| Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) R Koide, T Ikeuchi, O Onodera, H Tanaka, S Igarashi, K Endo, ... Nature genetics 6 (1), 9-13, 1994 | 1393 | 1994 |
| Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease K Hara, A Shiga, T Fukutake, H Nozaki, A Miyashita, A Yokoseki, ... New England Journal of Medicine 360 (17), 1729-1739, 2009 | 536 | 2009 |
| Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription T Shimohata, T Nakajima, M Yamada, C Uchida, O Onodera, S Naruse, ... Nature genetics 26 (1), 29-36, 2000 | 489 | 2000 |
| The gene for Machado–Joseph disease maps to human chromosome 14q Y Takiyama, M Nishizawa, H Tanaka, S Kawashima, H Sakamoto, ... Nature genetics 4 (3), 300-304, 1993 | 464 | 1993 |
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| Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene H Date, O Onodera, H Tanaka, K Iwabuchi, K Uekawa, S Igarashi, ... Nature genetics 29 (2), 184-188, 2001 | 426 | 2001 |
| TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation CF Tan, H Eguchi, A Tagawa, O Onodera, T Iwasaki, A Tsujino, ... Acta neuropathologica 113, 535-542, 2007 | 365 | 2007 |
| Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy H Ishiura, K Doi, J Mitsui, J Yoshimura, MK Matsukawa, A Fujiyama, ... Nature genetics 50 (4), 581-590, 2018 | 288 | 2018 |
| Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic T Takahashi, S Kikuchi, S Katada, Y Nagai, M Nishizawa, O Onodera Human molecular genetics 17 (3), 345-356, 2008 | 276 | 2008 |
| Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy Multiple-System Atrophy Research Collaboration New England Journal of Medicine 369 (3), 233-244, 2013 | 257 | 2013 |
| Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese … N Hattori, M Yamamoto, T Yoshihara, H Koike, M Nakagawa, ... Brain 126 (1), 134-151, 2003 | 252 | 2003 |
| Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy S Igarashi, Y Tanno, O Onodera, M Yamazaki, S Sato, A Ishikawa, ... Neurology 42 (12), 2300-2300, 1992 | 247 | 1992 |
| Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease K Okuizumi, O Onodera, Y Namba, K Ikeda, T Yamamoto, K Seki, A Ueki, ... Nature genetics 11 (2), 207-209, 1995 | 232 | 1995 |
| Aprataxin, a novel protein that protects against genotoxic stress N Gueven, OJ Becherel, AW Kijas, P Chen, O Howe, JH Rudolph, R Gatti, ... Human molecular genetics 13 (10), 1081-1093, 2004 | 206 | 2004 |
| β-synuclein gene alterations in dementia with Lewy bodies H Ohtake, P Limprasert, Y Fan, O Onodera, A Kakita, H Takahashi, ... Neurology 63 (5), 805-811, 2004 | 203 | 2004 |
| Polyglutamine diseases: where does toxicity come from? what is toxicity? where are we going? T Takahashi, S Katada, O Onodera Journal of molecular cell biology 2 (4), 180-191, 2010 | 198 | 2010 |
| Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions Y Nishihira, CF Tan, O Onodera, Y Toyoshima, M Yamada, T Morita, ... Acta neuropathologica 116, 169-182, 2008 | 197 | 2008 |
| Dentatorubral‐pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat T Ikeuchi, R Koide, H Tanaka, O Onodera, S Igarashi, H Takahashi, ... Annals of Neurology: Official Journal of the American Neurological …, 1995 | 191 | 1995 |
| ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19 Y Takahashi, Y Fukuda, J Yoshimura, A Toyoda, K Kurppa, H Moritoyo, ... The American Journal of Human Genetics 93 (5), 900-905, 2013 | 169 | 2013 |
| Early development of autonomic dysfunction may predict poor prognosis in patients with multiple system atrophy M Tada, O Onodera, M Tada, T Ozawa, YS Piao, A Kakita, H Takahashi, ... Archives of neurology 64 (2), 256-260, 2007 | 169 | 2007 |
Takeshi IkeuchiNiigata University, Brain Research InstituteVerified email at bri.niigata-u.ac.jp
