Associated Papers
Influence of DRD2 Polymorphisms on the Clinical Outcomes of Opioiddependent Patients on Methadone Maintenance Therapy.
Zahari Z et al.
Journal of Pharmacy & Bioallied Sciences, 2020
Evolutionary conservation and functional impact of dopamine D2 receptor.
Yuan J et al.
Neuroscience Letters, 2020
Tridimensional personalities and polymorphism of dopamine D2 receptor among heroin addicts.
Teh LK et al.
Biological Research for Nursing, 2012
A Nested Allele-Specific Multiplex Polymerase Chain Reaction Method for the Detection of DRD2 Polymorphisms.
Zahari Z et al.
The Malaysian Journal of Medical Sciences : Mjms, 2011
Influence of DRD2 polymorphisms on the clinical outcomes of patients with schizophrenia.
Zahari Z et al.
Psychiatric Genetics, 2011
TorsinA immunoreactivity in inclusion bodies in trinucleotide repeat diseases.
Walker RH et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2003
Analysis of transmission of novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene in patients with autism.
Lauritsen MB et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2003
Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor.
Duan J et al.
Human Molecular Genetics, 2003
Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutations.
Klein C et al.
Annals of Neurology, 2002
A major locus for several phenotypes of myoclonus--dystonia on chromosome 7q.
Vidailhet M et al.
Neurology, 2001
Inherited myoclonus-dystonia: evidence supporting genetic heterogeneity.
Grimes DA et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2001
[Angelman syndrome--from the phenotype of a developmental disorder to the genes].
Holopainen IE et al.
Duodecim; Laaketieteellinen Aikakauskirja, 2001
A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.
Klein C et al.
American Journal of Human Genetics, 2000
Association studies of Parkinson's disease and parkin polymorphisms.
Klein C et al.
Annals of Neurology, 2000
Association of early-onset Alzheimer's disease with an interleukin-1alpha gene polymorphism.
Grimaldi LM et al.
Annals of Neurology, 2000
Association of interleukin-1 gene polymorphisms with Alzheimer's disease.
Nicoll JA et al.
Annals of Neurology, 2000
Association of a missense change in the D2 dopamine receptor with myoclonus dystonia.
Klein C et al.
Proceedings of the National Academy of Sciences of the United States of America, 1999
Detection of altered methylation of MB-COMT promotor and DRD2 gene in cannabinoid or synthetic cannabinoid use disorder regarding gene variants and clinical parameters.
Oyaci Y et al.
Journal of Addictive Diseases, 0