Yoshino Hiroyo 吉野浩代

… Alternative Names

吉野浩代ヨシノヒロヨ

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Researcher Number	80338417
Other IDs
Affiliation (Current)	2025: 順天堂大学, 大学院医学研究科, 助教
Affiliation (based on the past Project Information) *help	2022 – 2023: 順天堂大学, 大学院医学研究科, 助教 2018 – 2020: 順天堂大学, 医学(系)研究科(研究院), 助教 2008: 順天堂大学, 医学(系)研究科(研究院), 助教
Review Section/Research Field	Principal Investigator Basic Section 52020:Neurology-related Except Principal Investigator Neurology
Keywords	Principal Investigator レアバリアント / パーキンソン病 / 発症リスク / VPS13遺伝子 / 遺伝的要因 / VPS13A/B/C/D / VPS13C遺伝子 / 感受性遺伝子 / risk variant / ミトコンドリア機能 … More / iPS細胞由来神経細胞 / VPS13A/B/D / 疾患感受性遺伝子 / 発症危険因子 / ＶPS13遺伝子 / VPS13C … More Except Principal Investigator α-synuclein / グアム島 / 紀伊半島 / 遺伝子解析 / TDP-43 / タウオパチー / パーキンソン認知症複合 / 筋萎縮性側索硬化症 Less

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Principal Investigator
- Principal Investigator
  
  吉野浩代
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Juntendo University
Genetic analysis of VPS13C in Parkinson's diseasePrincipal Investigator
- Principal Investigator
  
  Yoshino Hiroyo
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Juntendo University
Gene analysis of amyotrophic lateral sclerosis/parkinsonism-dementia complex, Kii, Japan
- Principal Investigator
  
  KOKUBO Yasumasa
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Mie University

All 2023 2022 2020 2018 2010

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] Long-read sequencing resolves a complex structural variant in PRKN Parkinson’s disease2023
- Author(s)
  Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N
- Journal Title
  
  Movement Disorders
  
  Volume: 38 Issue: 12 Pages: 2249-2257
- DOI
  10.1002/mds.29610
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K07542, KAKENHI-PROJECT-22H04925, KAKENHI-PROJECT-21H02814
[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] 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] 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] Nobutaka HattoriNo evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients Neuroscience Letters Neuroscience2010
- Author(s)
  Lin Li, Manabu Funayama, Hiroyuki Tomiyama, Yuanzhe Li, Hiroyo Yoshino, Ryogen Sasaki,Yasumasa Yasumasa Kokubo, Shigeki Kuzuhara, Yoshikuni Mizuno
- Journal Title
  
  Letters 479
  
  Pages: 245-248
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590994
[Journal Article] No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients Neuroscience Letters2010
- Author(s)
  Lin Li, Manabu Funayama, Hiroyuki Tomiyama, Yuanzhe Li, Hiroyo Yoshino, Ryogen Sasaki, Yasumasa Kokubo, Shigeki Kuzuhara, Yoshikuni Mizuno, Nobutaka Hattori
- Journal Title
  
  Neuroscience Letters
  
  Volume: 479 Pages: 245-248
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20590994
[Presentation] Comprehensive genetic analysis in Japanese Parkinson’s disease2023
- Author(s)
  Hiroyo Yoshino
- Organizer
  68th Annual Meeting of the Japan Society of Human Genetics（JSHG）
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K07542
[Presentation] Comprehensive genetic analysis in Japanese Parkinson's diseas2023
- Author(s)
  Hiroyo Yoshino
- Organizer
  第64回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-22K07542
[Presentation] Genotype-phenotype correlation of Parkinson’s disease with PRKN variants2022
- Author(s)
  Hiroyo Yoshino, Yuanzhe Li, Kenya Nishioka, Kensuke Daida, Arisa Hayashida, Yuta Ishiguro, Daisuke Yamada, Nana Izawa, Katsunori Nishi, Noriko Nishikawa, Genko Oyama, Taku Hatano, Shinichiro Nakamura, Asako Yoritaka, Yumiko Motoi, Manabu Funayama, Nobutaka Hattori
- Organizer
  日本人類遺伝学会第67回大会
- Data Source
  KAKENHI-PROJECT-22K07542
[Presentation] GCH1 variants in dopa-responsive dystonia and Parkinson’s disease2022
- Author(s)
  Hiroyo Yoshino, Kensuke Daida, Kenya Nishioka, Nobutaka Hattori
- Organizer
  第63回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-22K07542
[Presentation] Genetic analysis of VPS13A/B/D: paralogous genes of VPS13C in Parkinson's disease2020
- Author(s)
  吉野浩代
- Organizer
  第61回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-18K07536
[Presentation] Genetic analysis of VPS13A/B/D: paralogous genes of VPS13C in Parkinson’s disease2020
- Author(s)
  吉野浩代
- Organizer
  第61回日本神経学会学術大会
- Data Source
  KAKENHI-PROJECT-18K07536
[Presentation] Mutation analysis of VPS13C in Japanese patients with Parkinson's disease2018
- Author(s)
  Arisa Hayashida, Yuanzhe Li, Hiroyo Yoshino, Aya Ikeda, Manabu Funayama, Kenya Nishioka, Nobutaka Hattori
- Organizer
  13th International Meeting on Genetic Epidemiology of Parkinson's Disease
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07536
[Presentation] 日本人パーキンソン病患者におけるGIGYF2の変異解析2010
- Author(s)
  李林、舩山学、富山弘幸、李元哲、吉野浩代、佐々木良元、小久保康昌、葛原茂樹、水野美邦、服部信孝
- Organizer
  第4回 MDSJ
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20590994
[Presentation] 日本人パーキンソン病患者におけるGIGYF2の変異解析2010
- Author(s)
  李林、舩山学、富山弘幸、李元哲、吉野浩代、佐々木良元、小久保康昌、葛原茂樹、水野美邦、服部信孝
- Organizer
  第4回MDSJ
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20590994
[Presentation] パーキンソン病におけるPLA2G6 p.P806R2010
- Author(s)
  富山弘幸、吉野浩代、大垣光太郎、李林、李元哲、舩山学、佐々木良元、小久保康昌、葛原茂樹、服部信孝
- Organizer
  日本人類遺伝学会総会
- Place of Presentation
  大宮
- Data Source
  KAKENHI-PROJECT-20590994
[Presentation] FTDP-17が疑われた日本人71症例におけるMAPT、PGRN遺伝子解析2010
- Author(s)
  大垣光太郎、李元哲、高梨雅史、石川景一、小林智則、中西淳、野中隆、長谷川成人、岸雅彦、吉野浩代、舩山学、塩屋敬一、横地正之、佐々木良元、小久保康昌、葛原茂樹、本井ゆみ子、富山幸、服部信孝
- Organizer
  第4回MDSJ
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20590994
[Presentation] 孤発性パーキンソン病におけるPLA2G6 p.P806R2010
- Author(s)
  富山弘幸、吉野浩代、大垣光太郎、李林、李元哲、舩山学、佐々木良元、小久保康昌、葛原茂樹、服部信孝
- Organizer
  第4回 MDSJ
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20590994
[Presentation] FTDP-17が疑われた日本人71症例におけるMAPT、PGRN遺伝子解析2010
- Author(s)
  大垣光太郎、李元哲、高梨雅史、石川景一、小林智則、中西淳、野中隆、長谷川成人、岸雅彦、吉野浩代、舩山学、塩屋敬一、横地正之、佐々木良元、小久保康昌、葛原茂樹、本井ゆみ子、富山弘幸、服部信孝
- Organizer
  第4回 MDSJ
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20590994
[Presentation] パーキンソン病におけるPLA2G6p.P806R2010
- Author(s)
  富山弘幸、吉野浩代、大垣光太郎、李林、李元哲、舩山学、佐々木良元、小久保康昌、葛原茂樹、服部信孝
- Organizer
  日本人類遺伝学会総会
- Place of Presentation
  大宮
- Data Source
  KAKENHI-PROJECT-20590994
[Presentation] 孤発性パーキンソン病におけるPLA2G6 p.P806R2010
- Author(s)
  富山弘幸、吉野浩代、大垣光太郎、李林、李元哲、舩山学、佐々木良元、小久保康昌、葛原茂樹、服部信孝
- Organizer
  第4回MDSJ
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20590994

1. KOKUBO Yasumasa (60263000)

# of Collaborated Projects: 1 results

# of Collaborated Products: 10 results
2. KUZUHARA Sigeki (70111383)

# of Collaborated Projects: 1 results

# of Collaborated Products: 10 results
3. TOMIYAMA Hiroyuki (20515069)

# of Collaborated Projects: 1 results

# of Collaborated Products: 10 results
4. KAHORI Shiba

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
5. FUNAYAMA Manabu

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. 西岡健弥

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
7. 李元哲

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Yoshino Hiroyo 吉野 浩代

吉野 浩代 ヨシノ ヒロヨ

Research Projects

Research Products

Co-Researchers

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Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Genetic analysis of VPS13C in Parkinson's diseasePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Gene analysis of amyotrophic lateral sclerosis/parkinsonism-dementia complex, Kii, Japan

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] Long-read sequencing resolves a complex structural variant in PRKN Parkinson’s disease2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] α-Synuclein V15A variant in familial Parkinson's disease exhibits a weaker lipid-binding property.2022

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

Author(s)

Journal Title

DOI

Data Source

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

Author(s)

Journal Title

DOI

Data Source

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

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Nobutaka HattoriNo evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients Neuroscience Letters Neuroscience2010

Author(s)

Journal Title

Data Source

[Journal Article] No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients Neuroscience Letters2010

Author(s)

Journal Title

Data Source

[Presentation] Comprehensive genetic analysis in Japanese Parkinson’s disease2023

Author(s)

Organizer

Data Source

[Presentation] Comprehensive genetic analysis in Japanese Parkinson's diseas2023

Author(s)

Organizer

Data Source

[Presentation] Genotype-phenotype correlation of Parkinson’s disease with PRKN variants2022

Author(s)

Organizer

Data Source

[Presentation] GCH1 variants in dopa-responsive dystonia and Parkinson’s disease2022

Author(s)

Yoshino Hiroyo 吉野浩代

吉野浩代ヨシノヒロヨ