Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder-Reference-Cited by-同舟云学术

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Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder

Published:2016 Issue:1 Volume:15 Page:
ISSN:1676-5680
Container-title:Genetics and Molecular Research
language:
Short-container-title:Genet. Mol. Res.

Author:

Nascimento P.P.,Bossolani-Martins A.L.,Rosan D.B.A.,Mattos L.C.,Brandão-Mattos C.,Fett-Conte A.C.

Publisher

Genetics and Molecular Research

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.funpecrp.com.br/gmr/year2016/vol15-1/pdf/gmr7422.pdf

Cited by 26 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A common genetic variant in the Neurexin family member CNTNAP2 is related to language but not communication skills in youth with Autism Spectrum Disorder;Autism Research;2024-07-10

2. The role of the CNTNAP2 gene in the development of autism spectrum disorder;Research in Autism Spectrum Disorders;2024-06

3. Properties of the Caudal Pontine Reticular Nucleus Neurons Determine the Acoustic Startle Response in Cntnap2 KO Rats;Journal of Integrative Neuroscience;2024-03-20

4. 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

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

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