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SURF1 deficiency: a multi-centre natural history study

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

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2 tweeters

Citations

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69 Dimensions

Readers on

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62 Mendeley
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Title
SURF1 deficiency: a multi-centre natural history study
Published in
Orphanet Journal of Rare Diseases, July 2013
DOI 10.1186/1750-1172-8-96
Pubmed ID
Authors

Wedatilake Y, Brown R, McFarland R, Yaplito-Lee J, Morris AA, Champion M, Jardine PE, Clarke A, Thorburn DR, Taylor RW, Land JM, Forrest K, Dobbie A, Simmons L, Aasheim ET, Ketteridge D, Hanrahan D, Chakrapani A, Brown GK, Rahman S, Yehani Wedatilake, Ruth M Brown, Robert McFarland, Joy Yaplito-Lee, Andrew A M Morris, Mike Champion, Phillip E Jardine, Antonia Clarke, David R Thorburn, Robert W Taylor, John M Land, Katharine Forrest, Angus Dobbie, Louise Simmons, Erlend T Aasheim, David Ketteridge, Donncha Hanrahan, Anupam Chakrapani, Garry K Brown, Shamima Rahman

Abstract

SURF1 deficiency, a monogenic mitochondrial disorder, is the most frequent cause of cytochrome c oxidase (COX) deficient Leigh syndrome (LS). We report the first natural history study of SURF1 deficiency.

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

Geographical breakdown

Country Count As %
Spain 1 2%
Colombia 1 2%
Unknown 60 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 15 24%
Researcher 12 19%
Student > Bachelor 9 15%
Other 6 10%
Professor 4 6%
Other 10 16%
Unknown 6 10%
Readers by discipline Count As %
Medicine and Dentistry 24 39%
Biochemistry, Genetics and Molecular Biology 14 23%
Agricultural and Biological Sciences 9 15%
Neuroscience 5 8%
Computer Science 1 2%
Other 3 5%
Unknown 6 10%

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 12 July 2013.
All research outputs
#4,382,539
of 6,230,816 outputs
Outputs from Orphanet Journal of Rare Diseases
#708
of 957 outputs
Outputs of similar age
#62,847
of 99,011 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#34
of 47 outputs
Altmetric has tracked 6,230,816 research outputs across all sources so far. This one is in the 26th percentile – i.e., 26% of other outputs scored the same or lower than it.
So far Altmetric has tracked 957 research outputs from this source. They receive a mean Attention Score of 4.3. 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 99,011 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 47 others from the same source and published within six weeks on either side of this one. This one is in the 19th percentile – i.e., 19% of its contemporaries scored the same or lower than it.