Sano Sinichiro 佐野伸一朗

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佐野伸一朗サノシンイチロウ

Sano Shinichiro 佐野伸一朗

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Researcher Number	60535574
Affiliation (Current)	2025: 地方独立行政法人静岡県立病院機構静岡県立こども病院(臨床研究室), 臨床研究室, 医長
Affiliation (based on the past Project Information) *help	2020 – 2023: 地方独立行政法人静岡県立病院機構静岡県立こども病院(臨床研究室), 臨床研究室, 医長 2016 – 2017: 浜松医科大学, 医学部, 協定訪問共同研究員 2015: 国立研究開発法人国立成育医療研究センター, その他部局等, 研究員 2014: 独立行政法人国立成育医療研究センター, 分子内分泌研究部, 研究員
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics
Keywords	Principal Investigator GNAS / 偽性副甲状腺機能低下症 / エキソーム解析 / ゲノムワイド解析 / インプリンティング疾患 / PHP / レトロトランスポゾン / メチル化異常 / PHP-Ib / Pseudohypoparathyroidism … More / AHO徴候 / GNAS-DMRメチル化異常 / ＧＮＡＳ－ＤＭＲメチル化異常 / GNAS遺伝子変異 / ＧＮＡＳ構造異常 / ＧＮＡＳメチル化異常 / ＧＮＡＳ遺伝子 / インプリンティング Less

Exploration of clinical phenotype and pathogenic mechanisms of GNAS related diseasePrincipal Investigator
- Principal Investigator
  
  佐野伸一朗
- Project Period (FY)
  2020 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Shizuoka Prefectural Hospital Organization
Molecular evolutionary genetics analysis and elucidation of pathogenic mechanism of GNAS related imprinting diseasePrincipal Investigator
- Principal Investigator
  
  Sano Shinichiro
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hamamatsu University School of Medicine
  National Center for Child Health and Development

All 2024 2023 2022 2021 2020 2018 2017 2016 2015 Other

All Journal Article Presentation Book

[Book] エピゲノムで新たな解明が進む「先天性疾患」2021
- Author(s)
  佐野伸一朗
- Total Pages
  218
- Publisher
  メディカルデゥ
- ISBN
  9784909508119
- Data Source
  KAKENHI-PROJECT-20K08178
[Book] 医学のあゆみ2017
- Author(s)
  佐野伸一朗
- Total Pages
  70
- Publisher
  医歯薬出版株式会社
- Data Source
  KAKENHI-PROJECT-26461537
[Journal Article] A novel GNAS-Gsα splice donor site variant in a girl with pseudohypoparathyroidism type 1A and her mother with pseudopseudohypoparathyroidism2024
- Author(s)
 Sano Shinichiro、Iwamoto Shotaro、Matsushita Rie、Masunaga Yohei、Fujisawa Yasuko、Ogata Tsutomu
- Journal Title
 
 Clinical Pediatric Endocrinology
 
 Volume: 33 Issue: 2 Pages: 66-70
- DOI
 10.1297/cpe.2023-0065
- ISSN
 0918-5739, 1347-7358
- Language
 English
- Peer Reviewed
- Data Source
 KAKENHI-PROJECT-20K08178
[Journal Article] (Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B2023
- Author(s)
  Urakawa Tatsuki、Sano Shinichiro、Kawashima Sayaka、Nakamura Akie、Shima Hirohito、Ohta Motoki、Yamada Yuki、Nishida Ai、Narusawa Hiromune、Ohtsu Yoshiaki、Matsubara Keiko、Dateki Sumito、Maruo Yoshihiro、Fukami Maki、Ogata Tsutomu、Kagami Masayo
- Journal Title
  
  European Journal of Endocrinology
  
  Volume: 189 Issue: 6 Pages: 590-600
- DOI
  10.1093/ejendo/lvad163
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K08178, KAKENHI-PROJECT-22K07858, KAKENHI-PROJECT-23K07288
[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
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K08178, KAKENHI-PROJECT-21K07334, KAKENHI-PROJECT-22K07858, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-20H03641, KAKENHI-PUBLICLY-21H00342, KAKENHI-PROJECT-23K24490
[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
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-19H03628, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-20K08178
[Journal Article] (Epi)genotype-Phenotype Analysis in 69 Japanese Patients With Pseudohypoparathyroidism Type I2017
- Author(s)
  Sano Shinichiro、Nakamura Akie、Matsubara Keiko、Nagasaki Keisuke、Fukami Maki、Kagami Masayo、Ogata Tsutomu
- Journal Title
  
  J Endocr Soc
  
  Volume: 2 Issue: 1 Pages: 9-23
- DOI
  10.1210/js.2017-00293
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17H04204, KAKENHI-PROJECT-15K09734, KAKENHI-PROJECT-26461537, KAKENHI-PROJECT-15K15096
[Journal Article] A de novo 50-bp GNAS Intragenic Duplication in a Patient with Pseudohypoparathyroidism Type 1a2017
- Author(s)
 Suzuki Erina、Bo Ryosuke、Sue Kaori、Awano Hiroyuki、Ogata Tsutomu、Narumi Satoshi、Kagami Masayo、Sano Shinichiro、Fukami Maki
- Journal Title
 
 Cytogenetic and Genome Research
 
 Volume: 153 Issue: 3 Pages: 125-130
- DOI
 10.1159/000485644
- Peer Reviewed
- Data Source
 KAKENHI-PROJECT-17H03616, KAKENHI-PROJECT-26461537, KAKENHI-PROJECT-15K15096, KAKENHI-PROJECT-17H04204
[Journal Article] Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1b.2016
- Author(s)
  Nakamura A, Hamaguchi E, Horikawa R, Nishimura Y, Matsubara K, Sano S, Nagasaki K, Matsubara Y, Umezawa A, Tajima T, Ogata T, Kagami M, Okamura K, Fukami M.
- Journal Title
  
  J Clin Endocrinol Metab
  
  Volume: 101(7) Issue: 7 Pages: 2623-7
- DOI
  10.1210/jc.2016-1725
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09734, KAKENHI-PROJECT-16K07137, KAKENHI-PROJECT-26461537, KAKENHI-PROJECT-15K15096, KAKENHI-PROJECT-16K21665
[Journal Article] Sporadic pseudohypoparathyroidism type-1b with asymptomatic hypocalcemia.2016
- Author(s)
  Goto M, Sano S, et al
- Journal Title
  
  Pediatr Int
  
  Volume: 58 Issue: 11 Pages: 1229-1231
- DOI
  10.1111/ped.13096
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461537, KAKENHI-PROJECT-15K15096
[Journal Article] Growth hormone deficiency in monozygotic twins with autosomal dominant pseudohypoparathyroidism type Ib.2015
- Author(s)
  Shinicihro Sano
- Journal Title
  
  Endocrine Jouranal
  
  Volume: 未定
- NAID
  130005085768
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] インプリンティング疾患発症に対する生殖補助医療および母親の年齢の影響の解明2023
- Author(s)
  原　香織、松原　圭子、中村　明枝、佐野　伸一朗、井上　毅信、川嶋　明香、福家　智子、山澤　一樹、深見　真紀、緒方　勤、鏡　雅代
- Organizer
  第56回日本小児内分泌学会
- Data Source
  KAKENHI-PROJECT-20K08178
[Presentation] 新規GNASスプライスバリアントによる偽性副甲状腺機能低下症Iaの女児例2023
- Author(s)
  佐野伸一朗, 岩本彰太郎、松下理恵、加藤芙弥子、増永陽平、.藤澤泰子、緒方勤
- Organizer
  第56回日本小児内分泌学会
- Data Source
  KAKENHI-PROJECT-20K08178
[Presentation] GNASスプライスバリアントによる偽性副甲状腺機能低下症Iaの１例2023
- Author(s)
  佐野伸一朗,松下理恵、加藤芙弥子、増永陽平、.藤澤泰子、緒方勤
- Organizer
  第96回日本内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08178
[Presentation] GNAS 遺伝子座へのレトロトランスポゾン挿入によって発症した偽性副甲状腺機能低下症1B 型兄妹例2022
- Author(s)
  川嶋明日香、湯野暁子、佐野伸一朗、中村明枝、緒方勤、鏡雅代
- Organizer
  第55回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08178
[Presentation] 81名のメチル化異常を有する偽性副甲状腺機能低下症低下症におけるメチル化パターンの臨床像の検討2022
- Author(s)
  浦川立貴、成澤宏宗、佐野伸一朗、川嶋明日香、鏡雅代
- Organizer
  第55回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08178
[Presentation] GNASスプライスバリアントによる偽性副甲状腺機能低下症Iaの１例2022
- Author(s)
  佐野伸一朗、岩本彰太郎、増永陽平、藤澤泰子、緒方勤
- Organizer
  第22回日本内分泌学会東海支部学術集会
- Data Source
  KAKENHI-PROJECT-20K08178
[Presentation] 副甲状腺ホルモン抵抗性を伴うPDE4D 変異によるAcrodysostosisの2例2021
- Author(s)
  佐野伸一朗
- Organizer
  第54回日本小児内分泌学会
- Data Source
  KAKENHI-PROJECT-20K08178
[Presentation] PHPにおける（エピ）遺伝子型ー表現型解析2018
- Author(s)
  佐野伸一朗
- Organizer
  第40回日本小児遺伝学会
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] Beckwith-Wiedemann syndromeとPHP-Ib の臨床像を呈したMultilocus imprinting disturbance の女児例2017
- Author(s)
  佐野伸一朗
- Organizer
  第90回日本内分泌学会学術総会
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] PHPにおける(epi)genotype-phenotype correlationの検討2017
- Author(s)
  佐野伸一朗
- Organizer
  第51回日本小児内分泌学会学術集会
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] 偽性副甲状腺機能低下症の69例における（エピ）遺伝子型ー表現型解析2017
- Author(s)
  佐野伸一朗
- Organizer
  日本人類遺伝学会第62回大会
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] 先天性甲状腺機能低下症が先行した偽性副甲状腺機能低下症の臨床像2016
- Author(s)
  佐野伸一朗
- Organizer
  第16回日本内分泌学会東海支部学術集会
- Place of Presentation
  静岡県浜松市
- Year and Date
  2016-09-10
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with Multilocus methylation disturbance2016
- Author(s)
  Shinichiro Sano
- Organizer
  The 9th Biennial scientific meeting of the Asia Pacific Paediatric Endocrine Society
- Place of Presentation
  Tokyo
- Year and Date
  2016-11-17
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] 偽性副甲状腺機能低下症における分子遺伝学的分類に基づいたTSH抵抗性に関する検2016
- Author(s)
  佐野伸一朗
- Organizer
  第49回日本内分泌学会学術集会
- Place of Presentation
  タワーホール船堀
- Year and Date
  2016-10-08
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with Multilocus methylation disturbance2016
- Author(s)
  Shinichiro Sano
- Organizer
  The 13th International Congress of Human Genetics
- Place of Presentation
  Kyoto
- Year and Date
  2016-04-03
- Data Source
  KAKENHI-PROJECT-26461537
[Presentation] 分子遺伝学的診断からみた偽性副甲状腺機能低下症の臨床的特徴
- Author(s)
  佐野　伸一朗
- Organizer
  第48会日本小児内分泌学会
- Place of Presentation
  静岡県浜松市
- Year and Date
  2014-09-25 – 2014-09-27
- Data Source
  KAKENHI-PROJECT-26461537

1. 鏡雅代 (70399484)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
2. OGATA Tsutomu

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
3. FUKAMI Maki

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
4. MATSUBARA Keiko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Sano Sinichiro 佐野 伸一朗

佐野 伸一朗 サノ シンイチロウ

Sano Shinichiro 佐野 伸一朗

Research Projects

Research Products

Co-Researchers

Exploration of clinical phenotype and pathogenic mechanisms of GNAS related diseasePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Molecular evolutionary genetics analysis and elucidation of pathogenic mechanism of GNAS related imprinting diseasePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] エピゲノムで新たな解明が進む「先天性疾患」2021

Author(s)

Total Pages

Publisher

ISBN

Data Source

[Book] 医学のあゆみ2017

Author(s)

Total Pages

Publisher

Data Source

[Journal Article] A novel <i>GNAS</i>-Gsα splice donor site variant in a girl with pseudohypoparathyroidism type 1A and her mother with pseudopseudohypoparathyroidism2024

Author(s)

Journal Title

DOI

ISSN

Language

Data Source

[Journal Article] (Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Familial Pseudohypoparathyroidism Type IB Associated with an SVA Retrotransposon Insertion in the GNAS Locus2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] (Epi)genotype-Phenotype Analysis in 69 Japanese Patients With Pseudohypoparathyroidism Type I2017

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A de novo 50-bp <b><i>GNAS</i></b> Intragenic Duplication in a Patient with Pseudohypoparathyroidism Type 1a2017

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1b.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Sporadic pseudohypoparathyroidism type-1b with asymptomatic hypocalcemia.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Growth hormone deficiency in monozygotic twins with autosomal dominant pseudohypoparathyroidism type Ib.2015

Author(s)

Journal Title

NAID

Data Source

[Presentation] インプリンティング疾患発症に対する生殖補助医療および母親の年齢の影響の解明2023

Author(s)

Organizer

Data Source

Sano Sinichiro 佐野伸一朗

佐野伸一朗サノシンイチロウ

Sano Shinichiro 佐野伸一朗