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American Journal of Human Genetics|December 13, 2006
Functional variants in the promoter region of Chitinase 3-like 1 (CHI3L1) and susceptibility to schizophreniaXinzhi Zhao, Ruqi Tang, Bo Gao, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 29, 2010
Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorderElaine K Green, Detelina Grozeva, Valentina Moskvina, et al.Progress in Neuro-Psychopharmacology & Biological Psychiatry|June 29, 2010
Pharacogenetic effects of dopamine transporter gene polymorphisms on response to chlorpromazine and clozapine and on extrapyramidal syndrome in schizophreniaMingqing Xu, Qinghe Xing, Sheng Li, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 7, 2023
Establishment of a consensus protocol to explore the brain pathobiome in patients with mild cognitive impairment and Alzheimer's disease: Research outline and call for collaborationRichard Lathe, Nikki M Schultek, Brian J Balin, et al.Journal of Psychiatric Research|February 27, 2010
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohortLavinia Athanasiu, Morten Mattingsdal, Anna K Kähler, 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.Genome Biology|August 31, 2016
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylationEilis Hannon, Emma Dempster, Joana Viana, et al.Neuroscience Letters|March 18, 2004
Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's diseaseLynnette J Cook, Luk W Ho, Alison E Taylor, et al.Molecular Psychiatry|November 8, 2018
Reversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imagingMandy Johnstone, Navneet A Vasistha, Miruna C Barbu, et al.American Journal of Human Genetics|December 1, 2009
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depressionHelen M Knight, Benjamin S Pickard, Alan Maclean, et al.Pageof 17