DUF1220 copy number is associated with schizophrenia risk and severity: implications for understanding autism and schizophrenia as related diseases

Replicated linear association between DUF1220 copy number and severity of social impairment in autism

(2015) J. M. Davis et al.   HUMAN GENETICS

Mediators of the association between parental severe mental illness and offspring neurodevelopmental problems

(2014) Brittany M. McCoy et al.   ANNALS OF EPIDEMIOLOGY

Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome

(2014) Majesta O’Bleness et al.   BMC GENOMICS

DUF1220 protein domains drive proliferation in human neural stem cells and are associated with increased cortical volume in anthropoid primates

(2014) J. G. Keeney et al.   Brain Structure & Function

The case for DUF1220 domain dosage as a primary contributor to anthropoid brain expansion

(2014) Jonathon G. Keeney et al.   Frontiers in Human Neuroscience

DUF1220 copy number is linearly associated with increased cognitive function as measured by total IQ and mathematical aptitude scores

(2014) Jonathon M. Davis et al.   HUMAN GENETICS

Biological insights from 108 schizophrenia-associated genetic loci

(2014)   NATURE

White matter pathway organization of the reward system is related to positive and negative symptoms in schizophrenia

(2014) Tobias Bracht et al.   SCHIZOPHRENIA RESEARCH

DUF1220 Dosage Is Linearly Associated with Increasing Severity of the Three Primary Symptoms of Autism

(2014) Jonathan M. Davis et al.   PLoS Genetics

Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population

(2013) Nori Matsunami et al.   PLoS One

Evolutionary History and Genome Organization of DUF1220 Protein Domains

(2013) Majesta S. O’Bleness et al.   G3-Genes Genomes Genetics

DUF1220-Domain Copy Number Implicated in Human Brain-Size Pathology and Evolution

(2012) Laura J. Dumas et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic architecture in autism spectrum disorder

(2012) Bernie Devlin et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Association testing of copy number variants in schizophrenia and autism spectrum disorders

(2012) Bernard J Crespi et al.   Journal of Neurodevelopmental Disorders

Brain Volumes in Schizophrenia: A Meta-Analysis in Over 18 000 Subjects

(2012) Sander V. Haijma et al.   SCHIZOPHRENIA BULLETIN

Hippocampal subfields predict positive symptoms in schizophrenia: First evidence from brain morphometry

(2012) S Kühn et al.   Translational Psychiatry

Progressive loss of cortical gray matter in schizophrenia: a meta-analysis and meta-regression of longitudinal MRI studies

(2012) A Vita et al.   Translational Psychiatry

After GWAS: Searching for Genetic Risk for Schizophrenia and Bipolar Disorder

(2011) Elliot S. Gershon et al.   AMERICAN JOURNAL OF PSYCHIATRY

Brain growth across the life span in autism: Age-specific changes in anatomical pathology

(2010) Eric Courchesne et al.   BRAIN RESEARCH

REVIEW: Genome-Wide Findings in Schizophrenia and the Role of Gene-Environment Interplay

(2010) Ruud Van Winkel et al.   CNS Neuroscience & Therapeutics

Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies

(2010) Heather C. Mefford et al.   PLoS Genetics

Comparative genomics of autism and schizophrenia

(2009) B. Crespi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

(2009) Jonathan Sebat et al.   TRENDS IN GENETICS

Sex differences in schizophrenia and other psychotic disorders: a 20-year longitudinal study of psychosis and recovery

(2008) Linda S. Grossman et al.   COMPREHENSIVE PSYCHIATRY

Autism Spectrum Disorders and Childhood-Onset Schizophrenia: Clinical and Biological Contributions to a Relation Revisited

(2008) Judith Rapoport et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

(2008) Nicola Brunetti-Pierri et al.   NATURE GENETICS

Copy Number Variation and Schizophrenia

(2008) D. St Clair   SCHIZOPHRENIA BULLETIN