Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations-Reference-Cited by-同舟云学术

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

Published:2011-05-15 Issue:6 Volume:43 Page:585-589
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

O'Roak Brian J,Deriziotis Pelagia,Lee Choli,Vives Laura,Schwartz Jerrod J,Girirajan Santhosh,Karakoc Emre,MacKenzie Alexandra P,Ng Sarah B,Baker Carl,Rieder Mark J,Nickerson Deborah A,Bernier Raphael,Fisher Simon E,Shendure Jay,Eichler Evan E

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.835.pdf

Reference52 articles.

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3. Girirajan, S. et al. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nat. Genet. 42, 203–209 (2010).

4. Abrahams, B.S. & Geschwind, D.H. Advances in autism genetics: on the threshold of a new neurobiology. Nat. Rev. Genet. 9, 341–355 (2008).

5. Sebat, J. et al. Strong association of de novo copy number mutations with autism. Science 316, 445–449 (2007).

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