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EXPLAIN Fragile-X: an explorative, longitudinal study on the characterization, treatment pathways, and patient-related outcomes of Fragile X Syndrome

Overview of attention for article published in BMC Psychiatry, December 2013
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Title
EXPLAIN Fragile-X: an explorative, longitudinal study on the characterization, treatment pathways, and patient-related outcomes of Fragile X Syndrome
Published in
BMC Psychiatry, December 2013
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.

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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%