Author details

Full Name

FranÃ§ois Cambien

Affiliation

ORCID

Career Start Year

1979

Papers

316

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
33677556	Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.	Eur Heart J	2021
32059048	Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.	PLoS One	2020
29540468	Genetic Reduction in Left Ventricular Protein Kinase C-Î± and Adverse Ventricular Remodeling in Human Subjects.	Circ Genom Precis Med	2018
28296976	Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.	PLoS One	2017
28903782	Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy.	Genome Biol	2017
27558669	Preservation Analysis of Macrophage Gene Coexpression Between Human and Mouse Identifies PARK2 as a Genetically Controlled Master Regulator of Oxidative Phosphorylation in Humans.	G3 (Bethesda)	2016
27694435	Role of lipid phosphate phosphatase 3 in human aortic endothelial cell function.	Cardiovasc Res	2016
26160806	Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3.	Circulation: Cardiovascular Genetics	2015
25772935	Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism.	Am J Hum Genet	2015
26318107	SASH1, a new potential link between smoking and atherosclerosis.	Atherosclerosis	2015
26166477	Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages.	Am J Hum Genet	2015
25053723	Adrenomedullin and arterial stiffness: integrative approach combining monocyte ADM expression, plasma MR-Pro-ADM, and genome-wide association study.	Circulation: Cardiovascular Genetics	2014
25326100	Allelic expression mapping across cellular lineages to establish impact of non-coding SNPs.	Mol Syst Biol	2014
25424692	Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation.	Epigenetics	2014
24357727	A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential.	Blood	2014
24630777	DNA methylation and body-mass index: a genome-wide analysis.	Lancet	2014
25025429	Single nucleotide polymorphisms with cis-regulatory effects on long non-coding transcripts in human primary monocytes.	PLoS One	2014
24958846	Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleeding.	Journal of Experimental Medicine	2014
23202125	Large-scale association analysis identifies new risk loci for coronary artery disease.	Nat Genet	2013
23950726	GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm.	PLoS Genet	2013
24075742	Increased monocyte adhesion by endothelial expression of VCAM-1 missense variation inÂ vitro.	Atherosclerosis	2013
23382694	Genome-wide haplotype analysis of cis expression quantitative trait loci in monocytes.	PLoS Genet	2013
23137784	Cytokine phenotype, genotype, and renal outcomes at cardiac surgery.	Cytokine	2013
23372645	Graphical modeling of gene expression in monocytes suggests molecular mechanisms explaining increased atherosclerosis in smokers.	PLoS ONE	2013
21989056	Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene.	Hum Mol Genet	2012
22421339	Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies.	Lancet	2012
22675575	Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis.	PLoS One	2012
22325189	Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome.	Lancet	2012
22990020	Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.	Blood	2012
22403184	Statistical colocalization of monocyte gene expression and genetic risk variants for type 1 diabetes.	Human Molecular Genetics	2012
23300628	Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression.	PLoS One	2012
23029284	Comprehensive exploration of the effects of miRNA SNPs on monocyte gene expression.	PLoS One	2012
22106312	Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk.	Proc Natl Acad Sci U S A	2011
21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Nat Genet	2011
21157371	A pharmacogenetic analysis of determinants of hypertension and blood pressure response to angiotensin-converting enzyme inhibitor therapy in patients with vascular disease and healthy individuals.	J Hypertens	2011
21459883	A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.	Eur Heart J	2011
21507037	EDNRB gene variants and melanoma risk in two southern European populations.	Clinical and Experimental Dermatology	2011
20376705	Contribution of SELP and PSGL-1 genotypes and haplotypes to the presence of coronary heart disease in Tunisians.	Molecular Biology Reports	2011
21926303	Bayesian detection of expression quantitative trait loci hot spots.	Genetics	2011
21965548	Four genetic loci influencing electrocardiographic indices of left ventricular hypertrophy.	Circ Cardiovasc Genet	2011
21763416	Influence of sex and genetic variability on expression of X-linked genes in human monocytes.	Genomics	2011
21712549	Heritability, weak effects, and rare variants in genomewide association studies.	Clinical Chemistry	2011
21912656	The choice of the filtering method in microarrays affects the inference regarding dosage compensation of the active X-chromosome.	PLoS ONE	2011
22144904	Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans.	PLoS Genet	2011
21606135	A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.	Circ Cardiovasc Genet	2011
21980494	Genetics of venous thrombosis: insights from a new genome wide association study.	PLoS One	2011
22139419	New gene functions in megakaryopoiesis and platelet formation.	Nature	2011
20364137	Genome-wide association study of intracranial aneurysm identifies three new risk loci.	Nat Genet	2010
19660753	Low plasma retinol predicts coronary events in healthy middle-aged men: the PRIME Study.	Atherosclerosis	2010
19373437	Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population.	Journal of Thrombosis and Thrombolysis	2010