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Kenya Nishioka
Kenya Nishioka
Juntendo University School of Medicine
Verified email at juntendo.ac.jp
Title
Cited by
Cited by
Year
Genomic investigation of α‐synuclein multiplication and parkinsonism
OA Ross, AT Braithwaite, LM Skipper, J Kachergus, MM Hulihan, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
3982008
Translation initiator EIF4G1 mutations in familial Parkinson disease
MC Chartier-Harlin, JC Dachsel, C Vilariño-Güell, SJ Lincoln, F Leprêtre, ...
The American Journal of Human Genetics 89 (3), 398-406, 2011
3922011
Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease
K Nishioka, S Hayashi, MJ Farrer, AB Singleton, H Yoshino, H Imai, ...
Annals of Neurology: Official Journal of the American Neurological …, 2006
3922006
CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
M Funayama, K Ohe, T Amo, N Furuya, J Yamaguchi, S Saiki, Y Li, ...
The Lancet Neurology 14 (3), 274-282, 2015
3592015
LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors
KM Hinkle, M Yue, B Behrouz, JC Dächsel, SJ Lincoln, EE Bowles, ...
Molecular neurodegeneration 7, 1-17, 2012
2102012
Progress in the pathogenesis and genetics of Parkinson's disease
Y Mizuno, N Hattori, S Kubo, S Sato, K Nishioka, T Hatano, H Tomiyama, ...
Philosophical Transactions of the Royal Society B: Biological Sciences 363 …, 2008
1572008
Prognosis of Parkinson's disease: time to stage III, IV, V, and to motor fluctuations
K Sato, T Hatano, K Yamashiro, M Kagohashi, K Nishioka, N Izawa, ...
Movement disorders: official journal of the Movement Disorder Society 21 (9 …, 2006
1512006
Expanding the clinical phenotype of SNCA duplication carriers
K Nishioka, OA Ross, K Ishii, JM Kachergus, K Ishiwata, M Kitagawa, ...
Movement disorders 24 (12), 1811-1819, 2009
1482009
Homozygous alpha-synuclein p. A53V in familial Parkinson's disease
H Yoshino, M Hirano, AJ Stoessl, Y Imamichi, A Ikeda, Y Li, M Funayama, ...
Neurobiology of aging 57, 248. e7-248. e12, 2017
1132017
CLINICOPATHOLOGIC STUDY OF A SNCA GENE DUPLICATION PATIENT WITH PARKINSON DISEASE AND DEMENTIA
T Obi, K Nishioka, OA Ross, T Terada, K Yamazaki, A Sugiura, ...
Neurology 70 (3), 238-241, 2008
932008
Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease
Y Li, T Sekine, M Funayama, L Li, H Yoshino, K Nishioka, H Tomiyama, ...
Neurobiology of aging 35 (4), 935. e3-935. e8, 2014
872014
An epidemiologic internet survey of fibromyalgia and chronic pain in Japan
I Nakamura, K Nishioka, C Usui, K Osada, H Ichibayashi, M Ishida, ...
Arthritis care & research 66 (7), 1093-1101, 2014
852014
Association of α-, β-, and γ-synuclein with diffuse Lewy body disease
K Nishioka, C Wider, C Vilarino-Güell, AI Soto-Ortolaza, SJ Lincoln, ...
Archives of neurology 67 (8), 970-975, 2010
852010
Variants in saposin D domain of prosaposin gene linked to Parkinson’s disease
Y Oji, T Hatano, SI Ueno, M Funayama, K Ishikawa, A Okuzumi, S Noda, ...
Brain 143 (4), 1190-1205, 2020
802020
The E3 ligase synoviolin controls body weight and mitochondrial biogenesis through negative regulation of PGC‐1β
H Fujita, N Yagishita, S Aratani, T Saito‐Fujita, S Morota, Y Yamano, ...
The EMBO journal 34 (8), 1042-1055, 2015
772015
DNAJC12 and dopa‐responsive nonprogressive parkinsonism
L Straniero, I Guella, R Cilia, L Parkkinen, V Rimoldi, A Young, R Asselta, ...
Annals of neurology 82 (4), 640-646, 2017
682017
Familial Parkinsonism with digenic parkin and PINK1 mutations
M Funayama, Y Li, TH Tsoi, CW Lam, T Ohi, S Yazawa, E Uyama, ...
Movement disorders: official journal of the Movement Disorder Society 23 (10 …, 2008
652008
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders
K Ogaki, S Koga, MG Heckman, FC Fiesel, M Ando, C Labbé, ...
Neurology 85 (23), 2016-2025, 2015
642015
Molecular genetics of Parkinson’s disease: Contributions and global trends
M Funayama, K Nishioka, Y Li, N Hattori
Journal of human genetics 68 (3), 125-130, 2023
622023
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease
K Nishioka, M Kefi, B Jasinska-Myga, C Wider, C Vilariño-Güell, OA Ross, ...
Journal of Neurology, Neurosurgery & Psychiatry 81 (4), 391-395, 2010
612010
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