| 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 | 411 | 2011 |
| 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 | 409 | 2008 |
| 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 | 408 | 2006 |
| 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 | 384 | 2015 |
| 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 | 222 | 2012 |
| 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 | 164 | 2008 |
| 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 | 161 | 2006 |
| 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 | 151 | 2017 |
| 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 | 147 | 2009 |
| 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 | 128 | 2023 |
| 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 | 98 | 2008 |
| 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 | 96 | 2020 |
| 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 | 92 | 2014 |
| 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 | 90 | 2014 |
| 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 | 87 | 2010 |
| 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 | 80 | 2015 |
| 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 | 74 | 2017 |
| FBXO7 mutations in Parkinson's disease and multiple system atrophy S Conedera, H Apaydin, Y Li, H Yoshino, A Ikeda, T Matsushima, ... Neurobiology of aging 40, 192. e1-192. e5, 2016 | 68 | 2016 |
| 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 | 68 | 2015 |
| 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 | 68 | 2008 |
Matt FarrerUniversity of FloridaVerified email at can.ubc.ca