Association between NR4A2 genetic variation and schizophrenia: A comprehensive systematic review and meta-analysis-Reference-Cited by-同舟云学术

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Association between NR4A2 genetic variation and schizophrenia: A comprehensive systematic review and meta-analysis

Published:2015-06 Issue: Volume:598 Page:85-90
ISSN:0304-3940
Container-title:Neuroscience Letters
language:en
Short-container-title:Neuroscience Letters

Author:

Liu Hongmei,Fu Yingmei,Ren Juanjuan,Yu Shunying,Liu Hongbo,Jiang Ping,Dong Yi,Li Huafang

Funder

Shanghai Key Laboratory of Psychotic Disorders

National Major Project for IND

Shanghai Health Talent Professional Project

Shanghai Natural Science Fund Project

Shanghai Clinical Center for Mental Disorders

Publisher

Elsevier BV

Subject

General Neuroscience

Reference47 articles.

1. NR4A2: effects of an orphan receptor on sustained attention in a schizophrenic population;Ancin;Schizophr. Bull.,2013

2. Co-ordinate transcriptional regulation of dopamine synthesis genes by alpha-synuclein in human neuroblastoma cell lines;Baptista;J. Neurochem.,2003

3. Operating characteristics of a rank correlation test for publication bias;Begg;Biometrics,1994

4. Multiple significance tests: the Bonferroni method;Bland;Br. Med. J.,1995

5. NURR1 mutations in cases of schizophrenia and manic-depressive disorder;Buervenich;Am. J. Med. Genet.,2000

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1. Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment;Human Molecular Genetics;2023-08-16

2. Association Between NR4A2 Gene Polymorphism and Depressive Symptoms and Antidepressant Effect;Neuropsychiatric Disease and Treatment;2021-08

3. DNA Hypermethylation Induced by L-Methionine Leads to Oligodendroglial and Myelin Deficits and Schizophrenia-Like Behaviors in Adolescent Mice;Frontiers in Neuroscience;2021-04-20

4. Working memory deficits in schizophrenia are associated with the rs34884856 variant and expression levels of the NR4A2 gene in a sample Mexican population: a case control study;BMC Psychiatry;2021-02-09

5. De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy;Genetics in Medicine;2020-08

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