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Ichikawa Yaeko  市川 弥生子

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… Alternative Names

ICHIKAWA Yaeko  市川 弥生子

市川 弥生子  イチカワ ヤエコ

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Researcher Number 90341081
Other IDs
Affiliation (Current) 2025: 杏林大学, 医学部, 教授
Affiliation (based on the past Project Information) *help 2019 – 2023: 杏林大学, 医学部, 教授
2016 – 2018: 杏林大学, 医学部, 准教授
2010 – 2013: 東京大学, 医学部附属病院, 助教
2002 – 2003: 川崎医科大学, 医学部, 講師
Review Section/Research Field
Principal Investigator
Basic Section 59040:Nutrition science and health science-related / Epidemiology and preventive medicine / Neurology
Except Principal Investigator
Neurology / Neurology
Keywords
Principal Investigator
ショウジョウバエ / GLUT4 / 疾患関連遺伝子 / 2型糖尿病 / pollux / TBC1D4 / 寒冷ストレス / 飢餓耐性 / ストレス / 寒冷 … More / 飢餓 / drosophila / type 2 diabetes mellitus / 新規経口抗凝固薬 / 脳塞栓 / 経口抗凝固薬 / DOAC / ABCB1 / CES1 / 一塩基多型 / ファーマコゲノミクス / 脳塞栓症 / 脳梗塞 / 直接阻害型経口抗凝固薬 / ミオパチー / 原因遺伝子 / ゲノム解析研究 / 次世代シークエンサー / 網羅的ゲノム解析 / 拡張型心筋症 / ネマリンミオパチー … More
Except Principal Investigator
myostatin / nNOS / caveolin-3 / signal transduction / muscular dystrophy / モデル動物 / 肥大型心筋症 / eNOS / Smad2 / マイオスタチン / カベオリン / トランスジェニックマウス / シグナル伝達 / 筋ジストロフィー / SNP / 遺伝子同定 / 遺伝性疾患 / 一塩基多型(SNP) / 連鎖解析 Less
  • Research Projects

    (6 results)
  • Research Products

    (52 results)
  • Co-Researchers

    (12 People)
  •  2型糖尿病の高リスク疾患関連遺伝子による新しい病態―栄養・寒冷環境との関連―Principal Investigator

    • Principal Investigator
      市川 弥生子
    • Project Period (FY)
      2022 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 59040:Nutrition science and health science-related
    • Research Institution
      Kyorin University
  •  Exploring the molecular mechanism and the clinical features of carriers with a variant of a high-risk disease-associated gene of type 2 diabetes mellitusPrincipal Investigator

    • Principal Investigator
      Yaeko Ichikawa
    • Project Period (FY)
      2019 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 59040:Nutrition science and health science-related
    • Research Institution
      Kyorin University
  •  Pharmacogenomic study for bleeding risk of direct oral anticoagulants in ischemic cerebral stroke patientsPrincipal Investigator

    • Principal Investigator
      Ichikawa Yaeko
    • Project Period (FY)
      2016 – 2018
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Epidemiology and preventive medicine
    • Research Institution
      Kyorin University
  •  Exploring gene for a Japanese family of an autosomal dominant nemaline myopathy associated with dilated cardiomyopathyPrincipal Investigator

    • Principal Investigator
      ICHIKAWA Yaeko
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
  •  Identification of genes for hereditary neurological diseases by the high throughput SNP chip linkage system

    • Principal Investigator
      GOTO Jun
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
  •  Basic research developing a therapy for muscular dystrophy by modulating intracellular signal transduction

    • Principal Investigator
      SUNADA Yoshihide
    • Project Period (FY)
      2002 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      Kawasaki Medical School

All 2023 2020 2019 2014 2013 2012 2011 2010 2009 Other

All Journal Article Presentation Book

  • [Book] アクチュアル脳・神経疾患の臨床小脳と運動失調「JAMSAC研究」2013

    • Author(s)
      市川弥生子
    • Publisher
      中山書店
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Book] アクチュアル 脳・神経疾患の臨床 小脳と運動失調2013

    • Author(s)
      市川弥生子 (総編集:辻 省次)
    • Total Pages
      336
    • Publisher
      中山書店
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Book] カラー版 内科学2012

    • Author(s)
      市川弥生子 (総編集:門脇 孝、永井良三)
    • Total Pages
      1929
    • Publisher
      西村書店
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Book] Annual Review神経2012各種疾患変性疾患「MSA update」2012

    • Author(s)
      市川弥生子
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Book] Annual Review 神経 2012 「MSA update」2012

    • Author(s)
      市川弥生子
    • Publisher
      中外医学社
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Book] カラー版内科学「脊髄小脳変性症」2012

    • Author(s)
      市川弥生子
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] Novel SLC20A2 variant in a Japanese patient with idiopathic basal ganglia calcification-1 (IBGC1) associated with dopa-responsive parkinsonism2019

    • Author(s)
      Yaeko Ichikawa, Masaki Tanaka, Eriko Kurita, Masanori Nakajima, Masaki Tanaka, Chizuko Oishi, Jun Goto, Shoji Tsuji, Atsuro Chiba
    • Journal Title

      Human Genome Variation

      Volume: 6 Issue: 1 Pages: 44-44

    • DOI

      10.1038/s41439-019-0073-7

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K11723
  • [Journal Article] Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing2014

    • Author(s)
      Doi K, Monjo T, Hoang PH, Yoshimura J, Yurino H, Mitsui J, Ishiura H, Takahashi Y, Ichikawa Y, Goto J, Tsuji S, Morishita S
    • Journal Title

      Bioinformatics

      Volume: 30 Pages: 815-22

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] An open trial of long-term testosterone suppression in spinal and bulbar muscular atrophy2013

    • Author(s)
      Yamamoto T, Yokota K, Amao R, Maeno T, Haga N, Taguri M, Ohtsu H, Ichikawa Y, Goto J, Tsuji S
    • Journal Title

      Muscle Nerve

      Volume: 47 Pages: 816-22

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 12013

    • Author(s)
      Ichikawa Y, Ishiura H, Mitsui J, Takahashi Y, Kobayashi S, Takuma H, Kanazawa I, Doi K, Yoshimura J, Morishita S, Goto J, Tsuji S
    • Journal Title

      J Neurol Sci

      Volume: 331 Pages: 158-60

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 192013

    • Author(s)
      Takahashi Y, Fukuda Y, Yoshimura J, Toyoda A, Kurppa K, Moritoyo H, Belzil VV, Dion PA, Higasa K, Doi K, Ishiura H, Mitsui J, Date H, Ahsan B, Matsukawa T, Ichikawa Y, Moritoyo T, Ikoma M, Hashimoto T, Kimura F, Murayama S, Onodera O, Nishizawa M, Yoshida M, Atsuta N, Sobue G; JaCALS, Fifita JA, Williams KL, Blair IP, Nicholson GA, Gonzalez-Perez P, Brown RH Jr, Nomoto M, Elenius K, Rouleau GA, Fujiyama A, Morishita S, Goto J, Tsuji S
    • Journal Title

      Am J Hum Genet

      Volume: 93 Pages: 900-5

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth disease2012

    • Author(s)
      Maeda MH, Ishiura H, et al
    • Journal Title

      Ann Neurol

      Volume: 71 Issue: 1 Pages: 84-92

    • DOI

      10.1002/ana.22658

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-10J05639, KAKENHI-PROJECT-22240090, KAKENHI-PROJECT-23591233, KAKENHI-PROJECT-23790384
  • [Journal Article] Mutations in KCND3 cause spinocerebellar ataxia type 222012

    • Author(s)
      Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung MY, Mundwiller E, Shakkottai V, Liu TT, Tesson C, Lu YC, Brice A, Tsuji S, Burmeister M, Stevanin G, Soong BW
    • Journal Title

      Ann Neurol

      Volume: 72 Pages: 859-69

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan.2012

    • Author(s)
      Ishiura H, Kokubo Y.
    • Journal Title

      Arch Neurol.

      Volume: 69(9) Issue: 9 Pages: 1154-1158

    • DOI

      10.1001/archneurol.2012.1219

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21256005, KAKENHI-PROJECT-23591233, KAKENHI-PROJECT-23790384
  • [Journal Article] Mutations in KCND3 cause spinocerebellar ataxia type 22.2012

    • Author(s)
      Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y et al., ,
    • Journal Title

      Ann Neurol.

      Volume: 72 Issue: 6 Pages: 859-69

    • DOI

      10.1002/ana.23701

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement.2012

    • Author(s)
      Ishiura H
    • Journal Title

      Am J Hum Genet.

      Volume: 91(2) Issue: 2 Pages: 320-9

    • DOI

      10.1016/j.ajhg.2012.07.014

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22300118, KAKENHI-PROJECT-23500428, KAKENHI-PROJECT-23591233, KAKENHI-PROJECT-23659458, KAKENHI-PROJECT-23790384, KAKENHI-PROJECT-24300133, KAKENHI-PROJECT-24390220, KAKENHI-PROJECT-24406030, KAKENHI-PROJECT-24790348, KAKENHI-ORGANIZER-22129001, KAKENHI-PLANNED-22129002
  • [Journal Article] Increased gene dosage of myelin protein zero causes Charcot-Marie- Tooth disease2012

    • Author(s)
      Maeda MH, Mitsui J, Soong BW, Takahashi Y, Ishiura H, Hayashi S, Shirota Y, Ichikawa Y, Matsumoto H, Arai M, Okamoto T, Miyama S, Shimizu J, Inazawa J, Goto J, Tsuji S
    • Journal Title

      Ann Neurol

      Volume: 71 Pages: 84-92

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement2012

    • Author(s)
      Ishiura H, Sako W, Yoshida M, Kawarai T, Tanabe O, Goto J, Takahashi Y, Date H, Mitsui J, Ahsan B, Ichikawa Y, Iwata A, Yoshino H, Izumi Y, Fujita K, Maeda K, Goto S, Koizumi H, Morigaki R, Ikemura M, Yamauchi N, Murayama S, Nicholson GA, Ito H, Sobue G, Nakagawa M, Kaji R, Tsuji S
    • Journal Title

      Am J Hum Genet

      Volume: 91 Pages: 320-9

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] 多系統萎縮症 臨床試験に向けての現況と課題2012

    • Author(s)
      市川弥生子
    • Journal Title

      BRAIN and NERVE

      Volume: 64 Pages: 1141-1149

    • NAID

      40019456431

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan2012

    • Author(s)
      Ishiura H, Takahashi Y, Mitsui J, Yoshida S, Kihira T, Kokubo Y, Kuzuhara S, Ranum LP, Tamaoki T, Ichikawa Y, Date H, Goto J, Tsuji S
    • Journal Title

      Arch Neurol

      Volume: 69 Pages: 1154-8

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] Culture-negative Brain Abscess with <i>Streptococcus intermedius</i> Infection with Diagnosis Established by Direct Nucleotide Sequence Analysis of the 16S Ribosomal RNA Gene2012

    • Author(s)
      N.Saito, et al
    • Journal Title

      Intern. Med.

      Volume: 51 Issue: 2 Pages: 211-216

    • DOI

      10.2169/internalmedicine.51.6419

    • NAID

      130002062067

    • ISSN
      0918-2918, 1349-7235
    • Language
      English
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23310144, KAKENHI-PROJECT-23591233
  • [Journal Article] Culture-negative brain abscess with Streptococcus intermedius infection with diagnosis established by direct nucleotide sequence analysis of the 16s ribosomal RNA gene2012

    • Author(s)
      Saito N, Hida A, Koide Y, Ooka T, Ichikawa Y, Shimizu J, Mukasa A, Nakatomi H, Hatakeyama S, Hayashi T, Tsuji S
    • Journal Title

      Intern Med

      Volume: 51 Pages: 211-6

    • NAID

      130002062067

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1.2011

    • Author(s)
      Ishiura H, Fukuda Y, Mitsui J, Nakahara Y, Ahsan B, Takahashi Y, Ichikawa Y, Goto J, Sakai T, Tsuji S
    • Journal Title

      Neurogenetics. 12(2)

      Pages: 117-21

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Journal Article] Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR12011

    • Author(s)
      Ishiura H, Fukuda Y, Mitsui J, Nakahara Y, Ahsan B, Takahashi Y, Ichikawa Y, Goto J, Sakai T, Tsuji S
    • Journal Title

      Neurogenetics

      Volume: 12 Pages: 117-21

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] Therapeutic trial design issues for future disease-modifying therapy of multiple system atrophy2011

    • Author(s)
      Ichikawa Y, Goto J, Nakahara Y, Mitsui J, Tsuji S
    • Journal Title

      Rinsho Shinkeigaku

      Volume: 51 Pages: 910-913

    • NAID

      130004504910

    • Data Source
      KAKENHI-PROJECT-23591233
  • [Journal Article] A Japanese family of a novel autosomal dominant nemaline myopathy associated with dilated cardiomyopathy.2011

    • Author(s)
      Ichikawa Y, Ishiura H, Goto J, Kowa H, Oya Y, Date H, Tsuji S
    • Journal Title

      Neurology

      Volume: 76 (Suppl 4)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] Functional analysis of pollux Drosophila homolog of the human TBC1D4 a gene involved in an increased risk of type 2 diabetes in the Inuit population2023

    • Author(s)
      Awasaki T Sato S Ushimaru M Kato K Ichikawa Y
    • Organizer
      第46回日本分子生物学会
    • Data Source
      KAKENHI-PROJECT-22K11785
  • [Presentation] イヌイット集団で2型糖尿病発症リスク増加に関与するTBC1D4のショウジョウバエ相同遺伝子polluxの機能解析2023

    • Author(s)
      粟崎 健 佐藤 世都子,丑丸 真,加藤 健太郎,市川 弥生子
    • Organizer
      第95回日本遺伝学会
    • Data Source
      KAKENHI-PROJECT-22K11785
  • [Presentation] 2型糖尿病発症の高リスク疾患関連遺伝子バリアントを有する日本人の臨床像2020

    • Author(s)
      市川弥生子, 宮崎泰, 炭谷由計, 茂呂直紀, 渋谷裕彦, 永井健太郎, 石本麻衣, 徳重真一, 内堀歩, 石浦浩之, 三井純, 辻省次, 戸田達史, 安田和基, 千葉厚郎
    • Organizer
      日本人類遺伝学会第65回大会
    • Data Source
      KAKENHI-PROJECT-19K11723
  • [Presentation] 脳梗塞患者における直接阻害型経口抗凝固薬の出血性副作用とゲノム薬理学的検討2019

    • Author(s)
      市川弥生子, 丸岡響, 山下ひとみ, 齋藤幹人, 城野喬史, 上月直樹, 白鳥嵩之, 渋谷裕彦, 中島昌典, 本田有子, 天野達雄, 鳥居正剛, 岡野晴子, 河野浩之, 海野佳子, 平野照之
    • Organizer
      第60回日本神経学会学術大会
    • Data Source
      KAKENHI-PROJECT-16K09070
  • [Presentation] 神経・筋疾患における遺伝子検査の有用性2013

    • Author(s)
      市川弥生子,石浦浩之,三井純,松川敬志,田中真生,高橋祐二,後藤順,辻省次
    • Organizer
      第20回日本遺伝子診療学会大会
    • Place of Presentation
      浜松
    • Year and Date
      2013-07-20
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 神経内科領域における遺伝子診断の現況と課題.2013

    • Author(s)
      市川弥生子, 西垣昌和, 今井 靖, 平田恭信, 辻 省次, 後藤 順
    • Organizer
      第54回日本神経学会学術大会
    • Place of Presentation
      東京(東京国際フォーラム)
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 神経内科領域における遺伝子診断の現況と課題2013

    • Author(s)
      市川弥生子,西垣昌和,今井靖,平田恭信,辻省次,後藤順
    • Organizer
      第54回日本神経学会学術大会
    • Place of Presentation
      東京
    • Year and Date
      2013-05-24
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 神経内科・循環器内科領域における遺伝子診断の状況2012

    • Author(s)
      市川弥生子,西垣昌和,今井靖,平田恭信,辻省次,後藤順
    • Organizer
      第57回日本人類遺伝学会大
    • Place of Presentation
      東京
    • Year and Date
      2012-10-25
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 神経内科・循環器内科領域における遺伝子診断の状況2012

    • Author(s)
      市川弥生子、西垣昌和、今井 靖、平田恭信、辻 省次、後藤 順
    • Organizer
      第57回 日本人類遺伝学会大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 多系統萎縮症の早期症例における診断基準の検討2012

    • Author(s)
      市川 弥生子, 中原 康雄, 百瀬 義雄, 後藤 順, 辻 省次
    • Organizer
      第53回 日本神経学会学術大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 多系統萎縮症の早期症例における診断基準の検討2012

    • Author(s)
      市川弥生子,中原康雄,百瀬義雄,後藤順,辻省次
    • Organizer
      第53回日本神経学会学術大会
    • Place of Presentation
      東京
    • Year and Date
      2012-05-24
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] A four-generation Japanese family with autosomal dominant nemaline myopathy associated with dilated cardiomyopathy2012

    • Author(s)
      Y. Ichikawa, J. Goto, H. Ishiura, Y. Oya, H. Kowa, J. Shimizu, H. Date, S. Tsuji
    • Organizer
      17^<th> International congress of the world muscle society
    • Place of Presentation
      Perth, Australia
    • Year and Date
      2012-10-11
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] A four-generation Japanese family with autosomal dominant nemaline myopathy associated with dilated cardiomyopathy2012

    • Author(s)
      Y. Ichikawa, J. Goto, H. Ishiura, Y. Oya, H. Kowa, J. Shimizu, H. Date, S. Tsuji
    • Organizer
      17th International congress of the world muscle society
    • Place of Presentation
      Perth, Australia
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 多系統萎縮症の運動機能における経時的推移2011

    • Author(s)
      市川弥生子,百瀬義雄,中原康雄,後藤順,辻省次, JAMSAC (Japan MSA research consortium)
    • Organizer
      第52回日本神経学会学術大会
    • Place of Presentation
      名古屋
    • Year and Date
      2011-05-18
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] A Japanese family of a novel autosomal dominant nemaline myopathy associated with dilated cardiomyopathy2011

    • Author(s)
      Ichikawa Y, Ishiura H, Goto J, Kowa H, Oya Y, Date H, Tsuji S
    • Organizer
      American Academy of Neurology 63^<rd> Annual Meeting
    • Place of Presentation
      Honolulu, Hawaii
    • Year and Date
      2011-04-13
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] A Japanese family of a novel autosomal dominant nemaline myopathy associated with dilated cardiomyopathy2011

    • Author(s)
      Ichikawa Y, Ishiura H, Goto J, Kowa H, Oya Y, Date H, Tsuji S
    • Organizer
      American Academy of Neurology 63rd Annual Meeting
    • Place of Presentation
      Honolulu, USA
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 神経内科領域における前方向的コホート研究から見えてきたもの. MSAに対するdisease-modifying therapy実現のための臨床治験デザイン2011

    • Author(s)
      市川弥生子,後藤順,中原康雄,三井純,辻省次
    • Organizer
      第52回日本神経学会学術大会シンポジウム
    • Place of Presentation
      名古屋
    • Year and Date
      2011-05-19
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] MSAに対するdisease-modifying therapy 実現のための臨床治験デザイン2011

    • Author(s)
      市川弥生子 、後藤 順、中原康雄、三井 純、辻 省次
    • Organizer
      第52回日本神経学会 シンポジウム
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] Assessment of clinical usefulness of genetic diagnosis in neurology department of hospital2011

    • Author(s)
      Y. Ichikawa, H. Ishiura, J. Mitsui, T. Matsukawa, Y. Takahashi, H. Naruse, M. Taira, S. Tsuji, J. Goto
    • Organizer
      12^<th> International Conference of Human Genetics
    • Place of Presentation
      Montreal, Canada
    • Year and Date
      2011-10-13
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] Assessment of clinical usefulness of genetic diagnosis in neurology department of hospital2011

    • Author(s)
      Y. Ichikawa, H. Ishiura, J. Mitsui, T. Matsukawa, Y. Takahashi, H. Naruse, M. Taira, S. Tsuji, J. Goto
    • Organizer
      12th International Conference of Human Genetics
    • Place of Presentation
      Montreal, Canada
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] 多系統萎縮症の運動機能における経時的推移2011

    • Author(s)
      JAMSAC, 市川弥生子、百瀬義雄、中原康雄、後藤 順、辻 省次
    • Organizer
      第52回日本神経学会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-23591233
  • [Presentation] Clinical features of spinocerebellar ataxia type 31 in Japanese population.2010

    • Author(s)
      Ichikawa Y, (4名略), Goto J
    • Organizer
      60^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Washington, DC USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] A Japanese family ofnemaline myopathy which is caused by TPM2 mutation.2010

    • Author(s)
      Goto J, Ishiura H, Fukuda Y, Nagashima Y, Shimizu J, Takahashi Y, Ichikawa Y, Tsuji S
    • Organizer
      60^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Washington DC, USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] Siblings of pathologically proven multiple system atrophy : an application of whole genome analysis toward finding strong genetic factors for sporadic diseases.2010

    • Author(s)
      Ishiura H, Ahsan B, Mitsui J, Takahashi Y, Fukuda Y, Ichikawa Y, Nakahara Y, Kara K, Takahashi T, Kakita A, Onodera O, Nishizawa M, Goto J, Tsuji S
    • Organizer
      60^<th> Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Washington DC, USA
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] Molecular epidemiology of spinocerebellar ataxias in Japanese population.2009

    • Author(s)
      Ichikawa Y, Tsuji S, Goto J
    • Organizer
      59th Annual Meeting of the American Society of Human Genetics
    • Place of Presentation
      Honolulu, Hawaii, USA
    • Year and Date
      2009-10-21
    • Data Source
      KAKENHI-PROJECT-20590989
  • [Presentation] 神経・筋疾患における遺伝子検査の有用性

    • Author(s)
      市川弥生子, 石浦浩之, 三井 純, 松川敬志, 田中真生, 高橋祐二, 後藤 順, 辻 省次
    • Organizer
      第20回日本遺伝子診療学会大会
    • Place of Presentation
      東京(アクトシティ浜松コングレスセンター)
    • Data Source
      KAKENHI-PROJECT-23591233
  • 1.  粟崎 健 (60359669)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 2 results
  • 2.  GOTO Jun (10211252)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 5 results
  • 3.  TAKAHASHI Yuji (00372392)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 4.  FUKUDA Yoko (60396744)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 5.  SUNADA Yoshihide (00240713)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 6.  MURAKAMI Tatsuhumi (30330591)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 7.  HAGIWARA Hiroki (80276732)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 8.  NUKINA Nobuyuki (10134595)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 9.  GOTO Yuichi (20225668)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 10.  大沢 裕 (80246511)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 11.  平野 照之 (50346996)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 12.  小久保 康昌
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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