Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database-Reference-Cited by-同舟云学术

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Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

Published:2015-04-07 Issue:2 Volume:21 Page:290-297
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Li Jinchen,Cai Tao,Jiang Yi,Chen Huiqian,He Xin,Chen Chao,Li Xianfeng,Shao Qianzhi,Ran Xia,Li Zhongshan,Xia Kun,Liu Chunyu,Sun Zhong Sheng,Wu Jinyu

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://www.nature.com/articles/mp201540.pdf

Reference73 articles.

1. Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA et al. Exome sequencing as a tool for Mendelian disease gene discovery. Nat Rev Genet 2011; 12: 745–755.

2. Goldstein DB, Allen A, Keebler J, Margulies EH, Petrou S, Petrovski S et al. Sequencing studies in human genetics: design and interpretation. Nat Rev Genet 2013; 14: 460–470.

3. MacArthur D, Manolio T, Dimmock D, Rehm H, Shendure J, Abecasis G et al. Guidelines for investigating causality of sequence variants in human disease. Nature 2014; 508: 469–476.

4. Ku C, Polychronakos C, Tan E, Naidoo N, Pawitan Y, Roukos D et al. A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease. Mol Psychiatry 2013; 18: 141–153.

5. Michaelson JJ, Shi Y, Gujral M, Zheng H, Malhotra D, Jin X et al. Whole-genome sequencing in autism identifies hot spots for de novo germline mutation. Cell 2012; 151: 1431–1442.

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