These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

75 related articles for article (PubMed ID: 27325954)

  • 1. Genome-wide association analysis and replication of coronary artery disease in South Korea suggests a causal variant common to diverse populations.
    Cho EY; Jang Y; Shin ES; Jang HY; Yoo YK; Kim S; Jang JH; Lee JY; Yun MH; Park MY; Chae JS; Lim JW; Shin DJ; Park S; Lee JH; Han BG; Rae KH; Cardon LR; Morris AP; Lee JE; Clarke GM
    Heart Asia; 2010; 2(1):104-8. PubMed ID: 27325954
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.
    Shen GQ; Li L; Rao S; Abdullah KG; Ban JM; Lee BS; Park JE; Wang QK
    Arterioscler Thromb Vasc Biol; 2008 Feb; 28(2):360-5. PubMed ID: 18048766
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide association study of coronary artery disease in the Japanese.
    Takeuchi F; Yokota M; Yamamoto K; Nakashima E; Katsuya T; Asano H; Isono M; Nabika T; Sugiyama T; Fujioka A; Awata N; Ohnaka K; Nakatochi M; Kitajima H; Rakugi H; Nakamura J; Ohkubo T; Imai Y; Shimamoto K; Yamori Y; Yamaguchi S; Kobayashi S; Takayanagi R; Ogihara T; Kato N
    Eur J Hum Genet; 2012 Mar; 20(3):333-40. PubMed ID: 21971053
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.
    Erdmann J; Willenborg C; Nahrstaedt J; Preuss M; König IR; Baumert J; Linsel-Nitschke P; Gieger C; Tennstedt S; Belcredi P; Aherrahrou Z; Klopp N; Loley C; Stark K; Hengstenberg C; Bruse P; Freyer J; Wagner AK; Medack A; Lieb W; Grosshennig A; Sager HB; Reinhardt A; Schäfer A; Schreiber S; El Mokhtari NE; Raaz-Schrauder D; Illig T; Garlichs CD; Ekici AB; Reis A; Schrezenmeir J; Rubin D; Ziegler A; Wichmann HE; Doering A; Meisinger C; Meitinger T; Peters A; Schunkert H
    Eur Heart J; 2011 Jan; 32(2):158-68. PubMed ID: 21088011
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population.
    Kalpana B; Murthy DK; Balakrishna N; Aiyengar MT
    Indian Heart J; 2019; 71(3):263-271. PubMed ID: 31543200
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Independent association of the variant rs1333049 at the 9p21 locus and coronary heart disease.
    Mendonça I; dos Reis RP; Pereira A; Café H; Serrão M; Sousa AC; Freitas AI; Guerra G; Freitas S; Freitas C; Ornelas I; Brehm A; Araújo JJ
    Rev Port Cardiol; 2011 Jun; 30(6):575-91. PubMed ID: 21874923
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variant on 9p21 is strongly associated with coronary artery disease but lacks association with myocardial infarction and disease severity in a population in Western India.
    Bhanushali AA; Parmar N; Contractor A; Shah VT; Das BR
    Arch Med Res; 2011 Aug; 42(6):469-74. PubMed ID: 21925557
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi Consortium.
    Assimes TL; Lee IT; Juang JM; Guo X; Wang TD; Kim ET; Lee WJ; Absher D; Chiu YF; Hsu CC; Chuang LM; Quertermous T; Hsiung CA; Rotter JI; Sheu WH; Chen YD; Taylor KD
    PLoS One; 2016; 11(3):e0138014. PubMed ID: 26982883
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Common SNP-based haplotype analysis of the 9p21.3 gene locus as predictor coronary artery disease in Tanzanian population.
    Akan G; Kisenge P; Sanga TS; Mbugi E; Adolf I; Turkcan MK; Janabi M; Atalar F
    Cell Mol Biol (Noisy-le-grand); 2019 Jul; 65(6):33-43. PubMed ID: 31472045
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population.
    Yamada Y; Yasukochi Y; Kato K; Oguri M; Horibe H; Fujimaki T; Takeuchi I; Sakuma J
    Biomed Rep; 2018 Nov; 9(5):383-404. PubMed ID: 30402224
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-Wide Association Analysis for Severity of Coronary Artery Disease Using the Gensini Scoring System.
    Zeller T; Seiffert M; Müller C; Scholz M; Schäffer A; Ojeda F; Drexel H; Mündlein A; Kleber ME; März W; Sinning C; Brunner FJ; Waldeyer C; Keller T; Saely CH; Sydow K; Thiery J; Teupser D; Blankenberg S; Schnabel R
    Front Cardiovasc Med; 2017; 4():57. PubMed ID: 28979897
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
    Wakil SM; Ram R; Muiya NP; Mehta M; Andres E; Mazhar N; Baz B; Hagos S; Alshahid M; Meyer BF; Morahan G; Dzimiri N
    Atherosclerosis; 2016 Feb; 245():62-70. PubMed ID: 26708285
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of polymorphisms in 9p21 region with CAD in North Indian population: replication of SNPs identified through GWAS.
    Kumar J; Yumnam S; Basu T; Ghosh A; Garg G; Karthikeyan G; Sengupta S
    Clin Genet; 2011 Jun; 79(6):588-93. PubMed ID: 20718794
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gene dosage of the common variant 9p21 predicts severity of coronary artery disease.
    Dandona S; Stewart AF; Chen L; Williams K; So D; O'Brien E; Glover C; Lemay M; Assogba O; Vo L; Wang YQ; Labinaz M; Wells GA; McPherson R; Roberts R
    J Am Coll Cardiol; 2010 Aug; 56(6):479-86. PubMed ID: 20670758
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease.
    Muendlein A; Saely CH; Rhomberg S; Sonderegger G; Loacker S; Rein P; Beer S; Vonbank A; Winder T; Drexel H
    Atherosclerosis; 2009 Jul; 205(1):174-80. PubMed ID: 19135198
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The cardiovascular implication of single nucleotide polymorphisms of chromosome 9p21 locus among Arab population.
    El-Menyar AA; Rizk NM; Al-Qahtani A; AlKindi F; Elyas A; Farag F; Bakhsh FD; Ebrahim S; Ahmed E; Al-Khinji M; Al-Thani H; Suwaidi JA
    J Res Med Sci; 2015 Apr; 20(4):346-52. PubMed ID: 26109989
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association Study between Coronary Artery Disease and rs1333049 and rs10757274 Polymorphisms at 9p21 Locus in South-West Iran.
    Foroughmand AM; Nikkhah E; Galehdari H; Jadbabaee MH
    Cell J; 2015; 17(1):89-98. PubMed ID: 25870838
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic variants associated with celiac disease and the risk for coronary artery disease.
    Jansen H; Willenborg C; Schlesinger S; Ferrario PG; König IR; Erdmann J; Samani NJ; Lieb W; Schunkert H
    Mol Genet Genomics; 2015 Oct; 290(5):1911-7. PubMed ID: 25893417
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Variant at 9p21 rs1333049 is associated with age of onset of coronary artery disease in a Western Indian population: a case control association study.
    Bhanushali AA; Contractor A; Das BR
    Genet Res (Camb); 2013 Oct; 95(5):138-45. PubMed ID: 24246088
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study.
    Smith JG; Melander O; Lövkvist H; Hedblad B; Engström G; Nilsson P; Carlson J; Berglund G; Norrving B; Lindgren A
    Circ Cardiovasc Genet; 2009 Apr; 2(2):159-64. PubMed ID: 20031580
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.