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Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, July 2013
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1 tweeter

Citations

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80 Mendeley
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Title
Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome
Published in
Orphanet Journal of Rare Diseases, July 2013
DOI 10.1186/1750-1172-8-106
Pubmed ID
Authors

Bruno Donadille, Pascal D’Anella, Martine Auclair, Nancy Uhrhammer, Marc Sorel, Romulus Grigorescu, Sophie Ouzounian, Gilles Cambonie, Pierre Boulot, Pascal Laforêt, Bruno Carbonne, Sophie Christin-Maitre, Yves-Jean Bignon, Corinne Vigouroux

Abstract

Laminopathies, due to mutations in LMNA, encoding A type-lamins, can lead to premature ageing and/or lipodystrophic syndromes, showing that these diseases could have close physiopathological relationships. We show here that lipodystrophy and extreme insulin resistance can also reveal the adult progeria Werner syndrome linked to mutations in WRN, encoding a RecQ DNA helicase.

Twitter Demographics

The data shown below were collected from the profile of 1 tweeter who shared this research output. Click here to find out more about how the information was compiled.

Mendeley readers

The data shown below were compiled from readership statistics for 80 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Chile 1 1%
Russia 1 1%
Unknown 78 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 12 15%
Student > Master 12 15%
Researcher 11 14%
Student > Doctoral Student 8 10%
Student > Bachelor 6 8%
Other 14 18%
Unknown 17 21%
Readers by discipline Count As %
Medicine and Dentistry 33 41%
Biochemistry, Genetics and Molecular Biology 12 15%
Agricultural and Biological Sciences 7 9%
Nursing and Health Professions 2 3%
Psychology 2 3%
Other 5 6%
Unknown 19 24%

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 November 2013.
All research outputs
#17,253,161
of 21,347,849 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,946
of 2,383 outputs
Outputs of similar age
#136,981
of 185,602 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#8
of 8 outputs
Altmetric has tracked 21,347,849 research outputs across all sources so far. This one is in the 11th percentile – i.e., 11% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,383 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 7.2. This one is in the 7th percentile – i.e., 7% 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 185,602 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 12th percentile – i.e., 12% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 8 others from the same source and published within six weeks on either side of this one.