S.E. Medland

Discipline

Anthropologie biologique (9) Psychologie (5)

Type de document

Articles (26) Recensions (1)

Co-auteur

Date

Source

Mot-clé

association (21) Social groups (21) Human beings (17) Phenotype (13) Genes (13) Meta-analysis (13) analyse (9) effet (9) Analysis (9) risque (8) Risk (8) Manufacturers' agents (8) Commission merchants (8) Heredity (7) Genealogy (7) Evidence (7) Diseases (7) Body mass index (7) spectacle (6) Educational attainment (6) Susceptibility (6) Family (6) corps (6) Variation (5) Diseases (5) Cases (5) Expression (5) Brain (5) Cases (5) Regions (5)

Documents écrit par S.E. Medland (26) | parle de S.E. Medland (0)

A saturated map of common genetic variants associated with human height.
L. Yengo et al.
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention.
Z. Wang et al.
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
I.E. Sønderby et al.
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
I.E. Sønderby et al. (22 mars 2021)
Associations of autozygosity with a broad range of human phenotypes.
D.W. Clark et al. (31 oct. 2019)
Analysis of shared heritability in common disorders of the brain.
V. Anttila et al. (22 juin 2018)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
N.R. Wray et al.
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
V. Turcot et al.
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)
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.
S.H. Witt et al. (20 juin 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)
Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance.
M. Li et al. (2016)
Meta-analysis of genome-wide association studies of anxiety disorders.
T. Otowa et al. (2016)
The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects.
W.J. Peyrot et al.
Genetic studies of body mass index yield new insights for obesity biology
A.E. Locke et al. (2015)
Directional dominance on stature and cognition in diverse human populations.
P.K. Joshi et al. (2015)
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
C.A. Rietveld et al. (2013)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
S.I. Berndt et al. (2013)
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.
J.C. Randall et al. (2013)
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
M. den Hoed et al. (2013)
Seventy-five genetic loci influencing the human red blood cell.
P. van der Harst et al. (2012)
Genome-wide meta-analysis of common variant differences between men and women.
V. Boraska 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)

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