V. Mooser

Discipline

Anthropologie biologique (9) Psychologie (5) Economies et finances (1)

Type de document

Articles (55) Recensions (1)

Co-auteur

Date

Source

Mot-clé

association (43) Social groups (43) Human beings (37) adulte (24) adulte (24) risque (23) Risk (23) Population (22) Population (22) Meta-analysis (20) Older people (17) âge (16) Women (16) Genealogy (16) Age (16) Women (16) Age (16) Genes (15) Heredity (15) Body mass index (15) gène (14) Methods (14) Men (14) Methods (14) roman (14) Diabetes (13) puits (12) maladie (12) Obesity (12) cohorte (12)

Documents écrit par V. Mooser (55) | parle de V. Mooser (0)

High participation rate among 25 721 patients with broad age range in a hospital-based research project involving whole-genome sequencing - the Lausanne Institutional Biobank.
M. Bochud et al. (2017)
Low birth weight leads to obesity, diabetes and increased leptin levels in adults: the CoLaus study.
F.R. Jornayvaz et al. (3 mai 2016)
Identification and molecular characterisation of Lausanne Institutional Biobank participants with familial hypercholesterolaemia - a proof-of-concept study.
F. Maurer et al. (2016)
Prevalence of sleep-disordered breathing in the general population: the HypnoLaus study.
R. Heinzer et al. (2015)
A Population-Based Model to Consider the Effect of Seasonal Variation on Serum 25(OH)D and Vitamin D Status.
P. Vuistiner et al. (2015)
Strong impact of smoking on multimorbidity and cardiovascular risk among human immunodeficiency virus-infected individuals in comparison with the general population.
B. Hasse et al. (2015)
Associations between mood, anxiety or substance use disorders and inflammatory markers after adjustment for multiple covariates in a population-based study.
J. Glaus et al. (2014)
The Lausanne Institutional Biobank: a new resource to catalyse research in personalised medicine and pharmaceutical sciences.
V. Mooser et al. (2014)
Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links.
R. Rueedi et al. (2014)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
S.I. Berndt et al. (2013)
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
A.K. Manning et al. (13 mai 2012)
A genome-wide association search for type 2 diabetes genes in African Americans.
N.D. Palmer et al. (2012)
Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.
A. Valsesia et al. (2012)
Plasma lipoprotein-associated phospholipase A2 activity in Alzheimer's disease, amnestic mild cognitive impairment, and cognitively healthy elderly subjects: a cross-sectional study.
J.E. Davidson et al. (2012)
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.
L. Stolk et al. (2012)
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
Z. Dastani et al. (2012)
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
R. Li et al. (2012)
Hyperhomocysteinemia is independently associated with albuminuria in the population-based CoLaus study.
F. Marti et al. (26 sept. 2011)
Genetic variation at CHRNA5-CHRNA3-CHRNB4 interacts with smoking status to influence body mass index.
R.M. Freathy et al. (2011)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
G.B. Ehret et al. (2011)
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.
T.O. Kilpeläinen et al. (2011)
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.
E.R. Fox et al. (2011)
Serum calcium levels are associated with novel cardiometabolic risk factors in the population-based CoLaus study.
I. Guessous et al. (2011)
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption.
G. Schumann et al. (2011)
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
S. Jacquemont et al. (2011)

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