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Adult expression of a 3q13.31 microdeletion

Overview of attention for article published in Molecular Cytogenetics, March 2014
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Title
Adult expression of a 3q13.31 microdeletion
Published in
Molecular Cytogenetics, March 2014
DOI 10.1186/1755-8166-7-23
Pubmed ID
Authors

Chelsea Lowther, Gregory Costain, Rebecca Melvin, Dimitri J Stavropoulos, Anath C Lionel, Christian R Marshall, Stephen W Scherer, Anne S Bassett

Abstract

The emerging 3q13.31 microdeletion syndrome appears to encompass diverse neurodevelopmental conditions. However, the 3q13.31 deletion is rare and few adult cases have yet been reported. We examined a cohort with schizophrenia (n = 459) and adult control subjects (n = 26,826) using high-resolution microarray technology for deletions and duplications at the 3q13.31 locus.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 41 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Hong Kong 1 2%
United States 1 2%
Denmark 1 2%
Italy 1 2%
Unknown 37 90%

Demographic breakdown

Readers by professional status Count As %
Researcher 9 22%
Other 6 15%
Student > Ph. D. Student 4 10%
Lecturer 3 7%
Student > Postgraduate 2 5%
Other 4 10%
Unknown 13 32%
Readers by discipline Count As %
Agricultural and Biological Sciences 9 22%
Biochemistry, Genetics and Molecular Biology 6 15%
Medicine and Dentistry 4 10%
Neuroscience 3 7%
Social Sciences 1 2%
Other 2 5%
Unknown 16 39%