WADA TAKAHITO 和田敬仁

… Alternative Names

和田敬仁ワダタカヒト

Wada Takahito 和田敬仁

WADA Takahito 和田敬仁

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Researcher Number	70359727
Other IDs
Affiliation (Current)	2023: 京都大学, 医学研究科, 特定教授
Affiliation (based on the past Project Information) *help	2022: 京都大学, 医学研究科, 特定教授 2020: 京都大学, 医学研究科, 特定教授 2018 – 2019: 京都大学, 医学研究科, 准教授 2016: 京都大学, 医学研究科, 准教授 2014 – 2016: 京都大学, 医学(系)研究科(研究院), 准教授 … More 2007 – 2008: Shinshu University, 医学部, 准教授 2007: 信州大学, 医学部, 助教 2003: Shinshu Univ. Sch. Med., Medical Genetics, Assistant Professor, 医学部, 助手 Less
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Human genetics / Pediatrics Except Principal Investigator 医療における生命倫理 / Biological Sciences / Human genetics / Hygiene / Medical pharmacy / Human genetics
Keywords	Principal Investigator 知的障害 / ATRX / 発達障害 / バイオマーカー / 視線計測 / ATR-X症候群 / 分子遺伝学 / エピジェネティクス / 細胞遺伝学 / クロマチンリモデリング … More / 染色体テリトリー / 3D-FISH / クレアチン / トランスポーター / 先天性代謝異常 / 脳クレアチン欠乏症候群 / 治療薬 / クレアチントランスポーター / iPS細胞 / グアニジノ化合物 / クレアチニン / グアニジノ酢酸 / 精神遅滞 / 自閉症 / 注視点分布計測装置 / 認知機能 / 社会性 / 言語能力 / 評価法 / 注視点分布計測 / 知的障がい / 発達障がい … More Except Principal Investigator 遺伝子 / 染色体構造異常 / Mendelian Cytogenetics / fluorescence in situ hybridization / FISH / DBCRs / 遺伝カウンセリング / 遺伝子診療 / ガイドライン / 遺伝情報 / ELSI / 性分化 / エピゲノム / マイクロアレイ / 性分化異常 / マイクロアレー / 細胞遺伝学 / 3D-FISH解析 / ゲノム / 位置効果 / フッ化スルフリル / 生物学的曝露指標 / 尿中代謝物 / くん蒸剤 / 生物学的モニタリング / 産業中毒 / クレアチン / トランスポーター / 輸送 / クレアチン欠乏症 / 細胞内局在 / 中枢疾患 / 脳関門 / 中秋疾患 / ポジショナルクローニング / 染色体異常 / 均衡型構造異常 / 相互転座 / 染色体均衡型構造異常 / 特発性思春期早発症 / FISH解析 / 思春期早発症 / BACクローン / ボジショナルクローニング / YAC / BAC / positional cloning / chromosome abnormality / chromosome rearrangement / balanced translocation Less

知的障害患者に対する治療や療育効果判定のための視線計測によるバイオマーカーの確立Principal Investigator
- Principal Investigator
  
  和田敬仁
- 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
  Kyoto University
Development of the method to evaluate the cognitive function of pediatic patients with genetic intellectual disability syndromes by Gazefinder, an all-in-one eye tracking systemPrincipal Investigator
- Principal Investigator
  
  Wada Takahito
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kyoto University
Mechanism of cellular localization of mutated creatine transporter toward therapy for creatine deficiency syndromes
- Principal Investigator
  
  Ohtsuki Sumio
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Medical pharmacy
- Research Institution
  Kumamoto University
Study for Pathogenesis of Cerebral Creatine Deficiency SyndromesPrincipal Investigator
- Principal Investigator
  
  WADA Takahito
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kyoto University
3D nuclear architecture of the regions close to the candidate gene (s) related to the constitutional chromosomal abnormalities
- Principal Investigator
  
  WAKUI Keiko
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Shinshu University
Subjective symptom prevalence among workers exposed to Sulfryl fluoride
- Principal Investigator
  
  TSUKAHARA Teruomi
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hygiene
- Research Institution
  Shinshu University
エピゲノム解析から迫るATR-X症候群の性分化異常発症機構の解明
- Principal Investigator
  
  松本直通
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Yokohama City University
Study of the effect on the chromosomal territory in the nucleus by the mutated chromatin remodeling protein, ATRXPrincipal Investigator
- Principal Investigator
  
  WADA Takahito
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Shinshu University
Establishment of Ethics Guideline in Medical Genetics
- Principal Investigator
  
  FUKUSHIMA Yoshimitsu
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  医療における生命倫理
- Research Institution
  Shinshu University
Registration of disease-associated balanced chromosome rearrangements (DBCRs) and FISH analyses of the breakpoints for positional cloning strategy.
- Principal Investigator
  
  FUKUSHIMA Yoshimitsu
- Project Period (FY)
  2000 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Shinshu University

All 2021 2020 2019 2017 2016 2015 2014 2010 2009 2008 2007 2006 Other

All Journal Article Presentation Book

[Book] ATRX and X-linked a-Thalassemia Mental Retardation Syndrome. Epstein CJ, et.al.(ed.)Inborn Errrors of Development2008
- Author(s)
  Gibbons RJ, Wada T
- Publisher
  Oxford University Press
- Data Source
  KAKENHI-PROJECT-19590331
[Book] Epstein CJ, et al. (ed. )lnborn Errrors of Development ; ATRX and X-linked α-Thalassemia Mental Retardation Syndrome.2008
- Author(s)
  Gibbons RJ, Wada T. (分担)
- Publisher
  Oxford University Press
- Data Source
  KAKENHI-PROJECT-19590331
[Journal Article] Cyclocreatine Transport by SLC6A8, the Creatine Transporter, in HEK293 Cells, a Human Blood-Brain Barrier Model Cell, and CCDSs Patient-Derived Fibroblasts2020
- Author(s)
  Uemura T, Ito S, Masuda T, Shimbo H, Goto T, Osaka H, Wada T, Couraud PO, Ohtsuki S.
- Journal Title
  
  Pharmaceutical Research
  
  Volume: 37 Pages: 1-11
- DOI
  10.1007/s11095-020-2779-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07819, KAKENHI-PROJECT-19K05544
[Journal Article] 5‐Aminolevulinic acid can ameliorate language dysfunction of patients with ATR‐X syndrome2020
- Author(s)
  Wada T, Suzuki S, Shioda N.
- Journal Title
  
  Congenital Anomalies
  
  Volume: - Pages: 147-148
- DOI
  10.1111/cga.12365
- NAID
  50014579011
- ISSN
  0914-3505, 1741-4520
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07819, KAKENHI-PUBLICLY-19H05221, KAKENHI-PROJECT-20K21400
[Journal Article] Pharmacological prospects of G-quadruplexes for neurological diseases using porphyrins2020
- Author(s)
  Asamitsu S, Yabuki Y, Ikenoshita S, Wada T, Shioda N.
- Journal Title
  
  Biochemical and Biophysical Research Communications
  
  Volume: - Pages: 51-55
- DOI
  10.1016/j.bbrc.2020.01.054
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07819, KAKENHI-PUBLICLY-19H05221, KAKENHI-PROJECT-19K23801, KAKENHI-PROJECT-20K21400, KAKENHI-PROJECT-20H03393
[Journal Article] 指定難病ペディア2019】個別の指定難病　染色体・遺伝子関連　ATR-X症候群[指定難病180]2019
- Author(s)
  和田敬仁
- Journal Title
  
  日本医師会雑誌
  
  Volume: 148
- Data Source
  KAKENHI-PROJECT-18K07819
[Journal Article] 指定難病最前線(Volume 84)　ATR-X(X連鎖αサラセミア・知的障がい)症候群2019
- Author(s)
  和田敬仁
- Journal Title
  
  新薬と臨牀
  
  Volume: 84 Pages: 672-676
- Data Source
  KAKENHI-PROJECT-18K07819
[Journal Article] Abnormal <i>N</i>-Glycosylation of a Novel Missense Creatine Transporter Mutant, G561R, Associated with Cerebral Creatine Deficiency Syndromes Alters Transporter Activity and Localization2017
- Author(s)
  T. Uemura, S. Ito, Y. Ohta, M. Tachikawa, T. Wada, T. Terasaki, S. Ohtsuki
- Journal Title
  
  Biol. Pharm. Bull.
  
  Volume: 40 Issue: 1 Pages: 49-55
- DOI
  10.1248/bpb.b16-00582
- NAID
  130005188881
- ISSN
  0918-6158, 1347-5215
- Language
  English
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26293035, KAKENHI-PROJECT-26461544
[Journal Article] 脳クレアチン欠乏症候群2016
- Author(s)
  和田敬仁
- Journal Title
  
  小児科診療
  
  Volume: 79 Pages: 290-290
- Data Source
  KAKENHI-PROJECT-26461544
[Journal Article] 尿中クレアチン/クレアチニン比と家族歴により診断に至ったクレチントランスポーター欠損症の1家系：本邦3家系目．2015
- Author(s)
  野崎章仁、熊田友浩、柴田実、藤井達哉、和田敬仁、小坂仁．
- Journal Title
  
  脳と発達
  
  Volume: 47 Pages: 49-52
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461544
[Journal Article] Urine screening for patients with developmental disabilities detected a patient with creatine transporter deficiency due to a novel missense mutation in SLC6A8.2014
- Author(s)
  Kato H, Miyake F, Shimbo H, Ohya M, Sugawara H, Aida N, Anzai R, Takagi M, Okuda M, Takano K, Wada T*, Iai M, Yamashita S, Osaka H.
- Journal Title
  
  Brain Dev.
  
  Volume: 36 Pages: 630-633
- DOI
  10.1016/j.braindev.2013.08.004
- Data Source
  KAKENHI-PROJECT-26461544
[Journal Article] Mutations in the chromatin-associated protein ATRX2008
- Author(s)
  Gibbons RJ, Wada T, others
- Journal Title
  
  Hum Mut 29
  
  Pages: 796-802
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19040023
[Journal Article] Mutations in the chromatin-associated protein ATRX.2008
- Author(s)
  Gibbons RJ, Wada T, et al.
- Journal Title
  
  Human Mutation 29
  
  Pages: 796-802
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590331
[Journal Article] Mutations in the chromatin-associated protein ATRX2008
- Author(s)
  Gibbons RJ, Wada T, et.al
- Journal Title
  
  Hum Mut 29
  
  Pages: 796-802
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590331
[Journal Article] Nation wide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan2007
- Author(s)
  Yoshida K, Wada T, Sakurai A, Wakui K, Ikeda S, Fukushima Y
- Journal Title
  
  J Hum Genet 52
  
  Pages: 675-679
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18612003
[Journal Article] Nationwide survey on predictive genetic testing for late-onset,incurable neurological diseases in Japan.2007
- Author(s)
  Yoshida K, Wada T, others
- Journal Title
  
  J Hum Genet 52
  
  Pages: 675-679
- NAID
  10019812864
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19040023
[Journal Article] Mandibuloacral dysplasia and a novel LMNA mutation in a woman with severe progressive skeletal changes.2007
- Author(s)
  Kosho T, others, Wada T, others
- Journal Title
  
  Am J Med Genet 143A
  
  Pages: 2598-2603
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19040023
[Journal Article] 近親婚のリスクと遺伝カウンセリング2007
- Author(s)
  和田敬仁, 福嶋義光
- Journal Title
  
  日本医事新報 4338
  
  Pages: 96-97
- Data Source
  KAKENHI-PROJECT-18612003
[Journal Article] A new detection method for ATRX gene mutations using a mismatch-specific endonuclease2006
- Author(s)
  Wada T, Fukushima Y, Saitoh S
- Journal Title
  
  Am J Med Genet 140A
  
  Pages: 1519-1523
- Data Source
  KAKENHI-PROJECT-18612003
[Presentation] ダウン症候群の乳幼児の視線位置の特徴探索と発達の関連2021
- Author(s)
  岡本麻里、植田彰彦、小島諒介、毎原敏郎、土屋賢治、和田敬仁、奥野恭史
- Organizer
  第43回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07819
[Presentation] 5-Aminolevulinic acid can be a treatment for ATR-X syndrome.2019
- Author(s)
  Wada T, and Shioda N.
- Organizer
  19th International Workshop on Fragile X and other Neurodevelopmental Disorders, Sorrento Italy, 2019/9/18-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07819
[Presentation] 「脳クレアチン欠乏症候群」研究班の概要2017
- Author(s)
  和田敬仁
- Organizer
  平成28年度「脳クレアチン欠乏症候群」班会議及び研究会
- Place of Presentation
  東京
- Year and Date
  2017-03-17
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] 脳クレアチン欠乏症候群に関連する新規変異クレアチントランスポーターのクレアチン輸送活性低下とそのメカニズムの解明2016
- Author(s)
  上村立記、伊藤慎悟、太田悠介、立川正憲、平山未央、和田敬仁、寺崎哲也、大槻純男
- Organizer
  第40回　蛋白質と酵素の構造と機能に関する九州シンポジウム
- Place of Presentation
  鹿児島
- Year and Date
  2016-08-26
- Data Source
  KAKENHI-PROJECT-26293035
[Presentation] 脳クレアチン欠乏症の臨床研究2016
- Author(s)
  和田敬仁
- Organizer
  第58回日本小児神経学会学術集会
- Place of Presentation
  東京
- Year and Date
  2016-06-04
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] 新規変異クレアチントランスポーターのクレアチン輸送活性低下とそのメカニズムの解明2016
- Author(s)
  上村立記、伊藤慎悟、太田悠介、立川正憲、黒木未央、和田敬仁、寺崎哲也、大槻純男
- Organizer
  第9回トランスポーター研究会九州部会
- Place of Presentation
  宮崎
- Data Source
  KAKENHI-PROJECT-26293035
[Presentation] 「脳クレアチン欠乏症候群の臨床研究班」の取り組み2015
- Author(s)
  和田敬仁，小坂仁，相田典子，後藤知英，露崎悠，新保裕子，加藤秀一，高野亨子，大槻純男，伊藤慎悟，立川正憲，黒澤裕子
- Organizer
  第57回日本小児神経学会
- Place of Presentation
  大阪
- Year and Date
  2015-05-27
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] 新規変異クレアチントランスポーターの機能と発現解析2015
- Author(s)
  上村立記、伊藤慎悟、落合祐介、立川正憲、平山未央、和田敬仁、大槻純男
- Organizer
  第31回日本薬学会九州支部大会
- Place of Presentation
  神戸
- Year and Date
  2015-03-28
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] 脳クレアチン欠乏症候群に関連する新規変異クレアチントランスポーターの発現・局在と輸送機能特性の解析2015
- Author(s)
  上村立記、伊藤慎悟、太田悠介、立川正憲、平山未央、和田敬仁、寺崎哲也、大槻純男
- Organizer
  日本薬学会第135年会
- Place of Presentation
  神戸
- Year and Date
  2015-03-28
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] Tatsuki Uemura, Shingo Ito, Yusuke Ota, Masanori Tachikawa, Takahito Wada, Mio Hirayama, Tetsuya Terasaki, Sumio Ohtsuki: Changes in transport activity and cellular localization by a novel missense mutation in human creatine transporter found in Japanese cerebral creatine deficiency syndromes patients2015
- Author(s)
  Tatsuki Uemura, Shingo Ito, Yusuke Ota, Masanori Tachikawa, Takahito Wada, Mio Hirayama, Tetsuya Terasaki, Sumio Ohtsuki
- Organizer
  Barcelona BioMed Conference Blood Braine Barrier
- Place of Presentation
  Barcelona, Spain
- Year and Date
  2015-10-02
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] Molecular genetic study and urine analysis of Japanese patients with cerebral creatine deficiency syndromes.2015
- Author(s)
  H. Shimbo, H. Osaka, M. Tachikawa, S. Ohtsuki, S. Ito, T. Goto, Y. Tsuyusaki, N. Aida, K. Kurosawa, Y. Kurosawa, H. Kato, K. Takano, T. Wada.
- Organizer
  65th American Society of Human Genetics
- Place of Presentation
  Baltimore
- Year and Date
  2015-10-06
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] Changes of cellular localization and transport activity by a novel mutation in creatine transporter associated with chronic cerebral creatine depletion2015
- Author(s)
  Tatsuki Uemura, Shingo Ito, Yusuke Ota, Masanori Tachikawa, Takahito Wada, Mio Hirayama, Tetsuya Terasaki, Sumio Ohtsuki
- Organizer
  International Symposium on Chronic Inflammatory Diseases
- Place of Presentation
  Kumamoto
- Year and Date
  2015-10-16
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] 脳クレアチン欠乏症への取り組み2014
- Author(s)
  和田敬仁
- Organizer
  第35回グアニジノ化合物研究会
- Place of Presentation
  筑波
- Year and Date
  2014-10-11
- Data Source
  KAKENHI-PROJECT-26461544
[Presentation] 3D-FISH法による15q11.2-q12領域の細胞核内配置の解析2010
- Author(s)
  河村理恵, 涌井敬子, 田辺秀之, 和田敬仁, 斉藤伸治, 福嶋義光
- Organizer
  日本人類遺伝学会第55回大会
- Place of Presentation
  埼玉
- Year and Date
  2010-10-28
- Data Source
  KAKENHI-PROJECT-20590328
[Presentation] 3D-FISH法による15q11.2-q12領域の細胞核内配置の解析2010
- Author(s)
  河村理恵, 涌井敬子, 田辺透之, 和田敬仁, 斉藤伸治, 福嶋義光
- Organizer
  日本人類遺伝学会第55回大会
- Place of Presentation
  さいたま
- Year and Date
  2010-10-28
- Data Source
  KAKENHI-PROJECT-20590328
[Presentation] 3D-FISH法による細胞核内染色体テリトリー計測における細胞周期の影響にいて2009
- Author(s)
  河村理恵, 涌井敬子, 和田敬仁, 田辺秀之, 福嶋義光
- Organizer
  日本人類遺伝学会第54回大会
- Place of Presentation
  東京
- Year and Date
  2009-09-24
- Data Source
  KAKENHI-PROJECT-20590328
[Presentation] 3D-FISH法による細胞核内染色体テリトリー計測における細胞周期の影響について2009
- Author(s)
  河村理恵, 涌井敬子, 和田敬仁, 田辺透之, 福嶋義光
- Organizer
  日本人類遺伝学会第54回大会
- Place of Presentation
  東京
- Year and Date
  2009-09-24
- Data Source
  KAKENHI-PROJECT-20590328
[Presentation] 3D-FISH解析における細胞核内染色体間距離の計測について2009
- Author(s)
  涌井敬子、河村理恵、和田敬仁、田辺秀之、福嶋義光
- Organizer
  定量生物学の会第1回キャラバン遺伝研
- Place of Presentation
  静岡
- Year and Date
  2009-03-13
- Data Source
  KAKENHI-PROJECT-19590331
[Presentation] 3D-FISH法における細胞核内染色体間距離の計測について2009
- Author(s)
  涌井敬子, 河村理恵, 和田敬仁, 田辺透之, 福嶋義光
- Organizer
  定量生物の会第1回キャラバン遺伝研
- Place of Presentation
  三島
- Year and Date
  2009-03-14
- Data Source
  KAKENHI-PROJECT-20590328
[Presentation] 3D-FISH解析における細胞核内染色体間距離の計測について.2009
- Author(s)
  涌井敬子, 河村理恵, 和田敬仁, 田辺秀之, 福嶋義光.
- Organizer
  定量生物学の会第1回キャラバン
- Place of Presentation
  静岡
- Year and Date
  2009-03-13
- Data Source
  KAKENHI-PROJECT-19590331
[Presentation] 3D-FISH解析における細胞核内染色体間距離の計測について2009
- Author(s)
  涌井敬子, 河村理恵, 和田敬仁, 田辺秀之, 福嶋義光
- Organizer
  定量生物学の会第1回キャラバン遺伝研
- Place of Presentation
  静岡
- Year and Date
  2009-03-13
- Data Source
  KAKENHI-PROJECT-20590328
[Presentation] ヘッドスペースサンプラ付ガスクロマトグラフ質量分析計を用いた尿中フッ素分析方法の確立2008
- Author(s)
  大塚貴生、内山隆文、津田洋子、宮内博幸、塚原照臣、和田敬仁、野見山哲生
- Organizer
  日本産業衛生学会北陸甲信越地方会総会
- Data Source
  KAKENHI-PROJECT-20590596
[Presentation] 新規変異クレアチントランスポーターの機能と発現解析
- Author(s)
  上村立記、伊藤慎悟、落合祐介、立川正憲、平山未央、和田敬仁、大槻純男
- Organizer
  第31回日本薬学会九州支部大会
- Place of Presentation
  福岡
- Year and Date
  2014-12-05 – 2014-12-06
- Data Source
  KAKENHI-PROJECT-26293035
[Presentation] ヒトクレアチントランスポーター変異症例におけるクレアチン輸送機能の解明
- Author(s)
  上村立記、伊藤慎悟、落合祐介、立川正憲、平山未央、和田敬仁、大槻純男
- Organizer
  日本薬学会第135年会
- Place of Presentation
  神戸
- Year and Date
  2015-03-26 – 2015-03-28
- Data Source
  KAKENHI-PROJECT-26293035

1. FUKUSHIMA Yoshimitsu (70273084)

# of Collaborated Projects: 4 results

# of Collaborated Products: 11 results
2. WAKUI Keiko (50324249)

# of Collaborated Projects: 4 results

# of Collaborated Products: 9 results
3. KOSHO Tomoki (90276311)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
4. TANABE Hideyuki (50261178)

# of Collaborated Projects: 2 results

# of Collaborated Products: 8 results
5. Ohtsuki Sumio (60323036)

# of Collaborated Projects: 2 results

# of Collaborated Products: 11 results
6. 伊藤慎悟 (20466535)

# of Collaborated Projects: 2 results

# of Collaborated Products: 11 results
7. SAKURAI Akihiro (70262706)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
8. TAMAI Mariko (80283274)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. TSUKAHARA Teruomi (50377652)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
10. NOMIYAMA Tetsuo (70286441)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
11. MURAMATSU Tsukasa (10109423)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. MURASE Sumio (70200285)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. KUBOTA Takeo (70293511)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 松本直通 (80325638)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 立川正憲 (00401810)

# of Collaborated Projects: 1 results

# of Collaborated Products: 7 results
16. 新保裕子 (50724663)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
17. 小坂仁 (90426320)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
18. 坂爪悟 (70306174)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. 川目裕 (60246395)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 土屋賢治 (20362189)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
21. 小島諒介 (70807651)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. 吉田健司 (50790557)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
23. 川崎秀徳 (90468372)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. KAWAMURA Rie

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
25. MASUDA Takeshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 塩田倫史

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

WADA TAKAHITO 和田 敬仁

和田 敬仁 ワダ タカヒト

Wada Takahito 和田 敬仁

WADA Takahito 和田 敬仁

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知的障害患者に対する治療や療育効果判定のための視線計測によるバイオマーカーの確立Principal Investigator

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Development of the method to evaluate the cognitive function of pediatic patients with genetic intellectual disability syndromes by Gazefinder, an all-in-one eye tracking systemPrincipal Investigator

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Mechanism of cellular localization of mutated creatine transporter toward therapy for creatine deficiency syndromes

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Study for Pathogenesis of Cerebral Creatine Deficiency SyndromesPrincipal Investigator

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3D nuclear architecture of the regions close to the candidate gene (s) related to the constitutional chromosomal abnormalities

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Subjective symptom prevalence among workers exposed to Sulfryl fluoride

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エピゲノム解析から迫るATR-X症候群の性分化異常発症機構の解明

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Study of the effect on the chromosomal territory in the nucleus by the mutated chromatin remodeling protein, ATRXPrincipal Investigator

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Establishment of Ethics Guideline in Medical Genetics

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Registration of disease-associated balanced chromosome rearrangements (DBCRs) and FISH analyses of the breakpoints for positional cloning strategy.

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[Book] ATRX and X-linked a-Thalassemia Mental Retardation Syndrome. Epstein CJ, et.al.(ed.)Inborn Errrors of Development2008

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[Book] Epstein CJ, et al. (ed. )lnborn Errrors of Development ; ATRX and X-linked α-Thalassemia Mental Retardation Syndrome.2008

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[Journal Article] Cyclocreatine Transport by SLC6A8, the Creatine Transporter, in HEK293 Cells, a Human Blood-Brain Barrier Model Cell, and CCDSs Patient-Derived Fibroblasts2020

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WADA TAKAHITO 和田敬仁

和田敬仁ワダタカヒト

Wada Takahito 和田敬仁

WADA Takahito 和田敬仁

[Journal Article] 指定難病ペディア2019】個別の指定難病　染色体・遺伝子関連　ATR-X症候群[指定難病180]2019

[Journal Article] 指定難病最前線(Volume 84)　ATR-X(X連鎖αサラセミア・知的障がい)症候群2019