CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders

A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family

(2014) Setareh Moghadasi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Refining analyses of copy number variation identifies specific genes associated with developmental delay

(2014) Bradley P Coe et al.   NATURE GENETICS

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability

(2014) Anna A Kashevarova et al.   Molecular Cytogenetics

Shared genetics among major psychiatric disorders

(2013) Alessandro Serretti et al.   LANCET

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

(2013)   LANCET

Evidence for Shared Susceptibility to Epilepsy and Psychosis: A Population-Based Family Study

(2012) Mary C. Clarke et al.   BIOLOGICAL PSYCHIATRY

Disruption of Contactin 4 in two subjects with autism in Chinese population

(2012) Hui Guo et al.   GENE

A small homozygous microdeletion of 15q13.3 including the CHRNA7 gene in a girl with a spectrum of severe neurodevelopmental features

(2011) Jun Liao et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Contactin 4 as an autism susceptibility locus

(2011) Catherine E. Cottrell et al.   Autism Research

The chimeric gene CHRFAM7A, a partial duplication of the CHRNA7 gene, is a dominant negative regulator of α7*nAChR function

(2011) Tanguy Araud et al.   BIOCHEMICAL PHARMACOLOGY

Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism

(2011) Emma van Daalen et al.   NEUROGENETICS

Genome-Wide Association Study in Bipolar Patients Stratified by Co-Morbidity

(2011) Berit Kerner et al.   PLoS One

Molecular characterization and clinical features of a patient with an interstitial deletion of 3p25.3-p26.1

(2010) Cecilia Gunnarsson et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The genetics of neurodevelopmental disease

(2010) Kevin J Mitchell   CURRENT OPINION IN NEUROBIOLOGY

A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa

(2010) K Wang et al.   MOLECULAR PSYCHIATRY

Functional impact of global rare copy number variation in autism spectrum disorders

(2010) Dalila Pinto et al.   NATURE

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

(2009) Joseph T. Glessner et al.   NATURE

Contact in the genetics of autism and schizophrenia

(2009) J. Peter H. Burbach et al.   TRENDS IN NEUROSCIENCES

Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome

(2008) Thomas Fernandez et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

(2008) Dan E. Arking et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Parental Psychiatric Disorders Associated With Autism Spectrum Disorders in the Offspring

(2008) J. L. Daniels et al.   PEDIATRICS