Fukushi Daisuke 福士大輔

… Alternative Names

福士大輔フクシダイスケ

FUKUSHI Daisuke 福士大輔

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Researcher Number	90397159
Other IDs
Affiliation (Current)	2025: 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, 客員研究員
Affiliation (based on the past Project Information) *help	2019 – 2023: 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, 主任研究員 2013 – 2015: 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 2009: 愛知県心障者コロニー, 研究員 2008: 埼玉県立がんセンター, 臨床腫瘍研究所, 研究員 2007 – 2008: 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 2006: 埼玉県立がんセンター, 臨床腫瘍研究所, 研究員
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics Except Principal Investigator Pediatrics / Pediatric surgery
Keywords	Principal Investigator 染色体逆位 / 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 / R3HDM1 / 知的障害 / 先天異常 / マイクロRNA … More / R3HDM1欠損症 / 不均衡な発現 / 自閉症 / 欠失 / 逆位 / 均衡型相互転座 / サイトカラシンB / モナストロール / 染色体サイクル … More Except Principal Investigator 染色体異常 / コルネリアデランゲ症候群 / 先天性疾患 / モナストロール / 単極性染色体整列 / 染色体構築 / 染色体分配 / 染色体サイクル / M期チェックポイント遺伝子 / 倍数性異常 / 異数性異常 / MYCN / 倍数性・異数性染色体異常 / 細胞質不分離 / MYCN増幅 / 3極分裂 / 中心体異常 / 2倍体腫瘍 / 3倍体腫瘍 / 異数性染色体異常 / 倍数性 / 神経芽腫 Less

R3HDM1欠損症の発症機序として見出した遺伝子・マイクロRNA不均衡仮説の検証Principal Investigator
- Principal Investigator
  
  福士大輔
- Project Period (FY)
  2022 – 2024
- 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 disabilityPrincipal Investigator
- 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
Clinical and genetic characterization of patients with intellectual disability caused by chromosome structural abnormalities.Principal Investigator
- Principal Investigator
  
  Fukushi Daisuke
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Institute for Developmental Research, Aichi Human Service Center
染色体サイクルに異常のみられる原因不明の知的障害の病因解明Principal Investigator
- Principal Investigator
  
  福士大輔
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Institute for Developmental Research, Aichi Human Service Center
The mechanism of polyploidy and aneuploidy formation in neuroblastoma
- Principal Investigator
  
  KANEKO Yasuhiko
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatric surgery
- Research Institution
  Research Institute for Clinical Oncology, Saitama Cancer Center
染色体構築と分離に異常を示す先天性疾患の症例収集と早期診断法の確立
- Principal Investigator
  
  木村礼子
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Institute for Developmental Research, Aichi Human Service Center

All 2022 2021 2015 2014 2009 2008 2007 2006

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
[Journal Article] Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion2015
- Author(s)
  Yamada K, Aiba K, Kitaura Y, Kondo Y, Nomura N, Nakamura Y, Fukushi D, Murayama K, Shimomura Y, Pitt J, Yamaguchi S, Yokochi K, Wakamatsu N
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: 52 Issue: 10 Pages: 691-698
- DOI
  10.1136/jmedgenet-2015-103231
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09593, KAKENHI-PROJECT-15K09610, KAKENHI-PROJECT-26462225, KAKENHI-PROJECT-25461576
[Journal Article] Clinical characterization and identification of duplication breakpoints in a Japanese family with Xq28 duplication syndrome including MECP2.2014
- Author(s)
  Fukushi D, Yamada K, Nomura N, Naiki M, Kimura R, Yamada Y, Kumagai T, Yamaguchi K, Miyake Y, Wakamatsu N
- Journal Title
  
  Am J Med Genet A
  
  Volume: 164(4) Issue: 4 Pages: 924-933
- DOI
  10.1002/ajmg.a.36373
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23592636, KAKENHI-PROJECT-25461576, KAKENHI-PROJECT-26462225
[Journal Article] Centrosome amplification is correlated with ploidy divergence, but not with MYCN amplification in neuroblastoma tumors2009
- Author(s)
  Fukushi D, Watanabe N, Kasai F, Haruta M, Kikuchi A, Kikuta A, Kato K, Nakadate H, Tsunematsu Y, Kaneko Y
- Journal Title
  
  Cancer Genet Cytogenet 188
  
  Pages: 32-41
- Data Source
  KAKENHI-PROJECT-18390475
[Journal Article] Duplieation of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephrqma of the cellular or mixed type.2007
- Author(s)
  Watanabe N, Haruta M, Soejima H, Fukushi D, Yokomori K, Nakadate H, Okita H, Hata JI, Fukuzawa M, Kaneko Y
- Journal Title
  
  Genes Chromosomes Cancer 46
  
  Pages: 929-935
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390475
[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R3HDM1．2022
- 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-22K07860
[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] SF3B4の欠失が見られるNager症候群の1症例.2015
- Author(s)
  福士大輔, 水野誠司, 稲葉美枝, 鈴木　香, 野村紀子, 鈴木康予, 山田憲一郎, 若松延昭
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  東京
- Year and Date
  2015-10-16
- Data Source
  KAKENHI-PROJECT-25461576
[Presentation] 家族性Xq28重複症候群の染色体重複機構の解明2014
- Author(s)
  福士大輔、山田憲一郎、野村紀子ら
- Organizer
  日本人類遺伝学会第59回大会・日本遺伝子診療学会第21回大会
- Place of Presentation
  東京
- Year and Date
  2014-11-22
- Data Source
  KAKENHI-PROJECT-25461576
[Presentation] Centrosome amplification is correlated with ploidy instability in infant neuroblastoma (NB) tumors, but not with MYCN amplification in infant and childhood NB tumors or cell line2008
- Author(s)
  Kaneko Y, Fukushi D, Watanabe N, Kasai F, Haruta M, Kikuchi A, Kikuta A, Tsunematsu Y
- Organizer
  Advances in Neuroblastoma Research
- Place of Presentation
  千葉
- Data Source
  KAKENHI-PROJECT-18390475
[Presentation] 乳児と小児2倍体神経芽腫の特徴-中心体の増幅と異数性細胞の混在-2008
- Author(s)
  笠井文生、福士大輔、渡辺直樹、春田雅之、金子安比古
- Organizer
  第67回日本癌学会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-18390475
[Presentation] 神経芽腫のploidy異常の発生に3極分極が関与するのか?2007
- Author(s)
  福士大輔、渡辺直樹、春田雅之、金子安比古
- Organizer
  第66回日本癌学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-18390475
[Presentation] 神経芽腫のploidy異常の発生に中心体異常は関与するのか?2006
- Author(s)
  福士大輔、渡辺直樹、春田雅之、金子安比古
- Organizer
  第22回日本小児がん学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-18390475

1. KANEKO Yasuhiko (50373387)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
2. HARUTA Masayuki (80392190)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
3. KASAI Fumio (60393055)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
4. Yamada Yasukazu (70191343)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
5. Yamada Kenichiro (30291173)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
6. 木村礼子 (70393147)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. 小野教夫 (20291172)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. 加藤君子 (30598602)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
9. YAMADA Kenji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
10. 山口清次

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. 榎戸靖

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Fukushi Daisuke 福士 大輔

福士 大輔 フクシ ダイスケ

FUKUSHI Daisuke 福士 大輔

Research Projects

Research Products

Co-Researchers

R3HDM1欠損症の発症機序として見出した遺伝子・マイクロRNA不均衡仮説の検証Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidation of the brain pathology of R3HDM1 deficiency with mild intellectual disabilityPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Clinical and genetic characterization of patients with intellectual disability caused by chromosome structural abnormalities.Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

染色体サイクルに異常のみられる原因不明の知的障害の病因解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The mechanism of polyploidy and aneuploidy formation in neuroblastoma

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

染色体構築と分離に異常を示す先天性疾患の症例収集と早期診断法の確立

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

[Journal Article] Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Clinical characterization and identification of duplication breakpoints in a Japanese family with Xq28 duplication syndrome including MECP2.2014

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Centrosome amplification is correlated with ploidy divergence, but not with MYCN amplification in neuroblastoma tumors2009

Author(s)

Journal Title

Data Source

[Journal Article] Duplieation of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephrqma of the cellular or mixed type.2007

Author(s)

Journal Title

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R3HDM1．2022

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] SF3B4の欠失が見られるNager症候群の1症例.2015

Author(s)

Organizer

Fukushi Daisuke 福士大輔

福士大輔フクシダイスケ

FUKUSHI Daisuke 福士大輔