M.M. Nöthen

Discipline

Psychologie (3) Anthropologie biologique (3)

Type de document

Articles (17)

Co-auteur

Date

Source

Mot-clé

association (15) Social groups (15) Genes (12) Human beings (12) risque (10) Risk (10) analyse (8) Analysis (8) Cases (7) Phenotype (7) Cases (7) roman (7) gène (6) Meta-analysis (6) Manic-depressive illness (6) Evidence (6) Susceptibility (6) Disease susceptibility (5) Depression, Mental (5) Brain (5) cerveau (5) spectacle (4) architecture (4) Development (4) Patients (4) Diseases (4) Comprehension (4) Architecture (4) Case-control method (4) Patients (4)

Documents écrit par M.M. Nöthen (17) | parle de M.M. Nöthen (0)

A saturated map of common genetic variants associated with human height.
L. Yengo et al.
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
A. Gialluisi et al.
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
I. de Rojas et al. (7 juin 2021)
Synaptic processes and immune-related pathways implicated in Tourette syndrome.
F. Tsetsos et al. (18 janv. 2021)
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 association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.
S.H. Witt et al. (20 juin 2017)
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)
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)
Genetic studies of body mass index yield new insights for obesity biology
A.E. Locke et al. (2015)
Defining the role of common variation in the genomic and biological architecture of adult human height.
A.R. Wood et al.
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)
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
R. Li et al. (2012)
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.
F.J. McMahon et al.
Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14
Bruno Etain et al. (2006)