↓ Skip to main content

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2020
Altmetric Badge

About this Attention Score

  • In the top 5% of all research outputs scored by Altmetric
  • Among the highest-scoring outputs from this source (#23 of 1,841)
  • High Attention Score compared to outputs of the same age (96th percentile)

Mentioned by

news
8 news outlets
blogs
1 blog
twitter
3 tweeters
facebook
1 Facebook page

Citations

dimensions_citation
9 Dimensions

Readers on

mendeley
77 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
Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum
Published in
Orphanet Journal of Rare Diseases, February 2020
DOI 10.1186/s13023-020-1317-9
Pubmed ID
Authors

Roser Urreizti, Estrella Lopez-Martin, Antonio Martinez-Monseny, Montse Pujadas, Laura Castilla-Vallmanya, Luis Alberto Pérez-Jurado, Mercedes Serrano, Daniel Natera-de Benito, Beatriz Martínez-Delgado, Manuel Posada-de-la-Paz, Javier Alonso, Purificación Marin-Reina, Mar O’Callaghan, Daniel Grinberg, Eva Bermejo-Sánchez, Susanna Balcells

Twitter Demographics

The data shown below were collected from the profiles of 3 tweeters 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 77 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 77 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 14%
Student > Ph. D. Student 8 10%
Student > Bachelor 7 9%
Other 5 6%
Student > Doctoral Student 3 4%
Other 14 18%
Unknown 29 38%
Readers by discipline Count As %
Medicine and Dentistry 24 31%
Biochemistry, Genetics and Molecular Biology 5 6%
Agricultural and Biological Sciences 4 5%
Nursing and Health Professions 3 4%
Neuroscience 3 4%
Other 6 8%
Unknown 32 42%

Attention Score in Context

This research output has an Altmetric Attention Score of 73. 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 17 March 2020.
All research outputs
#348,956
of 17,377,895 outputs
Outputs from Orphanet Journal of Rare Diseases
#23
of 1,841 outputs
Outputs of similar age
#10,292
of 265,048 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#1
of 1 outputs
Altmetric has tracked 17,377,895 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 98th percentile: it's in the top 5% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 1,841 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.5. This one has done particularly well, scoring higher than 98% of its peers.
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 265,048 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 96% of its contemporaries.
We're also able to compare this research output to 1 others from the same source and published within six weeks on either side of this one. This one has scored higher than all of them