Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets-Reference-Cited by-同舟云学术

Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets

Published:2013-11 Issue:11 Volume:3 Page:e326-e326
ISSN:2158-3188
Container-title:Translational Psychiatry
language:en
Short-container-title:Transl Psychiatry

Author:

Degenhardt F, ,Priebe L,Meier S,Lennertz L,Streit F,Witt S H,Hofmann A,Becker T,Mössner R,Maier W,Nenadic I,Sauer H,Mattheisen M,Buizer-Voskamp J,Ophoff R A,Rujescu D,Giegling I,Ingason A,Wagner M,Delobel B,Andrieux J,Meyer-Lindenberg A,Heinz A,Walter H,Moebus S,Corvin A,Rietschel M,Nöthen M M,Cichon S,

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://www.nature.com/articles/tp2013101.pdf

Reference32 articles.

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3. Xu B, Roos JL, Dexheimer P, Boone B, Plummer B, Levy SGo et al Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat Genet 2011; 43: 864–868.

4. The International Schizophrenia Consortium. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008; 455: 237–241.

5. Stefansson H, Rujescu D, Cichon S, Pietiläinen OP, Ingason A, Steinberg S et al Large recurrent microdeletions associated with schizophrenia. Nature 2008; 455: 232–236.

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