Osamu Onodera

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Takeshi IkeuchiNiigata University, Brain Research InstituteGeverifieerd e-mailadres voor bri.niigata-u.ac.jp
Masato KanazawaBrain Research Institute, Niigata UniversityGeverifieerd e-mailadres voor bri.niigata-u.ac.jp
Mari TadaDepartment of pathology, BRI, Niigata UniversityGeverifieerd e-mailadres voor bri.niigata-u.ac.jp
Takuya KonnoBrain Research Institute, Niigata UniversityGeverifieerd e-mailadres voor bri.niigata-u.ac.jp
Akihiro SugaiBrain Research Institute, Niigata UniversityGeverifieerd e-mailadres voor bri.niigata-u.ac.jp
Warren J. StrittmatterProfessor Emeritus of Neurology, Duke University; Chief Scientific Officer, T3D TherapeuticsGeverifieerd e-mailadres voor t3dtherapeutics.com
Yoshitaka NagaiDepartment of Neurotherapeutics, Osaka University Graduate School of MedicineGeverifieerd e-mailadres voor neurother.med.osaka-u.ac.jp
Takashi NakajimaNational Hospital Organization Niigata National HospitalGeverifieerd e-mailadres voor mqb.biglobe.ne.jp
Tetsuya TakahashiProfessor of Mathematics Geverifieerd e-mailadres voor las.osakafu-u.ac.jp
Yuya HatanoNiigata UniversityGeverifieerd e-mailadres voor mail.cc.niigata-u.ac.jp
Satoshi KuwabaraDepartment of Neurology, Chiba UniversityGeverifieerd e-mailadres voor faculty.chiba-u.jp
Jun MitsuiDepartment of Neurology, The University of TokyoGeverifieerd e-mailadres voor umin.ac.jp
Tetsuya TakahashiNiigata UniversityGeverifieerd e-mailadres voor bri.niigata-u.ac.jp
Haruo ShimazakiJichi MedicalGeverifieerd e-mailadres voor jichi.ac.jp
Nadezhda MaksimovaChief Researcher, North-Eastern Federal UniversityGeverifieerd e-mailadres voor s-vfu.ru
Masafumi IharaNational Cerebral and Cardiovascular CenterGeverifieerd e-mailadres voor ncvc.go.jp
masamitsu nakazato大阪大学、宮崎大学Geverifieerd e-mailadres voor med.miyazaki-u.ac.jp
Fumiaki MoriHirosaki UniversityGeverifieerd e-mailadres voor hirosaki-u.ac.jp
Hideaki MatsuiProfessor, Dept. Neuroscience of Disease, Brain Research Institute, Niigata UniversityGeverifieerd e-mailadres voor bri.niigata-u.ac.jp
Atchayaram NaliniProfessor of Neurology, NIMHANSGeverifieerd e-mailadres voor nimhans.ac.in

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Osamu Onodera

Andere namenO. Onodera

Dept. of Neurology, Brain Research Institute, Niigata University

Geverifieerd e-mailadres voor bri.niigata-u.ac.jp - Homepage

Neurodegenerative disorders Cerebral small vessel disease ALS


Titel Sorteren op citaties Sorteren op jaar Sorteren op titel	Geciteerd door Geciteerd door	Jaar
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	1419	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	573	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	493	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	480	1993
TDP‐43 mutation in familial amyotrophic lateral sclerosis A Yokoseki, A Shiga, CF Tan, A Tagawa, H Kaneko, A Koyama, H Eguchi, ... Annals of Neurology: Official Journal of the American Neurological …, 2008	464	2008
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	434	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	376	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	309	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	290	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	267	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	255	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	248	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	240	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	214	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	213	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	207	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	204	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	195	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	185	2013
Sporadic ataxias in Japan–a population-based epidemiological study S Tsuji, O Onodera, J Goto, M Nishizawa, ... The Cerebellum 7, 189-197, 2008	182	2008

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