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Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant

Overview of attention for article published in European Journal of Medical Genetics, July 2018
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Mentioned by

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2 X users

Citations

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14 Dimensions

Readers on

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23 Mendeley
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1 CiteULike
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Title
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant
Published in
European Journal of Medical Genetics, July 2018
DOI 10.1016/j.ejmg.2018.07.019
Pubmed ID
Authors

Valtter B Virtanen, Perttu P Salo, Jia Cao, Anna Löf-Granström, Lili Milani, Andres Metspalu, Risto J Rintala, Outi Saarenpää-Heikkilä, Tiina Paunio, Tomas Wester, Agneta Nordenskjöld, Markus Perola, Mikko P Pakarinen

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 23 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 23 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 3 13%
Researcher 3 13%
Professor 3 13%
Librarian 2 9%
Student > Bachelor 2 9%
Other 4 17%
Unknown 6 26%
Readers by discipline Count As %
Medicine and Dentistry 9 39%
Biochemistry, Genetics and Molecular Biology 4 17%
Nursing and Health Professions 1 4%
Social Sciences 1 4%
Agricultural and Biological Sciences 1 4%
Other 0 0%
Unknown 7 30%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. 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 01 August 2018.
All research outputs
#20,567,353
of 26,017,215 outputs
Outputs from European Journal of Medical Genetics
#729
of 1,114 outputs
Outputs of similar age
#253,677
of 344,088 outputs
Outputs of similar age from European Journal of Medical Genetics
#21
of 42 outputs
Altmetric has tracked 26,017,215 research outputs across all sources so far. This one is in the 18th percentile – i.e., 18% of other outputs scored the same or lower than it.
So far Altmetric has tracked 1,114 research outputs from this source. They receive a mean Attention Score of 3.2. This one is in the 30th percentile – i.e., 30% 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 344,088 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 21st percentile – i.e., 21% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 42 others from the same source and published within six weeks on either side of this one. This one is in the 42nd percentile – i.e., 42% of its contemporaries scored the same or lower than it.