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Automated Author Profile

Ma, Xu

National Health and Family Planning Commission

Current S-Index

9.1

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

0.8

Average Dataset Index per dataset

Total Datasets

12

Total datasets for this author

Average FAIR Score

73.1%

Average FAIR Score per dataset

Total Citations

12

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 1 of A novel 1.38-kb deletion combined with a single nucleotide variant in KIAA0586 as a cause of Joubert syndrome

Additional file 1.  Table S1. Primers for verification of candidate variants.

Authors

  • Shen, Yue ;
  • Lu, Chao ;
  • Cheng, Tingting ;
  • Cao, Zongfu ;
  • Chen, Cuixia ;
  • Ma, Xu ;
  • Gao, Huafang ;
  • Luo, Minna
1 Citation0 Mentions85% FAIR0.8 Dataset Index
10.6084/m9.figshare.226112452023

Additional file 1 of A novel 1.38-kb deletion combined with a single nucleotide variant in KIAA0586 as a cause of Joubert syndrome

Additional file 1.  Table S1. Primers for verification of candidate variants.

Authors

  • Shen, Yue ;
  • Lu, Chao ;
  • Cheng, Tingting ;
  • Cao, Zongfu ;
  • Chen, Cuixia ;
  • Ma, Xu ;
  • Gao, Huafang ;
  • Luo, Minna
1 Citation0 Mentions85% FAIR0.9 Dataset Index
10.6084/m9.figshare.22611245.v12023

Additional file 2 of A novel 1.38-kb deletion combined with a single nucleotide variant in KIAA0586 as a cause of Joubert syndrome

Additional file 2.  Table S2. Results of qPCR for the 1.38kb deletion.

Authors

  • Shen, Yue ;
  • Lu, Chao ;
  • Cheng, Tingting ;
  • Cao, Zongfu ;
  • Chen, Cuixia ;
  • Ma, Xu ;
  • Gao, Huafang ;
  • Luo, Minna
1 Citation0 Mentions85% FAIR0.8 Dataset Index
10.6084/m9.figshare.226112482023

Additional file 2 of A novel 1.38-kb deletion combined with a single nucleotide variant in KIAA0586 as a cause of Joubert syndrome

Additional file 2.  Table S2. Results of qPCR for the 1.38kb deletion.

Authors

  • Shen, Yue ;
  • Lu, Chao ;
  • Cheng, Tingting ;
  • Cao, Zongfu ;
  • Chen, Cuixia ;
  • Ma, Xu ;
  • Gao, Huafang ;
  • Luo, Minna
1 Citation0 Mentions85% FAIR0.8 Dataset Index
10.6084/m9.figshare.22611248.v12023

Additional file 7 of NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree

Additional file 7 Table S4. 255 differentially expressed transcripts bewteen the Mut and WT groups

Authors

  • Li, Lin ;
  • Feng, Fan ;
  • Zhao, Minying ;
  • Li, Tengyan ;
  • Yue, Wentao ;
  • Ma, Xu ;
  • Wang, Binbin ;
  • Yin, Chenghong
1 Citation0 Mentions85% FAIR0.8 Dataset Index
10.6084/m9.figshare.121600742020

Additional file 7 of NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree

Additional file 7 Table S4. 255 differentially expressed transcripts bewteen the Mut and WT groups

Authors

  • Li, Lin ;
  • Feng, Fan ;
  • Zhao, Minying ;
  • Li, Tengyan ;
  • Yue, Wentao ;
  • Ma, Xu ;
  • Wang, Binbin ;
  • Yin, Chenghong
1 Citation0 Mentions85% FAIR0.8 Dataset Index
10.6084/m9.figshare.12160074.v12020

Additional file 4 of NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree

Additional file 4 Table S1. Heterozygous sequence variants found in the two patients

Authors

  • Li, Lin ;
  • Feng, Fan ;
  • Zhao, Minying ;
  • Li, Tengyan ;
  • Yue, Wentao ;
  • Ma, Xu ;
  • Wang, Binbin ;
  • Yin, Chenghong
1 Citation0 Mentions85% FAIR0.8 Dataset Index
10.6084/m9.figshare.121600532020

Additional file 1 of Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome

Additional file 1.

Authors

  • Shen, Yue ;
  • Wang, Hao ;
  • Liu, Zhimin ;
  • Luo, Minna ;
  • Ma, Siyu ;
  • Lu, Chao ;
  • Cao, Zongfu ;
  • Yu, Yufei ;
  • Cai, Ruikun ;
  • Chen, Cuixia ;
  • Li, Qian ;
  • Gao, Huafang ;
  • Peng, Yun ;
  • Xu, Baoping ;
  • Ma, Xu
1 Citation0 Mentions85% FAIR0.9 Dataset Index
10.6084/m9.figshare.130408892020

Additional file 1 of Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome

Additional file 1.

Authors

  • Shen, Yue ;
  • Wang, Hao ;
  • Liu, Zhimin ;
  • Luo, Minna ;
  • Ma, Siyu ;
  • Lu, Chao ;
  • Cao, Zongfu ;
  • Yu, Yufei ;
  • Cai, Ruikun ;
  • Chen, Cuixia ;
  • Li, Qian ;
  • Gao, Huafang ;
  • Peng, Yun ;
  • Xu, Baoping ;
  • Ma, Xu
1 Citation0 Mentions85% FAIR0.9 Dataset Index
10.6084/m9.figshare.13040889.v12020

Additional file 4 of NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree

Additional file 4 Table S1. Heterozygous sequence variants found in the two patients

Authors

  • Li, Lin ;
  • Feng, Fan ;
  • Zhao, Minying ;
  • Li, Tengyan ;
  • Yue, Wentao ;
  • Ma, Xu ;
  • Wang, Binbin ;
  • Yin, Chenghong
1 Citation0 Mentions85% FAIR0.8 Dataset Index
10.6084/m9.figshare.12160053.v12020