Genetic associations between voltage-gated calcium channels and autism spectrum disorder: a systematic review

Genetic Associations between Voltage-Gated Calcium Channels and Psychiatric Disorders

(2019) Arturo Andrade et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy

(2017) Alexandra Pinggera et al.   HUMAN MOLECULAR GENETICS

High-throughput screen detects calcium signaling dysfunction in typical sporadic autism spectrum disorder

(2017) Galina Schmunk et al.   Scientific Reports

CACNA1D De Novo Mutations in Autism Spectrum Disorders Activate Cav1.3 L-Type Calcium Channels

(2015) Alexandra Pinggera et al.   BIOLOGICAL PSYCHIATRY

CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms

(2015) Lena Damaj et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Whole-genome sequencing of quartet families with autism spectrum disorder

(2015) Ryan K C Yuen et al.   NATURE MEDICINE

Targeting voltage-gated calcium channels in neurological and psychiatric diseases

(2015) Gerald W. Zamponi   NATURE REVIEWS DRUG DISCOVERY

Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders

(2015) Samuel Heyes et al.   PROGRESS IN NEUROBIOLOGY

Shared functional defect in IP3R-mediated calcium signaling in diverse monogenic autism syndromes

(2015) G Schmunk et al.   Translational Psychiatry

Management of bipolar depression with lamotrigine: an antiepileptic mood stabilizer

(2015) Kedar S. Prabhavalkar et al.   Frontiers in Pharmacology

Synaptic, transcriptional and chromatin genes disrupted in autism

(2014) Silvia De Rubeis et al.   NATURE

Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

(2013) Yong-hui Jiang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder

(2013) Santhosh Girirajan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Monogenic mouse models of social dysfunction: Implications for autism

(2013) D. Oddi et al.   BEHAVIOURAL BRAIN RESEARCH

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

(2013)   LANCET

Activity-dependent neuronal signalling and autism spectrum disorder

(2013) Daniel H. Ebert et al.   NATURE

Exploring the Multifactorial Nature of Autism Through Computational Systems Biology: Calcium and the Rho GTPase RAC1 Under the Spotlight

(2013) Fares Zeidán-Chuliá et al.   NEUROMOLECULAR MEDICINE

Mitochondrial and ion channel gene alterations in autism

(2012) Moyra Smith et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage–fusion–bridge for telomere stabilization

(2012) Svetlana A. Yatsenko et al.   HUMAN GENETICS

Predicting the diagnosis of autism spectrum disorder using gene pathway analysis

(2012) E Skafidas et al.   MOLECULAR PSYCHIATRY

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

(2012) Brian J. O’Roak et al.   NATURE

De Novo Gene Disruptions in Children on the Autistic Spectrum

(2012) Ivan Iossifov et al.   NEURON

Support for calcium channel gene defects in autism spectrum disorders

(2012) Ake Tzu-Hui Lu et al.   Molecular Autism

A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing

(2011) Rachel A. Myers et al.   PLoS Genetics

The genetics of neurodevelopmental disease

(2010) Kevin J Mitchell   CURRENT OPINION IN NEUROBIOLOGY

Scaffold-based design and synthesis of potent N-type calcium channel blockers

(2009) Gerald W. Zamponi et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Calcium channel diversity: multiple roles of calcium channel subunits

(2009) Annette C Dolphin   CURRENT OPINION IN NEUROBIOLOGY

High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene

(2009) S P Strom et al.   MOLECULAR PSYCHIATRY

Common genetic variants on 5p14.1 associate with autism spectrum disorders

(2009) Kai Wang et al.   NATURE

Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1

(2008) L Palmieri et al.   MOLECULAR PSYCHIATRY