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Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability

Overview of attention for article published in BMC Medical Genomics, January 2011
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Title
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability
Published in
BMC Medical Genomics, January 2011
DOI 10.1186/1471-2350-12-17
Pubmed ID
Authors

Cecile Pagan, Hany Goubran Botros, Karine Poirier, Anne Dumaine, Stéphane Jamain, Sarah Moreno, Arjan de Brouwer, Hilde Van Esch, Richard Delorme, Jean-Marie Launay, Andreas Tzschach, Vera Kalscheuer, Didier Lacombe, Sylvain Briault, Frédéric Laumonnier, Martine Raynaud, Bregje W van Bon, Marjolein H Willemsen, Marion Leboyer, Jamel Chelly, Thomas Bourgeron

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 74 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 1%
Mexico 1 1%
Netherlands 1 1%
Unknown 71 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 12 16%
Student > Ph. D. Student 9 12%
Student > Doctoral Student 7 9%
Professor 5 7%
Student > Bachelor 5 7%
Other 22 30%
Unknown 14 19%
Readers by discipline Count As %
Medicine and Dentistry 19 26%
Agricultural and Biological Sciences 11 15%
Psychology 6 8%
Neuroscience 5 7%
Biochemistry, Genetics and Molecular Biology 4 5%
Other 10 14%
Unknown 19 26%