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Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

Overview of attention for article published in BMC Medical Genomics, March 2013
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Title
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
Published in
BMC Medical Genomics, March 2013
DOI 10.1186/1755-8794-6-10
Pubmed ID
Authors

Bente A Talseth-Palmer, Elizabeth G Holliday, Tiffany-Jane Evans, Mark McEvoy, John Attia, Desma M Grice, Amy L Masson, Cliff Meldrum, Allan Spigelman, Rodney J Scott

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 56 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Finland 1 2%
Spain 1 2%
Canada 1 2%
Unknown 53 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 14 25%
Researcher 9 16%
Student > Doctoral Student 8 14%
Professor > Associate Professor 5 9%
Student > Master 5 9%
Other 10 18%
Unknown 5 9%
Readers by discipline Count As %
Agricultural and Biological Sciences 15 27%
Biochemistry, Genetics and Molecular Biology 13 23%
Medicine and Dentistry 10 18%
Neuroscience 3 5%
Computer Science 2 4%
Other 7 13%
Unknown 6 11%