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Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies

Overview of attention for article published in Nucleic Acids Research, October 2016
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Title
Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies
Published in
Nucleic Acids Research, October 2016
DOI 10.1093/nar/gkw949
Pubmed ID
Authors

Emmanouil Viennas, Angeliki Komianou, Clint Mizzi, Maja Stojiljkovic, Christina Mitropoulou, Juha Muilu, Mauno Vihinen, Panagiota Grypioti, Styliani Papadaki, Cristiana Pavlidis, Branka Zukic, Theodora Katsila, Peter J. van der Spek, Sonja Pavlovic, Giannis Tzimas, George P. Patrinos

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 31 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Sweden 1 3%
Unknown 30 97%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 26%
Student > Ph. D. Student 5 16%
Student > Bachelor 4 13%
Professor 2 6%
Student > Master 2 6%
Other 4 13%
Unknown 6 19%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 10 32%
Computer Science 7 23%
Engineering 2 6%
Medicine and Dentistry 2 6%
Mathematics 1 3%
Other 4 13%
Unknown 5 16%