Genetic associations between voltage-gated calcium channels and autism spectrum disorder: a systematic review
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Title
Genetic associations between voltage-gated calcium channels and autism spectrum disorder: a systematic review
Authors
Keywords
-
Journal
Molecular Brain
Volume 13, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-06-22
DOI
10.1186/s13041-020-00634-0
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- (2019) Arturo Andrade et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
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- (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
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