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A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2015
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  • Average Attention Score compared to outputs of the same age and source

Mentioned by

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2 X users
facebook
1 Facebook page

Citations

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103 Dimensions

Readers on

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95 Mendeley
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Title
A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy
Published in
Orphanet Journal of Rare Diseases, February 2015
DOI 10.1186/s13023-015-0233-x
Pubmed ID
Authors

Andrea Zanichelli, Francesco Arcoleo, Maria Pina Barca, Paolo Borrelli, Maria Bova, Mauro Cancian, Marco Cicardi, Enrico Cillari, Caterina De Carolis, Tiziana De Pasquale, Isabella Del Corso, Paola Cesinaro Di Rocco, Maria Domenica Guarino, Ilaria Massaro, Paola Minale, Vincenzo Montinaro, Sergio Neri, Roberto Perricone, Stefano Pucci, Paolina Quattrocchi, Oliviero Rossi, Massimo Triggiani, Giuseppina Zanierato, Alessandra Zoli

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 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 95 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Turkey 1 1%
Unknown 94 99%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 12%
Student > Ph. D. Student 10 11%
Student > Doctoral Student 9 9%
Other 9 9%
Student > Bachelor 8 8%
Other 16 17%
Unknown 32 34%
Readers by discipline Count As %
Medicine and Dentistry 31 33%
Pharmacology, Toxicology and Pharmaceutical Science 10 11%
Agricultural and Biological Sciences 9 9%
Biochemistry, Genetics and Molecular Biology 2 2%
Immunology and Microbiology 2 2%
Other 9 9%
Unknown 32 34%
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 09 July 2016.
All research outputs
#16,721,208
of 25,373,627 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,955
of 3,105 outputs
Outputs of similar age
#211,461
of 360,790 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#20
of 35 outputs
Altmetric has tracked 25,373,627 research outputs across all sources so far. This one is in the 32nd percentile – i.e., 32% of other outputs scored the same or lower than it.
So far Altmetric has tracked 3,105 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.2. This one is in the 34th percentile – i.e., 34% 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 360,790 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 38th percentile – i.e., 38% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 35 others from the same source and published within six weeks on either side of this one. This one is in the 37th percentile – i.e., 37% of its contemporaries scored the same or lower than it.