4.2 Article

Analysis of CHRNA7 Rare Variants in Autism Spectrum Disorder Susceptibility

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

Dalila Pinto et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2014)

Article Biochemistry & Molecular Biology

CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree

Claudia Soler-Alfonso et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2014)

Article Biochemistry & Molecular Biology

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

D. Moreno-De-Luca et al.

MOLECULAR PSYCHIATRY (2013)

Article Multidisciplinary Sciences

Clinical Characteristics of Children with Autism Spectrum Disorder and Co-Occurring Epilepsy

Emma W. Viscidi et al.

PLOS ONE (2013)

Article Cell Biology

Genetic architecture in autism spectrum disorder

Bernie Devlin et al.

CURRENT OPINION IN GENETICS & DEVELOPMENT (2012)

Article Genetics & Heredity

Common genetic variants, acting additively, are a major source of risk for autism

Lambertus Klei et al.

MOLECULAR AUTISM (2012)

Review Clinical Neurology

Epilepsy and Autism: Neurodevelopmental Perspective

Roberto Tuchman et al.

CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2011)

Article Biochemistry & Molecular Biology

15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain

Dag H. Yasui et al.

HUMAN MOLECULAR GENETICS (2011)

Article Biochemistry & Molecular Biology

Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome

Makiko Meguro-Horike et al.

HUMAN MOLECULAR GENETICS (2011)

Article Genetics & Heredity

A copy number variation morbidity map of developmental delay

Gregory M. Cooper et al.

NATURE GENETICS (2011)

Article Genetics & Heredity

Understanding the impact of 1q21.1 copy number variant

Chansonette Harvard et al.

ORPHANET JOURNAL OF RARE DISEASES (2011)

Article Genetics & Heredity

Delineation of 15q13.3 microdeletions

A. Masurel-Paulet et al.

CLINICAL GENETICS (2010)

Article Genetics & Heredity

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

Santhosh Girirajan et al.

NATURE GENETICS (2010)

Article Biochemistry & Molecular Biology

A 15q13.3 microdeletion segregating with autism

Alistair T. Pagnamenta et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2009)

Article Biochemistry & Molecular Biology

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Leanne M. Dibbens et al.

HUMAN MOLECULAR GENETICS (2009)

Article Genetics & Heredity

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

Ingo Helbig et al.

NATURE GENETICS (2009)

Review Physiology

Mammalian Nicotinic Acetylcholine Receptors: From Structure to Function

Edson X. Albuquerque et al.

PHYSIOLOGICAL REVIEWS (2009)

Article Genetics & Heredity

Structural variation of chromosomes in autism spectrum disorder

Christian R. Marshall et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2008)

Article Multidisciplinary Sciences

Large recurrent microdeletions associated with schizophrenia

Hreinn Stefansson et al.

NATURE (2008)

Article Genetics & Heredity

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

Andrew J. Sharp et al.

NATURE GENETICS (2008)