Associated Papers
RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism.
Errichiello E et al.
Molecular Genetics & Genomic Medicine, 2021
Phenotypic features of patients with schizophrenia carrying de novo gene mutations: a pilot study.
Malherbe PJ et al.
Psychiatry Research, 2015
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.
Xu B et al.
Nature Genetics, 2012
23042115 (PubMed )
Supplement: NIHMS410678-supplement-5.xls › suppl_table_2
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