↓ Skip to main content

Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2022
Altmetric Badge

About this Attention Score

  • Average Attention Score compared to outputs of the same age

Mentioned by

twitter
2 X users

Readers on

mendeley
10 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Title
Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis
Published in
Orphanet Journal of Rare Diseases, February 2022
DOI 10.1186/s13023-022-02248-2
Pubmed ID
Authors

Lauriane Le Collen, Brigitte Delemer, Marta Spodenkiewicz, Pascale Cornillet Lefebvre, Emmanuelle Durand, Emmanuel Vaillant, Alaa Badreddine, Mehdi Derhourhi, Tarik Ait Mouhoub, Guillaume Jouret, Pauline Juttet, Pierre François Souchon, Martine Vaxillaire, Philippe Froguel, Amélie Bonnefond, Martine Doco Fenzy

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

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 1 10%
Student > Bachelor 1 10%
Professor 1 10%
Student > Master 1 10%
Professor > Associate Professor 1 10%
Other 0 0%
Unknown 5 50%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 30%
Medicine and Dentistry 2 20%
Psychology 1 10%
Mathematics 1 10%
Unknown 3 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 02 March 2022.
All research outputs
#15,633,726
of 23,243,271 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,831
of 2,667 outputs
Outputs of similar age
#252,253
of 441,287 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#87
of 141 outputs
Altmetric has tracked 23,243,271 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,667 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.7. This one is in the 23rd percentile – i.e., 23% 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 441,287 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 32nd percentile – i.e., 32% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 141 others from the same source and published within six weeks on either side of this one. This one is in the 26th percentile – i.e., 26% of its contemporaries scored the same or lower than it.