A molecular model for neurodevelopmental disorders-Reference-Cited by-同舟云学术

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A molecular model for neurodevelopmental disorders

Published:2015-05 Issue:5 Volume:5 Page:e565-e565
ISSN:2158-3188
Container-title:Translational Psychiatry
language:en
Short-container-title:Transl Psychiatry

Author:

Gigek C O,Chen E S,Ota V K,Maussion G,Peng H,Vaillancourt K,Diallo A B,Lopez J P,Crapper L,Vasuta C,Chen G G,Ernst C

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://www.nature.com/articles/tp201556.pdf

Reference81 articles.

1. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY . Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 1999; 23: 185–188.

2. Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE et al. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nat Genet 1993; 3: 36–43.

3. Schanen NC . Epigenetics of autism spectrum disorders. Hum Mol Genet 2006; 15, Spec No 2 R138–R150.

4. Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O et al. Disruptive CHD8 mutations define a subtype of autism early in development. Cell 2014; 158: 263–276.

5. Talkowski ME, Rosenfeld JA, Blumenthal I, Pillalamarri V, Chiang C, Heilbut A et al. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell 2012; 149: 525–537.

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