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A Pilot study of the Sharing Risk Information Tool (ShaRIT) for Families with Hereditary Breast and Ovarian Cancer Syndrome

Overview of attention for article published in Hereditary Cancer in Clinical Practice, April 2012
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Mentioned by

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2 tweeters

Citations

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18 Dimensions

Readers on

mendeley
26 Mendeley
Title
A Pilot study of the Sharing Risk Information Tool (ShaRIT) for Families with Hereditary Breast and Ovarian Cancer Syndrome
Published in
Hereditary Cancer in Clinical Practice, April 2012
DOI 10.1186/1897-4287-10-4
Pubmed ID
Abstract

Individuals who carry deleterious BRCA mutations face significantly elevated risks of breast, ovarian, and other cancers. These individuals are also responsible for informing relatives of their increased risk for carrying the family BRCA mutation. Few interventions have been developed to facilitate this family communication process.

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

Geographical breakdown

Country Count As %
Philippines 1 4%
Brazil 1 4%
Unknown 24 92%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 19%
Student > Master 5 19%
Student > Postgraduate 4 15%
Student > Ph. D. Student 3 12%
Professor 2 8%
Other 6 23%
Unknown 1 4%
Readers by discipline Count As %
Medicine and Dentistry 11 42%
Agricultural and Biological Sciences 3 12%
Social Sciences 2 8%
Biochemistry, Genetics and Molecular Biology 2 8%
Psychology 2 8%
Other 4 15%
Unknown 2 8%

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 April 2012.
All research outputs
#3,029,038
of 4,508,238 outputs
Outputs from Hereditary Cancer in Clinical Practice
#50
of 80 outputs
Outputs of similar age
#47,258
of 76,709 outputs
Outputs of similar age from Hereditary Cancer in Clinical Practice
#2
of 2 outputs
Altmetric has tracked 4,508,238 research outputs across all sources so far. This one is in the 20th percentile – i.e., 20% of other outputs scored the same or lower than it.
So far Altmetric has tracked 80 research outputs from this source. They receive a mean Attention Score of 2.2. 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 76,709 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 19th percentile – i.e., 19% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 2 others from the same source and published within six weeks on either side of this one.