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A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

Overview of attention for article published in Genome Medicine, July 2019
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (87th percentile)
  • Good Attention Score compared to outputs of the same age and source (65th percentile)

Mentioned by

twitter
29 X users

Citations

dimensions_citation
60 Dimensions

Readers on

mendeley
72 Mendeley
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Title
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing
Published in
Genome Medicine, July 2019
DOI 10.1186/s13073-019-0658-2
Pubmed ID
Authors

Ye Cao, Mari J. Tokita, Edward S. Chen, Rajarshi Ghosh, Tiansheng Chen, Yanming Feng, Elizabeth Gorman, Federica Gibellini, Patricia A. Ward, Alicia Braxton, Xia Wang, Linyan Meng, Rui Xiao, Weimin Bi, Fan Xia, Christine M. Eng, Yaping Yang, Tomasz Gambin, Chad Shaw, Pengfei Liu, Pawel Stankiewicz

X Demographics

X Demographics

The data shown below were collected from the profiles of 29 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 72 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 72 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 15 21%
Other 12 17%
Student > Ph. D. Student 8 11%
Student > Master 7 10%
Student > Bachelor 2 3%
Other 6 8%
Unknown 22 31%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 24 33%
Medicine and Dentistry 11 15%
Agricultural and Biological Sciences 6 8%
Neuroscience 2 3%
Immunology and Microbiology 1 1%
Other 2 3%
Unknown 26 36%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 17. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 30 September 2019.
All research outputs
#2,194,524
of 25,998,826 outputs
Outputs from Genome Medicine
#481
of 1,612 outputs
Outputs of similar age
#44,410
of 363,352 outputs
Outputs of similar age from Genome Medicine
#7
of 20 outputs
Altmetric has tracked 25,998,826 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 91st percentile: it's in the top 10% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 1,612 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 26.7. This one has gotten more attention than average, scoring higher than 70% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 363,352 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 87% of its contemporaries.
We're also able to compare this research output to 20 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 65% of its contemporaries.