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
Association between NR4A2 genetic variation and schizophrenia: A comprehensive systematic review and meta-analysis.
Liu H et al.
Neuroscience Letters, 2015
NR4A2 and schizophrenia: lack of association in a Portuguese/Brazilian study.
Ruano D et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2004
Myoclonus-dystonia: detection of novel, recurrent, and de novo SGCE mutations.
Hedrich K et al.
Neurology, 2004
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.
Hering R 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
NURR1 mutations in cases of schizophrenia and manic-depressive disorder.
Buervenich S et al.
American Journal of Medical Genetics, 2000
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