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The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and NRXN1 Deletions

Overview of attention for article published in Frontiers in Neuroscience, February 2022
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Title
The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and NRXN1 Deletions
Published in
Frontiers in Neuroscience, February 2022
DOI 10.3389/fnins.2022.806990
Pubmed ID
Authors

Jennifer Cooke, Ciara J. Molloy, Antonia San José Cáceres, Thomas Dinneen, Thomas Bourgeron, Declan Murphy, Louise Gallagher, Eva Loth

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 30 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 30 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 13%
Researcher 4 13%
Student > Bachelor 3 10%
Unspecified 2 7%
Student > Master 1 3%
Other 1 3%
Unknown 15 50%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 17%
Unspecified 2 7%
Psychology 2 7%
Medicine and Dentistry 2 7%
Arts and Humanities 1 3%
Other 4 13%
Unknown 14 47%