Rchr
J-GLOBAL ID:201801018252036371   Update date: Jun. 12, 2024

Nishioka Kenya

Nishioka Kenya | Nishioka Kenya
Affiliation and department:
Job title: Associate Professor
Research field  (1): Neuroscience - general
Research keywords  (6): Clinical Neurology ,  Chronic pain ,  Clinical genetics ,  Hereditary leukoencephalopathy ,  Dementia ,  Parkinson disease
Research theme for competitive and other funds  (5):
  • 2020 - 2023 Aim to identify a novel gene related to familial Parkinson's disease
  • 2016 - 2019 Aim to detect a novel pathogenic mutation in a familial Parkinson's disease
  • 2014 - 2017 Clinical Analysis of Neurodegenerative Dementia Using Cerebrospinal Fluid Biomarkers
  • 2013 - 2017 The detection of modifier gens in alpha-synuclein multiplications
  • 2013 - 2015 若手研究(B)
Papers (149):
  • Kei-ichi Ishikawa, Takahiro Shiga, Hiroyo Yoshino, Kenya Nishioka, Nobutaka Hattori, Wado Akamatsu. Generation of three clones (JUCGRMi002-A, B, C) of induced pluripotent stem cells from a Parkinson’s disease patient with SNCA duplication. Stem Cell Research. 2024
  • Kensuke Daida, Manabu Funayama, Kimberley J Billingsley, Laksh Malik, Abigail Miano-Burkhardt, Hampton L Leonard, Mary B Makarious, Hirotaka Iwaki, Jinhui Ding, J Raphael Gibbs, et al. Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease. Movement disorders : official journal of the Movement Disorder Society. 2023. 38. 12. 2249-2257
  • Kensuke Daida, Manabu Funayama, Kimberley J Billingsley, Laksh Malik, Abigail Miano-Burkhardt, Hampton L Leonard, Mary B Makarious, Hirotaka Iwaki, Jinhui Ding, J Raphael Gibbs, et al. Long-read sequencing resolves a complex structural variant in PRKN Parkinson's disease. medRxiv : the preprint server for health sciences. 2023
  • Hajime Yasuda, Yoshiki Furukawa, Kenya Nishioka, Makoto Sasaki, Yutaka Tsukune, Shuichi Shirane, Nobutaka Hattori, Miki Ando, Norio Komatsu. Vitamin B6 deficiency as a cause of polyneuropathy in POEMS syndrome: rapid recovery with supplementation in two cases. Hematology (Amsterdam, Netherlands). 2022. 27. 1. 463-468
  • 間瀬 智子, 阿部 奈那子, 岩井 正勝, 佐藤 靖子, 漆戸 由紀子, 品田 淳子, 井関 賛, 小川 崇, 上野 真一, 西岡 健弥, et al. 多系統萎縮症患者の重症度に合わせた看護支援の方策の検討. 臨床神経学. 2022. 62. Suppl. S407-S407
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MISC (64):
  • 西岡健弥, 山下由莉, 互健二, 島田斉, 吉野浩代, 李元哲, 舩山学, 舩山学, 樋口真, 服部信孝, et al. 新規変異MAPT p.K298_H299insQのタウイメージングと臨床遺伝学的解析. 日本人類遺伝学会大会プログラム・抄録集. 2021. 66th
  • 王子悠, 波田野琢, 上野真一, 舩山学, 石川景一, 石川景一, 奥住文美, 野田幸子, 佐藤栄人, 李元哲, et al. プロサポシン遺伝子サポシンD領域変異によるパーキンソン病. パーキンソン病・運動障害疾患コングレスプログラム・抄録集. 2021. 14th
  • 三嶋崇靖, 藤岡伸助, 佐藤和則, 保前英希, 矢部一郎, 塩見一剛, 西岡健弥, 波田野琢, 服部信孝, 坪井義夫. 日本におけるPerry病の特徴. 日本神経学会学術大会プログラム・抄録集. 2020. 61st
  • Masashi Takanashi, Manabu Funayama, Kenya Nishioka, Daisuke Taniguchi, Takashi Ogawa, Sho Tsuyama, Nobutaka Hattori. Isolated nigral degeneration not associated with a-synuclein pathologies in the familial Parkinson's disease with LRRK2 p.R1441H mutation. BRAIN PATHOLOGY. 2019. 29. 92-92
  • 田中 淳, 飯田 紘太郎, 林田 有沙, 西岡 健弥, 服部 信孝, 原 英夫. VPS13C遺伝子変異を認めた家族性パーキンソン病の1例. 臨床神経学. 2018. 58. 8. 545-545
more...
Education (7):
  • 2022 - 現在 Department of Neurology, Juntendo Tokyo Koto Geriatric Medical Center
  • 2013 - 現在 Juntendo University School of Medicine Medicine Neurology
  • 2010 - 2013 Juntendo Urayasu Hospital Medicine Neurology
  • 2008 - 2009 Mayo Clinic Jacksonville Department of Neuroscience
  • 2004 - 2007 Graduate School of Medicine, Juntendo University School of Medicine Medicine Neurology
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Association Membership(s) (5):
Genetic epidemiology of Parkinson's disease ,  Japan College of Fibromyalgia Investigation ,  The Japan Stroke Society ,  The Japanese Society of Internal Medicine ,  Japanese Society of Neurology
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