ONO Hiroyuki 小野裕之

… Alternative Names

小野裕之オノヒロユキ

Less

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

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

ONO Hiroyuki 小野 裕之

小野 裕之 オノ ヒロユキ

Research Projects

Research Products

Co-Researchers

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

Project Period (FY)

Research Category

Review Section

Research Institution

Clarification of underlying factors for disorders of sex development and reproductive dysfunction as multifactorial disorders

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[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)

Journal Title

DOI

Data Source

[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)

Journal Title

DOI

Data Source

[Journal Article] Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse2022

Author(s)

Journal Title

Data Source

[Journal Article] Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A case of siblings with juvenile retinitis pigmentosa associated with <i>NEK1</i> gene variants2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Intrauterine hyponutrition reduces fetal testosterone production and postnatal sperm count in the mouse.2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Retinitis pigmentosa with optic neuropathy and COQ2 mutations: A case report2022

Author(s)

Journal Title

DOI

Data Source

[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)

Journal Title

Data Source

[Journal Article] Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndrome2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] 思春期早発症が先行した松果体胚細胞腫瘍2021

Author(s)

Journal Title

NAID

Data Source

[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)

Journal Title

DOI

Data Source

[Journal Article] Insulin resistant diabetes mellitus in SHORT syndrome: case report and literature review2021

Author(s)

Journal Title

DOI

NAID

ISSN

Language

Data Source

[Journal Article] ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance2021

Author(s)

ONO Hiroyuki 小野裕之

小野裕之オノヒロユキ