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Mendeley readers
Title |
EXPLAIN Fragile-X: an explorative, longitudinal study on the characterization, treatment pathways, and patient-related outcomes of Fragile X Syndrome
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Published in |
BMC Psychiatry, December 2013
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DOI | 10.1186/1471-244x-13-339 |
Pubmed ID | |
Authors |
Frank Haessler, Franziska Gaese, Michael Colla, Michael Huss, Christoph Kretschmar, Marc Brinkman, Heike Schieb, Helmut Peters, Samuel Elstner, David Pittrow |
Abstract |
Fragile X syndrome (FXS), caused by a mutation of the FMR1 gene on the X chromosome, is the most common inherited form of intellectual disability and autism spectrum disorders. Comprehensive data are lacking, however, on the characteristics and management patients with FXS in Germany. |
Mendeley readers
The data shown below were compiled from readership statistics for 92 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 1 | 1% |
Australia | 1 | 1% |
Unknown | 90 | 98% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Researcher | 16 | 17% |
Student > Ph. D. Student | 10 | 11% |
Student > Master | 10 | 11% |
Other | 7 | 8% |
Student > Doctoral Student | 7 | 8% |
Other | 17 | 18% |
Unknown | 25 | 27% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 18 | 20% |
Psychology | 18 | 20% |
Social Sciences | 7 | 8% |
Nursing and Health Professions | 6 | 7% |
Agricultural and Biological Sciences | 5 | 5% |
Other | 12 | 13% |
Unknown | 26 | 28% |