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Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Overview of attention for article published in Hereditary Cancer in Clinical Practice, August 2021
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1 X user

Citations

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19 Mendeley
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Title
Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants
Published in
Hereditary Cancer in Clinical Practice, August 2021
DOI 10.1186/s13053-021-00190-1
Pubmed ID
Authors

Krithika Murali, Tanya M. Dwarte, Mehrdad Nikfarjam, Katherine M. Tucker, Rhys B. Vaughan, Marios Efthymiou, Allison Collins, Allan D. Spigelman, Lucinda Salmon, Amber L. Johns, David B. Williams, Martin B. Delatycki, Thomas John, Alina Stoita

X Demographics

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

Geographical breakdown

Country Count As %
Unknown 19 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 16%
Student > Doctoral Student 1 5%
Other 1 5%
Professor 1 5%
Professor > Associate Professor 1 5%
Other 0 0%
Unknown 12 63%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 21%
Nursing and Health Professions 1 5%
Medicine and Dentistry 1 5%
Engineering 1 5%
Unknown 12 63%
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 17 August 2021.
All research outputs
#22,774,430
of 25,392,582 outputs
Outputs from Hereditary Cancer in Clinical Practice
#216
of 261 outputs
Outputs of similar age
#362,901
of 421,288 outputs
Outputs of similar age from Hereditary Cancer in Clinical Practice
#5
of 9 outputs
Altmetric has tracked 25,392,582 research outputs across all sources so far. This one is in the 1st percentile – i.e., 1% of other outputs scored the same or lower than it.
So far Altmetric has tracked 261 research outputs from this source. They receive a mean Attention Score of 4.8. This one is in the 1st percentile – i.e., 1% 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 421,288 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 9 others from the same source and published within six weeks on either side of this one. This one has scored higher than 4 of them.