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De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment

Overview of attention for article published in Human Genetics, December 2018
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2 X users

Citations

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Readers on

mendeley
47 Mendeley
Title
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
Published in
Human Genetics, December 2018
DOI 10.1007/s00439-018-1965-1
Pubmed ID
Authors

Jeroen J. Smits, Jaap Oostrik, Andy J. Beynon, Sarina G. Kant, Pia A. M. de Koning Gans, Liselotte J. C. Rotteveel, Jolien S. Klein Wassink-Ruiter, Rolien H. Free, Saskia M. Maas, Jiddeke van de Kamp, Paul Merkus, Wouter Koole, Ilse Feenstra, Ronald J. C. Admiraal, Cornelis P. Lanting, Margit Schraders, Helger G. Yntema, Ronald J. E. Pennings, Hannie Kremer

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 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 47 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 47 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 17%
Researcher 7 15%
Student > Bachelor 5 11%
Student > Master 5 11%
Student > Doctoral Student 4 9%
Other 4 9%
Unknown 14 30%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 11 23%
Medicine and Dentistry 9 19%
Agricultural and Biological Sciences 3 6%
Nursing and Health Professions 2 4%
Computer Science 1 2%
Other 2 4%
Unknown 19 40%
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 19 December 2018.
All research outputs
#14,433,178
of 23,117,738 outputs
Outputs from Human Genetics
#2,450
of 2,966 outputs
Outputs of similar age
#235,572
of 436,781 outputs
Outputs of similar age from Human Genetics
#10
of 20 outputs
Altmetric has tracked 23,117,738 research outputs across all sources so far. This one is in the 35th percentile – i.e., 35% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,966 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.2. This one is in the 15th percentile – i.e., 15% 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 436,781 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 43rd percentile – i.e., 43% of its contemporaries scored the same or lower than it.
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 is in the 40th percentile – i.e., 40% of its contemporaries scored the same or lower than it.