Association between CNTNAP2 polymorphisms and autism: A family-based study in the chinese han population and a meta-analysis combined with GWAS data of psychiatric genomics consortium

Dysfunctional Autism Risk Genes Cause Circuit-Specific Connectivity Deficits With Distinct Developmental Trajectories

(2018) Valerio Zerbi et al.   CEREBRAL CORTEX

Genetic variants in autism-related CNTNAP2 impair axonal growth of cortical neurons

(2018) Giorgia Canali et al.   HUMAN MOLECULAR GENETICS

CNTNAP2 stabilizes interneuron dendritic arbors through CASK

(2018) Ruoqi Gao et al.   MOLECULAR PSYCHIATRY

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population

(2017) Sahar Zare et al.   JOURNAL OF CLINICAL NEUROSCIENCE

Identifying specific prefrontal neurons that contribute to autism-associated abnormalities in physiology and social behavior

(2017) A C Brumback et al.   MOLECULAR PSYCHIATRY

Family-based genetic association study of CNTNAP2 polymorphisms and sociality endophenotypes in Korean patients with autism spectrum disorders

(2017) Hee Jeong Yoo et al.   PSYCHIATRIC GENETICS

Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder

(2016) P.P. Nascimento et al.   GENETICS AND MOLECULAR RESEARCH

CNTNAP2 gene in high functioning autism: no association according to family and meta-analysis approaches

(2015) Anna Maria Werling et al.   JOURNAL OF NEURAL TRANSMISSION

Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2knockout neurons

(2015) Olga Varea et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample

(2015) Emma Colvert et al.   JAMA Psychiatry

Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10

(2015) Lina Jonsson et al.   Molecular Autism

Zinc finger protein 804A (ZNF804A) and verbal deficits in individuals with autism

(2014) Ayyappan Anitha et al.   JOURNAL OF PSYCHIATRY & NEUROSCIENCE

Defining the Contribution of CNTNAP2 to Autism Susceptibility

(2013) Srirangan Sampath et al.   PLoS One

A failure of left temporal cortex to specialize for language is an early emerging and fundamental property of autism

(2012) Lisa T. Eyler et al.   BRAIN

Individual common variants exert weak effects on the risk for autism spectrum disorders

(2012) Richard Anney et al.   HUMAN MOLECULAR GENETICS

Analysis of two language-related genes in autism

(2012) Claudio Toma et al.   PSYCHIATRIC GENETICS

Synapse dysfunction in autism: a molecular medicine approach to drug discovery in neurodevelopmental disorders

(2012) Will Spooren et al.   TRENDS IN PHARMACOLOGICAL SCIENCES

Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder

(2011) Andrea K. Vaags et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals

(2011) Heather C. Whalley et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits

(2011) Olga Peñagarikano et al.   CELL

Genetics in psychiatry: common variant association studies

(2010) Joseph D Buxbaum et al.   Molecular Autism

Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

(2008) Maricela Alarcón 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

Disruption of Neurexin 1 Associated with Autism Spectrum Disorder

(2008) Hyung-Goo Kim et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders

(2008) Betul Bakkaloglu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A 12Mb deletion at 7q33–q35 associated with autism spectrum disorders and primary amenorrhea

(2008) Elena Rossi et al.   European Journal of Medical Genetics