H. Stefansson

Discipline

Psychologie (4)

Type de document

Articles (9) Recensions (1)

Co-auteur

Date

Source

Mot-clé

risque (7) Risk (7) association (5) Social groups (5) Human beings (5) analyse (4) Cases (4) Schizophrenia (4) Meta-analysis (4) Brain (4) Cases (4) Analysis (4) cerveau (4) Deletion (3) Phenotype (3) Genes (3) Magnetic resonance imaging (3) Diseases (3) Carriers (3) Buildings (3) Regions (3) Susceptibility (3) Magnetic resonance imaging (3) Number (3) maladie (3) spectacle (2) mortalité (2) gène (2) effet (2) dose (2)

Documents écrit par H. Stefansson (9) | parle de H. Stefansson (0)

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.
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
I.E. Sønderby et al. (22 mars 2021)
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
I.E. Sønderby et al.
Genomic and clinical predictors of lacosamide response in refractory epilepsies.
S.B. Heavin et al.
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
N.R. Wray 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)
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
R. Li et al. (2012)
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
S. Jacquemont et al. (2011)
Male-pattern baldness susceptibility locus at 20p11.
J.B. Richards et al. (2008)