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A possible cranio-oro-facial phenotype in Cockayne syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2013
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Mentioned by

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2 tweeters

Citations

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8 Dimensions

Readers on

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47 Mendeley
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Title
A possible cranio-oro-facial phenotype in Cockayne syndrome
Published in
Orphanet Journal of Rare Diseases, January 2013
DOI 10.1186/1750-1172-8-9
Pubmed ID
Abstract

Cockayne Syndrome CS (Type A - CSA; or CS Type I OMIM #216400) (Type B - CSB; or CS Type II OMIM #133540) is a rare autosomal recessive neurological disease caused by defects in DNA repair characterized by progressive cachectic dwarfism, progressive intellectual disability with cerebral leukodystrophy, microcephaly, progressive pigmentary retinopathy, sensorineural deafness photosensitivity and possibly orofacial and dental anomalies.

Twitter Demographics

The data shown below were collected from the profiles of 2 tweeters who shared this research output. Click here to find out more about how the information was compiled.

Mendeley readers

The data shown below were compiled from readership statistics for 47 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Brazil 1 2%
Egypt 1 2%
Unknown 45 96%

Demographic breakdown

Readers by professional status Count As %
Student > Master 10 21%
Student > Ph. D. Student 6 13%
Other 5 11%
Student > Bachelor 5 11%
Student > Doctoral Student 4 9%
Other 13 28%
Unknown 4 9%
Readers by discipline Count As %
Medicine and Dentistry 27 57%
Agricultural and Biological Sciences 8 17%
Nursing and Health Professions 1 2%
Biochemistry, Genetics and Molecular Biology 1 2%
Psychology 1 2%
Other 1 2%
Unknown 8 17%

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 17 January 2013.
All research outputs
#2,930,890
of 4,507,280 outputs
Outputs from Orphanet Journal of Rare Diseases
#608
of 775 outputs
Outputs of similar age
#181,309
of 284,039 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#38
of 54 outputs
Altmetric has tracked 4,507,280 research outputs across all sources so far. This one is in the 31st percentile – i.e., 31% of other outputs scored the same or lower than it.
So far Altmetric has tracked 775 research outputs from this source. They receive a mean Attention Score of 3.5. This one is in the 16th percentile – i.e., 16% 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 284,039 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 54 others from the same source and published within six weeks on either side of this one. This one is in the 18th percentile – i.e., 18% of its contemporaries scored the same or lower than it.