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X Demographics
Mendeley readers
Attention Score in Context
| Title |
Socioeconomic burden of hereditary angioedema: results from the hereditary angioedema burden of illness study in Europe
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, July 2014
|
| DOI | 10.1186/1750-1172-9-99 |
| Pubmed ID | |
| Authors |
Emel Aygören-Pürsün, Anette Bygum, Kathleen Beusterien, Emily Hautamaki, Zlatko Sisic, Suzanne Wait, Henrik B Boysen, Teresa Caballero |
| Abstract |
Hereditary angioedema (HAE) due to C1 inhibitor deficiency is a rare but serious and potentially life-threatening disease marked by spontaneous, recurrent attacks of swelling. The study objective was to characterize direct and indirect resource utilization associated with HAE from the patient perspective in Europe. |
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.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 2 | 100% |
Demographic breakdown
| Type | Count | As % |
|---|---|---|
| Members of the public | 1 | 50% |
| Scientists | 1 | 50% |
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 | 16 | 17% |
| Other | 11 | 12% |
| Student > Master | 10 | 11% |
| Student > Doctoral Student | 8 | 8% |
| Student > Ph. D. Student | 7 | 7% |
| Other | 14 | 15% |
| Unknown | 29 | 31% |
| Readers by discipline | Count | As % |
|---|---|---|
| Medicine and Dentistry | 34 | 36% |
| Economics, Econometrics and Finance | 6 | 6% |
| Pharmacology, Toxicology and Pharmaceutical Science | 5 | 5% |
| Nursing and Health Professions | 4 | 4% |
| Agricultural and Biological Sciences | 4 | 4% |
| Other | 13 | 14% |
| Unknown | 29 | 31% |
Attention Score in Context
This research output has an Altmetric Attention Score of 8. 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 11 March 2021.
All research outputs
#4,659,159
of 25,371,288 outputs
Outputs from Orphanet Journal of Rare Diseases
#644
of 3,105 outputs
Outputs of similar age
#42,817
of 242,211 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#14
of 48 outputs
Altmetric has tracked 25,371,288 research outputs across all sources so far. Compared to these this one has done well and is in the 81st percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
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 has done well, scoring higher than 79% 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 242,211 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 82% of its contemporaries.
We're also able to compare this research output to 48 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 70% of its contemporaries.