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Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, March 2022
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2 X users

Citations

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3 Dimensions

Readers on

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7 Mendeley
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Title
Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome
Published in
Orphanet Journal of Rare Diseases, March 2022
DOI 10.1186/s13023-022-02244-6
Pubmed ID
Authors

Aboulfazl Rad, Maryam Najafi, Fatemeh Suri, Soheila Abedini, Stephen Loum, Ehsan Ghayoor Karimiani, Narsis Daftarian, David Murphy, Mohammad Doosti, Afrooz Moghaddasi, Hamid Ahmadieh, Hamideh Sabbaghi, Mohsen Rajati, Narges Hashemi, Barbara Vona, Miriam Schmidts

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

Geographical breakdown

Country Count As %
Unknown 7 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 29%
Student > Bachelor 1 14%
Unspecified 1 14%
Unknown 3 43%
Readers by discipline Count As %
Unspecified 1 14%
Nursing and Health Professions 1 14%
Psychology 1 14%
Medicine and Dentistry 1 14%
Unknown 3 43%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. 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 March 2022.
All research outputs
#15,659,831
of 23,269,984 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,832
of 2,669 outputs
Outputs of similar age
#252,192
of 440,991 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#86
of 140 outputs
Altmetric has tracked 23,269,984 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,669 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.7. This one is in the 23rd percentile – i.e., 23% 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 440,991 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 32nd percentile – i.e., 32% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 140 others from the same source and published within six weeks on either side of this one. This one is in the 27th percentile – i.e., 27% of its contemporaries scored the same or lower than it.