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Nature Communications|August 2, 2025
Whole-exome sequencing analysis identifies risk genes for schizophreniaSophie L Chick, Peter Holmans, Darren Cameron, et al.
Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
JCPP Advances|July 8, 2026
The role of rare copy number variants in early-onset depressionCharlotte A Dennison, Ida Sønderby, Miguel Garcia-Argibay, et al.
Translational Psychiatry|February 27, 2019
Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structuresMark Drakesmith, Greg D Parker, Jacqueline Smith, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 23, 2009
P2RX7: A bipolar and unipolar disorder candidate susceptibility gene?Elaine K Green, Detelina Grozeva, Rachel Raybould, et al.
Archives of General Psychiatry|June 9, 2005
Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorderElaine K Green, Rachel Raybould, Stuart Macgregor, et al.
Biological Psychiatry|April 12, 2005
Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1)Rachel Raybould, Elaine K Green, Stuart MacGregor, et al.
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