T. Meitinger

Discipline

Anthropologie biologique (8) Géographie (1) Economies et finances (1)

Type de document

Articles (34) Autres (1)

Co-auteur

Date

Source

Mot-clé

association (26) Social groups (26) Human beings (23) Heredity (18) Genealogy (18) Genes (17) Meta-analysis (17) Family (16) roman (14) risque (13) Risk (13) effet (11) adulte (11) Phenotype (11) adulte (11) analyse (10) Analysis (10) Evidence (9) génétique (8) Genetics (8) Genetics (8) Regions (8) Influence (8) cohorte (8) corps (8) gène (7) règlement (7) Variation (7) Older people (7) Regulation (7)

Documents écrit par T. Meitinger (34) | parle de T. Meitinger (0)

Stroke genetics informs drug discovery and risk prediction across ancestries.
A. Mishra et al.
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
L. de Las Fuentes et al.
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.
R. Noordam et al. (12 nov. 2019)
Associations of autozygosity with a broad range of human phenotypes.
D.W. Clark et al. (31 oct. 2019)
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
T.O. Kilpeläinen et al. (22 janv. 2019)
Genetic Factors Explain a Major Fraction of the 50% Lower Lipoprotein(a) Concentrations in Finns.
G. Erhart et al.
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.
M.F. Feitosa et al. (2018)
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies.
R.G. Feichtinger et al. (5 oct. 2017)
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.
A. Macé et al. (29 sept. 2017)
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.
E. Wheeler et al.
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms.
S. Mack et al.
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.
M.C. Zillikens et al. (19 juil. 2017)
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
M. Gorski et al. (26 mai 2017)
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
M. Gorski et al. (28 avr. 2017)
A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.
C. Lamina et al. (15 août 2016)
Genome-wide association study identifies 74 loci associated with educational attainment.
A. Okbay et al. (2016)
Directional dominance on stature and cognition in diverse human populations.
P.K. Joshi et al. (2015)
Defining the role of common variation in the genomic and biological architecture of adult human height.
A.R. Wood et al.
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis
B. Benyamin et al.
Novel calmodulin mutations associated with congenital arrhythmia susceptibility.
N. Makita et al. (2014)
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
O'Seaghdha C.M. et al. (2013)
A genome-wide association search for type 2 diabetes genes in African Americans.
N.D. Palmer et al. (2012)
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled.
H. Attar 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)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
G.B. Ehret et al. (2011)

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