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Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set

Overview of attention for article published in BMC Proceedings, November 2011
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Title
Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set
Published in
BMC Proceedings, November 2011
DOI 10.1186/1753-6561-5-s9-s21
Pubmed ID
Authors

Wai-Ki Yip, Gourab De, Benjamin A Raby, Nan Laird

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Korea, Republic of 1 6%
Unknown 16 94%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 29%
Student > Ph. D. Student 4 24%
Professor > Associate Professor 4 24%
Student > Master 2 12%
Professor 1 6%
Other 0 0%
Unknown 1 6%
Readers by discipline Count As %
Agricultural and Biological Sciences 8 47%
Medicine and Dentistry 4 24%
Biochemistry, Genetics and Molecular Biology 2 12%
Computer Science 1 6%
Nursing and Health Professions 1 6%
Other 0 0%
Unknown 1 6%