A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development-Reference-Cited by-同舟云学术

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

Published:2018-02-20 Issue:7 Volume:24 Page:1065-1078
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Eising Else^ORCID,Carrion-Castillo Amaia^ORCID,Vino Arianna,Strand Edythe A.,Jakielski Kathy J.,Scerri Thomas S.^ORCID,Hildebrand Michael S.^ORCID,Webster Richard,Ma Alan,Mazoyer Bernard^ORCID,Francks Clyde^ORCID,Bahlo Melanie^ORCID,Scheffer Ingrid E.^ORCID,Morgan Angela T.^ORCID,Shriberg Lawrence D.,Fisher Simon E.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://www.nature.com/articles/s41380-018-0020-x.pdf

Reference70 articles.

1. Fisher SE, Marcus GF. The eloquent ape: genes, brains and the evolution of language. Nat Rev Genet. 2006;7:9–20.

2. Graham SA, Fisher SE. Understanding language from a genomic perspective. Annu Rev Genet. 2015;49:131–60.

3. Fisher SE, Scharff C. FOXP2 as a molecular window into speech and language. Trends Genet: TIG. 2009;25:166–77.

4. American Speech-Language-Hearing Association. Childhood apraxia of speech. 2007. http://www.asha.org Accessed in April 2017.

5. Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 2001;413:519–23.

Cited by 119 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. Identification of gene co-expression modules from zebrafish brain data: Applications in psychiatry illustrated through alcohol-related traits;Progress in Neuro-Psychopharmacology and Biological Psychiatry;2024-12

2. Considerations for identifying subtypes of speech sound disorder;International Journal of Language & Communication Disorders;2024-09-04

3. O-GlcNAc transferase congenital disorder of glycosylation (OGT-CDG): Potential mechanistic targets revealed by evaluating the OGT interactome;Journal of Biological Chemistry;2024-09

4. Incorporating core concepts into an undergraduate neuroscience program in a resource-restricted environment;Frontiers in Education;2024-08-15

5. Identification of the synonymous variant c.3141G > A in TNRC6B gene that altered RNA splicing by minigene assay;Molecular Biology Reports;2024-08-08