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