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Automated Author Profile

Matsubara, Keiko

Current S-Index

29.4

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

0.9

Average Dataset Index per dataset

Total Datasets

32

Total datasets for this author

Average FAIR Score

38.1%

Average FAIR Score per dataset

Total Citations

20

Total citations to the author's datasets

Total Mentions

0

Total mentions of the author's datasets

S-Index Interpretation

S-Index Over Time

Cumulative Citations Over Time

Cumulative Mentions Over Time

Datasets

Additional file 3 of Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome

Additional file 3.: Table S3. Methylation indices (%) for CpGs within four iDMRs determined by target analysis using pyrosequencing.

Authors

  • 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
0 Citations0 Mentions13% FAIR0.3 Dataset Index
10.6084/m9.figshare.13142314January 2020

Additional file 1 of Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

Additional file 1: Table S1. File format: Excel spreadsheet. Gene list screened in this study.

Authors

  • Takanobu Inoue ;
  • Akie Nakamura ;
  • Iwahashi-Odano, Megumi ;
  • Tanase-Nakao, Kanako ;
  • Matsubara, Keiko ;
  • Nishioka, Junko ;
  • Maruo, Yoshihiro ;
  • Hasegawa, Yukihiro ;
  • Suzumura, Hiroshi ;
  • Sato, Seiji ;
  • Kobayashi, Yoshiyuki ;
  • Murakami, Nobuyuki ;
  • Nakabayashi, Kazuhiko ;
  • Yamazawa, Kazuki ;
  • Fuke, Tomoko ;
  • Narumi, Satoshi ;
  • Oka, Akira ;
  • Ogata, Tsutomu ;
  • Fukami, Maki ;
  • Kagami, Masayo
1 Citation0 Mentions13% FAIR0.7 Dataset Index
10.6084/m9.figshare.12495251January 2020

Additional file 1 of Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

Additional file 1: Table S1. File format: Excel spreadsheet. Gene list screened in this study.

Authors

  • Takanobu Inoue ;
  • Akie Nakamura ;
  • Iwahashi-Odano, Megumi ;
  • Tanase-Nakao, Kanako ;
  • Matsubara, Keiko ;
  • Nishioka, Junko ;
  • Maruo, Yoshihiro ;
  • Hasegawa, Yukihiro ;
  • Suzumura, Hiroshi ;
  • Sato, Seiji ;
  • Kobayashi, Yoshiyuki ;
  • Murakami, Nobuyuki ;
  • Nakabayashi, Kazuhiko ;
  • Yamazawa, Kazuki ;
  • Fuke, Tomoko ;
  • Narumi, Satoshi ;
  • Oka, Akira ;
  • Ogata, Tsutomu ;
  • Fukami, Maki ;
  • Kagami, Masayo
1 Citation0 Mentions13% FAIR0.5 Dataset Index
10.6084/m9.figshare.12495251.v1January 2020

Additional file 3 of Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

Additional file 3: Table S2. File format: Excel spreadsheet. Summary of multigene screening studies for etiology-unknown patients with SRS phenotype using next-generation sequencing

Authors

  • Takanobu Inoue ;
  • Akie Nakamura ;
  • Iwahashi-Odano, Megumi ;
  • Tanase-Nakao, Kanako ;
  • Matsubara, Keiko ;
  • Nishioka, Junko ;
  • Maruo, Yoshihiro ;
  • Hasegawa, Yukihiro ;
  • Suzumura, Hiroshi ;
  • Sato, Seiji ;
  • Kobayashi, Yoshiyuki ;
  • Murakami, Nobuyuki ;
  • Nakabayashi, Kazuhiko ;
  • Yamazawa, Kazuki ;
  • Fuke, Tomoko ;
  • Narumi, Satoshi ;
  • Oka, Akira ;
  • Ogata, Tsutomu ;
  • Fukami, Maki ;
  • Kagami, Masayo
1 Citation0 Mentions13% FAIR0.7 Dataset Index
10.6084/m9.figshare.12495266January 2020

Additional file 3 of Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

Additional file 3: Table S2. File format: Excel spreadsheet. Summary of multigene screening studies for etiology-unknown patients with SRS phenotype using next-generation sequencing

Authors

  • Takanobu Inoue ;
  • Akie Nakamura ;
  • Iwahashi-Odano, Megumi ;
  • Tanase-Nakao, Kanako ;
  • Matsubara, Keiko ;
  • Nishioka, Junko ;
  • Maruo, Yoshihiro ;
  • Hasegawa, Yukihiro ;
  • Suzumura, Hiroshi ;
  • Sato, Seiji ;
  • Kobayashi, Yoshiyuki ;
  • Murakami, Nobuyuki ;
  • Nakabayashi, Kazuhiko ;
  • Yamazawa, Kazuki ;
  • Fuke, Tomoko ;
  • Narumi, Satoshi ;
  • Oka, Akira ;
  • Ogata, Tsutomu ;
  • Fukami, Maki ;
  • Kagami, Masayo
1 Citation0 Mentions13% FAIR0.5 Dataset Index
10.6084/m9.figshare.12495266.v1January 2020

Additional file 4 of Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

Additional file 4: Table S3. File format: Excel spreadsheet. Primers utilized to detect mutations in PLAG1

Authors

  • Takanobu Inoue ;
  • Akie Nakamura ;
  • Iwahashi-Odano, Megumi ;
  • Tanase-Nakao, Kanako ;
  • Matsubara, Keiko ;
  • Nishioka, Junko ;
  • Maruo, Yoshihiro ;
  • Hasegawa, Yukihiro ;
  • Suzumura, Hiroshi ;
  • Sato, Seiji ;
  • Kobayashi, Yoshiyuki ;
  • Murakami, Nobuyuki ;
  • Nakabayashi, Kazuhiko ;
  • Yamazawa, Kazuki ;
  • Fuke, Tomoko ;
  • Narumi, Satoshi ;
  • Oka, Akira ;
  • Ogata, Tsutomu ;
  • Fukami, Maki ;
  • Kagami, Masayo
1 Citation0 Mentions13% FAIR0.7 Dataset Index
10.6084/m9.figshare.12495269.v1January 2020

Additional file 4 of Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

Additional file 4: Table S3. File format: Excel spreadsheet. Primers utilized to detect mutations in PLAG1

Authors

  • Takanobu Inoue ;
  • Akie Nakamura ;
  • Iwahashi-Odano, Megumi ;
  • Tanase-Nakao, Kanako ;
  • Matsubara, Keiko ;
  • Nishioka, Junko ;
  • Maruo, Yoshihiro ;
  • Hasegawa, Yukihiro ;
  • Suzumura, Hiroshi ;
  • Sato, Seiji ;
  • Kobayashi, Yoshiyuki ;
  • Murakami, Nobuyuki ;
  • Nakabayashi, Kazuhiko ;
  • Yamazawa, Kazuki ;
  • Fuke, Tomoko ;
  • Narumi, Satoshi ;
  • Oka, Akira ;
  • Ogata, Tsutomu ;
  • Fukami, Maki ;
  • Kagami, Masayo
1 Citation0 Mentions48% FAIR1.5 Dataset Index
10.6084/m9.figshare.12495269January 2020

Additional file 1 of Assisted reproductive technology represents a possible risk factor for development of epimutation-mediated imprinting disorders for mothers aged ≥ 30 years

Additional file 1: Table S1. Frequency of epimutation in the eight representative imprinting disorders.

Authors

  • Hara-Isono, Kaori ;
  • Matsubara, Keiko ;
  • Mikami, Masashi ;
  • Arima, Takahiro ;
  • Ogata, Tsutomu ;
  • Fukami, Maki ;
  • Kagami, Masayo
0 Citations0 Mentions85% FAIR2.1 Dataset Index
10.6084/m9.figshare.12695438January 2020

Additional file 1 of Assisted reproductive technology represents a possible risk factor for development of epimutation-mediated imprinting disorders for mothers aged ≥ 30 years

Additional file 1: Table S1. Frequency of epimutation in the eight representative imprinting disorders.

Authors

  • Hara-Isono, Kaori ;
  • Matsubara, Keiko ;
  • Mikami, Masashi ;
  • Arima, Takahiro ;
  • Ogata, Tsutomu ;
  • Fukami, Maki ;
  • Kagami, Masayo
0 Citations0 Mentions85% FAIR2.1 Dataset Index
10.6084/m9.figshare.12695438.v1January 2020

Additional file 1 of Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome

Additional file 1.: Table S1. Clinical features of patients.

Authors

  • 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
0 Citations0 Mentions13% FAIR0.1 Dataset Index
10.6084/m9.figshare.13142308.v1January 2020