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Lynch syndrome: barriers to and facilitators of screening and disease management

Overview of attention for article published in Hereditary Cancer in Clinical Practice, September 2011
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Title
Lynch syndrome: barriers to and facilitators of screening and disease management
Published in
Hereditary Cancer in Clinical Practice, September 2011
DOI 10.1186/1897-4287-9-8
Pubmed ID
Authors

Kathy E Watkins, Christine Y Way, Jacqueline J Fiander, Robert J Meadus, Mary Jane Esplen, Jane S Green, Valerie C Ludlow, Holly A Etchegary, Patrick S Parfrey

Abstract

Lynch syndrome is a hereditary cancer with confirmed carriers at high risk for colorectal (CRC) and extracolonic cancers. The purpose of the current study was to develop a greater understanding of the factors influencing decisions about disease management post-genetic testing.

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X Demographics

The data shown below were collected from the profile of 1 X user 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 49 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Pakistan 1 2%
Switzerland 1 2%
Unknown 47 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 22%
Student > Master 10 20%
Student > Bachelor 5 10%
Other 4 8%
Student > Ph. D. Student 4 8%
Other 7 14%
Unknown 8 16%
Readers by discipline Count As %
Medicine and Dentistry 18 37%
Psychology 6 12%
Nursing and Health Professions 5 10%
Biochemistry, Genetics and Molecular Biology 5 10%
Agricultural and Biological Sciences 2 4%
Other 4 8%
Unknown 9 18%
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 10 January 2016.
All research outputs
#19,945,185
of 25,374,917 outputs
Outputs from Hereditary Cancer in Clinical Practice
#165
of 260 outputs
Outputs of similar age
#111,616
of 136,358 outputs
Outputs of similar age from Hereditary Cancer in Clinical Practice
#3
of 3 outputs
Altmetric has tracked 25,374,917 research outputs across all sources so far. This one is in the 18th percentile – i.e., 18% of other outputs scored the same or lower than it.
So far Altmetric has tracked 260 research outputs from this source. They receive a mean Attention Score of 4.8. This one is in the 33rd percentile – i.e., 33% 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 136,358 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 16th percentile – i.e., 16% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 3 others from the same source and published within six weeks on either side of this one.