Literature DB >> 21672533

Cardiovascular diseases and genome-wide association studies.

Ndeye Coumba Ndiaye1, Mohsen Azimi Nehzad, Said El Shamieh, Maria G Stathopoulou, Sophie Visvikis-Siest.   

Abstract

Genome-Wide Association Studies (GWAS) on cardiovascular diseases and related quantitative traits revealed numerous genetic variants, which however have been partially replicated, probably due to the heterogeneity of the clinical phenotypes and the populations studied. Even if novel biological pathways have been identified through these studies, there is still a long way until the validation of causal variants and their use in clinical practice as factors for prevention, risk assessment and as targets for the development of new medications. GWAS methodologies should, in the following years, integrate gene-gene and gene-environment interaction analyses in a global research strategy and also involve subsequent transcriptomic and proteomic investigations. The GWAS era is very promising but it is just at the beginning.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21672533     DOI: 10.1016/j.cca.2011.05.035

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  7 in total

1.  Do we need diagnostic strategies enhanced with genetic information for ischemic heart disease?

Authors:  Pierre-Yves Marie; Sophie Visvikis-Siest
Journal:  J Nucl Cardiol       Date:  2018-03-06       Impact factor: 5.952

2.  Integromic analysis of genetic variation and gene expression identifies networks for cardiovascular disease phenotypes.

Authors:  Chen Yao; Brian H Chen; Roby Joehanes; Burcak Otlu; Xiaoling Zhang; Chunyu Liu; Tianxiao Huan; Oznur Tastan; L Adrienne Cupples; James B Meigs; Caroline S Fox; Jane E Freedman; Paul Courchesne; Christopher J O'Donnell; Peter J Munson; Sunduz Keles; Daniel Levy
Journal:  Circulation       Date:  2014-12-22       Impact factor: 29.690

Review 3.  Personalized cardiovascular medicine: concepts and methodological considerations.

Authors:  Henry Völzke; Carsten O Schmidt; Sebastian E Baumeister; Till Ittermann; Glenn Fung; Janina Krafczyk-Korth; Wolfgang Hoffmann; Matthias Schwab; Henriette E Meyer zu Schwabedissen; Marcus Dörr; Stephan B Felix; Wolfgang Lieb; Heyo K Kroemer
Journal:  Nat Rev Cardiol       Date:  2013-03-26       Impact factor: 32.419

4.  A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C.

Authors:  Maria G Stathopoulou; Amélie Bonnefond; Ndeye Coumba Ndiaye; Mohsen Azimi-Nezhad; Said El Shamieh; Abdelsalam Saleh; Marc Rancier; Gerard Siest; John Lamont; Peter Fitzgerald; Sophie Visvikis-Siest
Journal:  J Lipid Res       Date:  2012-12-02       Impact factor: 5.922

5.  Functional epistatic interaction between rs6046G>A in F7 and rs5355C>T in SELE modifies systolic blood pressure levels.

Authors:  Said El Shamieh; Ndeye Coumba Ndiaye; Maria G Stathopoulou; Helena A Murray; Christine Masson; John V Lamont; Peter Fitzgerald; Athanase Benetos; Sophie Visvikis-Siest
Journal:  PLoS One       Date:  2012-07-18       Impact factor: 3.240

Review 6.  A Matter of the Heart: The African Clawed Frog Xenopus as a Model for Studying Vertebrate Cardiogenesis and Congenital Heart Defects.

Authors:  Annemarie Hempel; Michael Kühl
Journal:  J Cardiovasc Dev Dis       Date:  2016-06-04

7.  Plasma proteomic analysis reveals altered protein abundances in cardiovascular disease.

Authors:  Vasiliki Lygirou; Agnieszka Latosinska; Manousos Makridakis; William Mullen; Christian Delles; Joost P Schanstra; Jerome Zoidakis; Burkert Pieske; Harald Mischak; Antonia Vlahou
Journal:  J Transl Med       Date:  2018-04-17       Impact factor: 5.531

  7 in total

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