Li Gentetsu 李元哲

… Alternative Names

李元哲リゲンテツ

LI Yuanzhe 李元哲

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Researcher Number	40549292
Other IDs
Affiliation (Current)	2025: 順天堂大学, 大学院医学研究科, 特任助教
Affiliation (based on the past Project Information) *help	2021 – 2023: 順天堂大学, 大学院医学研究科, 特任助教 2017 – 2018: 順天堂大学, 医学(系)研究科(研究院), 特任助教 2016: 順天堂大学, 医学(系)研究科(研究院), 非常勤助教 2016: 順天堂大学, 医学部 2013 – 2015: 順天堂大学, 医学(系)研究科(研究院), 助教 … More 2012: 順天堂大学, 医学(系)研究科(研究院), 研究員 2012: 順天堂大学, 医学研究科, 博士研究員 2011: 順天堂大学, 医学(系)研究科(研究院), 博士研究員 Less
Review Section/Research Field	Principal Investigator Neurology / Basic Section 51030:Pathophysiologic neuroscience-related Except Principal Investigator Neurology
Keywords	Principal Investigator パーキンソン病 / 家族性パーキンソン病 / 劣性遺伝性PD / 血族婚 / オート接合性マッピング / 次世代シーケンサー / 神経変性疾患 / 次世代シークエンサー / GBA遺伝子 / CHCHD2 / 劣性遺伝子パーキンソン病 … More Except Principal Investigator … More SNCS / 重複 / 変異 / duplication / Gene chip / 二倍体 / DNA / 遺伝子 / 認知症 / びまん性レビー小体病 / 遺伝子重複 / SNCA / alpha-synuclein / パーキンソン病 Less

パーキンソン病関連遺伝子の網羅的解析による遺伝的リスク因子の解明Principal Investigator
- Principal Investigator
  
  李元哲
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 51030:Pathophysiologic neuroscience-related
- Research Institution
  Juntendo University
Mutational analysis of the CHCHD2 gene in neurodegenerative diseasesPrincipal Investigator
- Principal Investigator
  
  Li Yuanzhe
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Juntendo University
Search for the causative gene in consanguineous families with Parkinson's diseasePrincipal Investigator
- Principal Investigator
  
  Li Yuanzhe
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neurology
- Research Institution
  Juntendo University
The detection of modifier gens in alpha-synuclein multiplications
- Principal Investigator
  
  Nishioka Kenya
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neurology
- Research Institution
  Juntendo University
Autozygosity mapping in consanguineous families with Parkinson's diseasePrincipal Investigator
- Principal Investigator
  
  LI Yuanzhe
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neurology
- Research Institution
  Juntendo University

All 2023 2022 2021 2019 2018 2017 2016 2015 2014 2013 2012 2011 Other

All Journal Article Presentation

[Journal Article] Analysis of LIN28A variants in patients with Parkinson’s disease2023
- Author(s)
  Peng Hao、Li Yuanzhe、Yoshino Hiroyo、Shimizu Mai、Nishioka Kenya、Funayama Manabu、Hattori Nobutaka
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 68 Issue: 5 Pages: 329-331
- DOI
  10.1038/s10038-022-01109-x
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-22K07542
[Journal Article] Investigation of 22q11.2 Deletion in Japanese Early‐Onset Parkinsonism2023
- Author(s)
  Ong Stephanie、Funayama Manabu、Mangyoku Yuki、Kawai Hiromichi、Yoshino Hiroyo、Li Yuanzhe、Nishioka Kenya、Hattori Nobutaka
- Journal Title
  
  Movement Disorders
  
  Volume: 39 Issue: 3 Pages: 626-627
- DOI
  10.1002/mds.29692
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07283
[Journal Article] Propagative α-synuclein seeds as serum biomarkers for synucleinopathies.2023
- Author(s)
  Ayami Okuzumi Taku Hatano Gen Matsumoto Nobutaka Hattori et al
- Journal Title
  
  Nature medicine
  
  Volume: 29 Issue: 6 Pages: 1448-1455
- DOI
  10.1038/s41591-023-02358-9
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K14785, KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-21K07424, KAKENHI-PROJECT-21K07444, KAKENHI-PUBLICLY-22H04651, KAKENHI-PROJECT-21H04820, KAKENHI-PROJECT-23K24214
[Journal Article] Generation of three hiPSC clones from a Parkinson's disease patient with a heterozygous variant of VPS35 p.D620N2022
- Author(s)
  Kei-Ichi Ishikawa, Mayu Ishiguro, Yuanzhe Li , Kenya Nishioka, Nobutaka Hattori, Wado Akamatsu
- Journal Title
  
  Stem Cell Research
  
  Volume: 60 Pages: 102739-102739
- DOI
  10.1016/j.scr.2022.102739
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-20K07873
[Journal Article] Genotype-phenotype correlation of Parkinson's disease with PRKN variants2022
- Author(s)
  Yoshino Hiroyo、Li Yuanzhe、Nishioka Kenya、Daida Kensuke、Hayashida Arisa、Ishiguro Yuta、Yamada Daisuke、Izawa Nana、Nishi Katsunori、Nishikawa Noriko、Oyama Genko、Hatano Taku、Nakamura Shinichiro、Yoritaka Asako、Motoi Yumiko、Funayama Manabu、Hattori Nobutaka
- Journal Title
  
  Neurobiology of Aging
  
  Volume: 114 Pages: 117-128
- DOI
  10.1016/j.neurobiolaging.2021.12.014
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-22K07542, KAKENHI-PROJECT-21H04820, KAKENHI-PROJECT-20K07893
[Journal Article] Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration2022
- Author(s)
  Riku Yuichi、Iwasaki Yasushi、Ishigaki Shinsuke、Akagi Akio、Hasegawa Masato、Nishioka Kenya、Li Yuanzhe、Riku Miho、Ikeuchi Takeshi、Fujioka Yusuke、Miyahara Hiroaki、Sone Jun、Hattori Nobutaka、Yoshida Mari、Katsuno Masahisa、Sobue Gen
- Journal Title
  
  Brain
  
  Volume: - Issue: 8 Pages: 2769-2784
- DOI
  10.1093/brain/awac091
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K16586, KAKENHI-PROJECT-20K16182, KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-21K15622, KAKENHI-PROJECT-22H04923, KAKENHI-PROJECT-23K21410
[Journal Article] Clinical Manifestations and Molecular Backgrounds of Parkinson's Disease Regarding Genes Identified From Familial and Population Studies2022
- Author(s)
  Nishioka Kenya、Imai Yuzuru、Yoshino Hiroyo、Li Yuanzhe、Funayama Manabu、Hattori Nobutaka
- Journal Title
  
  Frontiers in Neurology
  
  Volume: 13 Pages: 764917-764917
- DOI
  10.3389/fneur.2022.764917
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-22K07542, KAKENHI-PROJECT-21H04820, KAKENHI-PROJECT-20H03453, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-20K21531
[Journal Article] Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson’s disease.2022
- Author(s)
  Tezuka T, Taniguchi D, Sano M, Shimada T, Oji Y, Tsunemi T, Ikeda A, Li Y, Yoshino H, Ogata J, Shiba-Fukushima K, Funayama M, Nishioka K, Imai Y, Hattori N.
- Journal Title
  
  NPJ Parkinsons Dis.
  
  Volume: 8 Issue: 1 Pages: 97-97
- DOI
  10.1038/s41531-022-00367-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K07910, KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-21K07444, KAKENHI-PROJECT-22K07542, KAKENHI-PROJECT-22K15649, KAKENHI-PROJECT-20H03453, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-20K21531
[Journal Article] A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the SPG11 gene2022
- Author(s)
  Daida Kensuke、Nishioka Yosuke、Li Yuanzhe、Yoshino Hiroyo、Funayama Manabu、Hattori Nobutaka、Nishioka Kenya
- Journal Title
  
  eNeurologicalSci
  
  Volume: 26 Pages: 100391-100391
- DOI
  10.1016/j.ensci.2021.100391
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-22K07542, KAKENHI-PROJECT-21H04820
[Journal Article] A Novel LRRK2 Variant p.G2294R in the WD40 Domain Identified in Familial Parkinson’s Disease Affects LRRK2 Protein Levels2021
- Author(s)
  Ogata Jun、Hirao Kentaro、Nishioka Kenya、Hayashida Arisa、Li Yuanzhe、Yoshino Hiroyo、Shimizu Soichiro、Hattori Nobutaka、Imai Yuzuru
- Journal Title
  
  International Journal of Molecular Sciences
  
  Volume: 22 Issue: 7 Pages: 3708-3708
- DOI
  10.3390/ijms22073708
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K16929, KAKENHI-PROJECT-20H03453, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21K07283, KAKENHI-PROJECT-20K21531
[Journal Article] Genetic analysis of ATP10B for Parkinson's disease in Japan2021
- Author(s)
  Ishiguro Mayu、Yoshino Hiroyo、Li Yuanzhe、Ikeda Aya、Funayama Manabu、Nishioka Kenya、Hattori Nobutaka
- Journal Title
  
  Parkinsonism and Related Disorders
  
  Volume: 88 Pages: 10-12
- DOI
  10.1016/j.parkreldis.2021.05.020
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21K07283
[Journal Article] Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features2019
- Author(s)
  Ikeda Aya、Shimada Hitoshi、Nishioka Kenya、Takanashi Masashi、Hayashida Arisa、Li Yuanzhe、Yoshino Hiroyo、Funayama Manabu、Ueno Yuji、Hatano Taku、Sahara Naruhiko、Suhara Tetsuya、Higuchi Makoto、Hattori Nobutaka
- Journal Title
  
  Movement Disorders
  
  Volume: 34 Issue: 4 Pages: 568-574
- DOI
  10.1002/mds.27623
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-26117008, KAKENHI-PROJECT-16H05324, KAKENHI-PROJECT-16K09675, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-19K08003, KAKENHI-PUBLICLY-19H05437, KAKENHI-PROJECT-18H04043
[Journal Article] Isolated nigral degeneration without pathological protein aggregation in autopsied brains with LRRK2 p.R1441H homozygous and heterozygous mutations2018
- Author(s)
  Takanashi M, Funayama M (Contributed equally), Matsuura E, Yoshino H, Li Y, Tsuyama S, Takashima H, Nishioka K, Hattori N
- Journal Title
  
  Acta Neuropathologica Communications
  
  Volume: 6 Issue: 1 Pages: 105-105
- DOI
  10.1186/s40478-018-0617-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700
[Journal Article] Serum caffeine and metabolites are reliable biomarkers of early Parkinson disease.2018
- Author(s)
  Fujimaki M, Saiki S, Li Y, Kaga N, Taka H, Hatano T, Ishikawa KI, Oji Y, Mori A, Okuzumi A, Koinuma T, Ueno SI, Imamichi Y, Ueno T, Miura Y, Funayama M, Hattori N.
- Journal Title
  
  Neurology.
  
  Volume: 90 Issue: 5 Pages: 1-8
- DOI
  10.1212/wnl.0000000000004888
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K01834, KAKENHI-PROJECT-16K09675, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-17K07797, KAKENHI-PROJECT-15KK0354, KAKENHI-PROJECT-18K07829, KAKENHI-PROJECT-18H04043
[Journal Article] GCH1 mutations in dopa-responsive dystonia and Parkinson's disease.2018
- Author(s)
  Yoshino H, Nishioka K, Li Y, Oji Y, Oyama G, Hatano T, Machida Y, Shimo Y, Hayashida A, Ikeda A, Mogushi K, Shibagaki Y, Hosaka A, Iwanaga H, Fujitake J, Ohi T, Miyazaki D, Sekijima Y, Oki M, Kusaka H, Fujimoto KI Ugawa Y, Funayama M, Hattori N.
- Journal Title
  
  Journal of Neurology
  
  Volume: 265(8) Issue: 8 Pages: 1860-1870
- DOI
  10.1007/s00415-018-8930-8
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10552, KAKENHI-PROJECT-17K07797, KAKENHI-PROJECT-18K08798, KAKENHI-PROJECT-16K09675, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700
[Journal Article] COQ2 variants in Parkinson's disease and multiple system atrophy.2018
- Author(s)
  Mikasa M, Kanai K, Li Y, Yoshino H, Mogushi K, Hayashida A, Ikeda A, Kawajiri S, Okuma Y, Kashihara K, Sato T, Kondo H, Funayama M, Nishioka K, Hattori N.
- Journal Title
  
  J Neural Transm (Vienna)
  
  Volume: - Issue: 6 Pages: 938-944
- DOI
  10.1007/s00702-018-1885-1
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-26461319, KAKENHI-PROJECT-15KK0354, KAKENHI-PROJECT-16K10476, KAKENHI-PROJECT-16K10552, KAKENHI-PROJECT-17K09811, KAKENHI-PROJECT-17K10652, KAKENHI-PROJECT-18K08798, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-20K18340
[Journal Article] Genetic analysis of TMEM230 in Japanese patients with familial Parkinson’s disease.2018
- Author(s)
  Conedera SA, Li Y, Funayama M, Yoshino H, Nishioka K, Hattori N.
- Journal Title
  
  Parkinsonism Relat Disord
  
  Volume: 48 Pages: 107-108
- DOI
  10.1016/j.parkreldis.2017.12.020
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-15KK0354, KAKENHI-PROJECT-16K09678
[Journal Article] Dystonia due to bilateral caudate hemorrhage associated with a COL4A1 mutation.2017
- Author(s)
  Hatano T, Daida K, Hoshino Y, Li Y, Saitsu H, Matsumoto N, Hattori N.
- Journal Title
  
  Parkinsonism and Related Disorders
  
  Volume: 40 Pages: 80-82
- DOI
  10.1016/j.parkreldis.2017.04.009
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09675, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-17H01539
[Journal Article] A novel mutation of CHCHD2 p.R8H in a sporadic case of Parkinson's disease2017
- Author(s)
  Ikeda, Aya; Matsushima, Takashi; Daida, Kensuke; Nakajima, Sho; Conedera, Silvio; Li, Yuanzhe; Yoshino, Hiroyo; Oyama, Genko; Funayama, Manabu; Nishioka, Kenya; Hattori, Nobutaka
- Journal Title
  
  PARKINSONISM & RELATED DISORDERS
  
  Volume: 34 Pages: 66-68
- DOI
  10.1016/j.parkreldis.2016.10.018
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-15K19498, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-15KK0354
[Journal Article] Genotype-phenotype correlations of cysteine replacement in CADASIL2017
- Author(s)
  Matsushima, Takashi; Conedera, Silvio; Tanaka, Ryota; Li, Yuanzhe; Yoshino, Hiroyo; Funayama, Manabu; Ikeda, Aya; Hosaka, Yuka; Okuzumi, Ayame; Shimada, Yoshiaki; Yamashiro, Kazuo; Motoi, Yumiko; Nishioka, Kenya; Hattori, Nobutaka
- Journal Title
  
  NEUROBIOLOGY OF AGING
  
  Volume: 50 Pages: 169.e7-169.e14
- DOI
  10.1016/j.neurobiolaging.2016.10.026
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-16K09678
[Journal Article] Lysosomal defects in ATP13A2 and GBA associated familial Parkinson's disease.2017
- Author(s)
  Sato S, Li Y, Hattori N.
- Journal Title
  
  J Neural Transm
  
  Volume: 124 Issue: 11 Pages: 1395-1400
- DOI
  10.1007/s00702-017-1779-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-15H04842
[Journal Article] Mutation screening of PLA2G6 in Japanese patients with early onset dystonia-parkinsonism.2017
- Author(s)
  Yamashita C, Funayama M, Li Y, Yoshino H, Yamada H, Seino Y, Tomiyama H, Hattori N.
- Journal Title
  
  J Neural Transm
  
  Volume: 4 Issue: 4 Pages: 431-435
- DOI
  10.1007/s00702-016-1658-7
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-15KK0354
[Journal Article] Parkinsonism in a patient with valosin-containing protein gene mutation showing: a case report.2017
- Author(s)
  Fujimaki M, Kanai K, Funabe S, Takanashi M, Yokoyama K, Li Y, Hattori N.
- Journal Title
  
  J Neurol
  
  Volume: 264 Issue: 6 Pages: 1284-1286
- DOI
  10.1007/s00415-017-8467-2
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09700, KAKENHI-PROJECT-17K09811, KAKENHI-PROJECT-26461319
[Journal Article] Homozygous alpha-synuclein p.A53V in familial Parkinson's disease.2017
- Author(s)
  Yoshino H, Hirano M, Stoessl AJ, Imamichi Y, Ikeda A, Li Y, Funayama M, Yamada I, Nakamura Y, Sossi V, Farrer MJ, Nishioka K, Hattori N.
- Journal Title
  
  Neurobiology of Aging
  
  Volume: 57 Pages: 248.e7-248.e12
- DOI
  10.1016/j.neurobiolaging.2017.05.022
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700
[Journal Article] <i>CSF1R</i> Mutation p.G589R and the Distribution Pattern of Brain Calcification2017
- Author(s)
  Daida K, Nishioka K, Li Y, Nakajima S, Tanaka R, Hattori N.
- Journal Title
  
  Intern. Med.
  
  Volume: 56 Issue: 18 Pages: 2507-2512
- DOI
  10.2169/internalmedicine.8462-16
- NAID
  130006078597
- ISSN
  0918-2918, 1349-7235
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-16K09700
[Journal Article] Involvement of the caudate nucleus head and its networks in sporadic amyotrophic lateral sclerosis-frontotemporal dementia continuum.2016
- Author(s)
  Masuda, M., Senda, J., Watanabe, H., Epifanio, B., Tanaka, Y., Imai, K., Riku, Y., Li, Y., Nakamura, R., Ito, M., Ishigaki, S., Atsuta, N., Koike, H., Katsuno, M., Hattori, N., Naganawa, S., and Sobue, G.
- Journal Title
  
  Amyotroph Lateral Scler Frontotemporal Degener
  
  Volume: 17 Issue: 7-8 Pages: 571-579
- DOI
  10.1080/21678421.2016.1211151
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-26117002, KAKENHI-PROJECT-25293263, KAKENHI-PROJECT-15K15338, KAKENHI-PROJECT-15K19485, KAKENHI-PROJECT-16K09700, KAKENHI-ORGANIZER-26117001
[Journal Article] Schizophrenia as a prodromal symptom in a patient harboring SNCA duplication.2016
- Author(s)
  Takamura S, Ikeda A, Nishioka K, Furuya H, Tashiro M, Matsushima T, Li Y, Yoshino H, Funayama M, Morinobu S, Hattori N.
- Journal Title
  
  Parkinsonism Relat Disord.
  
  Volume: S1353-8020 Pages: 30028-1
- DOI
  10.1016/j.parkreldis.2016.01.028
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-26461311, KAKENHI-PROJECT-15KK0354
[Journal Article] FBXO7 mutations in Parkinson's disease and multiple system atrophy.2016
- Author(s)
  Conedera S, Apaydin H, Li Y, et al.
- Journal Title
  
  Neurobiol Aging.
  
  Volume: 40 Pages: 192.e1-192.e5
- DOI
  10.1016/j.neurobiolaging.2016.01.003
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25860726, KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-16K09676, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-15KK0354
[Journal Article] A family with hereditary diffuse leukoencephalopathy with spheroids caused by a novel c.2442+2T>C mutation in the CSF1R gene.2016
- Author(s)
  Kawakami I, Iseki E, Kasanuki K, Minegishi M, Sato K, Hino H, Shibuya K, Fujisawa K, Higashi S, Akiyama H, Furuta A, Takanashi M, Li Y, Hattori N, Mitsuyama Y, Arai H.
- Journal Title
  
  Journal of Neuroogicall Science
  
  Volume: 15;367 Pages: 349-55
- DOI
  10.1016/j.jns.2016.06.013
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K19757, KAKENHI-PROJECT-15K09822, KAKENHI-PROJECT-16K09700
[Journal Article] Absence of Lewy pathology associated with PINK1 homozygous mutation.2016
- Author(s)
  Takanashi M, Li Y, Hattori N.
- Journal Title
  
  Neurology.
  
  Volume: 86 Issue: 23 Pages: 2212-2213
- DOI
  10.1212/wnl.0000000000002744
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-16K09700
[Journal Article] Fibromyalgia syndrome and cognitive dysfunction in elderly: a case series.2016
- Author(s)
  Nishioka K, Hayashi T, Suzuki M, et al.
- Journal Title
  
  Int J Rheum Dis.
  
  Volume: 19 Issue: 1 Pages: 21-29
- DOI
  10.1111/1756-185x.12734
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-25860725
[Journal Article] CHCHD2 mutations in autosomal dominant late-onset Parkinson’s disease: a genome-wide linkage and sequencing study.2015
- Author(s)
  Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Yuanzhe L, Ogaki K, Ando M, Yoshinon 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.
- Journal Title
  
  Lancet Neurol
  
  Volume: 14 Issue: 3 Pages: 274-282
- DOI
  10.1016/s1474-4422(14)70266-2
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-24390224, KAKENHI-PROJECT-24500868, KAKENHI-PROJECT-24790903, KAKENHI-PUBLICLY-25110720, KAKENHI-ORGANIZER-25111001, KAKENHI-PLANNED-25111007, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-26870175, KAKENHI-PROJECT-15K10050, KAKENHI-ORGANIZER-23111001, KAKENHI-PLANNED-23111003, KAKENHI-PLANNED-23111004, KAKENHI-PROJECT-25257507, KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-25305030
[Journal Article] High frequency of beta-propeller protein-associated neurodegeneration (BPAN) among patients with intellectual disability and young-onset parkinsonism.2015
- Author(s)
  Nishioka K, Oyama G, Yoshino H, Li Y, Matsushima T, Takeuchi C, Mochizuki Y, Mori-Yoshimura M, Murata M, Yamasita C, Nakamura N, Konishi Y, Ohi K, Ichikawa K, Terada T, Obi T, Funayama M, Saiki S, Hattori N.
- Journal Title
  
  Neurobiol Aging.
  
  Volume: S0197 Issue: 5 Pages: 54-58
- DOI
  10.1016/j.neurobiolaging.2015.01.020
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-ORGANIZER-25111001, KAKENHI-PLANNED-25111007, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-15K19498, KAKENHI-PROJECT-15H04842
[Journal Article] EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population2014
- Author(s)
  Nishioka K, Funayama M, Vilarino-GuellC, Ogaki K, Li Y, Sasaki R, Kokubo Y, Kuzuhara S, Kachergus JM, Cobb SA, Takahashi H, Mizuno Y, Farrer MJ, Ross OA, Hattori N
- Journal Title
  
  Parkinsonism Relat Disord.
  
  Volume: 20 Issue: 6 Pages: 659-61
- DOI
  10.1016/j.parkreldis.2014.03.004
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25257507, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726
[Journal Article] P150glued-associated disorders are caused by activation of intrinsic apoptotic pathway.2014
- Author(s)
  Ishikawa K, Saiki S, Furuya N, Yamada D, Imamichi Y, Li Y, Kawajiri S, Sasaki H, Koike M, Tsuboi Y, Hattori N.
- Journal Title
  
  PLoS One.
  
  Volume: 9 Issue: 4 Pages: e94645-e94645
- DOI
  10.1371/journal.pone.0094645
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-ORGANIZER-25111001, KAKENHI-PLANNED-25111007, KAKENHI-PROJECT-25460276, KAKENHI-PROJECT-25860725, KAKENHI-PUBLICLY-26111519
[Journal Article] The evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease.2014
- Author(s)
  Yamashita C, Tomiyama H, Funayama M, Inamizu S, Ando M, Li Y, Yoshino H, Araki T, Ichikawa T, Ehara Y, Ishikawa K, Mizusawa H, Hattori N.
- Journal Title
  
  Neurobiol Aging.
  
  Volume: 35 Issue: 7 Pages: 1779.e17-1779.e21
- DOI
  10.1016/j.neurobiolaging.2014.01.022
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-25129703, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25860725
[Journal Article] Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease.2014
- Author(s)
  Li Y, Sekine T, Funayama M, Li L, Yoshino H, Nishioka K, Tomiyama H, Hattori N
- Journal Title
  
  Neurobiol Aging.
  
  Volume: 35 Issue: 4 Pages: 935.e3-935.e8
- DOI
  10.1016/j.neurobiolaging.2013.09.019
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390224, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726
[Journal Article] Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, andCBS2013
- Author(s)
  Ogaki K
- Journal Title
  
  Parkinsonism & Related Disorders
  
  Volume: 19 Issue: 1 Pages: 15-20
- DOI
  10.1016/j.parkreldis.2012.06.019
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23240050, KAKENHI-PROJECT-23791003, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PUBLICLY-23110526, KAKENHI-PUBLICLY-23129506
[Journal Article] VPS35 Mutation in Japanese Patients with Typical Parkinson’s Disease2013
- Author(s)
  Ando　M, Kokubo Y.
- Journal Title
  
  Movement Disorders
  
  Volume: 15;27(11) Issue: 11 Pages: 175-182
- DOI
  10.1002/mds.25145
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21256005, KAKENHI-PROJECT-23700389, KAKENHI-PROJECT-23791003, KAKENHI-PROJECT-24390224, KAKENHI-PUBLICLY-23129506
[Journal Article] A TREX1 mutation causing cerebral vasculopathy in a patient with familial chilblain lupus.2013
- Author(s)
  Yamashiro K, Tanaka R, Li Y, Mikasa M, Hattori N.
- Journal Title
  
  J Neurol
  
  Volume: 260 Issue: 10 Pages: 2653-2655
- DOI
  10.1007/s00415-013-7084-y
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860725
[Journal Article] Pseudo-heterozygous rearrangement mutation of parkin2012
- Author(s)
  Fumayama M, et al
- Journal Title
  
  Movement Disorders
  
  Volume: vol.27 Issue: 4 Pages: 552-555
- DOI
  10.1002/mds.24906
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22790829, KAKENHI-PROJECT-23791003, KAKENHI-PUBLICLY-23129506
[Journal Article] Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis2012
- Author(s)
  Ogaki K, Li Y, Atsuta N, Tomiyama H, Funayama M, Watanabe H, Nakamura R, Yoshino H, Yato S, Tamura A, Naito Y, Taniguchi A, Fujita K, Izumi Y, Kaji R, Hattori N, Sobue G
- Journal Title
  
  Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis
  
  Volume: 33 Issue: 10 Pages: 2527.e11-2527.e16
- DOI
  10.1016/j.neurobiolaging.2012.05.011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23659458, KAKENHI-PROJECT-23791003, KAKENHI-PUBLICLY-23129506
[Journal Article] PLA2G6 variant in Parkinson's disease2011
- Author(s)
  Tomiyama H, Kokubo Y, Kuzuhara S
- Journal Title
  
  J Hum Genet
  
  Volume: 56(5) Issue: 5 Pages: 401-403
- DOI
  10.1038/jhg.2011.22
- NAID
  10030659472
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21256005, KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-23791003
[Journal Article] Prevalence of GJB2 causing recessive profound non-syndromic deafness in Japanese children2011
- Author(s)
  Hayashi C, Funayama M, Li Y, Kamiya K, Kawano A, Suzuki M, Hattori N, Ikeda K
- Journal Title
  
  Int J Pediatr Otorhinolaryngol
  
  Volume: 75(2) Issue: 2 Pages: 211-4
- DOI
  10.1016/j.ijporl.2010.11.001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791003
[Journal Article] Visual grasping in frontotemporal dementia and parkinsonism linked to chromosome 17 (microtubule-associated with protein tau) : a comparison of N-Isopropyl-p-[(123)I]-iodoamphetamine brain perfusion single photon emission computed tomography analysis with progressive supranuclear palsy2011
- Author(s)
  Ogaki K
- Journal Title
  
  Mov Disord
  
  Volume: 26(3) Issue: 3 Pages: 561-3
- DOI
  10.1002/mds.23461
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390272, KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-23791003
[Presentation] Genetic screening by targeted gene panel of the GBA1 gene in Parkinson’s disease.2023
- Author(s)
  李元哲
- Organizer
  第64回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-21K07283
[Presentation] Genetic screening by panel sequencing of the GBA gene in Parkinson’s disease2022
- Author(s)
  李元哲
- Organizer
  第63回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-21K07283
[Presentation] Genetic screening by panel sequencing of glucosylceramidase beta variants for Parkinson’s disease2021
- Author(s)
  李元哲
- Organizer
  第62回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-21K07283
[Presentation] パーキンソン病においてパネル解析によるGBA遺伝子変異のスクリにニング2021
- Author(s)
  李元哲
- Organizer
  日本人類遺伝学会第66回大会
- Data Source
  KAKENHI-PROJECT-21K07283
[Presentation] パーキンソン病における次世代シークエンサによる遺伝子解析2017
- Author(s)
  李元哲、吉野浩代、Silvio Conedera、舩山学、西岡健弥、服部信孝.
- Organizer
  日本人類遺伝学会第62回大会
- Data Source
  KAKENHI-PROJECT-16K09700
[Presentation] Analysis of GCH1 mutations in the patients with Parkinson’s disease in Japanese population2016
- Author(s)
  Hiroyo Yoshino, Kenya Nishioka, Aya Ikeda, Takashi Matsushima, Mitsuaki Oki, Daigo Miyazaki, Yoshiki Sekijima, Ai Hosaka, Takekazu Ohi, Hiroshi Iwanaga, Yuanzhe Li, Manabu Funayama, Nobutaka Hattori
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  神戸ポートピアホテル
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] Schizophrenia as a prodromal symptom in a patient harboring SNCA duplication2016
- Author(s)
  Silvio Conedera, Aya Ikeda, Kenya Nishioka, Shogo Takamura, Takashi Matsushima, Yuanzhe Li, Hiroyo Yoshino, Manabu Funayama, Shigeru Morinobu, Nobutaka Hattori
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  神戸ポートピアホテル
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] The analyze of four pedigrees with MAPT N279K mutation accompanying DAT scan and Tau imaging2016
- Author(s)
  Aya Ikeda (Manabe), Kenya Nishioka, Yuanzhe Li, Hiroyo Yoshino, Manabu Funayama, Takashi Matsushima, Shinichi Ueno, Naohide Kurita, Hitoshi Shimada, Naruhiko Sahara, Makoto Higuchi, Tetsuya Suhara, Yuji Ueno, Masashi Takanashi, Yumiko Motoi, Nobutaka Hattori
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  神戸ポートピアホテル
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] The comprehensive study of four pedigrees harboring MAPT N279K; genetics, pathology, and neuroimaging; DAT-scan and [¹¹C]PBB3 PET.2015
- Author(s)
  Kenya Nishioka, Aya Ikeda, Li Yuanzhe, et al.
- Organizer
  GEOPD
- Place of Presentation
  東京
- Year and Date
  2015-10-01
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] The Comprehensive study of genetics of Parkinson’s disease2015
- Author(s)
  Kenya Nishioka, Hiroyo Yoshino, Yuanzher Li et al.
- Organizer
  56th Annual Meeting of the Japanese Society of Neurology
- Place of Presentation
  新潟
- Year and Date
  2015-05-20
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] GBA遺伝子変異を伴う家族性パーキンソン病の臨床遺伝学的検討2014
- Author(s)
  李元哲
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡国際会議場
- Year and Date
  2014-05-21
- Data Source
  KAKENHI-PROJECT-25860725
[Presentation] 日本人若年性パーキンソン病におけるFBXO7遺伝子変異解析2012
- Author(s)
  李元哲
- Organizer
  第53回日本神経学会学術大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23791003
[Presentation] Genetic analysis of the GBA gene in Japanese familial Parkinson’s disease.2012
- Author(s)
  Li Y
- Organizer
  ASHG 2012 Annual Meeting
- Place of Presentation
  San Francisco, US.
- Data Source
  KAKENHI-PROJECT-23791003
[Presentation] Analysis of the FBXO7 gene in early-onset parkinsonism.2011
- Author(s)
  Yuanzhe Li
- Organizer
  国際人類遺伝学会第12回大会
- Place of Presentation
  カナダ・モントリオール
- Data Source
  KAKENHI-PROJECT-23791003
[Presentation] 血族婚のあるパーキンソン病におけるオート接合性マッピンクの検討（続報）2011
- Author(s)
  李元哲
- Organizer
  第５２回神経学会総会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-23791003
[Presentation] パーキンソン病の家族歴を有する多系統萎縮症患者におけるCOQ2変異解析
- Author(s)
  三笠道太、金井数明、李元哲、西岡健弥、舩山学、富山弘幸、服部信孝
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  福岡国際会議場
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] High frequency of WDR45 mutation in Japanese patients with beta- propeller protein-associated neurodegeneration (BPAN)
- Author(s)
  Nishioka K, Oyama G, Yoshino H, Li Y, Matsushima T, Takeuchi C, Mochizuki Y, Mori-Yoshimura M, Murata M, Yamasita C, Nakamura N, Konishi Y, Ohi K, Ichikawa K, Terada T, Obi T, Funayama M, Saiki S, Hattori N.
- Organizer
  9th Annual Genetics Epidemiology of Parkinson's Disease Consortium
- Place of Presentation
  Vancouver, British Columbia
- Year and Date
  2014-09-10 – 2014-09-13
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] 異染性白質ジストロフィー患者の家族に発症したパーキンソン病２症例の検討
- Author(s)
  金井数明、李元哲、中谷光良、藤巻基紀、舩山学、西岡健弥、服部信孝
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  福岡国際会議場
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] 日本人パーキンソン病患者におけるαシヌクレイン遺伝子新規変異の解析
- Author(s)
  吉野浩代、西岡健弥、李元哲、舩山学、服部信孝
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  福岡国際会議場
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] 日本人パーキンソン病におけるEIF4G1遺伝子変異の頻度
- Author(s)
  舩山学、西岡健弥、大垣光太郎、李元哲、佐々木良元、小久保康昌、葛原茂樹、高橋裕秀、富山弘幸、水野美邦、服部信孝
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  福岡国際会議場
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] GBA遺伝子変異を伴う家族性パーキンソン病の臨床遺伝学的検討
- Author(s)
  李元哲、舩山学、李林、吉野浩代、西岡健弥、富山弘幸、服部信孝
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  福岡国際会議場
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] 認知症と全身に広がる慢性疼痛を合併した症例の解析
- Author(s)
  林徹生、西岡健弥、鈴木通真、李元哲、本井ゆみ子、井関雅子、西岡久寿樹、服部信孝
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  福岡国際会議場
- Year and Date
  2014-05-21 – 2014-05-24
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] GBA遺伝子変異を伴う家族性パーキンソン病の臨床遺伝学的検討
- Author(s)
  李元哲
- Organizer
  第55回日本神経学会学術大会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-25860725

1. Nishioka Kenya (40348933)

# of Collaborated Projects: 1 results

# of Collaborated Products: 16 results
2. HATTORI Nobutaka (80218510)

# of Collaborated Projects: 1 results

# of Collaborated Products: 18 results
3. MANABU Funayama (70468578)

# of Collaborated Projects: 1 results

# of Collaborated Products: 16 results
4. TODA Tatsushi (30262025)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
5. IKEDA aya

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. Farrer Matthew J

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. Ross Owen A.

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. Kruger Rejko Kruger

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. WATANABE Hirohisa

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
10. ITO kengo

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. KATSUNO masahisa

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
12. ATSUTA naoki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
13. TANABE hiroki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
14. HATANO Taku

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
15. Higuchi Makoto

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
16. SATAKE Wataru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
17. TAKA Hikari

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. KAGA Naoko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
19. MOGUSHI Kaoru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
20. KAHORI Shiba

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
21. 祖父江元

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
22. 小久保康昌

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
23. 葛原茂樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 佐原成彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 緒方洵

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 秋山治彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 河上緒

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 梶龍兒

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. 陸雄一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
30. 奥住文美

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Li Gentetsu 李 元哲

李 元哲 リ ゲンテツ

LI Yuanzhe 李 元哲

Research Projects

Research Products

Co-Researchers

パーキンソン病関連遺伝子の網羅的解析による遺伝的リスク因子の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Mutational analysis of the CHCHD2 gene in neurodegenerative diseasesPrincipal Investigator

Principal Investigator

Project Period (FY)

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Research Field

Research Institution

Search for the causative gene in consanguineous families with Parkinson's diseasePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The detection of modifier gens in alpha-synuclein multiplications

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Autozygosity mapping in consanguineous families with Parkinson's diseasePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Analysis of LIN28A variants in patients with Parkinson’s disease2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Investigation of 22q11.2 Deletion in Japanese Early‐Onset Parkinsonism2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Propagative α-synuclein seeds as serum biomarkers for synucleinopathies.2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Generation of three hiPSC clones from a Parkinson's disease patient with a heterozygous variant of VPS35 p.D620N2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Genotype-phenotype correlation of Parkinson's disease with PRKN variants2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Clinical Manifestations and Molecular Backgrounds of Parkinson's Disease Regarding Genes Identified From Familial and Population Studies2022

Author(s)

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[Journal Article] Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson’s disease.2022

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[Journal Article] A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the SPG11 gene2022

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Li Gentetsu 李元哲

李元哲リゲンテツ

LI Yuanzhe 李元哲