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A deleterious mutation in the ALMS1 gene in a naturally occurring model of hypertrophic cardiomyopathy in the Sphynx cat

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2021
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About this Attention Score

  • Above-average Attention Score compared to outputs of the same age (62nd percentile)
  • Above-average Attention Score compared to outputs of the same age and source (61st percentile)

Mentioned by

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Citations

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Readers on

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59 Mendeley
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Title
A deleterious mutation in the ALMS1 gene in a naturally occurring model of hypertrophic cardiomyopathy in the Sphynx cat
Published in
Orphanet Journal of Rare Diseases, February 2021
DOI 10.1186/s13023-021-01740-5
Pubmed ID
Authors

Kathryn M. Meurs, Brian G. Williams, Dylan DeProspero, Steven G. Friedenberg, David E. Malarkey, J. Ashley Ezzell, Bruce W. Keene, Darcy B. Adin, Teresa C. DeFrancesco, Sandra Tou

X Demographics

X Demographics

The data shown below were collected from the profiles of 5 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 59 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 59 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 9 15%
Researcher 8 14%
Student > Doctoral Student 5 8%
Other 3 5%
Student > Ph. D. Student 3 5%
Other 6 10%
Unknown 25 42%
Readers by discipline Count As %
Veterinary Science and Veterinary Medicine 17 29%
Biochemistry, Genetics and Molecular Biology 5 8%
Neuroscience 2 3%
Agricultural and Biological Sciences 2 3%
Medicine and Dentistry 2 3%
Other 2 3%
Unknown 29 49%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 4. 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 07 May 2021.
All research outputs
#7,378,900
of 24,138,997 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,042
of 2,828 outputs
Outputs of similar age
#156,178
of 421,535 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#36
of 91 outputs
Altmetric has tracked 24,138,997 research outputs across all sources so far. This one has received more attention than most of these and is in the 69th percentile.
So far Altmetric has tracked 2,828 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.0. This one has gotten more attention than average, scoring higher than 62% 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 421,535 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 62% of its contemporaries.
We're also able to compare this research output to 91 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 61% of its contemporaries.