Rare deleterious mutations of the gene EFR3A in autism spectrum disorders-Reference-Cited by-同舟云学术

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders

Published:2014 Issue:1 Volume:5 Page:31
ISSN:2040-2392
Container-title:Molecular Autism
language:en
Short-container-title:Molecular Autism

Author:

Gupta Abha R,Pirruccello Michelle,Cheng Feng,Kang Hyo,Fernandez Thomas V,Baskin Jeremy M,Choi Murim,Liu Li,Ercan-Sencicek Adife,Murdoch John D,Klei Lambertus,Neale Benjamin M,Franjic Daniel,Daly Mark J,Lifton Richard P,De Camilli Pietro,Zhao Hongyu,Šestan Nenad,State Matthew W

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Developmental Biology,Developmental Neuroscience,Molecular Biology

Reference38 articles.

1. De novo mutations revealed by whole-exome sequencing are strongly associated with autism

2. De Novo Gene Disruptions in Children on the Autistic Spectrum

3. Patterns and rates of exonic de novo mutations in autism spectrum disorders

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

5. Assembly of the PtdIns 4-kinase Stt4 complex at the plasma membrane requires Ypp1 and Efr3

Cited by 28 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. Reovirus infection induces transcriptome-wide unique A-to-I editing changes in the murine fibroblasts.;Virus Research;2024-08

2. Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansion;Acta Neuropathologica;2024-04-19

3. Reovirus infection induces transcriptome-wide unique A-to-I editing changes in the murine fibroblasts;2024-02-12

4. Efr3b is essential for social recognition by modulating the excitability of CA2 pyramidal neurons;Proceedings of the National Academy of Sciences;2024-01-08

5. EFR3A: a new raft domain organizing protein?;Cellular & Molecular Biology Letters;2023-10-25