N.G. Martin

Discipline

Anthropologie biologique (17) Psychologie (6)

Type de document

Articles (57) Autres (2)

Co-auteur

Date

Source

Mot-clé

association (45) Social groups (45) Human beings (33) Genes (32) Meta-analysis (29) Heredity (23) Genealogy (23) risque (21) Phenotype (21) Risk (21) effet (19) Family (19) roman (17) Expression (15) Evidence (15) spectacle (14) corps (13) maladie (13) gène (12) maladie (12) adulte (12) Body mass index (12) Susceptibility (12) adulte (12) analyse (11) Manufacturers' agents (11) Diseases (11) Commission merchants (11) Regions (11) Analysis (11)

Documents écrit par N.G. Martin (57) | parle de N.G. Martin (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.
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention.
Z. Wang et al.
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
S. Ramdas et al. (4 août 2022)
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)
Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression.
J. Martin et al. (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)
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.
The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders.
H. Chang et al.
Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.
X. Xiao et al. (11 déc. 2017)
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 Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.
Y. Zeng et al. (1 sept. 2017)
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 meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
A.E. Justice et al. (26 avr. 2017)
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
M. Graff et al.
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.
S. Heilmann-Heimbach et al. (8 mars 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.
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
C. Pattaro et al. (2016)

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