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

Research Project

Project/Area Number 20H00539
Research Category

Grant-in-Aid for Scientific Research (A)

Allocation TypeSingle-year Grants
Section一般
Review Section Medium-sized Section 54:Internal medicine of the bio-information integration and related fields
Research InstitutionHamamatsu University School of Medicine

Principal Investigator

Ogata Tsutomu  浜松医科大学, 医学部, 特命研究教授 (40169173)

Co-Investigator(Kenkyū-buntansha) 深見 真紀  国立研究開発法人国立成育医療研究センター, 分子内分泌研究部, 部長 (40265872)
小野 裕之  浜松医科大学, 医学部附属病院, 助教 (40868866)
Project Period (FY) 2020-04-01 – 2023-03-31
Project Status Completed (Fiscal Year 2022)
Budget Amount *help
¥45,110,000 (Direct Cost: ¥34,700,000、Indirect Cost: ¥10,410,000)
Fiscal Year 2022: ¥14,820,000 (Direct Cost: ¥11,400,000、Indirect Cost: ¥3,420,000)
Fiscal Year 2021: ¥14,820,000 (Direct Cost: ¥11,400,000、Indirect Cost: ¥3,420,000)
Fiscal Year 2020: ¥15,470,000 (Direct Cost: ¥11,900,000、Indirect Cost: ¥3,570,000)
Keywords性分化疾患 / 生殖機能障害 / 多因子疾患 / 子宮内発育不全 / 内分泌撹乱環境化学物質感受性 / ESR1 / 微細欠失 / 絶対連鎖不平衡
Outline of Research at the Start

性分化疾患・生殖機能障害は、単一遺伝子疾患としてのみならず、環境因子と遺伝的感受性に支配される多因子疾患としても発症する。本研究では、環境因子として子宮内発育不全、遺伝的感受性としてエストロゲン受容体alpha遺伝子(ESR1)の微細欠失、環境因子と遺伝的感受性の協調作用解析モデルとして遺伝子改変マウスを対象する解析を行い、多因子疾患としての性分化疾患・生殖機能障害発症機序の解明に挑む。

Outline of Final Research Achievements

We have revealed that intrauterine hyponutrition causes significantly reduced intra-testicular testosterone production in association with significantly reduced expressions of steroidogenic genes during fetal life, and significantly decreased sperm count in association with significantly altered expressions of oxidation stress-related, apoptosis-related, and spermatogenesis-related genes in the postnatal life in the mouse. We have also showed that a 2,244 bp microdeletion at ESR1 intron 6 (ΔESR1) functions as a susceptibility factor for cryptorchidism and hypospadias by facilitating the ESR1 expression. We have also clarified the underlying cause for the generation of the absolute linkage disequilibrium between ΔESR1 and the susceptibility haplotype. The results provide highly valuable information regarding the development of disorders of sex development and reproductive dysfunction as multifactorial disorders.

Academic Significance and Societal Importance of the Research Achievements

本研究成果の学術的意義としては、多因子疾患としての性分化疾患・生殖機能障害発症機序を子宮内栄養不全という環境因子とエストロゲン受容体α遺伝子(ESR1) 発現を亢進させる微細欠失(ΔESR1)という遺伝的感受性の観点から明らかとしたことが挙げられる。本研究の社会的意義には、わが国で大きな問題となっている妊婦の痩せによる子宮内発育不全が、DoHAD仮説で研究されている将来のメタボリック症候群だけではなく性分化疾患や生殖機能障害発症リスクであることを世界で初めて示したこと、ならびに、ΔESR1が世界的に大きな問題となっている内分泌撹乱環境化学物質感受性にも関わることを明らかとしたことが挙げられる。

Report

(5 results)
  • 2022 Annual Research Report   Final Research Report ( PDF )
  • 2021 Annual Research Report
  • 2020 Comments on the Screening Results   Annual Research Report
  • Research Products

    (78 results)

All 2023 2022 2021 2020 Other

All Int'l Joint Research (1 results) Journal Article (60 results) (of which Int'l Joint Research: 7 results,  Peer Reviewed: 57 results,  Open Access: 32 results) Presentation (17 results) (of which Int'l Joint Research: 2 results,  Invited: 10 results)

  • [Int'l Joint Research] Pisa University(イタリア)

    • Related Report
      2022 Annual Research Report
  • [Journal Article] PORCN-related microphthalmia with limb anomalies: case report and literature review.2023

    • Author(s)
      Fukahori K, Yamoto K, Saitsu H, Ogata T, Nagasaki K
    • Journal Title

      Am J Med Genet A

      Volume: 191(2) Issue: 2 Pages: 636-639

    • DOI

      10.1002/ajmg.a.63048

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed
  • [Journal Article] A questionnaire-based survey of medical conditions in adults with Prader-Willi syndrome in Japan: implications for transitional care2023

    • Author(s)
      Kawai M, Muroya K, Murakami N, Ihara H, Takahashi Y, Horikawa R, Ogata T
    • Journal Title

      Endocrine Journal

      Volume: 70 Issue: 5 Pages: 519-528

    • DOI

      10.1507/endocrj.EJ22-0561

    • ISSN
      0918-8959, 1348-4540
    • Related Report
      2022 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] A deep intronic TCTN2 variant activating a cryptic exon predicted by SpliceRover in a patient with Joubert syndrome.2023

    • Author(s)
      Hiraide T, Shimizu K, Okumura Y, Miyamoto S, Nakashima M, Ogata T, Saistu H
    • Journal Title

      J Hum Genet

      Volume: - Issue: 7 Pages: 499-505

    • DOI

      10.1038/s10038-023-01143-3

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Microdeletion at ESR1 Intron 6 (DEL_6_75504) Is a Susceptibility Factor for Cryptorchidism and Hypospadias.2023

    • Author(s)
      Masunaga Y, Fujisawa Y, Massart F, Spinelli C, Kojima Y, Mizuno K, Hayashi Y, Sasagawa I, Yoshida R, Kato F, Fukami M, Kamatani N, Saitsu H, Ogata T.
    • Journal Title

      J Clin Endocrinol Metab.

      Volume: Apr 3 Issue: 10 Pages: 1-11

    • DOI

      10.1210/clinem/dgad187

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Molecular Autopsy Underlie COVID-19-Associated Sudden, Unexplained Child Mortality.2023

    • Author(s)
      Unuma K, Tomomasa D, Noma K, Yamamoto K, Matsuyama T, Makino Y, Hijikata A, Wen S, Ogata T, Okamoto N, Okada S, Ohashi K, Uemura K, Kanegane H
    • Journal Title

      Front Immunol (accepted)

      Volume: -

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] c.116G>A, p(Arg39His)ホモ接合性バリアントが同定された一過性眼振を伴う遊離シアル酸蓄積症の姉弟例2023

    • Author(s)
      伊藤あかね、平出拓也、古澤友花子、松本由香里、川崎知子、鶴井聡、才津浩智、緒方勤、福田冬季子
    • Journal Title

      浜松医科大学小児科学雑誌

      Volume: 3 (1) Pages: 36-44

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed
  • [Journal Article] インプリンティング2023

    • Author(s)
      緒方勤
    • Journal Title

      Genetics in CKD

      Volume: 94 (3) Pages: 339-345

    • Related Report
      2022 Annual Research Report
  • [Journal Article] Retrotransposition disrupting EBP in a girl and her mother with X-linked dominant chondrodysplasia punctata2022

    • Author(s)
      Hiraide T, Masunaga Y, Honda A, Kato F, Fukuda T, Fukami M, Nakashima M, Saitsu H, Ogata T
    • Journal Title

      J Hum Genet

      Volume: - Issue: 5 Pages: 303-306

    • DOI

      10.1038/s10038-021-01000-1

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] A novel intronic PORCN variant creating an alternative splice acceptor site in a mother and her daughter with focal dermal hypoplasia2022

    • Author(s)
      Yamoto K, Okada S, Kato F, Fujisawa Y, Fukami M, Saitsu H, Ogata T
    • Journal Title

      Am J Med Genet A

      Volume: - Issue: 5 Pages: 1612-1617

    • DOI

      10.1002/ajmg.a.62649

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Genome sequencing and RNA sequencing of urinary cells reveal an intronic FBN1 variant causing aberrant splicing2022

    • Author(s)
      Hiraide Takuya、Shimizu Kenji、Miyamoto Sachiko、Aoto Kazushi、Nakashima Mitsuko、Yamaguchi Tomomi、Kosho Tomoki、Ogata Tsutomu、Saitsu Hirotomo
    • Journal Title

      Journal of Human Genetics

      Volume: - Issue: 7 Pages: 387-392

    • DOI

      10.1038/s10038-022-01016-1

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed
  • [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

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed / Open Access
  • [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

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] ACAN biallelic variants in a girl with severe idiopathic short stature2022

    • Author(s)
      Masunaga Y, Ohkubo Y, Nishimura G, Ueno T, Fujisawa Y, Fukami M, Saitsu H, Ogata T
    • Journal Title

      J Hum Genet

      Volume: - Issue: 8 Pages: 481-486

    • DOI

      10.1038/s10038-022-01030-3

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed
  • [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

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] SHOX far-downstream deletion in a patient with non-syndromic short stature2022

    • Author(s)
      Fukami M, Shindo J, Ogata T, Kageyama I, Kamimaki T
    • Journal Title

      Am J Med Genet A

      Volume: - Issue: 7 Pages: 2173-2177

    • DOI

      10.1002/ajmg.a.62734

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed
  • [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

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences2022

    • Author(s)
      Eggermann T, Yapici E, Bliek J, Pereda A, Begemann M, Russo S, Tannorella P, Calzari L, de Nanclares GP, Lombardi P, Temple IK, Mackay D, Riccio A, Kagami M, Ogata T, Lapunzina P, Monk D, Maher ER, Tuemer Z
    • Journal Title

      Clin Epigenetics

      Volume: 14 Issue: 1 Pages: 41-41

    • DOI

      10.1186/s13148-022-01259-x

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] The first adult case of cytochrome P450 oxidoreductase deficiency with sufficient semen volume and sperm concentration2022

    • Author(s)
      Sato T, Ishii T, Fukami M, Ogata T, Hasegawa T
    • Journal Title

      Congenit Anom (Kyoto)

      Volume: - Issue: 3 Pages: 136-137

    • DOI

      10.1111/cga.12464

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Combined pituitary hormone deficiency in a patient with an <i>FGFR1</i> missense variant: case report and literature review2022

    • Author(s)
      Sano S, Masunaga Y, Kato F, Fujisawa Y, Saitsu H, Ogata T
    • Journal Title

      Clinical Pediatric Endocrinology

      Volume: 31 Issue: 3 Pages: 172-177

    • DOI

      10.1297/cpe.2022-0020

    • ISSN
      0918-5739, 1347-7358
    • Related Report
      2022 Annual Research Report
    • Peer Reviewed / Open Access
  • [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 &amp; Metabolism

      Volume: 107 Issue: 8 Pages: e3121-e3133

    • DOI

      10.1210/clinem/dgac319

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Familial Pseudohypoparathyroidism Type IB Associated with an SVA Retrotransposon Insertion in the GNAS Locus2022

    • Author(s)
      Sayaka Kawashima, Akiko Yuno, Shinichiro Sano, Masayo Kagami
    • Journal Title

      J Bone Miner Res .

      Volume: 10 Issue: 10 Pages: 1850-1859

    • DOI

      10.1002/jbmr.4652

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Clinical and molecular findings in three Japanese patients with N-acetylneuraminic acid synthetase-congenital disorder of glycosylation (NANS-CDG).2022

    • Author(s)
      Masunaga Y, Nishimura G, Hishiyama T, Imamura M, Kashimada K, Kadoya M, Wada Y, Okamoto N, Oba D, Ohashi H, Ikeno M, Sakamoto Y, Fukami M, Saitsu H, Ogata T
    • Journal Title

      Sci Rep

      Volume: 12 Pages: 17079-17079

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed / Open Access
  • [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

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed
  • [Journal Article] First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders2022

    • Author(s)
      Mackay Deborah、Bliek Jet、Kagami Masayo et al.
    • Journal Title

      Clinical Epigenetics

      Volume: 14 Issue: 1 Pages: 143-143

    • DOI

      10.1186/s13148-022-01358-9

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Characterization of KMT2A :: MATR3 fusion in a patient with acute lymphoblastic leukemia and monitoring of minimal residual disease by nanoplate digital PCR.2022

    • Author(s)
      Komatsu K, Sakaguchi K, Shimizu D, Yamoto K, Kato F, Ogata T, Saitsu H
    • Journal Title

      Pediatr Blood Cancer

      Volume: e30120 Issue: 4

    • DOI

      10.1002/pbc.30120

    • Related Report
      2022 Annual Research Report
    • Peer Reviewed
  • [Journal Article] MAMLD1 and differences/disorders of sex development: An update.2022

    • Author(s)
      Miyado M, Fukami M and Ogata T.
    • Journal Title

      Sexual Development

      Volume: 印刷中 Issue: 2-3 Pages: 1-12

    • DOI

      10.1159/000519298

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Congenital disorders of estrogen biosynthesis and action2022

    • Author(s)
      Fukami Maki、Ogata Tsutomu
    • Journal Title

      Best Practice and Research Clinical Endocrinology and Metabolism

      Volume: 36 Issue: 1 Pages: 101580-101580

    • DOI

      10.1016/j.beem.2021.101580

    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Silver-Russell症候群とその周辺2022

    • Author(s)
      緒方勤
    • Journal Title

      周産期医学特集:知っておくべき周産期・新生児領域の遺伝学的検査を展望する

      Volume: 52 (5) Pages: 761-764

    • Related Report
      2022 Annual Research Report
  • [Journal Article] ミュラー管発生異常2022

    • Author(s)
      緒方勤
    • Journal Title

      末岡浩(企画)AYA世代の補正ヘルスケア.産婦人科の実際.9月臨時増刊号

      Volume: 71 (10) Pages: 1034-1040

    • Related Report
      2022 Annual Research Report
  • [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: -

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Combined pituitary hormone deficiency in a patient with an FGFR1 missense variant: case report and literature review2022

    • Author(s)
      Shinichiro Sano1,2, Yohei Masunaga2, Fumiko Kato3, Yasuko Fujisawa2, Hirotomo Saitsu4, Tsutomu Ogata
    • Journal Title

      Clin Pediatr Endocrinol

      Volume: -

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed / Open Access
  • [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

      Endocrine Journal

      Volume: 68 Issue: 1 Pages: 111-117

    • DOI

      10.1507/endocrj.EJ20-0291

    • NAID

      130007975883

    • ISSN
      0918-8959, 1348-4540
    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Primary ovarian insufficiency in a female with phosphomannomutase-2 gene (<i>PMM2</i>) mutations for congenital disorder of glycosylation2021

    • Author(s)
      Masunaga Yohei、Mochizuki Mie、Kadoya Machiko、Wada Yoshinao、Okamoto Nobuhiko、Fukami Maki、Kato Fumiko、Saitsu Hirotomo、Ogata Tsutomu
    • Journal Title

      Endocrine Journal

      Volume: 68 Issue: 5 Pages: 605-611

    • DOI

      10.1507/endocrj.EJ20-0706

    • NAID

      130008044607

    • ISSN
      0918-8959, 1348-4540
    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] NDNF variants are rare in patients with congenital hypogonadotropic hypogonadism2021

    • Author(s)
      Tamaoka Satoshi、Suzuki Erina、Hattori Atsushi、Ogata Tsutomu、Fukami Maki、Katoh-Fukui Yuko
    • Journal Title

      Human Genome Variation

      Volume: 8 Issue: 1 Pages: 5-5

    • DOI

      10.1038/s41439-021-00137-x

    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Long-term Effect of Aromatase Inhibition in Aromatase Excess Syndrome2021

    • Author(s)
      Binder Gerhard、Nakamura Akie、Schweizer Roland、Ogata Tsutomu、Fukami Maki、Nagasaki Keisuke
    • Journal Title

      The Journal of Clinical Endocrinology & Metabolism

      Volume: 106 Issue: 5 Pages: 1491-1500

    • DOI

      10.1210/clinem/dgab054

    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation2021

    • Author(s)
      Saida K, Fukuda T, Scott DA, Sengoku T, Ogata K, Nicosia A, Hernandez-Garcia A, Lalani SR, Azamian MS, Streff H, Liu P, Dai H, Mizuguchi T, Miyatake S, Asahina M, Ogata T, Miyake N, Matsumoto N.
    • Journal Title

      Front Cell Dev Biol.

      Volume: 9 Pages: 631428-631428

    • DOI

      10.3389/fcell.2021.631428

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [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

    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole-exome sequencing2021

    • Author(s)
      Hiraide T, Yamoto K, Masunaga Y, Asahina M, Endoh Y, Ohkubo Y, Matsubayashi T, Tsurui S, Yamada H, Yanagi K, Nakashima M, Hirano K, Sugimura H, Fukuda T, Ogata T, Saistu T
    • Journal Title

      Clin Genet

      Volume: 100 Issue: 1 Pages: 40-50

    • DOI

      10.1111/cge.13951

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Parthenogenetic mosaicism: generation via second polar body retention and unmasking of a likely causative PER2 variant for hypersomnia2021

    • Author(s)
      Masunaga Yohei、Kagami Masayo、Kato Fumiko、Usui Takeshi、Yonemoto Takako、Mishima Kazuo、Fukami Maki、Aoto Kazushi、Saitsu Hirotomo、Ogata Tsutomu
    • Journal Title

      Clinical Epigenetics

      Volume: 13 Issue: 1 Pages: 73-73

    • DOI

      10.1186/s13148-021-01062-0

    • NAID

      120007042184

    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] SOX10 mutation screening for 117 patients with Kallmann syndrome2021

    • Author(s)
      Shima Hirohito、Tokuhiro Etsuro、Okamoto Shingo、Nagamori Mariko、Ogata Tsutomu、Narumi Satoshi、Nakamura Akie、Izumi Yoko、Jinno Tomoko、Suzuki Erina、Fukami Maki
    • Journal Title

      Journal of the Endocrine Society

      Volume: 5 Issue: 7

    • DOI

      10.1210/jendso/bvab056

    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [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

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [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

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Novel ALG12 variants and hydronephrosis in siblings with impaired N-glycosylation2021

    • Author(s)
      Hiraide T, Wada Y, Matsubayashi T, Kadoya M, Masunaga Y, Ohkubo Y, Nakashima M, Okamoto N, Ogata T, Saitsu H
    • Journal Title

      Brain Dev

      Volume: -

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Global developmental delay, systemic dysmorphism and epilepsy in a patient with a de novo U2AF2 variant.2021

    • Author(s)
      Hiraide T, Tanaka T, Masunaga Y, Ohkubo Y, Nakashima M, Fukuda T, Ogata T, Saitsu H
    • Journal Title

      J Hum Genet

      Volume: - Issue: 12 Pages: 1185-1187

    • DOI

      10.1038/s10038-021-00948-4

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [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

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] 新規ヒトインプリンティング疾患「Kagami-Ogata症候群」の樹立2021

    • Author(s)
      緒方勤
    • Journal Title

      浜松医科大学小児科学雑誌

      Volume: 1 Pages: 3-19

    • NAID

      120006975657

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] プラダーウイリ症候群とGH治療.特集:成長ホルモン (GH) 治療を考える2021

    • Author(s)
      緒方勤、村上信之、永井敏郎
    • Journal Title

      糖尿病・内分泌代謝内科

      Volume: 53 Pages: 178-186

    • NAID

      40022674665

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] GNAS-Gsα機能亢進型バリアントに起因する新たな先天性腎疾患の発見2021

    • Author(s)
      宮戸真美、緒方勤、深見真紀
    • Journal Title

      糖尿病・内分泌代謝内科

      Volume: 53 Pages: 71-77

    • NAID

      40022653122

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] 性分化分野で多用する遺伝学的検査2021

    • Author(s)
      緒方勤
    • Journal Title

      臨床遺伝専門医テキスト:各論I 臨床遺伝学生殖・周産期領域

      Volume: - Pages: 38-43

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [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

    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Kagami?Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG32020

    • Author(s)
      Omark Jessica、Masunaga Yohei、Hannibal Mark、Shaw Brandon、Fukami Maki、Kato Fumiko、Saitsu Hirotomo、Kagami Masayo、Ogata Tsutomu
    • Journal Title

      Journal of Human Genetics

      Volume: 66 Issue: 4 Pages: 439-443

    • DOI

      10.1038/s10038-020-00858-x

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum2020

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

      The Journal of Clinical Endocrinology & Metabolism

      Volume: 106 Issue: 3 Pages: 802-813

    • DOI

      10.1210/clinem/dgaa856

    • Related Report
      2021 Annual Research Report 2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Treatment approaches for congenital transverse limb deficiency: Data analysis from an epidemiological national survey in Japan2020

    • Author(s)
      Mano Hiroshi、Fujiwara Sayaka、Takamura Kazuyuki、Kitoh Hiroshi、Takayama Shinichiro、Ogata Tsutomu、Haga Nobuhiko
    • Journal Title

      Journal of Orthopaedic Science

      Volume: 20 Issue: 4 Pages: 650-654

    • DOI

      10.1016/j.jos.2020.05.008

    • Related Report
      2021 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Random X chromosome inactivation in patients with Klinefelter syndrome.2020

    • Author(s)
      Kinjo K, Yoshida T, Kobori Y, Okada H, Suzuki E, Ogata T, Miyado M and Fukami M.
    • Journal Title

      Mol Cell Pediatr.

      Volume: 7 Issue: 1 Pages: 1-1

    • DOI

      10.1186/s40348-020-0093-x

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients2020

    • Author(s)
      Inoue Takanobu、et al
    • Journal Title

      Clinical Epigenetics

      Volume: 12 Issue: 1 Pages: 86-86

    • DOI

      10.1186/s13148-020-00865-x

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency.2020

    • Author(s)
      Kinjo K, Nagasaki K, Muroya K, Suzuki E, Ishiwata K, Nakabayashi K, Hattori A, Nagao K, Nozawa R-S, Obuse C, Miyado K, Ogata T, Fukami M and Miyado M.
    • Journal Title

      Scientific Reports

      Volume: 10 Issue: 1 Pages: 10985-10985

    • DOI

      10.1038/s41598-020-67715-x

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [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

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [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

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Nonsense-associated altered splicing of MAP3K1 in two siblings with 46,XY disorders of sex development.2020

    • Author(s)
      Igarashi M, Masunaga Y, Hasegawa Y, Kinjo K, Miyado M, Saitsu H, Kato-Fukui Y, Horikawa R, Okubo Y, Ogata T and Fukami M.
    • Journal Title

      Scientific Reports

      Volume: 10 Issue: 1 Pages: 17375-17375

    • DOI

      10.1038/s41598-020-74405-1

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [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

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] 第6回論文執筆応援セミナー2023

    • Author(s)
      緒方勤
    • Organizer
      第45回日本小児遺伝学会
    • Related Report
      2022 Annual Research Report
    • Invited
  • [Presentation] Plenary Lecture: Genomic imprinting and its clinical relevance: lesson from Kagami-Ogata syndrome and Temple syndrome.2023

    • Author(s)
      Ogata T
    • Organizer
      11th International Meeting of Pediatric Endocrinology
    • Related Report
      2022 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] NIPT(新型出生前検査)について2023

    • Author(s)
      緒方勤
    • Organizer
      母子保健セミナー
    • Related Report
      2022 Annual Research Report
    • Invited
  • [Presentation] ヒト性分化疾患研究:遺伝と環境の観点から2023

    • Author(s)
      緒方勤
    • Organizer
      性の研究会 Beyond Sex Differentiation
    • Related Report
      2022 Annual Research Report
    • Invited
  • [Presentation] Microdeletion at ESR1 Intron 6 (DEL_6_75504) Is a Susceptibility Factor for Cryptorchidism and Hypospadias.2023

    • Author(s)
      Ogata T
    • Organizer
      11th International Meeting of Pediatric Endocrinology
    • Related Report
      2022 Annual Research Report
    • Int'l Joint Research
  • [Presentation] もっと研究しよう・論文も書こう2022

    • Author(s)
      緒方勤
    • Organizer
      第55回日本小児内分泌学会学術集会
    • Related Report
      2022 Annual Research Report
    • Invited
  • [Presentation] 生殖補助医療とインプリント異常:シンポジウムにより誕生した児の健康2022

    • Author(s)
      緒方勤
    • Organizer
      第67回日本生殖医学会学術講演会・総会
    • Related Report
      2022 Annual Research Report
    • Invited
  • [Presentation] 性染色体異常症と成長2022

    • Author(s)
      緒方勤
    • Organizer
      第40回 小児内分泌・代謝研究会信濃町フォーラム
    • Related Report
      2022 Annual Research Report 2021 Annual Research Report
    • Invited
  • [Presentation] 多因子疾患としての性分化疾患発症機序2022

    • Author(s)
      緒方勤
    • Organizer
      和3年度第4回周産期医療研究会
    • Related Report
      2022 Annual Research Report
    • Invited
  • [Presentation] SGA発症の遺伝的機序2022

    • Author(s)
      緒方勤
    • Organizer
      Next Generation Meeting Current and future management in growth disorders.
    • Related Report
      2022 Annual Research Report
    • Invited
  • [Presentation] ヌーナン症候群における成長・成熟2022

    • Author(s)
      緒方勤
    • Organizer
      ヌーナン症候群類縁疾患合同シンポジウム (AMED研究班主催)
    • Related Report
      2022 Annual Research Report
    • Invited
  • [Presentation] 多因子疾患としての性分化疾患発症機序2022

    • Author(s)
      緒方勤
    • Organizer
      令和3年度第4回周産期医療研究会
    • Related Report
      2021 Annual Research Report
  • [Presentation] ヌーナン症候群:診断と治療のupdate2021

    • Author(s)
      緒方勤
    • Organizer
      第43回日本小児遺伝学会学術集会企業共催セミナー
    • Related Report
      2021 Annual Research Report
  • [Presentation] IRUD拠点病院としての工夫:検体処理、NGS解析データマイニング、機能解析を主に2021

    • Author(s)
      緒方勤
    • Organizer
      IRUDワークショップ
    • Related Report
      2021 Annual Research Report
  • [Presentation] SGAをめぐって2021

    • Author(s)
      緒方勤
    • Organizer
      Next Generation Meeting Current and future management in growth disorders
    • Related Report
      2021 Annual Research Report
  • [Presentation] SGA:思春期・性分化を主に2021

    • Author(s)
      緒方勤
    • Organizer
      Next Generation Meeting Current and future management in growth disorders
    • Related Report
      2021 Annual Research Report
  • [Presentation] SGA: 遺伝的機序と思春期・性分化2021

    • Author(s)
      緒方勤
    • Organizer
      Next Generation Meeting Current and future management in growth disorders
    • Related Report
      2021 Annual Research Report

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Published: 2020-04-28   Modified: 2024-01-30  

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