Variants of the CNTNAP2 5′ promoter as risk factors for autism spectrum disorders: a genetic and functional approach

The grammar of transcriptional regulation

(2014) Shira Weingarten-Gabbay et al.   HUMAN GENETICS

Glutamatergic candidate genes in autism spectrum disorder: an overview

(2014) Andreas G. Chiocchetti et al.   JOURNAL OF NEURAL TRANSMISSION

A Sympathetic Neuron Autonomous Role for Egr3-Mediated Gene Regulation in Dendrite Morphogenesis and Target Tissue Innervation

(2013) D. H. Quach et al.   JOURNAL OF NEUROSCIENCE

Activity-dependent neuronal signalling and autism spectrum disorder

(2013) Daniel H. Ebert et al.   NATURE

Effects of GC Bias in Next-Generation-Sequencing Data on De Novo Genome Assembly

(2013) Yen-Chun Chen 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

Finding parallels in fronto-striatal organization

(2012) Theresa M. Desrochers et al.   TRENDS IN COGNITIVE SCIENCES

What does CNTNAP2 reveal about autism spectrum disorder?

(2012) Olga Peñagarikano et al.   TRENDS IN MOLECULAR MEDICINE

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

Epidemiology of Autism Spectrum Disorders in Adults in the Community in England

(2011) Traolach S. Brugha et al.   ARCHIVES OF GENERAL PSYCHIATRY

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

(2011) Olga Peñagarikano et al.   CELL

Reduced transcript expression of genes affected by inherited and de novo CNVs in autism

(2011) Alex S Nord et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

CNTNAP2variants affect early language development in the general population

(2011) A. J. O. Whitehouse et al.   GENES BRAIN AND BEHAVIOR

Normalization of gene expression using SYBR green qPCR: A case for paraoxonase 1 and 2 in Alzheimer's disease brains

(2011) Valérie Leduc et al.   JOURNAL OF NEUROSCIENCE METHODS

Modeling the functional genomics of autism using human neurons

(2011) G Konopka et al.   MOLECULAR PSYCHIATRY

Rare structural variation of synapse and neurotransmission genes in autism

(2011) X Gai et al.   MOLECULAR PSYCHIATRY

Spatio-temporal transcriptome of the human brain

(2011) Hyo Jung Kang et al.   NATURE

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

(2011) Brian J O'Roak et al.   NATURE GENETICS

Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case

(2010) Aline L. Petrin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Deletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features

(2010) Line T. Sehested et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

EGR3 as a potential susceptibility gene for schizophrenia in Korea

(2010) Se Hyun Kim et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

The Genetics of Autism Spectrum Disorders and Related Neuropsychiatric Disorders in Childhood

(2010) Paul Lichtenstein et al.   AMERICAN JOURNAL OF PSYCHIATRY

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

(2010) D. F. Newbury et al.   BEHAVIOR GENETICS

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

(2010) Dalila Pinto et al.   NATURE

Cerebellum and Nonmotor Function

(2009) Peter L. Strick et al.   Annual Review of Neuroscience

Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism

(2009) Valerie W. Hu et al.   Autism Research

Changes in the Developmental Trajectories of Striatum in Autism

(2009) Marieke Langen et al.   BIOLOGICAL PSYCHIATRY

Genetics of autistic disorders: review and clinical implications

(2009) Christine M. Freitag et al.   EUROPEAN CHILD & ADOLESCENT PSYCHIATRY

Adenosine A2A receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder

(2009) Christine M. Freitag et al.   EUROPEAN CHILD & ADOLESCENT PSYCHIATRY

Genomic Targets of the KRAB and SCAN Domain-containing Zinc Finger Protein 263

(2009) Seth Frietze et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Genome-wide linkage in Utah autism pedigrees

(2009) K Allen-Brady et al.   MOLECULAR PSYCHIATRY

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder

(2009) Martin Poot et al.   NEUROGENETICS

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

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

Delineation of the phenotype associated with 7q36.1q36.2 deletion: Long QT syndrome, renal hypoplasia and mental retardation

(2008) Rossella Caselli et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

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

Likelihood-Based Association Analysis for Nuclear Families and Unrelated Subjects with Missing Genotype Data

(2008) Frank Dudbridge   HUMAN HEREDITY

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE

Orientation-dependent interaction between Drosophila insulators is a property of this class of regulatory elements

(2008) O. Kyrchanova et al.   NUCLEIC ACIDS RESEARCH