Rchr
J-GLOBAL ID:201801018252036371   Update date: Mar. 26, 2025

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 (166):
  • 関根 智子, 石黒 麻由, 安藤 真矢, 石黒 雄太, 奥住 文美, 古川 芳明, 西岡 健弥. 自律神経障害を発症した抗MAG抗体・抗SGPG抗体陽性ニューロパチーの87歳男性例. 臨床神経学. 2025. 65. 1. 67-67
  • Kensuke Daida, Hiroyo Yoshino, Laksh Malik, Breeana Baker, Mayu Ishiguro, Rylee Genner, Kimberly Paquette, Yuanzhe Li, Kenya Nishioka, Satoshi Masuzugawa, et al. The Utility of Long-Read Sequencing in Diagnosing Early Onset Parkinson's Disease. Annals of neurology. 2024
  • 石黒 雄太, 安藤 真矢, 奥住 文美, 石黒 麻由, 古川 芳明, 西岡 健弥, 服部 信孝. ホスレボドパ・ホスカルビドパ水和物持続皮下注療法を導入したPRKN変異パーキンソン病の64歳女性例. 臨床神経学. 2024. 64. 11. 835-835
  • Mayu Ishiguro, Manabu Funayama, Taku Hatano, Hiroshi Nishida, Yuko Wada, Kazuyuki Noda, Masahiko Tomiyama, Hiroyo Yoshino, Yuanzhe Li, Stephanie Ong, et al. Genetic and clinical study of PARK7 in Japanese Parkinson's disease. Heliyon. 2024. 10. 15. e35271
  • Aya Ikeda, Hongrui Meng, Daisuke Taniguchi, Muneyo Mio, Manabu Funayama, Kenya Nishioka, Mari Yoshida, Yuanzhe Li, Hiroyo Yoshino, Tsuyoshi Inoshita, et al. CHCHD2 P14L, found in amyotrophic lateral sclerosis, exhibits cytoplasmic mislocalization and alters Ca2+ homeostasis. PNAS Nexus. 2024. 3. 8
more...
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
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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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