M.J. Owen

Discipline

Psychologie (5)

Discipline

Linguistique (1)

Type de document

Articles (15)

Type de document

Articles (1)

Co-auteur

Date

Date

Source

Source

Mot-clé

association (11) Social groups (11) Human beings (11) risque (10) Risk (10) Schizophrenia (9) Number (9) analyse (8) Depression, Mental (8) Analysis (8) effet (7) Case-control method (7) Deletion (6) Control (6) Cases (6) Cases (6) Variation (5) Symptoms (5) Carriers (5) Autism (5) Sizes (5) gène (4) ADN (4) adulte (4) Methods (4) Comorbidity (4) Genes (4) Weights and measures (4) Patients (4) Meta-analysis (4)

Mot-clé

Communication (1) Reading (1) Lectura (1) Information (1) Information (1) Lecture (1)

Documents écrit par M.J. Owen (15) | parle de M.J. Owen (1)

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia.
A.F. Pardiñas et al. (1 mars 2022)
Effects of eight neuropsychiatric copy number variants on human brain structure.
C. Modenato et al. (20 juil. 2021)
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
I.E. Sønderby et al. (22 mars 2021)
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
X. Zhang et al. (15 juin 2019)
Psychiatric disorders in children with 16p11.2 deletion and duplication.
M. Niarchou et al. (16 janv. 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.
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals.
M. Rivera 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 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)
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
D'Angelo D. et al. (2016)
Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder.
J.J. Rucker et al. (2016)
A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder.
C.F. Hung et al. (2015)
Genome-wide association analysis of copy number variation in recurrent depressive disorder.
J.J. Rucker et al. (2013)
Genomewide association scan of suicidal thoughts and behaviour in major depression.
A. Schosser et al. (2011)

Les troubles spécifiques de la lecture
Franck Ramus (2012)