R. Mägi

Discipline

Anthropologie biologique (20) Psychologie (1)

Type de document

Articles (53) Autres (2)

Co-auteur

Date

Source

Mot-clé

association (42) Social groups (42) Human beings (38) Genes (26) Meta-analysis (21) roman (21) Heredity (20) Genealogy (20) Family (19) risque (17) Risk (17) effet (16) Phenotype (15) Body mass index (15) analyse (14) adulte (14) Evidence (14) Analysis (14) adulte (14) spectacle (13) Obesity (13) corps (13) maladie (12) maladie (12) gène (11) Variation (11) Diabetes (11) Comprehension (11) Blood (11) Regions (11)

Documents écrit par R. Mägi (53) | parle de R. Mägi (0)

Genetic determinants of plasma protein levels in the Estonian population.
A. Kalnapenkis et al. (2 avr. 2024)
Rare copy-number variants as modulators of common disease susceptibility.
C. Auwerx et al. (8 janv. 2024)
Genetic insights into the age-specific biological mechanisms governing human ovarian aging.
S.E. Ojavee et al. (7 sept. 2023)
Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations.
M. Lepamets et al. (13 oct. 2022)
Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome.
M. Alver et al.
A saturated map of common genetic variants associated with human height.
L. Yengo et al.
Improving GWAS discovery and genomic prediction accuracy in biobank data.
E.J. Orliac et al. (2 août 2022)
A first update on mapping the human genetic architecture of COVID-19
G. A. Pathak et al.
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
T.W. Winkler et al. (13 juin 2022)
The trans-ancestral genomic architecture of glycemic traits.
J. Chen 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.
Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis.
S.E. Ojavee et al. (20 avr. 2021)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
V. Lagou et al. (8 févr. 2021)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
V. Lagou et al. (5 janv. 2021)
Genome-wide association study identifies 48 common genetic variants associated with handedness.
J.Y. Tung 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)
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
A.E. Justice et al.
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
T.O. Kilpeläinen et al. (22 janv. 2019)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
J.J. Lee et al. (23 juil. 2018)
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)
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.
P.K. Joshi et al. (13 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)
Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
M. Graff et al.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
M. Graff et al.

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