De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia
Xu, Bin, Ionita-Laza, Iuliana, Roos, J Louw, Boone, Braden, Woodrick, Scarlet, Sun, Yan, Levy, Shawn, Gogos, Joseph A +1 more·2012·Nature Genetics
DOI 10.1038/ng.2446
Cited by (442)
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- Manuscript Word Count: Abstract: 193; Text, with citations, without references: 3921 Number of Tables: 2; Supplemental Files: Yes Whole-genome sequencing suggests schizophrenia risk mechanisms in humans with 22q11.2 deletion syndromeDaniele Merico, Mehdi Zarrei, Gregory Costain, Lucas Ogura, Babak Alipanahi, Nancy J. Butcher, Bhooma Thiruvahindrapuram, Eva W.C. Chow, Danielle Molinari Andrade, Brendan J. Frey et al. · 2015
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- Increased Risk for Nonfamilial Schizophrenia from De Novo MutationsBarbara Geller · 2012 · Journal watch
- Genetic Epidemiology of Schizophrenia and Bipolar Disorder: a reviewA. Anuradha, V. Lakshmi Kalpana · 2018 · Indian Journal of Mental Health(IJMH)