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The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued

Overview of attention for article published in Orphanet Journal of Rare Diseases, May 2023
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About this Attention Score

  • Above-average Attention Score compared to outputs of the same age (53rd percentile)
  • Good Attention Score compared to outputs of the same age and source (73rd percentile)

Mentioned by

twitter
3 X users

Citations

dimensions_citation
1 Dimensions

Readers on

mendeley
4 Mendeley
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Title
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued
Published in
Orphanet Journal of Rare Diseases, May 2023
DOI 10.1186/s13023-023-02706-5
Pubmed ID
Authors

Simone Schröder, Gökhan Yigit, Yun Li, Janine Altmüller, Hans-Martin Büttel, Barbara Fiedler, Christoph Kretzschmar, Peter Nürnberg, Jürgen Seeger, Valentina Serpieri, Enza Maria Valente, Bernd Wollnik, Eugen Boltshauser, Knut Brockmann

X Demographics

X Demographics

The data shown below were collected from the profiles of 3 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 4 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 1 25%
Student > Doctoral Student 1 25%
Lecturer > Senior Lecturer 1 25%
Unknown 1 25%
Readers by discipline Count As %
Arts and Humanities 1 25%
Biochemistry, Genetics and Molecular Biology 1 25%
Medicine and Dentistry 1 25%
Unknown 1 25%
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 04 May 2023.
All research outputs
#14,498,056
of 23,668,780 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,571
of 2,733 outputs
Outputs of similar age
#92,951
of 208,199 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#11
of 42 outputs
Altmetric has tracked 23,668,780 research outputs across all sources so far. This one is in the 37th percentile – i.e., 37% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,733 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 40th percentile – i.e., 40% 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 208,199 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 53% of its contemporaries.
We're also able to compare this research output to 42 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 73% of its contemporaries.