I.J. Deary

Discipline

Anthropologie biologique (7) Psychologie (2)

Type de document

Articles (26)

Co-auteur

Date

Source

Mot-clé

association (22) Social groups (22) Genes (15) Human beings (13) Meta-analysis (12) effet (9) Phenotype (9) Heredity (9) Genealogy (9) risque (8) Risk (8) Family (8) Evidence (7) Blood (7) roman (7) adulte (6) Manufacturers' agents (6) Expression (6) Commission merchants (6) Regions (6) adulte (6) maladie (6) architecture (5) maladie (5) Serum (5) Diseases (5) Architecture (5) Educational attainment (5) Sizes (5) architecture (5)

Documents écrit par I.J. Deary (26) | parle de I.J. Deary (0)

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
L. de Las Fuentes et al.
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
T.S. Ahluwalia et al. (27 avr. 2021)
Bayesian reassessment of the epigenetic architecture of complex traits.
D.T. Banos et al. (9 oct. 2020)
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
R.F. Hillary et al. (8 juil. 2020)
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)
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.
A. Teumer et al. (26 oct. 2018)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
N.R. Wray 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)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
V. Turcot et al.
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.
Y. Zeng et al. (1 sept. 2017)
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.
R.A. Power et al. (15 févr. 2017)
Rare and low-frequency coding variants alter human adult height.
E. Marouli et al. (9 févr. 2017)
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
A. Okbay et al.
Genome-wide association study identifies 74 loci associated with educational attainment.
A. Okbay et al. (2016)
Modulation of genetic associations with serum urate levels by body-mass-index in humans.
J.E. Huffman et al. (2015)
Directional dominance on stature and cognition in diverse human populations.
P.K. Joshi et al. (2015)
DNA mismatch repair gene MSH6 implicated in determining age at natural menopause.
J.R. Perry et al. (2014)
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
C.A. Rietveld et al. (2013)
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
A. Köttgen et al. (2013)
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
O'Seaghdha C.M. et al. (2013)
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
N. Franceschini et al. (2012)
Seventy-five genetic loci influencing the human red blood cell.
P. van der Harst 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)
Childhood socioeconomic position and objectively measured physical capability levels in adulthood: a systematic review and meta-analysis.
K. Birnie et al. (2011)

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