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Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder

Overview of attention for article published in Orphanet Journal of Rare Diseases, May 2019
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  • Average Attention Score compared to outputs of the same age
  • Average Attention Score compared to outputs of the same age and source

Mentioned by

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4 X users
facebook
1 Facebook page

Citations

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5 Dimensions

Readers on

mendeley
49 Mendeley
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Title
Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder
Published in
Orphanet Journal of Rare Diseases, May 2019
DOI 10.1186/s13023-019-1094-5
Pubmed ID
Authors

Julie Masson, Caroline Demily, Nicolas Chatron, Audrey Labalme, Pierre-Antoine Rollat-Farnier, Caroline Schluth-Bolard, Brigitte Gilbert-Dussardier, Fabienne Giuliano, Renaud Touraine, Sylvie Tordjman, Alain Verloes, Giuseppe Testa, Damien Sanlaville, Patrick Edery, Gaetan Lesca, Massimiliano Rossi

X Demographics

X Demographics

The data shown below were collected from the profiles of 4 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 49 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 49 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 7 14%
Student > Master 5 10%
Other 4 8%
Student > Doctoral Student 4 8%
Professor 3 6%
Other 8 16%
Unknown 18 37%
Readers by discipline Count As %
Medicine and Dentistry 8 16%
Biochemistry, Genetics and Molecular Biology 8 16%
Psychology 5 10%
Nursing and Health Professions 3 6%
Computer Science 1 2%
Other 4 8%
Unknown 20 41%
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 04 June 2019.
All research outputs
#14,166,076
of 23,149,216 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,537
of 2,652 outputs
Outputs of similar age
#185,081
of 350,050 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#43
of 67 outputs
Altmetric has tracked 23,149,216 research outputs across all sources so far. This one is in the 37th percentile – i.e., 37% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,652 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.6. This one is in the 40th percentile – i.e., 40% 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 350,050 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 45th percentile – i.e., 45% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 67 others from the same source and published within six weeks on either side of this one. This one is in the 35th percentile – i.e., 35% of its contemporaries scored the same or lower than it.