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Human Heredity|July 10, 2010
Genetic differences between five European populationsValentina Moskvina, Michael Smith, Dobril Ivanov, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2006
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaLyudmila Georgieva, Valentina Moskvina, Tim Peirce, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 27, 2005
Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophreniaNadine Norton, Valentina Moskvina, Derek W Morris, et al.
Bipolar Disorders|August 20, 2009
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31Marian L Hamshere, Thomas G Schulze, Johannes Schumacher, et al.
Nature Communications|January 15, 2022
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variantsBret Sanders, Daniel D'Andrea, Mark O Collins, et al.
European Journal of Human Genetics : EJHG|January 17, 2013
Mosaic copy number variation in schizophreniaDouglas M Ruderfer, Kim Chambert, Jennifer Moran, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 22, 2008
Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samplesMichael E Talkowski, Lora McClain, Trina Allen, et al.
Biological Psychiatry|July 5, 2005
No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samplesBeate Glaser, Johannes Schumacher, Hywel J Williams, et al.
Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.
Human Molecular Genetics|January 30, 2014
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosisDerek W Morris, Richard D Pearson, Paul Cormican, et al.
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