Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism-Reference-Cited by-同舟云学术

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Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

Published:2013-10 Issue:5 Volume:23 Page:198-203
ISSN:0955-8829
Container-title:Psychiatric Genetics
language:en
Short-container-title:

Author:

Volaki Konstantina,Pampanos Andreas,Kitsiou-Tzeli Sophia,Vrettou Christina,Oikonomakis Vasilis,Sofocleous Christalena,Kanavakis Emmanuel

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Biological Psychiatry,Psychiatry and Mental health,Genetics(clinical),Genetics

Reference22 articles.

1. Advances in autism genetics: on the threshold of a new neurobiology.;Abrahams;Nat Rev Genet,2008

2. Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection.;Blasi;Am J Med Genet B Neuropsychiatr Genet,2006

3. A synaptic trek to autism.;Bourgeron;Curr Opin Neurobiol,2009

4. Control of excitatory and inhibitory synapse formation by neuroligins.;Chih;Science,2005

5. Alternative splicing controls selective trans-synaptic interactions of the neuroligin-neurexin complex.;Chih;Neuron,2006

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1. Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD;Nature Communications;2023-12-06

2. Unraveling the Role of Neuroligin3 in Autism Spectrum Disorders: Pathophysiological Insights and Targeted Therapies;CNS & Neurological Disorders - Drug Targets;2023-07-27

3. Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder;2022-09-23

4. Imbalance of flight–freeze responses and their cellular correlates in the Nlgn3−/y rat model of autism;Molecular Autism;2022-07-18

5. Genetic analysis of the postsynaptic transmembrane X-linked neuroligin 3 gene in autism;Genomics & Informatics;2021-12-31

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