

Jones, Gregory T. ;

Rinkel, Gabriel J. E. ;

Blankensteijn, Jan D. ;

Ronkainen, Antti ;

Jaaskelainen, Juha E. ;

Kyo, Yoshiki ;

Lenk, Guy M. ;

Sakalihasan, Natzi ;

Kostulas, Konstantinos ;

Gottsater, Anders ;

Flex, Andrea ;

Stefansson, Hreinn ;

Hansen, Torben ;

Andersen, Gitte ;

Weinsheimer, Shantel ;

Borch-Johnsen, Knut ;

Jorgensen, Torben ;

Shah, Svati H. ;

Quyyumi, Arshed A. ;

Granger, Christopher B. ;

Reilly, Muredach P. ;

Austin, Harland ;

Levey, Allan I. ;

Vaccarino, Viola ;

Palsdottir, Ebba ;

Walters, G. Bragi ;

Jonsdottir, Thorbjorg ;

Snorradottir, Steinunn ;

Magnusdottir, Dana ;

Gudmundsson, Gudmundur ;

Ferrell, Robert E. ;

Sveinbjornsdottir, Sigurlaug ;

Hernesniemi, Juha ;

Niemela, Mika ;

Limet, Raymond ;

Andersen, Karl ;

Sigurdsson, Gunnar ;

Benediktsson, Rafn ;

Verhoeven, Eric L. G. ;

Teijink, Joep A. W. ;

Grobbee, Diederick E. ;

Rader, Daniel J. ;

Collier, David A. ;

Pedersen, Oluf .

NATURE GENETICS, 2008, 40 (02) :217-224

[9] A common variant on chromosome 9p21 affects the risk of myocardial infarction [J].

Helgadottir, Anna ;

Thorleifsson, Gudmar ;

Manolescu, Andrei ;

Gretarsdottir, Solveig ;

Blondal, Thorarinn ;

Jonasdottir, Aslaug ;

Jonasdottir, Adalbjorg ;

Sigurdsson, Asgeir ;

Baker, Adam ;

Palsson, Arnar ;

Masson, Gisli ;

Gudbjartsson, Daniel F. ;

Magnusson, Kristinn P. ;

Andersen, Karl ;

Levey, Allan I. ;

Backman, Valgerdur M. ;

Matthiasdottir, Sigurborg ;

Jonsdottir, Thorbjorg ;

Palsson, Stefan ;

Einarsdottir, Helga ;

Gunnarsdottir, Steinunn ;

Gylfason, Arnaldur ;

Vaccarino, Viola ;

Hooper, W. Craig ;

Reilly, Muredach P. ;

Granger, Christopher B. ;

Austin, Harland ;

Rader, Daniel J. ;

Shah, Svati H. ;

Quyyumi, Arshed A. ;

Gulcher, Jeffrey R. ;

Thorgeirsson, Gudmundur ;

Thorsteinsdottir, Unnur ;

Kong, Augustine ;

Stefansson, Kari .

SCIENCE, 2007, 316 (5830) :1491-1493

[10] Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations [J].

Hinohara, Kunihiko ;

Nakajima, Toshiaki ;

Takahashi, Megumi ;

Hohda, Shigeru ;

Sasaoka, Taishi ;

Nakahara, Ken-ichi ;

Chida, Kouji ;

Sawabe, Motoji ;

Arimura, Takuro ;

Sato, Akinori ;

Lee, Bok-Soo ;

Ban, Ji-min ;

Yasunami, Michio ;

Park, Jeong-Euy ;

Izumi, Toru ;

Kimura, Akinori .

JOURNAL OF HUMAN GENETICS, 2008, 53 (04) :357-359

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