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Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID)

Overview of attention for article published in BMC Medical Genomics, July 2014
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Title
Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID)
Published in
BMC Medical Genomics, July 2014
DOI 10.1186/1471-2350-15-82
Pubmed ID
Authors

Ying Qiao, Eloi Mercier, Jila Dastan, Jane Hurlburt, Barbara McGillivray, Albert E Chudley, Sandra Farrell, Francois P Bernier, ME Suzanne Lewis, Paul Pavlidis, Evica Rajcan-Separovic

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 47 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 47 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 11 23%
Student > Bachelor 7 15%
Student > Master 6 13%
Researcher 5 11%
Student > Doctoral Student 4 9%
Other 7 15%
Unknown 7 15%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 11 23%
Medicine and Dentistry 11 23%
Agricultural and Biological Sciences 6 13%
Nursing and Health Professions 3 6%
Computer Science 2 4%
Other 7 15%
Unknown 7 15%