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GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients

Overview of attention for article published in Orphanet Journal of Rare Diseases, October 2013
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About this Attention Score

  • Good Attention Score compared to outputs of the same age (74th percentile)
  • Above-average Attention Score compared to outputs of the same age and source (64th percentile)

Mentioned by

twitter
5 tweeters
facebook
1 Facebook page
googleplus
1 Google+ user

Citations

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12 Dimensions

Readers on

mendeley
31 Mendeley
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Title
GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients
Published in
Orphanet Journal of Rare Diseases, October 2013
DOI 10.1186/1750-1172-8-170
Pubmed ID
Authors

Maria E de la Morena-Barrio, Trinidad Hernández-Caselles, Javier Corral, Roberto García-López, Irene Martínez-Martínez, Belen Pérez-Dueñas, Carmen Altisent, Teresa Sevivas, Soren R Kristensen, Encarna Guillén-Navarro, Antonia Miñano, Vicente, Jaak Jaeken, Maria L Lozano

Abstract

Mutations in PMM2 impair phosphomannomutase-2 activity and cause the most frequent congenital disorder of glycosylation, PMM2-CDG. Mannose-1-phosphate, that is deficient in this disorder, is also implicated in the biosynthesis of glycosylphosphatidyl inositol (GPI) anchors.

Twitter Demographics

The data shown below were collected from the profiles of 5 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 31 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 3%
Vietnam 1 3%
Unknown 29 94%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 7 23%
Researcher 7 23%
Student > Master 4 13%
Other 3 10%
Professor 3 10%
Other 4 13%
Unknown 3 10%
Readers by discipline Count As %
Medicine and Dentistry 11 35%
Agricultural and Biological Sciences 7 23%
Biochemistry, Genetics and Molecular Biology 6 19%
Immunology and Microbiology 1 3%
Unknown 6 19%

Attention Score in Context

This research output has an Altmetric Attention Score of 4. 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 21 July 2014.
All research outputs
#3,248,801
of 12,378,406 outputs
Outputs from Orphanet Journal of Rare Diseases
#439
of 1,338 outputs
Outputs of similar age
#42,130
of 170,472 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#12
of 37 outputs
Altmetric has tracked 12,378,406 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 1,338 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 7.0. This one has gotten more attention than average, scoring higher than 66% 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 170,472 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 74% of its contemporaries.
We're also able to compare this research output to 37 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 64% of its contemporaries.