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X Demographics
Mendeley readers
Attention Score in Context
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 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. |
X Demographics
The data shown below were collected from the profiles of 5 X users who shared this research output. Click here to find out more about how the information was compiled.
Geographical breakdown
Country | Count | As % |
---|---|---|
Spain | 2 | 40% |
United Kingdom | 1 | 20% |
Mexico | 1 | 20% |
France | 1 | 20% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 3 | 60% |
Scientists | 2 | 40% |
Mendeley readers
The data shown below were compiled from readership statistics for 32 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 | 30 | 94% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 7 | 22% |
Researcher | 7 | 22% |
Student > Master | 5 | 16% |
Other | 3 | 9% |
Professor | 3 | 9% |
Other | 4 | 13% |
Unknown | 3 | 9% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 11 | 34% |
Agricultural and Biological Sciences | 7 | 22% |
Biochemistry, Genetics and Molecular Biology | 6 | 19% |
Immunology and Microbiology | 2 | 6% |
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
#6,769,383
of 22,727,570 outputs
Outputs from Orphanet Journal of Rare Diseases
#930
of 2,604 outputs
Outputs of similar age
#62,621
of 211,692 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#11
of 34 outputs
Altmetric has tracked 22,727,570 research outputs across all sources so far. This one has received more attention than most of these and is in the 69th percentile.
So far Altmetric has tracked 2,604 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.5. This one has gotten more attention than average, scoring higher than 63% 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 211,692 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 70% of its contemporaries.
We're also able to compare this research output to 34 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.