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Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

Overview of attention for article published in Genetics in Medicine, October 2018
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About this Attention Score

  • Above-average Attention Score compared to outputs of the same age (62nd percentile)

Mentioned by

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6 X users

Citations

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14 Dimensions

Readers on

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35 Mendeley
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Title
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease
Published in
Genetics in Medicine, October 2018
DOI 10.1038/s41436-018-0345-5
Pubmed ID
Authors

Stijn Van de Sompele, Claire Smith, Marianthi Karali, Marta Corton, Kristof Van Schil, Frank Peelman, Timothy Cherry, Toon Rosseel, Hannah Verdin, Julien Derolez, Thalia Van Laethem, Kamron N. Khan, Martin McKibbin, Carmel Toomes, Manir Ali, Annalaura Torella, Francesco Testa, Belen Jimenez, Francesca Simonelli, Julie De Zaeytijd, Jenneke Van den Ende, Bart P. Leroy, Frauke Coppieters, Carmen Ayuso, Chris F. Inglehearn, Sandro Banfi, Elfride De Baere

X Demographics

X Demographics

The data shown below were collected from the profiles of 6 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 35 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 35 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 17%
Student > Postgraduate 4 11%
Student > Ph. D. Student 4 11%
Other 3 9%
Student > Doctoral Student 2 6%
Other 7 20%
Unknown 9 26%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 20%
Medicine and Dentistry 4 11%
Agricultural and Biological Sciences 4 11%
Business, Management and Accounting 2 6%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Other 5 14%
Unknown 12 34%
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 06 November 2018.
All research outputs
#7,901,007
of 25,385,509 outputs
Outputs from Genetics in Medicine
#1,943
of 2,945 outputs
Outputs of similar age
#134,122
of 363,318 outputs
Outputs of similar age from Genetics in Medicine
#67
of 90 outputs
Altmetric has tracked 25,385,509 research outputs across all sources so far. This one has received more attention than most of these and is in the 68th percentile.
So far Altmetric has tracked 2,945 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 19.0. This one is in the 33rd percentile – i.e., 33% 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 363,318 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 62% of its contemporaries.
We're also able to compare this research output to 90 others from the same source and published within six weeks on either side of this one. This one is in the 25th percentile – i.e., 25% of its contemporaries scored the same or lower than it.