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 *

137 related articles for article (PubMed ID: 27240780)

  • 21. The chromosome 9p21 variant interacts with vegetable and wine intake to influence the risk of cardiovascular disease: a population based cohort study.
    Hindy G; Ericson U; Hamrefors V; Drake I; Wirfält E; Melander O; Orho-Melander M
    BMC Med Genet; 2014; 15():1220. PubMed ID: 25551366
    [TBL] [Abstract][Full Text] [Related]  

  • 22. IL1RL1 single nucleotide polymorphism predicts sST2 level and mortality in coronary and peripheral artery disease.
    Lin JF; Wu S; Juang JJ; Chiang FT; Hsu LA; Teng MS; Cheng ST; Huang HL; Sun YC; Liu PY; Ko YL
    Atherosclerosis; 2017 Feb; 257():71-77. PubMed ID: 28110258
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.
    Chan K; Patel RS; Newcombe P; Nelson CP; Qasim A; Epstein SE; Burnett S; Vaccarino VL; Zafari AM; Shah SH; Anderson JL; Carlquist JF; Hartiala J; Allayee H; Hinohara K; Lee BS; Erl A; Ellis KL; Goel A; Schaefer AS; El Mokhtari NE; Goldstein BA; Hlatky MA; Go AS; Shen GQ; Gong Y; Pepine C; Laxton RC; Whittaker JC; Tang WH; Johnson JA; Wang QK; Assimes TL; Nöthlings U; Farrall M; Watkins H; Richards AM; Cameron VA; Muendlein A; Drexel H; Koch W; Park JE; Kimura A; Shen WF; Simpson IA; Hazen SL; Horne BD; Hauser ER; Quyyumi AA; Reilly MP; Samani NJ; Ye S
    J Am Coll Cardiol; 2013 Mar; 61(9):957-70. PubMed ID: 23352782
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Lower Circulating Folate Induced by a Fidgetin Intronic Variant Is Associated With Reduced Congenital Heart Disease Susceptibility.
    Wang D; Wang F; Shi KH; Tao H; Li Y; Zhao R; Lu H; Duan W; Qiao B; Zhao SM; Wang H; Zhao JY
    Circulation; 2017 May; 135(18):1733-1748. PubMed ID: 28302752
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Variants on Chromosome 9p21 Confer Risks of Noncardioembolic Cerebral Infarction and Carotid Plaque in the Chinese Han Population.
    Lu Z; Zhang Y; Maimaiti Y; Feng Y; Sun J; Zhuang J; Zeng L; Fu Y
    J Atheroscler Thromb; 2015; 22(10):1061-70. PubMed ID: 25958930
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: results from a multicenter study in Italy.
    Silvestri V; Rizzolo P; Scarnò M; Chillemi G; Navazio AS; Valentini V; Zelli V; Zanna I; Saieva C; Masala G; Bianchi S; Manoukian S; Barile M; Pensotti V; Peterlongo P; Varesco L; Tommasi S; Russo A; Giannini G; Cortesi L; Viel A; Montagna M; Radice P; Palli D; Ottini L
    Eur J Cancer; 2015 Nov; 51(16):2289-95. PubMed ID: 26248686
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease.
    Temel ŞG; Ergören MÇ
    Anatol J Cardiol; 2019 Jan; 21(1):31-38. PubMed ID: 30587704
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Analysis on the Polymorphism of Chromosome Region 9p21 and the Susceptibility of Carotid Plaque.
    Sun J; Sun F; Yang K; Fu N; Li L
    Eur Neurol; 2017; 77(1-2):25-31. PubMed ID: 27846637
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Metallothionein 2A genetic polymorphism and its correlation to coronary heart disease.
    Yang XY; Sun JH; Ke HY; Chen YJ; Xu M; Luo GH
    Eur Rev Med Pharmacol Sci; 2014; 18(24):3747-53. PubMed ID: 25555862
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Associations between single nucleotide polymorphisms on chromosome 9p21 and risk of coronary heart disease in Chinese Han population.
    Zhou L; Zhang X; He M; Cheng L; Chen Y; Hu FB; Wu T
    Arterioscler Thromb Vasc Biol; 2008 Nov; 28(11):2085-9. PubMed ID: 18757290
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A common allele on chromosome 9 associated with coronary heart disease.
    McPherson R; Pertsemlidis A; Kavaslar N; Stewart A; Roberts R; Cox DR; Hinds DA; Pennacchio LA; Tybjaerg-Hansen A; Folsom AR; Boerwinkle E; Hobbs HH; Cohen JC
    Science; 2007 Jun; 316(5830):1488-91. PubMed ID: 17478681
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The association of functional polymorphisms in genes encoding growth factors for endothelial cells and smooth muscle cells with the severity of coronary artery disease.
    Osadnik T; Strzelczyk JK; Lekston A; Reguła R; Bujak K; Fronczek M; Gawlita M; Gonera M; Wasilewski J; Szyguła-Jurkiewicz B; Gierlotka M; Gąsior M
    BMC Cardiovasc Disord; 2016 Nov; 16(1):218. PubMed ID: 27835972
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Socioeconomic Status Interacts with the Genetic Effect of a Chromosome 9p21.3 Common Variant to Influence Coronary Artery Calcification and Incident Coronary Events in the Heinz Nixdorf Recall Study (Risk Factors, Evaluation of Coronary Calcium, and Lifestyle).
    Schmidt B; Frölich S; Dragano N; Frank M; Eisele L; Pechlivanis S; Forstner AJ; Nöthen MM; Mahabadi AA; Erbel R; Moebus S; Jöckel KH
    Circ Cardiovasc Genet; 2017 Apr; 10(2):. PubMed ID: 28411192
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Association between rs3088440 (G > A) polymorphism at 9p21.3 locus with the occurrence and severity of coronary artery disease in an Iranian population.
    Pourgholi M; Abazari O; Pourgholi L; Ghasemi-Kasman M; Boroumand M
    Mol Biol Rep; 2021 Aug; 48(8):5905-5912. PubMed ID: 34313925
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CYP11B2 gene polymorphism among coronary heart disease patients and blood donors in Malaysia.
    Normaznah Y; Azizah MR; Kuak SH; Rosli MA
    Malays J Pathol; 2015 Apr; 37(1):45-7. PubMed ID: 25890613
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues.
    Pilbrow AP; Folkersen L; Pearson JF; Brown CM; McNoe L; Wang NM; Sweet WE; Tang WH; Black MA; Troughton RW; Richards AM; Franco-Cereceda A; Gabrielsen A; Eriksson P; Moravec CS; Cameron VA
    PLoS One; 2012; 7(6):e39574. PubMed ID: 22768093
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The rs10757278 Polymorphism of the 9p21.3 Locus in Children with Arterial Ischemic Stroke: A Family-Based and Case-Control Study.
    Niemiec P; Balcerzyk A; Iwanicki T; Emich-Widera E; Kopyta I; Nowak T; Pilarska E; Pienczk-Ręcławowicz K; Kaciński M; Wendorff J; Gorczynska-Kosiorz S; Trautsolt W; Grzeszczak W; Zak I
    J Stroke Cerebrovasc Dis; 2017 Dec; 26(12):2763-2768. PubMed ID: 28778720
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Association of CDKN2BAS polymorphism rs4977574 with coronary heart disease: a case-control study and a meta-analysis.
    Huang Y; Ye H; Hong Q; Xu X; Jiang D; Xu L; Dai D; Sun J; Gao X; Duan S
    Int J Mol Sci; 2014 Sep; 15(10):17478-92. PubMed ID: 25268619
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chromosome 9p21.3 is associated with early-onset coronary heart disease in the Irish population.
    Meng W; Hughes AE; Patterson CC; Belton C; Kee F; McKeown PP
    Dis Markers; 2008; 25(2):81-5. PubMed ID: 18957718
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The Association Between Extracellular Matrix Metalloproteinase Inducer Polymorphisms and Coronary Heart Disease: A Potential Way to Predict Disease.
    Weng Y; Chen T; Ren J; Lu D; Liu X; Lin S; Xu C; Lou J; Chen X; Tang L
    DNA Cell Biol; 2020 Feb; 39(2):244-254. PubMed ID: 31928425
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.