K. Stefansson

Discipline

Anthropologie biologique (21) Psychologie (3)

Type de document

Articles (51) Recensions (1) Autres (1)

Co-auteur

Date

Source

Mot-clé

association (44) Social groups (44) Human beings (34) Meta-analysis (26) Genes (25) risque (23) Risk (23) Heredity (20) Genealogy (20) Body mass index (17) effet (16) Family (16) roman (15) Phenotype (14) Evidence (14) adulte (13) adulte (13) corps (13) Obesity (12) maladie (12) spectacle (11) gène (11) règlement (11) Women (11) Regulation (11) Women (11) analyse (10) maladie (10) âge (10) Diabetes (10)

Documents écrit par K. Stefansson (51) | parle de K. Stefansson (0)

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
S. Kanoni et al. (27 déc. 2022)
A saturated map of common genetic variants associated with human height.
L. Yengo et al.
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
S. Ramdas et al. (4 août 2022)
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.
The power of genetic diversity in genome-wide association studies of lipids.
S.E. Graham 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)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
V. Lagou et al. (5 janv. 2021)
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
I.E. Sønderby et al.
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.
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.
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.
M.C. Zillikens et al. (19 juil. 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)
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.
J.S. Ried et al. (23 nov. 2016)
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.
G.B. Ehret et al.
Genome-wide association study identifies 74 loci associated with educational attainment.
A. Okbay et al. (2016)
Correction: The influence of age and sex on genetic associations with adult body size and shape : a large-scale genome-wide interaction study.
T.W. Winkler et al. (2016)
Genetic studies of body mass index yield new insights for obesity biology
A.E. Locke et al. (2015)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
T.W. Winkler et al. (2015)
New genetic loci link adipose and insulin biology to body fat distribution.
D. Shungin et al. (2015)
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
F.R. Day et al. (2015)
Defining the role of common variation in the genomic and biological architecture of adult human height.
A.R. Wood et al.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
J.R. Perry et al. (2 oct. 2014)

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