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Causes of death in Prader-Willi syndrome: lessons from 11 years’ experience of a national reference center

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2019
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Mentioned by

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2 X users

Citations

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53 Dimensions

Readers on

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79 Mendeley
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Title
Causes of death in Prader-Willi syndrome: lessons from 11 years’ experience of a national reference center
Published in
Orphanet Journal of Rare Diseases, November 2019
DOI 10.1186/s13023-019-1214-2
Pubmed ID
Authors

Dibia Liz Pacoricona Alfaro, Perrine Lemoine, Virginie Ehlinger, Catherine Molinas, Gwénaëlle Diene, Marion Valette, Graziella Pinto, Muriel Coupaye, Christine Poitou-Bernert, Denise Thuilleaux, Catherine Arnaud, Maithé Tauber

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

Geographical breakdown

Country Count As %
Unknown 79 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 11 14%
Researcher 7 9%
Student > Postgraduate 7 9%
Student > Ph. D. Student 5 6%
Student > Master 5 6%
Other 17 22%
Unknown 27 34%
Readers by discipline Count As %
Medicine and Dentistry 22 28%
Nursing and Health Professions 13 16%
Biochemistry, Genetics and Molecular Biology 7 9%
Agricultural and Biological Sciences 2 3%
Engineering 2 3%
Other 4 5%
Unknown 29 37%
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 09 August 2021.
All research outputs
#16,495,581
of 24,273,038 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,920
of 2,865 outputs
Outputs of similar age
#230,885
of 368,637 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#21
of 36 outputs
Altmetric has tracked 24,273,038 research outputs across all sources so far. This one is in the 21st percentile – i.e., 21% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,865 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.9. This one is in the 25th percentile – i.e., 25% 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 368,637 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 28th percentile – i.e., 28% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 36 others from the same source and published within six weeks on either side of this one. This one is in the 36th percentile – i.e., 36% of its contemporaries scored the same or lower than it.