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Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease

Overview of attention for article published in BMC Medical Genomics, August 2011
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Title
Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease
Published in
BMC Medical Genomics, August 2011
DOI 10.1186/1471-2350-12-111
Pubmed ID
Authors

Ingeborg Brønstad, Anette SB Wolff, Kristian Løvås, Per M Knappskog, Eystein S Husebye

Abstract

Addison's disease (AD) is caused by an autoimmune destruction of the adrenal cortex. The pathogenesis is multi-factorial, involving genetic components and hitherto unknown environmental factors. The aim of the present study was to investigate if gene dosage in the form of copy number variation (CNV) could add to the repertoire of genetic susceptibility to autoimmune AD.

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

Geographical breakdown

Country Count As %
Unknown 23 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 26%
Student > Ph. D. Student 4 17%
Student > Doctoral Student 3 13%
Student > Postgraduate 3 13%
Professor > Associate Professor 3 13%
Other 3 13%
Unknown 1 4%
Readers by discipline Count As %
Agricultural and Biological Sciences 14 61%
Medicine and Dentistry 5 22%
Chemistry 1 4%
Computer Science 1 4%
Unknown 2 9%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. 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 28 October 2011.
All research outputs
#15,090,466
of 25,371,288 outputs
Outputs from BMC Medical Genomics
#964
of 2,444 outputs
Outputs of similar age
#86,523
of 133,392 outputs
Outputs of similar age from BMC Medical Genomics
#17
of 26 outputs
Altmetric has tracked 25,371,288 research outputs across all sources so far. This one is in the 40th percentile – i.e., 40% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,444 research outputs from this source. They receive a mean Attention Score of 4.4. This one has gotten more attention than average, scoring higher than 60% of its peers.
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 133,392 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 35th percentile – i.e., 35% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 26 others from the same source and published within six weeks on either side of this one. This one is in the 34th percentile – i.e., 34% of its contemporaries scored the same or lower than it.