Chromosome 9p21 and Cardiovascular Disease The Story Unfolds

被引:36
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
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
收藏
页码:81 / 84
页数:4
相关论文
共 20 条
  • [1] Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest)
    Abdullah, K. G.
    Li, L.
    Shen, G. -Q.
    Hu, Y.
    Yang, Y.
    MacKinlay, K. G.
    Topol, E. J.
    Wang, Q. K.
    [J]. 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
    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
    [J]. 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
    Bown, Matthew J.
    Braund, Peter S.
    Thompson, John
    London, Nicholas J. M.
    Samani, Nilesh J.
    Sayers, Robert D.
    [J]. 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
    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
    [J]. 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
    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.
    [J]. NATURE, 2007, 447 (7145) : 661 - 678
  • [6] P15(INK4B) IS A POTENTIAL EFFECTOR OF TGF-BETA-INDUCED CELL-CYCLE ARREST
    HANNON, GJ
    BEACH, D
    [J]. NATURE, 1994, 371 (6494) : 257 - 261
  • [7] Genetics of melanoma predisposition
    Hayward, NK
    [J]. ONCOGENE, 2003, 22 (20) : 3053 - 3062
  • [8] The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
    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
    [J]. NATURE GENETICS, 2008, 40 (02) : 217 - 224
  • [9] A common variant on chromosome 9p21 affects the risk of myocardial infarction
    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
    [J]. 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
    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
    [J]. JOURNAL OF HUMAN GENETICS, 2008, 53 (04) : 357 - 359