Association study between GNB1L and three major mental disorders in Chinese Han populations
Author:
Publisher
Elsevier BV
Subject
Biological Psychiatry,Psychiatry and Mental health
Reference13 articles.
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3. Folding of proteins with WD-repeats: comparison of six members of the WD-repeat superfamily to the G protein beta subunit;Garcia-Higuera;Biochemistry,1996
4. GNB1L a gene deleted in the critical region for DiGeorge syndrome on 22q11, encodes a G-protein β-subunit-like polypeptide;Gong;Biochimica et Biophysica Acta,2000
5. Supportive evidence for reduced expression of GNB1L in schizophrenia;Ishiguro;Schizophrenia Bulletin,2010
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1. Sequencing of the coding regions of GNBIL on chromosome 22q11.2 as a risk gene of schizophrenia;Psychiatry Research;2021-06
2. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother;Taiwanese Journal of Obstetrics and Gynecology;2021-01
3. A 31-bp indel in the 5′ UTR region of GNB1L is significantly associated with chicken body weight and carcass traits;BMC Genetics;2020-08-26
4. Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2017-01-31
5. Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder;PLOS ONE;2015-07-22
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