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Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity

Overview of attention for article published in Frontiers in Genetics, May 2021
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About this Attention Score

  • Above-average Attention Score compared to outputs of the same age (55th percentile)
  • High Attention Score compared to outputs of the same age and source (81st percentile)

Mentioned by

twitter
4 X users
peer_reviews
1 peer review site

Citations

dimensions_citation
6 Dimensions

Readers on

mendeley
19 Mendeley
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Title
Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity
Published in
Frontiers in Genetics, May 2021
DOI 10.3389/fgene.2021.641925
Pubmed ID
Authors

Mohd Fareed, Varun Sharma, Inderpal Singh, Sayeed Ur Rehman, Gurdarshan Singh, Mohammad Afzal

X Demographics

X Demographics

The data shown below were collected from the profiles of 4 X users who shared this research output. Click here to find out more about how the information was compiled.
As of 1 July 2024, you may notice a temporary increase in the numbers of X profiles with Unknown location. Click here to learn more.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 19 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 11%
Student > Ph. D. Student 1 5%
Student > Bachelor 1 5%
Student > Master 1 5%
Student > Postgraduate 1 5%
Other 0 0%
Unknown 13 68%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 1 5%
Agricultural and Biological Sciences 1 5%
Immunology and Microbiology 1 5%
Social Sciences 1 5%
Design 1 5%
Other 0 0%
Unknown 14 74%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. 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 20 April 2022.
All research outputs
#14,861,336
of 26,117,612 outputs
Outputs from Frontiers in Genetics
#3,037
of 13,856 outputs
Outputs of similar age
#205,363
of 463,926 outputs
Outputs of similar age from Frontiers in Genetics
#113
of 632 outputs
Altmetric has tracked 26,117,612 research outputs across all sources so far. This one is in the 42nd percentile – i.e., 42% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,856 research outputs from this source. They receive a mean Attention Score of 3.9. This one has done well, scoring higher than 77% 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 463,926 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 55% of its contemporaries.
We're also able to compare this research output to 632 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 81% of its contemporaries.