Yamamura Tomohiko 山村智彦

… Alternative Names

山村智彦ヤマムラトモヒコ

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Researcher Number	30770242
Other IDs
Affiliation (Current)	2025: 神戸大学, 医学研究科, 助教
Affiliation (based on the past Project Information) *help	2024: 神戸大学, 医学研究科, 助教 2019 – 2020: 神戸大学, 医学研究科, 助教 2017: 神戸大学, 医学部附属病院, 助教 2017: 神戸大学, 医学部附属病院, 特定助教 2016: 神戸大学, 医学研究科, 特命助教
Review Section/Research Field	Principal Investigator Basic Section 53040:Nephrology-related / Pediatrics
Keywords	Principal Investigator X染色体不活化 / レーザーキャプチャーマイクロダイセクション / X染色体不活化解析 / 重症化機序 / Ｘ染色体不活化 / アルポート症候群 / 診断 / 修飾遺伝子 / 高い診断能力 / 体細胞モザイク / 網羅的遺伝子解析 / 次世代シークエンサー / Alport症候群

A comprehensive X chromosome inactivation analysis for female patients with X-linked Alport syndromePrincipal Investigator
- Principal Investigator
  
  山村智彦
- Project Period (FY)
  2023 – 2024
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Kobe University
Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndromePrincipal Investigator
- Principal Investigator
  
  Yamamura Tomohiko
- Project Period (FY)
  2016 – 2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University

All 2018 2017 2016

All Journal Article Presentation

[Journal Article] Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases2018
- Author(s)
  Nagano C, Nozu K, Morisada N, Yazawa M, Ichikawa D, Numasawa K, Kourakata H, Matsumura C, Tazoe S, Tanaka R, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Sakakibara N, Nozu Y, Ye MJ, Kaito H, Iijima K
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 印刷中 Issue: 4 Pages: 881-888
- DOI
  10.1007/s10157-018-1534-x
- NAID
  120006624236
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K19642, KAKENHI-PROJECT-18K08243
[Journal Article] Natural History and Genotype?Phenotype Correlation in Female X-Linked Alport Syndrome2017
- Author(s)
  Yamamura Tomohiko、Nozu Kandai、Fu Xue Jun、Nozu Yoshimi、Ye Ming Juan、Shono Akemi、Yamanouchi Satoko、Minamikawa Shogo、Morisada Naoya、Nakanishi Koichi、Shima Yuko、Yoshikawa Norishige、Ninchoji Takeshi、Morioka Ichiro、Kaito Hiroshi、Iijima Kazumoto
- Journal Title
  
  Kidney Int Rep.
  
  Volume: 2 Issue: 5 Pages: 850-855
- DOI
  10.1016/j.ekir.2017.04.011
- NAID
  120006373817
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09695, KAKENHI-PROJECT-16K19642
[Journal Article] Female X-linked Alport syndrome with somatic mosaicism2016
- Author(s)
  Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K.
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 印刷中 Issue: 5 Pages: 877-883
- DOI
  10.1007/s10157-016-1352-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-16K19642
[Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2018
- Author(s)
  山村智彦
- Organizer
  第121回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-16K19642
[Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2017
- Author(s)
  山村智彦
- Organizer
  第60回日本腎臓学会学術集会
- Data Source
  KAKENHI-PROJECT-16K19642
[Presentation] Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome2017
- Author(s)
  山村智彦
- Organizer
  13th Asian Congress of Pediatric Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K19642
[Presentation] Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome2017
- Author(s)
  山村智彦
- Organizer
  第52回日本小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-16K19642

1. IIJIMA Kazumoto (00240854)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
2. NOZU Kandai (70362796)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
3. MINAMIKAWA Shogo (10772634)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. YOSHIKAWA Norishige

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
5. NAKANISHI Koichi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. SHIMA Yuko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
7. MORISADA Naoya

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
8. 庄野朱美

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Yamamura Tomohiko 山村 智彦

山村 智彦 ヤマムラ トモヒコ

Research Projects

Research Products

Co-Researchers

A comprehensive X chromosome inactivation analysis for female patients with X-linked Alport syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases2018

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Natural History and Genotype?Phenotype Correlation in Female X-Linked Alport Syndrome2017

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Female X-linked Alport syndrome with somatic mosaicism2016

Author(s)

Journal Title

DOI

Data Source

[Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2018

Author(s)

Organizer

Data Source

[Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2017

Author(s)

Organizer

Data Source

[Presentation] Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome2017

Author(s)

Organizer

Data Source

[Presentation] Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome2017

Author(s)

Organizer

Data Source

Yamamura Tomohiko 山村智彦

山村智彦ヤマムラトモヒコ