Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders-Reference-Cited by-同舟云学术

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Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders

Published:2018-12-26 Issue:12 Volume:14 Page:e1007535
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Toma Claudio^ORCID,Pierce Kerrie D.^ORCID,Shaw Alex D.,Heath Anna,Mitchell Philip B.,Schofield Peter R.^ORCID,Fullerton Janice M.^ORCID

Funder

National Health and Medical Research Council

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference106 articles.

1. Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1;S Poliak;The Journal of cell biology,2003

2. Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits;O Penagarikano;Cell,2011

3. Genome-wide analyses of human perisylvian cerebral cortical patterning;BS Abrahams;Proceedings of the National Academy of Sciences of the United States of America,2007

4. Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development;GR Anderson;Proceedings of the National Academy of Sciences of the United States of America,2012

5. Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2;KA Strauss;The New England journal of medicine,2006

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1. Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case–control association study reveals potential biomarkers;Molecular Biology Reports;2024-02-05

2. Inhibitory dysfunction and social processing difficulties in autism: A comprehensive narrative review;Journal of Psychiatric Research;2024-01

3. Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder;Gene;2023-12

4. Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder;Human Genetics;2023-05-14

5. Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis;Molecular Psychiatry;2022-10-17

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