↓ Skip to main content

Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2013
Altmetric Badge

About this Attention Score

  • Good Attention Score compared to outputs of the same age (73rd percentile)
  • High Attention Score compared to outputs of the same age and source (83rd percentile)

Mentioned by

twitter
7 tweeters

Citations

dimensions_citation
63 Dimensions

Readers on

mendeley
103 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
Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome
Published in
Orphanet Journal of Rare Diseases, January 2013
DOI 10.1186/1750-1172-8-78
Pubmed ID
Authors

Fransiska Malfait, Sofie Symoens, Nathalie Goemans, Yolanda Gyftodimou, Eva Holmberg, Vanesa López-González, Geert Mortier, Sheela Nampoothiri, Michael Petersen, Anne De Paepe

Abstract

Whereas mutations affecting the helical domain of type I procollagen classically cause Osteogenesis Imperfecta (OI), helical mutations near the amino (N)-proteinase cleavage site have been suggested to result in a mixed OI/Ehlers-Danlos syndrome (EDS)-phenotype.

Twitter Demographics

The data shown below were collected from the profiles of 7 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 103 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Portugal 1 <1%
Unknown 102 99%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 18 17%
Researcher 14 14%
Student > Ph. D. Student 12 12%
Other 11 11%
Student > Master 11 11%
Other 18 17%
Unknown 19 18%
Readers by discipline Count As %
Medicine and Dentistry 38 37%
Agricultural and Biological Sciences 16 16%
Biochemistry, Genetics and Molecular Biology 8 8%
Engineering 4 4%
Computer Science 2 2%
Other 12 12%
Unknown 23 22%

Attention Score in Context

This research output has an Altmetric Attention Score of 5. 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 13 November 2019.
All research outputs
#5,705,277
of 21,346,872 outputs
Outputs from Orphanet Journal of Rare Diseases
#731
of 2,383 outputs
Outputs of similar age
#45,556
of 175,743 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#3
of 12 outputs
Altmetric has tracked 21,346,872 research outputs across all sources so far. This one has received more attention than most of these and is in the 73rd percentile.
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 7.3. This one has gotten more attention than average, scoring higher than 68% 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 175,743 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 73% of its contemporaries.
We're also able to compare this research output to 12 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 83% of its contemporaries.