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Clinical characteristics in patients with hereditary amyloidosis with Glu54Gln transthyretin identified in the Romanian population

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2020
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About this Attention Score

  • Above-average Attention Score compared to outputs of the same age (63rd percentile)
  • Above-average Attention Score compared to outputs of the same age and source (57th percentile)

Mentioned by

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5 X users

Citations

dimensions_citation
14 Dimensions

Readers on

mendeley
34 Mendeley
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Title
Clinical characteristics in patients with hereditary amyloidosis with Glu54Gln transthyretin identified in the Romanian population
Published in
Orphanet Journal of Rare Diseases, January 2020
DOI 10.1186/s13023-020-1309-9
Pubmed ID
Authors

Andreea Jercan, Amalia Ene, Ruxandra Jurcut, Mirela Draghici, Sorina Badelita, Mihaela Dragomir, Camelia Dobrea, Monica Popescu, Dumitru Jardan, Emanuel Stoica, Speranta Iacob, Ionela Codita, Claudiu Stan, Daniel Coriu

X Demographics

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.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 34 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 34 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 7 21%
Researcher 5 15%
Other 3 9%
Student > Doctoral Student 2 6%
Student > Postgraduate 2 6%
Other 3 9%
Unknown 12 35%
Readers by discipline Count As %
Medicine and Dentistry 9 26%
Nursing and Health Professions 2 6%
Biochemistry, Genetics and Molecular Biology 2 6%
Neuroscience 2 6%
Social Sciences 2 6%
Other 3 9%
Unknown 14 41%
Attention Score in Context

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 26 August 2020.
All research outputs
#7,548,106
of 23,191,112 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,116
of 2,661 outputs
Outputs of similar age
#161,212
of 451,744 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#21
of 50 outputs
Altmetric has tracked 23,191,112 research outputs across all sources so far. This one has received more attention than most of these and is in the 67th percentile.
So far Altmetric has tracked 2,661 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.7. This one has gotten more attention than average, scoring higher than 57% 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 451,744 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 63% of its contemporaries.
We're also able to compare this research output to 50 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 57% of its contemporaries.