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Mendeley readers
Title |
Adult expression of a 3q13.31 microdeletion
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Published in |
Molecular Cytogenetics, March 2014
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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
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% |