Search Results - "Tregouet, David A."
-
1
Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension
Published in Nature genetics (01-05-2013)“…Florent Soubrier and colleagues report a genome-wide association study of pulmonary arterial hypertension. They identify a susceptibility locus near CBLN2…”
Get full text
Journal Article -
2
Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial Cardiomyopathy
Published in Circulation research (08-05-2020)“…Fibro-fatty infiltration of subepicardial layers of the atrial wall has been shown to contribute to the substrate of atrial fibrillation. Here, we examined if…”
Get full text
Journal Article -
3
Genetic Variations at the Endocannabinoid Type 1 Receptor Gene (CNR1) Are Associated with Obesity Phenotypes in Men
Published in The journal of clinical endocrinology and metabolism (01-06-2007)“…Context: The endocannabinoid system modulates food intake and body weight in animal models. Treatment with the cannabinoid type 1 receptor blocker, rimonabant,…”
Get full text
Journal Article -
4
Effect of cytochrome P450 2C19 genotype on voriconazole exposure in cystic fibrosis lung transplant patients
Published in European journal of clinical pharmacology (01-03-2011)“…Purpose Voriconazole is widely used to treat invasive aspergillosis after lung transplantation. In cystic fibrosis patients, the interindividual variability in…”
Get full text
Journal Article -
5
A large‐scale exome array analysis of venous thromboembolism
Published in Genetic epidemiology (01-06-2019)“…Although recent Genome‐Wide Association Studies have identified novel associations for common variants, there has been no comprehensive exome‐wide search for…”
Get full text
Journal Article -
6
The Factor XII −4C>T Variant and Risk of Common Thrombotic Disorders: A HuGE Review and Meta-Analysis of Evidence From Observational Studies
Published in American journal of epidemiology (15-01-2011)“…Coagulation factor XII is involved in thrombus formation and therefore may play a role in the etiology of thrombotic disorders. A common variant in the factor…”
Get full text
Journal Article -
7
Association between Angiotensin-Converting Enzyme gene polymorphisms and diabetic nephropathy : Case-control, haplotype, and family-based study in three European Populations
Published in Journal of the American Society of Nephrology (01-04-2007)“…Angiotensin 1-converting enzyme gene (ACE) is a risk factor for diabetic nephropathy (DN) in patients with type 1 diabetes. The selection of this candidate…”
Get full text
Journal Article -
8
Gender-Specific Association of a Perilipin Gene Haplotype with Obesity Risk in a White Population
Published in Obesity (Silver Spring, Md.) (01-11-2004)“…Objective: Perilipin is a class of protein‐coating lipid droplets in adipocytes and steroidogenic cells. Our purpose was to examine the association between…”
Get full text
Journal Article -
9
Common Risk Factors Add to Inherited Thrombophilia to Predict Venous Thromboembolism Risk in Families
Published in TH open : companion journal to thrombosis and haemostasis (01-01-2019)“…The clinical venous thromboembolism (VTE) pattern often shows wide heterogeneity within relatives of a VTE-affected family, although they carry the same…”
Get full text
Journal Article -
10
Combined Effects of Genetic and Environmental Factors on Insulin Resistance Associated With Reduced Fetal Growth
Published in Diabetes (New York, N.Y.) (01-12-2002)“…Combined Effects of Genetic and Environmental Factors on Insulin Resistance Associated With Reduced Fetal Growth Delphine Jaquet 1 , David A. Trégouët 2 ,…”
Get full text
Journal Article -
11
Associations of PPARGC1A haplotypes with plaque score but not with intima-media thickness of carotid arteries in middle-aged subjects
Published in Stroke (1970) (01-09-2006)“…Peroxisome proliferator activated receptor gamma coactivator 1alpha (PGC-1alpha, PPARGC1A) integrates the transcriptional program of mitochondrial biogenesis…”
Get full text
Journal Article -
12
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
Published in European heart journal (01-05-2011)“…Dilated cardiomyopathy (DCM) is a major cause of heart failure with a high familial recurrence risk. So far, the genetics of DCM remains largely unresolved. We…”
Get full text
Journal Article -
13
Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study
Published in Human genetics (01-07-2017)“…Observational studies have shown an association between obesity and venous thromboembolism (VTE) but it is not known if observed associations are causal, due…”
Get full text
Journal Article -
14
Exome Sequencing Studies Identify Mutations in STAB2 As a Genetic Risk for Venous Thromboembolic Disease
Published in Blood (08-12-2017)“…Deep vein thrombosis and pulmonary embolism, collectively referred to as venous thromboembolism (VTE), are the third leading cause of cardiovascular death in…”
Get full text
Journal Article -
15
A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients
Published in Nature communications (04-01-2018)“…To date, epimutations reported in man have been somatic and erased in germlines. Here, we identify a cause of the autosomal recessive cblC class of inborn…”
Get full text
Journal Article -
16
Abstract 564: Influence of Coronary Artery Disease-Associated Genetic Variants on Risk of Venous Thromboembolism
Published in Arteriosclerosis, thrombosis, and vascular biology (01-05-2013)“…Abstract only Objective To determine whether genetic variation robustly associated with coronary artery disease (CAD) also influences risk of venous…”
Get full text
Journal Article -
17
Cox proportional hazards survival regression in haplotype-based association analysis using the Stochastic-EM algorithm
Published in European journal of human genetics : EJHG (01-11-2004)“…It is now widely recognized that haplotype information inferred from genotypes can be of great interest to better characterize the role of a candidate gene in…”
Get full text
Journal Article