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Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2019
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  • Average Attention Score compared to outputs of the same age
  • Average Attention Score compared to outputs of the same age and source

Mentioned by

twitter
2 X users

Citations

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13 Dimensions

Readers on

mendeley
30 Mendeley
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Title
Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review
Published in
Orphanet Journal of Rare Diseases, April 2019
DOI 10.1186/s13023-019-1053-1
Pubmed ID
Authors

Fang Peng, Yi-Min Sun, Chao Quan, Jian Wang, Jian-Jun Wu

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 30 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 30 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 6 20%
Researcher 5 17%
Student > Master 4 13%
Other 1 3%
Unspecified 1 3%
Other 1 3%
Unknown 12 40%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 23%
Medicine and Dentistry 4 13%
Veterinary Science and Veterinary Medicine 1 3%
Agricultural and Biological Sciences 1 3%
Unspecified 1 3%
Other 2 7%
Unknown 14 47%
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 28 April 2019.
All research outputs
#14,887,818
of 24,417,958 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,585
of 2,898 outputs
Outputs of similar age
#188,832
of 355,153 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#27
of 46 outputs
Altmetric has tracked 24,417,958 research outputs across all sources so far. This one is in the 38th percentile – i.e., 38% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,898 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.0. This one is in the 44th percentile – i.e., 44% 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 355,153 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 45th percentile – i.e., 45% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 46 others from the same source and published within six weeks on either side of this one. This one is in the 36th percentile – i.e., 36% of its contemporaries scored the same or lower than it.