Yoshino Hiroyo

Research theme for competitive and other funds (3)：

2022 - 2025 神経変性疾患関連遺伝子VPS13のパーキンソン病におけるリスク因子の解明
2018 - 2021 Genetic analysis of VPS13C in Parkinson's disease
2008 - 2010 Gene analysis of amyotrophic lateral sclerosis/parkinsonism-dementia complex, Kii, Japan

Papers (101)：

Toshiki Tezuka, Mayu Ishiguro, Daisuke Taniguchi, Ehoto Osogaguchi, Kahori Shiba-Fukushima, Jun Ogata, Ryota Ishii, Aya Ikeda, Yuanzhe Li, Hiroyo Yoshino, et al. Clinical characteristics and pathophysiological properties of newly discovered LRRK2 variants associated with Parkinson's disease. Neurobiology of disease. 2024. 199. 106571-106571
Kei-Ichi Ishikawa, Ayami Okuzumi, Hiroyo Yoshino, Nobutaka Hattori, Wado Akamatsu. Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson's disease with PARK2 mutation. Stem cell research. 2024. 76. 103323-103323
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

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MISC (67)：

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
吉野浩代, 服部信孝. 【パーキンソン病(第2版)-基礎・臨床研究のアップデート-】病因原因・関連遺伝子 GCH1遺伝子. 日本臨床. 2018. 76. 増刊4 パーキンソン病. 135-139
Nakayama Sachiko, Shimonaka Shotaro, Elahi Montasir, Oji Yutaka, Li Yuanzhe, Hiroyo Yoshino, Nishioka Kenya, Hatano Taku, Motoi Yumiko, Hattori Nobutaka. 新規MAPT遺伝子変異臨床的および生化学的解析(New Mutations in the MAPT Gene: Clinical and Biochemical Characterization). 順天堂醫事雑誌. 2017. 63. 6. 489-490
服部達哉, 服部優子, 後藤洋二, 吉野浩代, 服部信孝. ドーパミントランスポーターSPECT(DAT SPECT)で高度集積低下のみられたbata-propeller protein-associated neurodegeneration(BPAN)の1例. 臨床神経学. 2017. 57. 12. 791-791
西岡健弥, 李元哲, 吉野浩代, 服部信孝. 【神経疾患のゲノム医療】 Parkinson病のゲノム医療. 神経内科. 2017. 86. 6. 660-666

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