Nisioka Kenya 西岡健弥

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Nishioka Kenya 西岡健弥

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Researcher Number	40348933
Other IDs
Affiliation (Current)	2025: 順天堂大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2022: 順天堂大学, 医学部, 先任准教授 2020 – 2022: 順天堂大学, 医学部, 准教授 2013 – 2018: 順天堂大学, 医学部, 准教授 2016: 順天堂大学, 脳神経内科, 准教授
Review Section/Research Field	Principal Investigator Neurology / Basic Section 52020:Neurology-related Except Principal Investigator General internal medicine(including psychosomatic medicine)
Keywords	Principal Investigator 遺伝子 / パーキンソン病 / 次世代シーケンサー / 遺伝子変異 / 全エクソームシーケンス / 全ゲノムシーケンス / 臨床遺伝学 / 家族性パーキンソン病 / Whole exome sequencing / Long read sequencing … More / Whole genome sequencing / Parkinson's disease / 神経変性疾患 / SNCS / 重複 / 変異 / duplication / Gene chip / 二倍体 / DNA / 認知症 / びまん性レビー小体病 / 遺伝子重複 / SNCA / alpha-synuclein … More Except Principal Investigator レビー小体型認知症 / 皮質基底核変性症 / 非流暢性失語 / 意味性認知症 / 髄液マーカー / 脳血流シンチ / ドパーミントランスポーターシンチグラフィ / 進行性失語症 / 皮質基底核症候群 / アルツハイマー病 Less

Aim to identify a novel gene related to familial Parkinson's diseasePrincipal Investigator
- Principal Investigator
  
  Nishioka Kenya
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Juntendo University
Aim to detect a novel pathogenic mutation in a familial Parkinson's diseasePrincipal Investigator
- Principal Investigator
  
  Nishioka Kenya
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Juntendo University
Clinical Analysis of Neurodegenerative Dementia Using Cerebrospinal Fluid Biomarkers
- Principal Investigator
  
  Yumiko Motoi
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  General internal medicine(including psychosomatic medicine)
- Research Institution
  Juntendo University
The detection of modifier gens in alpha-synuclein multiplicationsPrincipal Investigator
- 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

All 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 Other

All Journal Article Presentation Book

[Book] II. 病因　1. 関連遺伝子　(11) VPS13C パーキンソン病（第２版）　基礎・臨床研究のアップデート2018
- Author(s)
  林田有紗、西岡　健弥、服部信孝
- Total Pages
  5
- Publisher
  日本臨床社
- Data Source
  KAKENHI-PROJECT-16K09678
[Book] Parkinson病のゲノム医療2017
- Author(s)
  西岡健弥　李元哲　吉野浩代　服部信孝
- Publisher
  科学評論社
- ISBN
- Data Source
  KAKENHI-PROJECT-16K09678
[Book] 第17番染色体に連鎖するパーキソニズムを伴う前側頭葉型認知症（FTDP-17）2016
- Author(s)
  西岡健弥，池田彩，服部信孝
- Total Pages
  6
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-16K09678
[Book] 第17番染色体に連鎖するパーキソニズムを伴う前側頭葉型認知症（FTDP-17）2016
- Author(s)
  西岡健弥，池田彩，服部信孝
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-25860726
[Book] 家族性パーキンソン病　update annual review 20162016
- Author(s)
  松島隆史、西岡健弥、服部信孝
- Total Pages
  9
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-16K09678
[Book] 家族性パーキンソン病　update annual review 20162016
- Author(s)
  松島隆史、西岡健弥、服部信孝
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-25860726
[Book] 痛みのScience and Practice2015
- Author(s)
  西岡健弥　服部信孝
- Publisher
  文光堂
- Data Source
  KAKENHI-PROJECT-25860726
[Book] 神経症候群（第２版）（II）ーその他の神経疾患を含めてー2014
- Author(s)
  西岡健弥　服部信孝
- Publisher
  日本臨床社
- Data Source
  KAKENHI-PROJECT-25860726
[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] 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] 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] 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] 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] 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] α-Synuclein V15A variant in familial Parkinson's disease exhibits a weaker lipid-binding property.2022
- Author(s)
  Daida K, Shimonaka S, Shiba-Fukushima K, Ogata J, Yoshino H, Okuzumi A, Hatano T, Motoi Y, Hirunagi T, Katsuno M, Shindou H, Funayama M, Nishioka K, Hattori N, Imai Y.
- Journal Title
  
  Mov Disord.
  
  Volume: 37 Issue: 10 Pages: 2075-2085
- DOI
  10.1002/mds.29162
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K07910, KAKENHI-PROJECT-21K07424, KAKENHI-PROJECT-22K07542, KAKENHI-PROJECT-20K16160, KAKENHI-PROJECT-22K15649, KAKENHI-PROJECT-21H04820, KAKENHI-PROJECT-20H03453, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-20K21531, KAKENHI-PROJECT-21K19443
[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] PLA2G6 variants associated with the number of affected alleles in Parkinson’s disease in Japan2021
- Author(s)
  Daida Kensuke、Nishioka Kenya、Li Yuanzhe、Yoshino Hiroyo、Shimada Tomoyo、Dougu Nobuhiro、et al.
- Journal Title
  
  Neurobiology of Aging
  
  Volume: 97 Pages: 1-9
- DOI
  10.1016/j.neurobiolaging.2020.07.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21H04820
[Journal Article] Clinical manifestations of Parkinson's disease harboring VPS35 retromer complex component p.D620N with long-term follow-up2021
- Author(s)
  Ishiguro Mayu、Li Yuanzhe、Yoshino Hiroyo、Daida Kensuke、Ishiguro Yuta、Oyama Genko、Saiki Shinji、Funayama Manabu、Hattori Nobutaka、Nishioka Kenya
- Journal Title
  
  Parkinsonism & Related Disorders
  
  Volume: 84 Pages: 139-143
- DOI
  10.1016/j.parkreldis.2021.02.014
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-18H04043, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-21H04820
[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] The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK12021
- Author(s)
  Hayashida Arisa、Li Yuanzhe、Yoshino Hiroyo、Daida Kensuke、Ikeda Aya、et al.
- Journal Title
  
  Neurobiology of Aging
  
  Volume: 97 Pages: 3301-3301
- DOI
  10.1016/j.neurobiolaging.2020.06.017
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-19K17047, KAKENHI-PROJECT-18H04043, KAKENHI-PROJECT-18K15376, KAKENHI-PROJECT-18H02743, KAKENHI-PROJECT-21H04820
[Journal Article] Meta-iodobenzylguanidine myocardial scintigraphy in Perry disease2021
- Author(s)
  Mishima T, Fujioka S, Nishioka K, Li Y, Sato K, Houzen H, Yabe I, Shiomi K, Eriguchi M, Hara H, Hattori N, Tsuboi Y.
- Journal Title
  
  Parkinsonism and related disorders
  
  Volume: In press Pages: 49-53
- DOI
  10.1016/j.parkreldis.2020.12.017
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-18K15471, KAKENHI-PROJECT-20K07890
[Journal Article] Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan2020
- Author(s)
  Li Y、Ikeda A、Yoshino H、Oyama G、Kitani M、Daida K、Hayashida A、Ogaki K、Yoshida K、Kimura T、Nakayama Y、Ito H、Sugeno N、Aoki M、Miyajima H、Kimura K、Ueda N、Watanabe M、Urabe T、Takanashi M、Funayama M、Nishioka K、Hattori N
- Journal Title
  
  Journal of Human Genetics
  
  Volume: ー Issue: 9 Pages: 771-781
- DOI
  10.1038/s10038-020-0772-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K14966, KAKENHI-PROJECT-20K07862, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-19K17047
[Journal Article] Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease2020
- Author(s)
  Daida Kensuke、Funayama Manabu、Li Yuanzhe、Yoshino Hiroyo、Hayashida Arisa、Ikeda Aya、Ogaki Kotaro、Nishioka Kenya、Hattori Nobutaka
- Journal Title
  
  Frontiers in Neurology
  
  Volume: 11 Pages: 576465-576465
- DOI
  10.3389/fneur.2020.576465
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-19K17047, KAKENHI-PROJECT-18H04043
[Journal Article] A novel rare variant of LRRK2 associated with familial Parkinson's disease: p.R1501W2020
- Author(s)
  Masuzugawa S, Nishioka K, Imai Y, Ogata J, Shojima Y, Li Y, Yoshino H, Hattori N.
- Journal Title
  
  Parkinsonism and Related Disorders.
  
  Volume: 76 Pages: 46-48
- DOI
  10.1016/j.parkreldis.2020.05.035
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-17H04049
[Journal Article] Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy2020
- Author(s)
  Lin Chin-Hsien、Tsai Pei-I、Lin Han-Yi、Hattori Nobutaka、Funayama Manabu、Jeon Beomseok、et al.
- Journal Title
  
  Brain
  
  Volume: 143 Issue: 11 Pages: 3352-3373
- DOI
  10.1093/brain/awaa279
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08003, KAKENHI-PROJECT-20K07893
[Journal Article] Pathological findings in a patient with alpha-synuclein p.A53T and familial Parkinson's disease2020
- Author(s)
  Nishioka K, Hashizume Y, Takanashi M, Daida K, Li Y, Yoshino H, Tambasco N, Prontera P, Hattori Y, Ueda A, Watanabe H, Hattori N.
- Journal Title
  
  Parkinsonism and related disorders
  
  Volume: In press Pages: 183-187
- DOI
  10.1016/j.parkreldis.2020.11.001
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K07893, KAKENHI-PROJECT-18H04043
[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] Tau aggregation and seeding analyses of two novel MAPT variants found in patients with motor neuron disease and progressive parkinsonism.2019
- Author(s)
  Nakayama S, Shimonaka S, Elahi M, Nishioka K, Oji Y, Matsumoto SE, Li Y, Yoshino H, Mogushi K, Hatano T, Sato T, Ikura T, Ito N, Motoi Y, Hattori N.
- Journal Title
  
  Neurobiology of Aging
  
  Volume: 19 Pages: 240.e13-240.e22
- DOI
  10.1016/j.neurobiolaging.2019.02.016
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-18K06198
[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] 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] Association between abnormal nocturnal blood pressure profile and dementia in Parkinson's disease.2018
- Author(s)
  Tanaka R, Shimo Y, Yamashiro K, Ogawa T, Nishioka K, Oyama G, Umemura A, Hattori N.
- Journal Title
  
  Parkinsonism and Related Disorders
  
  Volume: 46 Pages: 24-29
- DOI
  10.1016/j.parkreldis.2017.10.014
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-15K09359
[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] Marked reduction in striatal dopamine transporter uptake during the early stage of motor symptoms in patients with the MAPT N279K mutation2018
- Author(s)
  Takeshige H, Nakayama S, Nishioka K, Li Y, Motoi Y, Hattori N.
- Journal Title
  
  Internal Medicine
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09678
[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] <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] 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] 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] DNAJC12 and dopa-responsive nonprogressive parkinsonism.2017
- Author(s)
  Straniero L, Guella I, Cilia R, Parkkinen L, Rimoldi V, Young A, Asselta R, Sold, G, Sossi V, Stoessl AJ, Priori A, Nishioka K, Hattori N, Follett J, Rajput A, Blau N, Pezzoli G, Farrer MJ, Goldwurm S, Rajput AH, Duga S.
- Journal Title
  
  Annals of Neurology
  
  Volume: 82 Issue: 4 Pages: 640-646
- DOI
  10.1002/ana.25048
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09678
[Journal Article] Anterior opercular syndrome induced by Epstein-Barr virus encephalitis.2016
- Author(s)
  Matsushima T, Nishioka K, Tanaka R, et al.
- Journal Title
  
  Neurocase.
  
  Volume: 22 Issue: 1 Pages: 103-108
- DOI
  10.1080/13554794.2015.1051054
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726
[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] 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] Genetic association between RAGE polymorphisms and Alzheimer's disease and Lewy body dementias in a Japanese cohort: a case-control study.2016
- Author(s)
  Takeshita Y, Shibata N, Kasanuki K, Nagata T, Shinagawa S, Kobayashi N, Ohnuma T, Suzuki A, Kawai E, Takayama T, Nishioka K, Motoi Y, Hattori N, Nakayama K, Yamada H, Arai H.
- Journal Title
  
  International Journal of Geriatric Psychiatry
  
  Volume: 4 Issue: 12 Pages: 1241-1246
- DOI
  10.1002/gps.4600
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-16K09678, KAKENHI-PROJECT-26860946
[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] Genetic Association between Presenilin 2 Polymorphisms and Alzheimer's Disease and Dementia of Lewy Body Type in a Japanese Population.2016
- Author(s)
  Suzuki A, Shibata N, Kasanuki K, et al.
- Journal Title
  
  Dement Geriatr Cogn Dis Extra.
  
  Volume: 16 Issue: 1 Pages: 90-97
- DOI
  10.1159/000444080
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-26860946, KAKENHI-PROJECT-16K09678
[Journal Article] Anterior opercular syndrome induced by Epstein-Barr virus encephalitis.2015
- Author(s)
  Matsushima T, Nishioka K, Tanaka R, Yokoyama K, Hattori N.
- Journal Title
  
  Neurocase
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726
[Journal Article] Beneficial therapeutic effects of spinal cord stimulation in advanced cases of Parkinson’s disease with intractable chronic pain: results of a case series2015
- Author(s)
  Nishioka K. Nakajima M.
- Journal Title
  
  Neuromodulation
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726
[Journal Article] Beneficial Therapeutic Effects of Spinal Cord Stimulation in Advanced Cases of Parkinson's Disease With Intractable Chronic Pain: A Case Series.2015
- Author(s)
  Nishioka K, Nakajima M.
- Journal Title
  
  Neuromodulation.
  
  Volume: 18 Issue: 8 Pages: 751-753
- DOI
  10.1111/ner.12315
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726
[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] An epidemiologic internet survey of fibromyalgia and chronic pain in Japan.2014
- Author(s)
  Nakamura I, Nishioka K, Usui C, Osada K, Ichibayashi H, Ishida M, Turk DC, Matsumoto Y, Nishioka K.
- Journal Title
  
  Arthritis Care and Research
  
  Volume: 66(7) Issue: 7 Pages: 1093-1101
- DOI
  10.1002/acr.22277
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726
[Journal Article] Cerebral dural sinus thrombosis associated with adenomyosis: a case report.2014
- Author(s)
  Nishioka K et al.
- Journal Title
  
  Journal of stroke and cerebrovascular diseases
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726
[Journal Article] Quantitative evaluation of electroconvulsive therapy for Parkinson’s disease with refractory psychiatric symptoms.2014
- Author(s)
  Nishioka K, Tanaka R, Shimura H, Hirano K, Hatano T, Miyakawa K, Arai H, Hattori N, Urabe T.
- Journal Title
  
  Journal of Neural Transmission
  
  Volume: 121 Issue: 11 Pages: 1405-1410
- DOI
  10.1007/s00702-014-1212-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461290, KAKENHI-PROJECT-25860726
[Journal Article] Quantitative evaluation of electroconvulsive therapy for Parkinson's disease with refractory psychiatric symptoms.2014
- Author(s)
  Nishioka K et al.
- Journal Title
  
  Journal of neural transmissoin
  
  Volume: in press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] Two novel variants in CHCHD2 associate with TDP-43 pathology among amyotrophic lateral sclerosis2022
- Author(s)
  Aya Ikeda, Manabu Funayama, Mari Yoshida, Kenya Nishioka, et al.
- Organizer
  第63会日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-20K07893
[Presentation] SNCA p.V15A a novel pathogenic variant for familial Parkinson’s disease2022
- Author(s)
  Kensuke Daida, Shotaro Shimonaka, Kahori Shiba-Fukushima, Jun Ogata, Hiroyo Yoshino, Ayami Okuzumi, Taku Hatano, Yumiko Motoi, Manabu Funayama, Tomoki Hirunagi, Kentaro Sahashi,　Masao Katsuno, Kenya Nishioka, Yuzuru Imai, Nobutaka Hattori
- Organizer
  第６３回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-20K07893
[Presentation] Two novel variants in CHCHD2 associate with TDP-43 pathology among amyotrophic lateral sclerosis2022
- Author(s)
  Aya Ikeda, Manabu Funayama, Mari Yoshida, Kenya Nishioka et al.
- Organizer
  第６３回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-20K07893
[Presentation] 白質脳症の画像を呈する患者群へのNOTCH3, HTRA1遺伝子変異の解析2022
- Author(s)
  西岡健弥　李元哲　吉野浩代　服部信孝
- Organizer
  Stroke 2022
- Data Source
  KAKENHI-PROJECT-20K07893
[Presentation] SNCA p.V15A a novel pathogenic variant for familial Parkinson’s disease2022
- Author(s)
  Kensuke Daida , Shotaro Shimonaka , Kahori Shiba-Fukushima , Jun Ogata , Hiroyo Yoshino , Ayami Okuzumi, Taku Hatano, Yumiko Motoi, Manabu Funayama, Tomoki Hirunagi, Kentaro Sahashi , Masao Katsuno , Kenya Nishioka, Yuzuru Imai, Nobutaka Hattori.
- Organizer
  第63会日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-20K07893
[Presentation] Genetic screening by panel sequencing of glucosylceramidase beta variants for Parkinson’s disease2021
- Author(s)
  Yuanzhe Li, Hiroyo Yoshino, Manabu Funayama, Kenya Nishioka, Nobutaka Hattori
- Organizer
  第62会日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-20K07893
[Presentation] Pathological findings in a patient with alpha-synuclein p.A53T and familial Parkinson's disease2021
- Author(s)
  Kenya Nishioka, Yoshio Hashizume, Masashi Takanashi, et al.
- Organizer
  第62会日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-20K07893
[Presentation] Comprehensive study of LRRK2 mutations in familial Parkinson's disease in Japan2018
- Author(s)
  Kenya Nishioka, Aya Ikeda, Hiroyo Yoshino, Yuanzhe Li, Manabu Funayama, Nobutaka Hattori
- Organizer
  日本人類遺伝学会　第63回大会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09678
[Presentation] Digenic mutations of parkin-PINK1, PINK1-LRRK2, and LRRK2-PINK1 in familial Parkinson’s disease2018
- Author(s)
  Kenya Nishioka, Yuanzhe Li, Hiroyo Yoshino, Arisa Hayashida, Aya Ikeda, Kotaro Ogaki, Manabu Funayama, Nobutaka Hattori
- Organizer
  第50回日本神経学会学術大会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09678
[Presentation] Brain pathology, functional analysis and fly models of CHCHD2 p.T61I2018
- Author(s)
  Kenya Nishioka1, Aya Ikeda, Hongrui Meng, Masashi Takanashi, Hiroyo Yoshino, Yuanzhe Li, Yuzuru Imai, Manabu Funayama, Nobutaka Hattori
- Organizer
  Genetic Epidemiology of Parkinson's Disease, Paris, 2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09678
[Presentation] The correlation of CHCHD2 mutations and alpha-synculein in the brain pathology and fly models2017
- Author(s)
  Kenya Nishioka, Aya Ikeda, Masashi Takanashi, Hiroyo Yoshino, Yuanzhe Li, Manabu Funayama, Yuzuru Imai, Nobutaka Hattori.
- Organizer
  Genetic Epidemiology of Parkinson’s disease
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09678
[Presentation] HOMOZYGOUS ALPHA-SYNUCLEIN A53V IN FAMILIAL PARKINSON'S DISEASE2017
- Author(s)
  Kenya Nishioka, Makito Hirano, A. Jon Stoessl, Hiroyo Yoshino, Yoko Imamichi, Aya Ikeda, Yuanzhe Li, Manabu Funayama, Ikuko Yamada, Yusaku Nakamura, Vesna Sossi, Matthew J. Farrer, Nobutaka Hattori.
- Organizer
  The XXIII World Congress of Neurology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09678
[Presentation] Missense mutations and multiplications of alpha-synuclein in familial Parkinson’s disease; genotype-phenotype correlation2017
- Author(s)
  Kenya Nishioka, Hiroyo Yoshino, Yuanzhe Li, Manabu Funayama, Tara Candido, A. Jon Stoessl, Matthew J Farrer, Nobutaka Hattori.
- Organizer
  The American Society of Human Genetics
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09678
[Presentation] Analysis of GCH1 mutations in the patients with Parkinson’s disease in Japanese population2016
- Author(s)
  Kenya Nishioka, Hiroyo Yoshino, Takashi Matsushima, Aya Ikeda, Manabu Funayama, Nobutaka Hattori
- Organizer
  11th Annual Meeting of the Genetic Epidemiology of Parkinson’s disease (GEOPD) Consortium
- Place of Presentation
  Campus Belval, Luxembourg
- Year and Date
  2016-10-06
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25860726
[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会日本神経学会学術大会
- Place of Presentation
  神戸コンベンションセンター
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-16K09678
[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] Analysis of GCH1 mutations in the patients with Parkinson’s disease in Japanese population2016
- Author(s)
  Kenya Nishioka, Hiroyo Yoshino, Takashi Matsushima, Aya Ikeda, Manabu Funayama, Nobutaka Hattori
- Organizer
  11th Annual Meeting of the Genetic Epidemiology of Parkinson’s disease (GEOPD) Consortium
- Place of Presentation
  Campus Belval, Luxembourg
- Year and Date
  2016-10-06
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09678
[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] 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会日本神経学会学術大会
- Place of Presentation
  神戸コンベンションセンター
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-16K09678
[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] Dopamine transporrter scanで顕著な結合低下を示したN279Kタウ変異の前頭側頭葉変性症の5例2016
- Author(s)
  竹重遥香、中山茶千子、林徹生、西岡健弥、波田野琢、本井ゆみ子、服部信孝
- Organizer
  第57回　日本神経学会総会学術総会
- Place of Presentation
  神戸コンベンションセンター、兵庫県
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-26460921
[Presentation] 教育講演ベーシック明日からの臨床に役立つパーキンソン病診断　up to date2015
- Author(s)
  西岡健弥　服部信孝
- Organizer
  第５６回　日本神経学会総会
- Place of Presentation
  新潟
- Year and Date
  2015-05-20
- 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] 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] 精神発達遅滞と片側パーキンソニズムを呈しWDR45遺伝子変異を認めたNBIAの36歳女性例2014
- Author(s)
  中里朋子、大山彦光、西岡健弥、吉野浩代、服部信孝
- Organizer
  日本神経学会関東地方会
- Place of Presentation
  砂防会館
- Year and Date
  2014-05-31
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] Genetic Analysis of Parkinson’s Disease in the Japanese population2013
- Author(s)
  Kenya Nishioka
- Organizer
  GEO-PD Genetic Epidemiology of Parkinson's disease
- Place of Presentation
  ドイツ　リューベック
- Data Source
  KAKENHI-PROJECT-25860726
[Presentation] 首下がり症候群　パーキンソン病と多系統萎縮症を対象とした後ろ向き解析
- Author(s)
  中村亮太、西岡健弥、山城一雄、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] 大脳皮質基底核症候群の髄液マーカーに基づいた臨床解析
- Author(s)
  中山茶千子、西岡健弥、原裕子、本井ゆみ子、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] 進行性失語症のバイオロジカルマーカーに基づいた臨床解析
- Author(s)
  城崇之、西岡健弥、原裕子、本井ゆみ子、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] 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] Parkinノックアウトマウスにおける細胞骨格蛋白異常による機能障害
- Author(s)
  江口博人、今泉美佳、塚口ケネス、舩山学、西岡健弥、波田野琢、斉木臣二、佐藤栄人、久保紳一郎、今井譲、永松信哉、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] 難治性の慢性疼痛を伴ったパーキンソン病患者へのSCS導入検討
- Author(s)
  松島隆史、西岡健弥、藤巻基紀、原毅、中島円、新井一、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] 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

1. HATTORI Nobutaka (80218510)

# of Collaborated Projects: 2 results

# of Collaborated Products: 30 results
2. MANABU Funayama (70468578)

# of Collaborated Projects: 1 results

# of Collaborated Products: 21 results
3. LI Yuanzhe (40549292)

# of Collaborated Projects: 1 results

# of Collaborated Products: 15 results
4. TODA Tatsushi (30262025)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
5. Yumiko Motoi (60338407)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
6. YORITAKA Asako (90245720)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. SHIMURA Hideki (50286746)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. MACHIDA Yu (90317470)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. Nakamura Shinishiro (80407296)

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. Higuchi Makoto

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
14. MOGUSHI Kaoru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
15. SATAKE Wataru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
16. HATANO Taku

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
17. KAHORI Shiba

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
18. 大垣光太郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
19. 緒方洵

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
21. 斉木臣二

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Nisioka Kenya 西岡 健弥

Nishioka Kenya 西岡 健弥

Research Projects

Research Products

Co-Researchers

Aim to identify a novel gene related to familial Parkinson's diseasePrincipal Investigator

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Aim to detect a novel pathogenic mutation in a familial Parkinson's diseasePrincipal Investigator

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Clinical Analysis of Neurodegenerative Dementia Using Cerebrospinal Fluid Biomarkers

Principal Investigator

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The detection of modifier gens in alpha-synuclein multiplicationsPrincipal Investigator

Principal Investigator

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[Book] II. 病因 1. 関連遺伝子 (11) VPS13C パーキンソン病（第２版） 基礎・臨床研究のアップデート2018

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[Book] Parkinson病のゲノム医療2017

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[Book] 第17番染色体に連鎖するパーキソニズムを伴う前側頭葉型認知症（FTDP-17）2016

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[Book] 第17番染色体に連鎖するパーキソニズムを伴う前側頭葉型認知症（FTDP-17）2016

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[Book] 家族性パーキンソン病 update annual review 20162016

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[Book] 家族性パーキンソン病 update annual review 20162016

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[Book] 痛みのScience and Practice2015

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[Book] 神経症候群（第２版）（II）ーその他の神経疾患を含めてー2014

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

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

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

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Nisioka Kenya 西岡健弥

Nishioka Kenya 西岡健弥

[Book] II. 病因　1. 関連遺伝子　(11) VPS13C パーキンソン病（第２版）　基礎・臨床研究のアップデート2018

[Book] 家族性パーキンソン病　update annual review 20162016

[Book] 家族性パーキンソン病　update annual review 20162016