Associated Papers
Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370S GBA Variant Carriers with and without Parkinson's Disease.
Grigor'eva EV et al.
International Journal of Molecular Sciences, 2023
Gene polymorphisms and motor levodopa-induced complications in Parkinson's disease.
Michałowska M et al.
Brain and Behavior, 2020
A novel germline ARMC5 mutation in a patient with bilateral macronodular adrenal hyperplasia: a case report.
Liu Q et al.
Bmc Medical Genetics, 2018
No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson's disease in nine ADHD candidate SNPs.
Geissler JM et al.
Attention Deficit and Hyperactivity Disorders, 2017
Missense dopamine transporter mutations associate with adult parkinsonism and ADHD.
Hansen FH et al.
The Journal of Clinical Investigation, 2014
SLC6A3 is a risk factor for Parkinson's disease: a meta-analysis of sixteen years' studies.
Zhai D et al.
Neuroscience Letters, 2014
Impact of COMT H108L, MAOB int 13 A>G and DRD2 haplotype on the susceptibility to Parkinson's disease in South Indian subjects.
Kumudini N et al.
Indian Journal of Biochemistry & Biophysics, 2013
SLC6A3 and body mass index in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial.
Azzato EM et al.
Bmc Medical Genetics, 2009
Polymorphism in environment responsive genes and association with Parkinson disease.
Singh M et al.
Molecular and Cellular Biochemistry, 2008
The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease.
Białecka M et al.
Acta Neurologica Scandinavica, 2004
Association study of dopamine transporter gene and schizophrenia in Korean population using multiple single nucleotide polymorphism markers.
Jeong SH et al.
Progress in Neuro-psychopharmacology & Biological Psychiatry, 2004
Association between dopamine transporter gene polymorphism and susceptibility to Parkinson's disease in Japan.
Nishimura M et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2002
Association study for Parkinson's disease and a dopamine transporter gene polymorphism (1215A/G).
Lin CN et al.
European Neurology, 2002
The human dopamine transporter gene: gene organization, transcriptional regulation, and potential involvement in neuropsychiatric disorders.
Bannon MJ et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology, 2001
No evidence of association between a dopamine transporter gene polymorphism (1215A/G) and Parkinson's disease.
Kimura M et al.
Annals of Neurology, 2001
[Association between genetic polymorphism of dopamine transporter gene and susceptibility to Parkinson's disease].
Wang J et al.
Zhonghua Yi Xue Za Zhi, 2000
Reversible brain creatine deficiency in two sisters with normal blood creatine level.
Bianchi MC et al.
Annals of Neurology, 2000
A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease.
Morino H et al.
Annals of Neurology, 2000