Associated Papers
Two novel heterozygous truncating variants in NR4A2 identified in patients with neurodevelopmental disorder and brief literature review.
Song X et al.
Frontiers in Neuroscience, 2022
Possible genes responsible for developmental delay observed in patients with rare 2q23q24 microdeletion syndrome: Literature review and description of an additional patient.
Shimojima K et al.
Congenital Anomalies, 2017
NR4A2 genetic variation and Parkinson's disease: Evidence from a systematic review and meta-analysis.
Liu H et al.
Neuroscience Letters, 2017
Association between NR4A2 genetic variation and schizophrenia: A comprehensive systematic review and meta-analysis.
Liu H et al.
Neuroscience Letters, 2015
BDNF 196 G/A and 270 C/T polymorphisms and susceptibility to Parkinson's disease: a meta-analysis.
Lee YH et al.
Journal of Motor Behavior, 2014
Genetic analysis of NR4A2 gene in a large population of Han Chinese patients with Parkinson's disease.
Liu H et al.
European Journal of Neurology, 2013
Nur-related receptor 1 gene polymorphisms and alcohol dependence in Mexican Americans.
Wei YM et al.
World Journal of Gastroenterology, 2012
Examination of the MSX1 gene in patients with Parkinson's disease.
Deng H et al.
Acta Neurologica Scandinavica, 2009
[Association of the polymorphisms in NURR1 gene with Parkinson's disease].
Wu Y et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2008
Nuclear receptor NR4A2 IVS6 +18insG and brain derived neurotrophic factor (BDNF) V66M polymorphisms and risk of Taiwanese Parkinson's disease.
Chen CM et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2007
Mitochondrial DNA polymorphisms and the risk of Parkinson's disease in Taiwan.
Chen CM et al.
Journal of Neural Transmission (vienna, Austria : 1996), 2007
Unraveling the pathogenesis of Parkinson's disease--the contribution of monogenic forms.
Bonifati V et al.
Cellular and Molecular Life Sciences : Cmls, 2004
Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease.
Ibáñez P et al.
Neurology, 2004
Distribution of haplotypes derived from three common variants of the NR4A2 gene in Japanese patients with schizophrenia.
Iwayama-Shigeno Y et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2003
Mutation analysis of the human NR4A2 gene, an essential gene for midbrain dopaminergic neurogenesis, in schizophrenic patients.
Chen YH et al.
American Journal of Medical Genetics, 2001