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 *

1204 related articles for article (PubMed ID: 26892958)

  • 21. Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
    Dichgans M; Malik R; König IR; Rosand J; Clarke R; Gretarsdottir S; Thorleifsson G; Mitchell BD; Assimes TL; Levi C; O'Donnell CJ; Fornage M; Thorsteinsdottir U; Psaty BM; Hengstenberg C; Seshadri S; Erdmann J; Bis JC; Peters A; Boncoraglio GB; März W; Meschia JF; Kathiresan S; Ikram MA; McPherson R; Stefansson K; Sudlow C; Reilly MP; Thompson JR; Sharma P; Hopewell JC; Chambers JC; Watkins H; Rothwell PM; Roberts R; Markus HS; Samani NJ; Farrall M; Schunkert H; ; ; ;
    Stroke; 2014 Jan; 45(1):24-36. PubMed ID: 24262325
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Whole-exome sequencing in individuals with multiple cardiovascular risk factors and normal coronary arteries.
    Abramowitz Y; Roth A; Keren G; Isakov O; Shomron N; Laitman Y; Weissglas-Volkov D; Arbel Y; Banai S; Finkelstein A; Friedman E
    Coron Artery Dis; 2016 Jun; 27(4):257-66. PubMed ID: 26905423
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.
    Jia Q; Han Y; Huang P; Woodward NC; Gukasyan J; Kettunen J; Ala-Korpela M; Anufrieva O; Wang Q; Perola M; Raitakari O; Lehtimäki T; Viikari J; Järvelin MR; Boehnke M; Laakso M; Mohlke KL; Fiehn O; Wang Z; Tang WHW; Hazen SL; Hartiala JA; Allayee H
    J Am Heart Assoc; 2019 May; 8(10):e011922. PubMed ID: 31070104
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction?
    Wong CW; Christen T; Pfenniger A; James RW; Kwak BR
    Atherosclerosis; 2007 Apr; 191(2):355-61. PubMed ID: 16677656
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Contribution of Gene Regulatory Networks to Heritability of Coronary Artery Disease.
    Zeng L; Talukdar HA; Koplev S; Giannarelli C; Ivert T; Gan LM; Ruusalepp A; Schadt EE; Kovacic JC; Lusis AJ; Michoel T; Schunkert H; Björkegren JLM
    J Am Coll Cardiol; 2019 Jun; 73(23):2946-2957. PubMed ID: 31196451
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Identification of novel SNPs associated with coronary artery disease and birth weight using a pleiotropic cFDR method.
    Wu X; Lin X; Li Q; Wang Z; Zhang N; Tian M; Wang X; Deng H; Tan H
    Aging (Albany NY); 2020 Dec; 13(3):3618-3644. PubMed ID: 33411684
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Functional Analysis of a Novel Genome-Wide Association Study Signal in SMAD3 That Confers Protection From Coronary Artery Disease.
    Turner AW; Martinuk A; Silva A; Lau P; Nikpay M; Eriksson P; Folkersen L; Perisic L; Hedin U; Soubeyrand S; McPherson R
    Arterioscler Thromb Vasc Biol; 2016 May; 36(5):972-83. PubMed ID: 26966274
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identification of susceptibility modules for coronary artery disease using a genome wide integrated network analysis.
    Duan S; Luo X; Dong C
    Gene; 2013 Dec; 531(2):347-54. PubMed ID: 23994195
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genome-wide significant loci: how important are they? Systems genetics to understand heritability of coronary artery disease and other common complex disorders.
    Björkegren JLM; Kovacic JC; Dudley JT; Schadt EE
    J Am Coll Cardiol; 2015 Mar; 65(8):830-845. PubMed ID: 25720628
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study.
    Karjalainen MK; Holmes MV; Wang Q; Anufrieva O; Kähönen M; Lehtimäki T; Havulinna AS; Kristiansson K; Salomaa V; Perola M; Viikari JS; Raitakari OT; Järvelin MR; Ala-Korpela M; Kettunen J
    Atherosclerosis; 2020 Apr; 299():56-63. PubMed ID: 32113648
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Polygenic risk for coronary artery disease in the Scottish and English population.
    Yang C; Starnecker F; Pang S; Chen Z; Güldener U; Li L; Heinig M; Schunkert H
    BMC Cardiovasc Disord; 2021 Dec; 21(1):586. PubMed ID: 34876023
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Predictive genetic testing for coronary artery disease.
    Johansen CT; Hegele RA
    Crit Rev Clin Lab Sci; 2009; 46(5-6):343-60. PubMed ID: 19958218
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Monocyte chemoattractant protein-1 gene (MCP-1) polymorphisms are associated with risk of premature coronary artery disease in Mexican patients from the Genetics of Atherosclerotic Disease (GEA) study.
    Angeles-Martínez J; Posadas-Sánchez R; Álvarez-León E; Villarreal-Molina T; Cardoso-Saldaña G; Fragoso JM; Juárez-Rojas JG; Medina-Urrutia A; Posadas-Romero C; Vargas-Alarcón G
    Immunol Lett; 2015 Oct; 167(2):125-30. PubMed ID: 26277553
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease.
    Tada H; Won HH; Melander O; Yang J; Peloso GM; Kathiresan S
    Circ Cardiovasc Genet; 2014 Oct; 7(5):583-7. PubMed ID: 25170055
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors.
    LeBlanc M; Zuber V; Andreassen BK; Witoelar A; Zeng L; Bettella F; Wang Y; McEvoy LK; Thompson WK; Schork AJ; Reppe S; Barrett-Connor E; Ligthart S; Dehghan A; Gautvik KM; Nelson CP; Schunkert H; Samani NJ; ; Ridker PM; Chasman DI; Aukrust P; Djurovic S; Frigessi A; Desikan RS; Dale AM; Andreassen OA
    Circ Res; 2016 Jan; 118(1):83-94. PubMed ID: 26487741
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genome-wide association study on coronary artery disease in type 1 diabetes suggests beta-defensin 127 as a risk locus.
    Antikainen AAV; Sandholm N; Trégouët DA; Charmet R; McKnight AJ; Ahluwalia TS; Syreeni A; Valo E; Forsblom C; Gordin D; Harjutsalo V; Hadjadj S; Maxwell AP; Rossing P; Groop PH
    Cardiovasc Res; 2021 Jan; 117(2):600-612. PubMed ID: 32077919
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetics-Current and Future Role in the Prevention and Management of Coronary Artery Disease.
    Roberts R
    Curr Atheroscler Rep; 2016 Dec; 18(12):78. PubMed ID: 27815829
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 61.