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Human Molecular Genetics|November 30, 2007
A network of dopaminergic gene variations implicated as risk factors for schizophreniaMichael E Talkowski, George Kirov, Mikhil Bamne, et al.American Journal of Human Genetics|October 9, 2012
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depthMenachem Fromer, Jennifer L Moran, Kimberly Chambert, et al.Journal of Human Genetics|January 23, 2009
Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian populationElitza T Betcheva, Taisei Mushiroda, Atsushi Takahashi, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 30, 2017
Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar typeElaine K Green, Arianna Di Florio, Liz Forty, et al.Human Molecular Genetics|July 15, 2025
Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palateAlexandros Rammos, Rachel Blakey, Charlotte A Dennison, et al.Thyroid : Official Journal of the American Thyroid Association|June 14, 2018
An InDel in Phospholipase-C-B-1 Is Linked with Euthyroid Multinodular GoiterAmeen D Bakhsh, Ioannis Ladas, Marian L Hamshere, et al.JAMA Psychiatry|August 4, 2021
Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in SchizophreniaSophie E Legge, Alastair G Cardno, Judith Allardyce, et al.Plos One|February 5, 2026
Genetics to Improve Outcomes in Schizophrenia (GENios): A within-case molecular genetic study protocolSophie E Smart, Eilidh Fenner, Rhys Humphreys, et al.Psychiatric Genetics|November 13, 2012
Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility geneElitza T Betcheva, Adelina G Yosifova, Taisei Mushiroda, et al.JAMA Psychiatry|January 18, 2013
Implication of a rare deletion at distal 16p11.2 in schizophreniaSaurav Guha, Elliott Rees, Ariel Darvasi, et al.Pageof 20