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PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies

Overview of attention for article published in Orphanet Journal of Rare Diseases, March 2014
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (86th percentile)
  • High Attention Score compared to outputs of the same age and source (81st percentile)

Mentioned by

twitter
7 X users
patent
2 patents
wikipedia
2 Wikipedia pages

Citations

dimensions_citation
123 Dimensions

Readers on

mendeley
263 Mendeley
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Title
PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies
Published in
Orphanet Journal of Rare Diseases, March 2014
DOI 10.1186/1750-1172-9-38
Pubmed ID
Authors

Barbara W van Paassen, Anneke J van der Kooi, Karin Y van Spaendonck-Zwarts, Camiel Verhamme, Frank Baas, Marianne de Visser

X Demographics

X Demographics

The data shown below were collected from the profiles of 7 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 263 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Croatia 1 <1%
Germany 1 <1%
Unknown 261 99%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 39 15%
Student > Master 35 13%
Student > Ph. D. Student 34 13%
Researcher 32 12%
Other 20 8%
Other 36 14%
Unknown 67 25%
Readers by discipline Count As %
Medicine and Dentistry 68 26%
Agricultural and Biological Sciences 32 12%
Neuroscience 32 12%
Biochemistry, Genetics and Molecular Biology 27 10%
Nursing and Health Professions 14 5%
Other 21 8%
Unknown 69 26%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 11. 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 24 February 2024.
All research outputs
#3,340,316
of 25,563,770 outputs
Outputs from Orphanet Journal of Rare Diseases
#474
of 3,150 outputs
Outputs of similar age
#32,177
of 237,192 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#10
of 48 outputs
Altmetric has tracked 25,563,770 research outputs across all sources so far. Compared to these this one has done well and is in the 86th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 3,150 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 84% 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 237,192 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 86% 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 done well, scoring higher than 81% of its contemporaries.