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A homozygous missense variant in CHRM3 associated with familial urinary bladder disease

Overview of attention for article published in Clinical Genetics, September 2019
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About this Attention Score

  • Average Attention Score compared to outputs of the same age
  • Above-average Attention Score compared to outputs of the same age and source (54th percentile)

Mentioned by

twitter
1 X user
peer_reviews
1 peer review site

Citations

dimensions_citation
8 Dimensions

Readers on

mendeley
8 Mendeley
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Title
A homozygous missense variant in CHRM3 associated with familial urinary bladder disease
Published in
Clinical Genetics, September 2019
DOI 10.1111/cge.13631
Pubmed ID
Authors

Glenda M. Beaman, Gabriella Galatà, Keng W. Teik, Jill E. Urquhart, Ali Aishah, James O'Sullivan, Sanjeev S. Bhaskar, Katherine A. Wood, Huw B. Thomas, Raymond T. O'Keefe, Adrian S. Woolf, Helen M. Stuart, William G. Newman

X Demographics

X Demographics

The data shown below were collected from the profile of 1 X user 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 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Other 2 25%
Student > Postgraduate 2 25%
Student > Ph. D. Student 1 13%
Researcher 1 13%
Unknown 2 25%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 25%
Medicine and Dentistry 2 25%
Unknown 4 50%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. 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 24 August 2019.
All research outputs
#13,654,141
of 23,154,520 outputs
Outputs from Clinical Genetics
#1,454
of 2,437 outputs
Outputs of similar age
#170,777
of 341,046 outputs
Outputs of similar age from Clinical Genetics
#13
of 37 outputs
Altmetric has tracked 23,154,520 research outputs across all sources so far. This one is in the 39th percentile – i.e., 39% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,437 research outputs from this source. They receive a mean Attention Score of 3.8. This one is in the 36th percentile – i.e., 36% of its peers scored the same or lower than it.
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 341,046 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 48th percentile – i.e., 48% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 37 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 54% of its contemporaries.