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Mendeley readers
Title |
Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?
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Published in |
Molecular Cytogenetics, September 2015
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DOI | 10.1186/s13039-015-0178-8 |
Pubmed ID | |
Authors |
Julia K. Ehret, Hartmut Engels, Kirsten Cremer, Jessica Becker, Johannes P. Zimmermann, Eva Wohlleber, Ute Grasshoff, Eva Rossier, Michael Bonin, Elisabeth Mangold, Andrea Bevot, Stefanie Schön, Stefanie Heilmann-Heimbach, Nicola Dennert, Michèle Mathieu-Dramard, Elodie Lacaze, Ghislaine Plessis, Alain de Broca, Guillaume Jedraszak, Benno Röthlisberger, Peter Miny, Isabel Filges, Andreas Dufke, Joris Andrieux, Jennifer A. Lee, Alexander M. Zink |
Mendeley readers
The data shown below were compiled from readership statistics for 35 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 35 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 7 | 20% |
Researcher | 5 | 14% |
Student > Bachelor | 4 | 11% |
Student > Master | 4 | 11% |
Professor | 2 | 6% |
Other | 5 | 14% |
Unknown | 8 | 23% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 10 | 29% |
Biochemistry, Genetics and Molecular Biology | 5 | 14% |
Agricultural and Biological Sciences | 3 | 9% |
Computer Science | 2 | 6% |
Neuroscience | 2 | 6% |
Other | 5 | 14% |
Unknown | 8 | 23% |