User profiles for MJ Owen
OwenEtudiant Verified email at 2027.icam.fr Cited by 358313 |
Analysis of shared heritability in common disorders of the brain
…, M Tsolaki, P Proitsi, NC Fox, H Hampel, MJ Owen… - Science, 2018 - science.org
INTRODUCTION Brain disorders may exhibit shared symptoms and substantial epidemiological
comorbidity, inciting debate about their etiologic overlap. However, detailed study of …
comorbidity, inciting debate about their etiologic overlap. However, detailed study of …
The genetic basis of complex human behaviors
Quantitative genetic research has built a strong case for the importance of genetic factors in
many complex behavioral disorders and dimensions in the domains of psychopathology, …
many complex behavioral disorders and dimensions in the domains of psychopathology, …
Definition and description of schizophrenia in the DSM-5
Although dementia praecox or schizophrenia has been considered a unique disease for
over a century, its definitions and boundaries have changed over this period and its etiology …
over a century, its definitions and boundaries have changed over this period and its etiology …
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Schizophrenia is a severe mental disorder with a lifetime risk of about 1%, characterized by
hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80% 1 , 2 . …
hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80% 1 , 2 . …
Biological insights from 108 schizophrenia-associated genetic loci
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of
alleles, including common alleles of small effect that might be detected by genome-wide …
alleles, including common alleles of small effect that might be detected by genome-wide …
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
…, W Gu, C Razquin, P Pastor, I Mateo, MJ Owen… - Nature …, 2013 - nature.com
Eleven susceptibility loci for late-onset Alzheimer's disease (LOAD) were identified by previous
studies; however, a large portion of the genetic risk for this disease remains unexplained. …
studies; however, a large portion of the genetic risk for this disease remains unexplained. …
Synaptic, transcriptional and chromatin genes disrupted in autism
The genetic architecture of autism spectrum disorder involves the interplay of common and
rare variants and their impact on hundreds of genes. Using exome sequencing, here we …
rare variants and their impact on hundreds of genes. Using exome sequencing, here we …
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
…, DR Nyholt, PF O'Reilly, H Oskarsson, MJ Owen… - Nature …, 2018 - nature.com
Major depressive disorder (MDD) is a common illness accompanied by considerable
morbidity, mortality, costs, and heightened risk of suicide. We conducted a genome-wide …
morbidity, mortality, costs, and heightened risk of suicide. We conducted a genome-wide …
[HTML][HTML] Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development
We have generated Cbfa1-deficient mice. Homozygous mutants die of respiratory failure
shortly after birth. Analysis of their skeletons revealed an absence of osteoblasts and bone. …
shortly after birth. Analysis of their skeletons revealed an absence of osteoblasts and bone. …
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
We undertook a two-stage genome-wide association study (GWAS) of Alzheimer's disease (AD)
involving over 16,000 individuals, the most powerful AD GWAS to date. In stage 1 (3,941 …
involving over 16,000 individuals, the most powerful AD GWAS to date. In stage 1 (3,941 …