Wang Zheng 王錚

Researcher Number	90794313
Other IDs
Affiliation (based on the past Project Information) *help	2022: 国立研究開発法人理化学研究所, 生命医科学研究センター, 研究員 2018: 国立研究開発法人理化学研究所, 生命医科学研究センター, 研究員 2017: 国立研究開発法人理化学研究所, 統合生命医科学研究センター, 研究員
Review Section/Research Field	Principal Investigator Orthopaedic surgery Except Principal Investigator Basic Section 56020:Orthopedics-related
Keywords	Principal Investigator WES / Exome解析 / シーケンス解析 / 原因遺伝子 / 遺伝子診断 / 分子病態 / エキソーム解析 / ゲノム解析 / 遺伝子変異 / 単一遺伝子病 / 骨系統疾患 … More Except Principal Investigator … More コホート / 遺伝的関連 / 思春期特発性側湾症 / 遺伝相関 / 後縦靱帯骨化症 / ゲノム解析 / 骨関節疾患 / 運動器疾患 / 遺伝的相関 / ゲノム / 骨関節 / 運動器 / GWAS Less

運動器疾患のMulti disease GWAS 解析
- Principal Investigator
  
  池川志郎
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 56020:Orthopedics-related
- Research Institution
  Institute of Physical and Chemical Research
Systematic sequence analysis for early onset skeletal dysplasiaPrincipal Investigator
- Principal Investigator
  
  Wang Zheng
- Project Period (FY)
  2017 – 2018
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  Institute of Physical and Chemical Research

All 2023 2019 2018 2017

All Journal Article Presentation

[Journal Article] Impaired glycine neurotransmission causes adolescent idiopathic scoliosis.2023
- Author(s)
  Wang X, Yue M, Cheung JPY, Cheung PWH, Fan Y, Wu M, Wang X, Zhao S, Khanshour AM, Rios JJ, Chen Z, Wang X, Tu W, Chan D, Yuan Q, Qin D, Qiu G, Wu Z, Zhang J, Ikegawa S, Wu N, Wise CA, Hu Y, Luk KDK, Song YQ, Gao B.
- Journal Title
  
  J Clin Invest
  
  Volume: 134 Issue: 2
- DOI
  10.1172/jci168783
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24466
[Journal Article] Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia2019
- Author(s)
  Chang HR, Cho SY, Lee JH, Lee E, Seo J, Lee HR, Cavalcanti DP, Makitie O, Valta H, Girisha KM, Lee C, Neethukrishna K, Bhavani GS, Shukla A, Nampoothiri S, Phadke SR, Park MJ, Ikegawa S, Wang Z, (以下15名省略）, Cho TJ.
- Journal Title
  
  The American Journal of Human Genetics
  
  Volume: 104 Issue: 3 Pages: 439-453
- DOI
  10.1016/j.ajhg.2019.01.009
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K16710
[Journal Article] Dysosteosclerosis is also caused by TNFRSF11A mutation.2018
- Author(s)
  Guo L, Elcioglu NH, Karalar OK, Topkar MO, Wang Z, Sakamoto Y, Matsumoto N, Miyake N, Nishimura G, Ikegawa S#.
- Journal Title
  
  J Hum Genet.
  
  Volume: 63(6) Issue: 6 Pages: 769-774
- DOI
  10.1038/s10038-018-0447-6
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-16H05357, KAKENHI-PROJECT-18H02932, KAKENHI-PROJECT-17K16710
[Journal Article] Further expansion of the mutational spectrum of spondylo-meta-epiphyseal dysplasia with abnormal calcification2018
- Author(s)
  ?rel-Demir Gizem、Simsek-Kiper Pelin Ozlem、Akg?n-Do?an ?zlem、G??men Rah?an、Wang Zheng、Matsumoto Naomichi、Miyake Noriko、Utine G?len Eda、Nishimura Gen、Ikegawa Shiro、Boduroglu Koray
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 63 Issue: 9 Pages: 1003-1007
- DOI
  10.1038/s10038-018-0473-4
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K16710
[Journal Article] Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies2017
- Author(s)
  Hammarsjo A.、Wang Z.、（以下24名）
- Journal Title
  
  Scientific Reports
  
  Volume: 7 Issue: 1 Pages: 15585-15585
- DOI
  10.1038/s41598-017-15442-1
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K16710, KAKENHI-PROJECT-16H05357
[Journal Article] Axial spondylometaphyseal dysplasia is also caused by NEK1 mutations2017
- Author(s)
  Wang Zheng、Horemuzova Eva、Iida Aritoshi、Guo Long、Liu Ying、Matsumoto Naomichi、Nishimura Gen、Nordgren Ann、Miyake Noriko、Tham Emma、Grigelioniene Giedre、Ikegawa Shiro
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 62 Issue: 4 Pages: 503-506
- DOI
  10.1038/jhg.2016.157
- NAID
  40021158326
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K16710, KAKENHI-PROJECT-16H05357
[Journal Article] Identification of biallelic EXTL3 mutations in a novel type of spondylo-epi-metaphyseal dysplasia2017
- Author(s)
  *Long Guo, *Nursel H Elcioglu, *Shuji Mizumoto, Zheng Wang, Bilge Noyan, Hatice M Albayrak, Shuhei Yamada, Naomichi Matsumoto, Noriko Miyake, Gen Nishimura, Shiro Ikegawa (equal contribution)
- Journal Title
  
  Journal of Human Genetics
  
  Volume: － Issue: 8 Pages: 797-801
- DOI
  10.1038/jhg.2017.38
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K08251, KAKENHI-PROJECT-17K16710, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-16H05357, KAKENHI-PROJECT-15K07951
[Presentation] New Discovery on the Basic Research of Camurati-Engelmann Disease2019
- Author(s)
  Wang Zheng
- Organizer
  第9回 Orthopedic Research Club
- Invited
- Data Source
  KAKENHI-PROJECT-17K16710

1. 池川志郎 (30272496)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
2. 寺尾知可史 (60610459)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. 郭竜 (50784055)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. GUO long

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
5. MIZUMOTO Shuji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. 松本直通

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
7. 三宅紀子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
8. 山田修平

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Wang Zheng 王 錚

Research Projects

Research Products

Co-Researchers

運動器疾患のMulti disease GWAS 解析

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Systematic sequence analysis for early onset skeletal dysplasiaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Impaired glycine neurotransmission causes adolescent idiopathic scoliosis.2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Dysosteosclerosis is also caused by TNFRSF11A mutation.2018

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Further expansion of the mutational spectrum of spondylo-meta-epiphyseal dysplasia with abnormal calcification2018

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies2017

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Axial spondylometaphyseal dysplasia is also caused by NEK1 mutations2017

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Identification of biallelic EXTL3 mutations in a novel type of spondylo-epi-metaphyseal dysplasia2017

Author(s)

Journal Title

DOI

Data Source

[Presentation] New Discovery on the Basic Research of Camurati-Engelmann Disease2019

Author(s)

Organizer

Data Source

Wang Zheng 王錚