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X Demographics
Mendeley readers
Attention Score in Context
Title |
Treatable inherited metabolic disorders causing intellectual disability: 2021 review and digital app
|
---|---|
Published in |
Orphanet Journal of Rare Diseases, April 2021
|
DOI | 10.1186/s13023-021-01727-2 |
Pubmed ID | |
Authors |
Eva M. M. Hoytema van Konijnenburg, Saskia B. Wortmann, Marina J. Koelewijn, Laura A. Tseng, Roderick Houben, Sylvia Stöckler-Ipsiroglu, Carlos R. Ferreira, Clara D. M. van Karnebeek |
X Demographics
The data shown below were collected from the profiles of 39 X users who shared this research output. Click here to find out more about how the information was compiled.
Geographical breakdown
Country | Count | As % |
---|---|---|
France | 13 | 33% |
Spain | 2 | 5% |
Colombia | 2 | 5% |
United Kingdom | 2 | 5% |
United States | 1 | 3% |
Canada | 1 | 3% |
Ireland | 1 | 3% |
Australia | 1 | 3% |
Mexico | 1 | 3% |
Other | 1 | 3% |
Unknown | 14 | 36% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 30 | 77% |
Scientists | 4 | 10% |
Practitioners (doctors, other healthcare professionals) | 4 | 10% |
Science communicators (journalists, bloggers, editors) | 1 | 3% |
Mendeley readers
The data shown below were compiled from readership statistics for 89 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 89 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Researcher | 10 | 11% |
Student > Master | 10 | 11% |
Student > Ph. D. Student | 7 | 8% |
Student > Bachelor | 5 | 6% |
Student > Postgraduate | 4 | 4% |
Other | 15 | 17% |
Unknown | 38 | 43% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 17 | 19% |
Biochemistry, Genetics and Molecular Biology | 13 | 15% |
Nursing and Health Professions | 3 | 3% |
Immunology and Microbiology | 2 | 2% |
Unspecified | 2 | 2% |
Other | 12 | 13% |
Unknown | 40 | 45% |
Attention Score in Context
This research output has an Altmetric Attention Score of 27. 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 06 May 2022.
All research outputs
#1,466,826
of 25,755,403 outputs
Outputs from Orphanet Journal of Rare Diseases
#162
of 3,187 outputs
Outputs of similar age
#39,371
of 458,289 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#8
of 86 outputs
Altmetric has tracked 25,755,403 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 94th percentile: it's in the top 10% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 3,187 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.2. This one has done particularly well, scoring higher than 94% 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 458,289 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 91% of its contemporaries.
We're also able to compare this research output to 86 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 90% of its contemporaries.