Katoh Kimiko 加藤君子

… Alternative Names

加藤君子カトウキミコ

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Researcher Number	30598602
Other IDs	https://orcid.org/0000-0003-3355-4678
Affiliation (Current)	2024: 愛知県医療療育総合センター発達障害研究所, 障害モデル研究部, 主任
Affiliation (based on the past Project Information) *help	2023: 愛知県医療療育総合センター発達障害研究所, 障害モデル研究部, 研究員 2019 – 2022: 愛知県医療療育総合センター発達障害研究所, 遺伝子医療研究部, 研究員 2017 – 2018: 愛知県心身障害者コロニー発達障害研究所, 遺伝学部, 研究員 2013: 大阪大学, たんぱく質研究所, 招へい研究員
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics / Genome biology Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator X染色体不活性化 / X連鎖性疾患 / skewed X染色体不活性化 / 脳・神経 / 遺伝子 / Skewed X染色体不活性化 / skewed X inactivation / Xq27.3q28欠失 / 網膜 / リプログラミング / ヒストンバリアント … More Except Principal Investigator … More 自閉症 / miR-128 / RNA結合タンパク質 / 神経突起 / 自閉症様行動 / 軽度知的障害 / 染色体逆位 / R3HDM1 Less

X染色体不活性化システムから迫る初期胚異常と疾患発症要因の新たな理解Principal Investigator
- Principal Investigator
  
  加藤君子
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Institute for Developmental Research Aichi Developmental Disability Center
新たなアプローチによるX連鎖性疾患に伴うskewed X染色体不活性化機構の解明Principal Investigator
- Principal Investigator
  
  加藤君子
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Institute for Developmental Research Aichi Developmental Disability Center
Elucidation of the brain pathology of R3HDM1 deficiency with mild intellectual disability
- Principal Investigator
  
  Fukushi Daisuke
- Project Period (FY)
  2019 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Institute for Developmental Research Aichi Developmental Disability Center
The analysis of X chromosome inactivation in X-linked disordersPrincipal Investigator
- Principal Investigator
  
  Katoh Kimiko
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Institute for Developmental Research Aichi Developmental Disability Center
細胞特性を決める分子基盤の解明Principal Investigator
- Principal Investigator
  
  加藤君子
- Project Period (FY)
  2013
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Genome biology
- Research Institution
  Osaka University

All 2022 2021 2019 2017

All Journal Article Presentation

[Journal Article] R3HDM1 haploinsufficiency is associated with mild intellectual disability.2021
- Author(s)
  Fukushi D, Inaba M, Katoh K, Suzuki Y, Enokido Y, Nomura N, Tokita Y, Hayashi S, Mizuno S, Yamada K, Wakamatsu N
- Journal Title
  
  Am J Med Genet A
  
  Volume: 185 Issue: 6 Pages: 1776-1786
- DOI
  10.1002/ajmg.a.62173
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08313, KAKENHI-PROJECT-19K08337
[Presentation] 染色体腕間逆位から同定した知的障害の新規原因遺伝子R3HDM1．2022
- Author(s)
  林　深, 福士大輔, 稲葉美枝, 加藤君子, 鈴木康予, 榎戸　靖, 野村紀子, 時田義人, 水野誠司, 山田憲一郎, 若松延昭
- Organizer
  第125回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-19K08337
[Presentation] 染色体腕間逆位から同定した知的障害の新規原因遺伝子R3HDM1.2021
- Author(s)
  福士大輔, 稲葉美枝, 加藤君子, 鈴木康予, 榎戸　靖, 野村紀子, 時田義人, 水野誠司, 山田憲一郎, 若松延昭, 林深
- Organizer
  日本人類遺伝学会第66回大会・第28回日本遺伝子診療学会大会
- Data Source
  KAKENHI-PROJECT-19K08337
[Presentation] 症状が異なるXq27.1q28欠失の2女児例のX染色体不活性化解析2019
- Author(s)
  加藤君子、相場佳織、福士大輔、鈴木康予、山田憲一郎、若松延昭
- Organizer
  第91回日本生化学会大会
- Data Source
  KAKENHI-PROJECT-17K16293
[Presentation] TWO FEMALE PATIENTS WITH Xq27.3q28 DELETION AND SKEWED X-INACTIVATION DISPLAY SIMILAR PHENOTYPES AS HUNTER SYNDROME2017
- Author(s)
  Kimiko KATOH
- Organizer
  第23 回世界神経学会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K16293

1. Fukushi Daisuke (90397159)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
2. 榎戸靖

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Katoh Kimiko 加藤 君子

加藤 君子 カトウ キミコ

Research Projects

Research Products

Co-Researchers

X染色体不活性化システムから迫る初期胚異常と疾患発症要因の新たな理解Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

新たなアプローチによるX連鎖性疾患に伴うskewed X染色体不活性化機構の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidation of the brain pathology of R3HDM1 deficiency with mild intellectual disability

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

The analysis of X chromosome inactivation in X-linked disordersPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

細胞特性を決める分子基盤の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] R3HDM1 haploinsufficiency is associated with mild intellectual disability.2021

Author(s)

Journal Title

DOI

Data Source

[Presentation] 染色体腕間逆位から同定した知的障害の新規原因遺伝子R3HDM1．2022

Author(s)

Organizer

Data Source

[Presentation] 染色体腕間逆位から同定した知的障害の新規原因遺伝子R3HDM1.2021

Author(s)

Organizer

Data Source

[Presentation] 症状が異なるXq27.1q28欠失の2女児例のX染色体不活性化解析2019

Author(s)

Organizer

Data Source

[Presentation] TWO FEMALE PATIENTS WITH Xq27.3q28 DELETION AND SKEWED X-INACTIVATION DISPLAY SIMILAR PHENOTYPES AS HUNTER SYNDROME2017

Author(s)

Organizer

Data Source

Katoh Kimiko 加藤君子

加藤君子カトウキミコ