J.J. Hottenga

Discipline

Anthropologie biologique (19) Psychologie (5)

Type de document

Articles (54) Autres (2) Recensions (1)

Co-auteur

Date

Source

Mot-clé

association (44) Social groups (44) Human beings (35) Meta-analysis (33) risque (24) Risk (24) Genes (23) Heredity (23) Genealogy (23) Phenotype (19) Family (18) effet (17) Evidence (14) roman (14) gène (13) Body mass index (13) Number (13) corps (13) Disease susceptibility (12) Blood (12) Obesity (11) Diabetes (11) Regions (11) maladie (11) analyse (10) adulte (10) Women (10) Manufacturers' agents (10) Expression (10) Diseases (10)

Documents écrit par J.J. Hottenga (54) | parle de J.J. Hottenga (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.
The trans-ancestral genomic architecture of glycemic traits.
J. Chen et al.
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
T.S. Ahluwalia et al. (27 avr. 2021)
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
I.E. Sønderby et al. (22 mars 2021)
Obesity and atypical depression symptoms: findings from Mendelian randomization in two European cohorts.
G. Pistis et al. (4 févr. 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.
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
X. Zhang et al. (15 juin 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.
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.
P.K. Joshi et al. (13 oct. 2017)
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.
Y. Zeng et al. (1 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.
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals.
M. Rivera et al.
Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
M. Graff et al.
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)
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
M. Graff et al.
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)
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.
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
A. Okbay et al.

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