User profiles for MJ Owen

Owen

Etudiant
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 …

The genetic basis of complex human behaviors

R Plomin, MJ Owen, P McGuffin - Science, 1994 - science.org
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, …

Definition and description of schizophrenia in the DSM-5

…, RE Gur, S Heckers, D Malaspina, MJ Owen… - Schizophrenia …, 2013 - Elsevier
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 …

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

…, A McQuillin, WJ Muir, MC O'Donovan, MJ Owen… - Nature, 2009 - nature.com
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 . …

Biological insights from 108 schizophrenia-associated genetic loci

…, BJ Mowry, MM Nöthen, RA Ophoff, MJ Owen… - Nature, 2014 - nature.com
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 …

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. …

Synaptic, transcriptional and chromatin genes disrupted in autism

…, CR Marshall, AL McInnes, B Neale, MJ Owen… - Nature, 2014 - nature.com
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 …

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 …

[HTML][HTML] Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

…, S Mundlos, BR Olsen, PB Selby, MJ Owen - Cell, 1997 - cell.com
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. …

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

…, SG Younkin, PA Holmans, M O'Donovan, MJ Owen… - Nature …, 2009 - nature.com
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 …