Rare and common variants at 16p11.2 are associated with schizophrenia
Author:
Publisher
Elsevier BV
Subject
Biological Psychiatry,Psychiatry and Mental health
Reference33 articles.
1. High rate of disease-related copy number variations in childhood onset schizophrenia;Ahn;Mol. Psychiatry,2014
2. Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients;Buizer-Voskamp;Biol. Psychiatry,2011
3. Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays;Costain;Hum. Mol. Genet.,2013
4. KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant;Golzio;Nature,2012
5. Implication of a rare deletion at distal 16p11.2 in schizophrenia;Guha;JAMA Psychiat.,2013
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