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ONO Hiroyuki  小野 裕之

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… Alternative Names

小野 裕之  オノ ヒロユキ

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Researcher Number 40868866
Affiliation (Current) 2025: 浜松医科大学, 医学部, 特任研究員
Affiliation (based on the past Project Information) *help 2022 – 2023: 浜松医科大学, 医学部, 特任研究員
2020 – 2022: 浜松医科大学, 医学部附属病院, 助教
Review Section/Research Field
Principal Investigator
Basic Section 52050:Embryonic medicine and pediatrics-related
Except Principal Investigator
Medium-sized Section 54:Internal medicine of the bio-information integration and related fields
Keywords
Principal Investigator
性分化疾患 / 性分化発症メカニズム / 妊娠母体低栄養 / 精巣形成不全症候群 (TDS) / 胎生期低栄養環境 / 精巣形成不全症候群 / 性分化
Except Principal Investigator
絶対連鎖不平衡 / 微細欠失 / ESR1 … More / 内分泌撹乱環境化学物質感受性 / 子宮内発育不全 / 多因子疾患 / 生殖機能障害 / 性分化疾患 Less
  • Research Projects

    (2 results)
  • Research Products

    (17 results)
  • Co-Researchers

    (7 People)
  •  性分化疾患・生殖機能障害における葉酸とメチル化変動の関係Principal Investigator

    • Principal Investigator
      小野 裕之
    • Project Period (FY)
      2021 – 2024
    • Research Category
      Grant-in-Aid for Early-Career Scientists
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Hamamatsu University School of Medicine
  •  Clarification of underlying factors for disorders of sex development and reproductive dysfunction as multifactorial disorders

    • Principal Investigator
      Ogata Tsutomu
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Review Section
      Medium-sized Section 54:Internal medicine of the bio-information integration and related fields
    • Research Institution
      Hamamatsu University School of Medicine

All 2022 2021 2020

All Journal Article

  • [Journal Article] Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system2022

    • Author(s)
      Fuke Tomoko、Nakamura Akie、Inoue Takanobu、Kawashima Sayaka、Hara-Isono Kaori、Matsubara Keiko、Sano Shinichiro、Yamazawa Kazuki、Fukami Maki、Ogata Tsutomu、Kagami Masayo
    • Journal Title

      Journal of Human Genetics

      Volume: 67 Issue: 10 Pages: 607-611

    • DOI

      10.1038/s10038-022-01048-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22K07858, KAKENHI-PROJECT-21K19751, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-23K24309
  • [Journal Article] Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa2022

    • Author(s)
      Tachibana Nobutaka、Hosono Katsuhiro、Nomura Shuhei、Arai Shinji、Torii Kaoruko、Kurata Kentaro、Sato Miho、Shimakawa Shuichi、Azuma Noriyuki、Ogata Tsutomu、Wada Yoshinao、Okamoto Nobuhiko、Saitsu Hirotomo、Nishina Sachiko、Hotta Yoshihiro
    • Journal Title

      Genes

      Volume: 13 Issue: 2 Pages: 359-359

    • DOI

      10.3390/genes13020359

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K10004, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-19H03810, KAKENHI-PROJECT-20H03641, KAKENHI-PROJECT-20K09825, KAKENHI-PROJECT-22K09848, KAKENHI-PROJECT-20H03845, KAKENHI-PROJECT-22K19606
  • [Journal Article] Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse2022

    • Author(s)
      Yasuko Fujisawa*, Hiroyuki Ono*, Alu Konno, Ikuko Yao, Hiroaki Itoh, Takashi Baba, Kenichirou Morohashi, Yuko Katoh-Fukui, Mami Miyado, Maki Fukami, Tsutomu Ogata
    • Journal Title

      Journal of the Endocrine Society

      Volume: 6 Pages: 1-11

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21K15879
  • [Journal Article] Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders2022

    • Author(s)
      Hara-Isono Kaori、Nakamura Akie、Fuke Tomoko、Inoue Takanobu、Kawashima Sayaka、Matsubara Keiko、Sano Shinichiro、Yamazawa Kazuki、Fukami Maki、Ogata Tsutomu、Kagami Masayo
    • Journal Title

      The Journal of Clinical Endocrinology & Metabolism

      Volume: 107 Issue: 8 Pages: e3121-e3133

    • DOI

      10.1210/clinem/dgac319

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-22K07858, KAKENHI-PROJECT-21K19751, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-23K24309
  • [Journal Article] A case of siblings with juvenile retinitis pigmentosa associated with <i>NEK1</i> gene variants2022

    • Author(s)
      Hikoya Akiko、Hosono Katsuhiro、Ono Kaoru、Arai Shinji、Tachibana Nobutaka、Kurata Kentaro、Torii Kaoruko、Sato Miho、Saitsu Hirotomo、Ogata Tsutomu、Hotta Yoshihiro
    • Journal Title

      Ophthalmic Genetics

      Volume: - Issue: 5 Pages: 1-6

    • DOI

      10.1080/13816810.2022.2141788

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20K09825, KAKENHI-PROJECT-20H00539
  • [Journal Article] Intrauterine hyponutrition reduces fetal testosterone production and postnatal sperm count in the mouse.2022

    • Author(s)
      Fujisawa Y, Ono H, Konno A, Yao I, Itoh H, Baba T, Morohashi K, Katoh-Fukui Y, Miyado M, Fukami M and Ogata T.
    • Journal Title

      Journal of the Endocrine Society

      Volume: 6 Issue: 4 Pages: 1-11

    • DOI

      10.1210/jendso/bvac022

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K09682, KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-20K08863, KAKENHI-PROJECT-21K18298, KAKENHI-PROJECT-20K08255, KAKENHI-PROJECT-20H03436, KAKENHI-PROJECT-20H03823, KAKENHI-PROJECT-22H00492
  • [Journal Article] Retinitis pigmentosa with optic neuropathy and COQ2 mutations: A case report2022

    • Author(s)
      Kurata K, Hosono K, Takayama M, Tatsuno M, Saitsu H, Ogata T, Hotta Y
    • Journal Title

      Am J Ophthalmol Case Rep

      Volume: - Pages: 101298-101298

    • DOI

      10.1016/j.ajoc.2022.101298

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-20H03641, KAKENHI-PROJECT-20K18340
  • [Journal Article] Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system2022

    • Author(s)
      Fuke T, Nakamura A, Inoue T, Kawashima S, Hara-Isono K, Matsubara K, Sano S, Yamazawa K, Fukami M, Ogata T, Kagami M
    • Journal Title

      J Hum Genet

      Volume: -

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20H00539
  • [Journal Article] Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndrome2021

    • Author(s)
      Nishina Sachiko、Hosono Katsuhiro、Ishitani Shizuka、Kosaki Kenjiro、Yokoi Tadashi、Yoshida Tomoyo、Tomita Kaoru、Fukami Maki、Saitsu Hirotomo、Ogata Tsutomu、Ishitani Tohru、Hotta Yoshihiro、Azuma Noriyuki
    • Journal Title

      Journal of Human Genetics

      Volume: - Issue: 10 Pages: 1021-1027

    • DOI

      10.1038/s10038-021-00909-x

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-20K09825, KAKENHI-PROJECT-20K21502, KAKENHI-PROJECT-19H03412, KAKENHI-PROJECT-19K10004, KAKENHI-PUBLICLY-20H05365, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-19H03810, KAKENHI-PLANNED-21H05287
  • [Journal Article] 思春期早発症が先行した松果体胚細胞腫瘍2021

    • Author(s)
      山本拓也、村松真由美、小野裕之、大髙幸之助、坂口公祥、緒方勤、藤澤泰子
    • Journal Title

      日小児会誌

      Volume: 125 Pages: 1316-1322

    • NAID

      40022707852

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20H00539
  • [Journal Article] A patient with Silver-Russell syndrome with multilocus imprinting disturbance, and Schimke immuno-osseous dysplasia unmasked by uniparental isodisomy of chromosome 22021

    • Author(s)
      Hara-Isono K, Matsubara K, Hamada R, Shimada S, Yamaguchi T, Wakui K, Miyazaki O, Kurosawa K, Fukami M, Ogata T, Kosho T, Kagami M
    • Journal Title

      J Hum Genet

      Volume: - Issue: 11 Pages: 1121-1126

    • DOI

      10.1038/s10038-021-00937-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20H00539
  • [Journal Article] Insulin resistant diabetes mellitus in SHORT syndrome: case report and literature review2021

    • Author(s)
      Masunaga Yohei、Fujisawa Yasuko、Muramatsu Mayumi、Ono Hiroyuki、Inoue Takanobu、Fukami Maki、Kagami Masayo、Saitsu Hirotomo、Ogata Tsutomu
    • Journal Title

      Endocr J

      Volume: 68 Issue: 1 Pages: 111-117

    • DOI

      10.1507/endocrj.EJ20-0291

    • NAID

      130007975883

    • ISSN
      0918-8959, 1348-4540
    • Language
      English
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-20H00539
  • [Journal Article] ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance2021

    • Author(s)
      Kagami M, Hara-Isono K, Matsubara K, Nakabayashi K, Narumi S, Fukami M, Ohkubo Y, Saitsu H, Takada S, Ogata T
    • Journal Title

      Clin Epigenetics

      Volume: 13 Issue: 1 Pages: 119-119

    • DOI

      10.1186/s13148-021-01106-5

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-20H03641
  • [Journal Article] Human Spermatogenesis Tolerates Massive Size Reduction of the Pseudoautosomal Region2020

    • Author(s)
      Fukami Maki、Fujisawa Yasuko、Ono Hiroyuki、Jinno Tomoko、Ogata Tsutomu
    • Journal Title

      Genome Biology and Evolution

      Volume: 12 Issue: 11 Pages: 1961-1964

    • DOI

      10.1093/gbe/evaa168

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-20H00539
  • [Journal Article] Assisted reproductive technology represents a possible risk factor for development of epimutation-mediated imprinting disorders for mothers aged ? 30?years2020

    • Author(s)
      Hara-Isono Kaori、Matsubara Keiko、Mikami Masashi、Arima Takahiro、Ogata Tsutomu、Fukami Maki、Kagami Masayo
    • Journal Title

      Clinical Epigenetics

      Volume: 12 Issue: 1 Pages: 111-111

    • DOI

      10.1186/s13148-020-00900-x

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-20H00539
  • [Journal Article] Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome2020

    • Author(s)
      Yamazawa K, Inoue T, Sakemi Y, Nakashima T, Yamashita H, Khono K, Fujita H, Enomoto K, Nakabayashi K, Hata K, Nakashima M, Matsunaga T, Nakamura A, Matsubara K, Ogata T, Kagami M.
    • Journal Title

      Journal of Medical Genetics

      Volume: - Issue: 6 Pages: 107019-107019

    • DOI

      10.1136/jmedgenet-2020-107019

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-20H00539
  • [Journal Article] Genome-wide methylation analysis in Silver?Russell syndrome, Temple syndrome, and Prader?Willi syndrome2020

    • Author(s)
      Hara-Isono Kaori、Matsubara Keiko、Fuke Tomoko、Yamazawa Kazuki、Satou Kazuhito、Murakami Nobuyuki、Saitoh Shinji、Nakabayashi Kazuhiko、Hata Kenichiro、Ogata Tsutomu、Fukami Maki、Kagami Masayo
    • Journal Title

      Clinical Epigenetics

      Volume: 12 Issue: 1 Pages: 159-159

    • DOI

      10.1186/s13148-020-00949-8

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-20H05700, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-19H03628
  • 1.  Ogata Tsutomu (40169173)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 8 results
  • 2.  深見 真紀 (40265872)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 6 results
  • 3.  KAGAMI Masayo
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 4.  NISHINA Sachiko
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 5.  HOTTA Yoshihiro
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 6.  宮戸 真美
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 7.  中林 一彦
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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