BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 21925557)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension.
    Wahlstrand B; Orho-Melander M; Delling L; Kjeldsen S; Narkiewicz K; Almgren P; Hedner T; Melander O
    J Hypertens; 2009 Apr; 27(4):769-73. PubMed ID: 19293724
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An association study of thrombospondin 1 and 2 SNPs with coronary artery disease and myocardial infarction among South Indians.
    Ashokkumar M; Anbarasan C; Saibabu R; Kuram S; Raman SC; Cherian KM
    Thromb Res; 2011 Oct; 128(4):e49-53. PubMed ID: 21762961
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.
    Horne BD; Carlquist JF; Muhlestein JB; Bair TL; Anderson JL
    Circ Cardiovasc Genet; 2008 Dec; 1(2):85-92. PubMed ID: 19956784
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of the platelet glycoprotein IIIa PlA1/A2 gene polymorphism to coronary artery disease but not to nonfatal myocardial infarction in low risk patients.
    Gardemann A; Humme J; Stricker J; Nguyen QD; Katz N; Philipp M; Tillmanns H; Hehrlein FW; Rau M; Haberbosch W
    Thromb Haemost; 1998 Aug; 80(2):214-7. PubMed ID: 9716139
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A common variant on chromosome 9p21 affects the risk of myocardial infarction.
    Helgadottir A; Thorleifsson G; Manolescu A; Gretarsdottir S; Blondal T; Jonasdottir A; Jonasdottir A; Sigurdsson A; Baker A; Palsson A; Masson G; Gudbjartsson DF; Magnusson KP; Andersen K; Levey AI; Backman VM; Matthiasdottir S; Jonsdottir T; Palsson S; Einarsdottir H; Gunnarsdottir S; Gylfason A; Vaccarino V; Hooper WC; Reilly MP; Granger CB; Austin H; Rader DJ; Shah SH; Quyyumi AA; Gulcher JR; Thorgeirsson G; Thorsteinsdottir U; Kong A; Stefansson K
    Science; 2007 Jun; 316(5830):1491-3. PubMed ID: 17478679
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Association between the coronary artery disease risk locus on chromosome 9p21.3 and abdominal aortic aneurysm.
    Bown MJ; Braund PS; Thompson J; London NJ; Samani NJ; Sayers RD
    Circ Cardiovasc Genet; 2008 Oct; 1(1):39-42. PubMed ID: 20031540
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. CDKN2B gene expression is affected by 9p21.3 rs10757278 in CAD patients, six months after the MI.
    Zivotić I; Djurić T; Stanković A; Milasinovic D; Stankovic G; Dekleva M; Marković Nikolić N; Alavantić D; Zivković M
    Clin Biochem; 2019 Nov; 73():70-76. PubMed ID: 31386834
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A customized genetic approach to the number one killer: coronary artery disease.
    Roberts R
    Curr Opin Cardiol; 2008 Nov; 23(6):629-33. PubMed ID: 18830080
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality.
    Ellis KL; Pilbrow AP; Frampton CM; Doughty RN; Whalley GA; Ellis CJ; Palmer BR; Skelton L; Yandle TG; Palmer SC; Troughton RW; Richards AM; Cameron VA
    Circ Cardiovasc Genet; 2010 Jun; 3(3):286-93. PubMed ID: 20400779
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease.
    Patel RS; Su S; Neeland IJ; Ahuja A; Veledar E; Zhao J; Helgadottir A; Holm H; Gulcher JR; Stefansson K; Waddy S; Vaccarino V; Zafari AM; Quyyumi AA
    Eur Heart J; 2010 Dec; 31(24):3017-23. PubMed ID: 20729229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population.
    Kashyap S; Kumar S; Agarwal V; Misra DP; Rai MK; Kapoor A
    Gene; 2018 Mar; 648():89-96. PubMed ID: 29309886
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The presence of apolipoprotein epsilon4 and epsilon2 alleles augments the risk of coronary artery disease in type 2 diabetic patients.
    Vaisi-Raygani A; Rahimi Z; Nomani H; Tavilani H; Pourmotabbed T
    Clin Biochem; 2007 Oct; 40(15):1150-6. PubMed ID: 17689519
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The impact of susceptibility loci for coronary artery disease on other vascular domains and recurrence risk.
    Tragante V; Doevendans PA; Nathoe HM; van der Graaf Y; Spiering W; Algra A; de Borst GJ; de Bakker PI; Asselbergs FW;
    Eur Heart J; 2013 Oct; 34(37):2896-904. PubMed ID: 23828831
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The coronary artery disease-associated 9p21 variant and later life 20-year survival to cohort extinction.
    Dutta A; Henley W; Lang IA; Murray A; Guralnik J; Wallace RB; Melzer D
    Circ Cardiovasc Genet; 2011 Oct; 4(5):542-8. PubMed ID: 21852414
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.