HATTORI Nobutaka, M.D., Ph.D. , FANA
Department of Neurology
Short Biography
| 1985-1986 | M.D. Juntendo University Faculty of Medicine
Intern, Juntendo University Hospital |
| 1986-1988 | Resident in Neurology, Department of Neurology, Fuji, National Hospital |
| 1988-1989 | Assistant Professor of Neurology, Juntendo University |
| 1990-1994 | Ph.D. Juntendo University Graduate School of Medicine |
| 1990-1993 | Study Molecular Biology as a Special Graduate Student at Department of Biological Chemistry at the Faculty of Medicine, University of Nagoya |
| 1994-1995 | Medical Staff, Department of Neurology, Tokyo Metropolitan Ebara Hospital |
| 1995-1998 | Assistant Professor, Department of Neurology, Juntendo University |
| 1999-2003 | Lecturer, Department of Neurology, Juntendo University |
| 2003-2006 | Associate Professor, Department of Neurology, Juntendo University |
| 2006-Present | Professor and Chairman, Department of Neurology, Juntendo University Faculty of Medicine |
| 2019-Present | Dean, Faculty of Medicine and Graduate School of Medicine, Juntendo University |
| 2020-Present | Team Leader, Neurodegenerative Disorders Collaborative Laboratory, RIKEN Center for Brain Science |
Keywords
- Parkinson's Disease
- Neuro-Genetics
- Autophagy Lysosome
- Ubiquitin proteasome
- Mitochondrial impairment
Main Research Topics and Interests
- Familial Parkinson's disease
- Ubiquitin proteasome
- Autophagy lysosome pathway
- Neurodegeneration
- Mitochondria
- iPS
- Telemedicine
Publications (in English)
- Original and Review Articles: 840
- Books: 16
- h-index: 80
- Sum of Times Cited: 34,318
Recent Main Publications
- Oji Y, Hatano T, Ueno SI, Funayama M, Ishikawa KI, Okuzumi A, Noda S, Sato S, Satake W, Toda T, Li Y, Hino-Takai T, Kakuta S, Tsunemi T, Yoshino H, Nishioka K, Hattori T, Mizutani Y, Mutoh T, Yokochi F, Ichinose Y, Koh K, Shindo K, Takiyama Y, Hamaguchi T, Yamada M, Farrer MJ, Uchiyama Y, Akamatsu W, Wu YR, Matsuda J, Hattori N. Variants in saposin D domain of prosaposin gene linked to Parkinson's disease. Brain. 2020 Apr 1;143(4):1190-1205.
- Mori A, Hatano T, Inoshita T, Shiba-Fukushima K, Koinuma T, Meng H, Kubo SI, Spratt S, Cui C, Yamashita C, Miki Y, Yamamoto K, Hirabayashi T, Murakami M, Takahashi Y, Shindou H, Nonaka T, Hasegawa M, Okuzumi A, Imai Y, Hattori N. Parkinson's disease-associated iPLA2-VIA/PLA2G6 regulates neuronal functions and α-synuclein stability through membrane remodeling. Proc Natl Acad Sci U S A. 2019 Oct 8;116(41):20689-20699.
- Meng H, Yamashita C, Shiba-Fukushima K, Inoshita T, Funayama M, Sato S, Hatta T, Natsume T, Umitsu M, Takagi J, Imai Y, Hattori N. Loss of Parkinson's disease-associated protein CHCHD2 affects mitochondrial crista structure and destabilizes cytochrome c. Nat Commun. 2017 Jun 7;8:15500.
- Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Li Y, Ogaki K, Ando M, Yoshino H, Tomiyama H, Nishioka K, Hasegawa K, Saiki H, Satake W, Mogushi K, Sasaki R, Kokubo Y, Kuzuhara S, Toda T, Mizuno Y, Uchiyama Y, Ohno K, Hattori N. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. Lancet Neurol. 2015 Mar;14(3):274-82.
- Hattori N, Mizuno Y. Pathogenetic mechanisms of parkin in Parkinson's disease. Lancet. 2004 Aug 21-27;364(9435):722-4.
- Shimura H, Schlossmacher MG, Hattori N, Frosch MP, Trockenbacher A, Schneider R, Mizuno Y, Kosik KS, Selkoe DJ. Ubiquitination of a new form of alpha-synuclein by parkin from human brain: implications for Parkinson's disease. Science. 2001 Jul 13;293(5528):263-9.
- Shimura H, Hattori N, Kubo Si, Mizuno Y, Asakawa S, Minoshima S, Shimizu N, Iwai K, Chiba T, Tanaka K, Suzuki T. Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase. Nat Genet. 2000 Jul;25(3):302-5.
- Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y. Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals. Ann Neurol. 1998 Dec;44(6):935-41.
- Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature. 1998 Apr 9;392(6676):605-8.
- Hattori N, Tanaka M, Ozawa T, Mizuno Y. Immunohistochemical studies on complexes I, II, III, and IV of mitochondria in Parkinson's disease. Ann Neurol.1991 Oct;30(4):563-71.
- More
Other Specific Comments
- The Commendation for Science and Technology by the Minister of Education, Culture, Sports, Science and Technology, Research Category, May 30, 2014
- Newsweek ranked the Department of Neurology in Juntendo University Hospital as the 10th best hospital in the world for neurology in 2021, the highest ranking for a Japanese hospital. Newsweek. "World’s Best Specialized Hospitals - Neurology." Newsweek, 2021 NEWSWEEK DIGITAL LLC, Nov 20, 2020,