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Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites

Overview of attention for article published in BMC Genomics, January 2009
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80 Mendeley
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2 CiteULike
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Title
Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites
Published in
BMC Genomics, January 2009
DOI 10.1186/1471-2164-10-59
Pubmed ID
Authors

Allison A Burrow, Laura E Williams, Levi CT Pierce, Yuh-Hwa Wang

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 80 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 1%
Unknown 79 99%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 28 35%
Researcher 19 24%
Student > Master 6 8%
Professor > Associate Professor 5 6%
Student > Bachelor 5 6%
Other 9 11%
Unknown 8 10%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 31 39%
Agricultural and Biological Sciences 31 39%
Medicine and Dentistry 6 8%
Chemistry 1 1%
Computer Science 1 1%
Other 0 0%
Unknown 10 13%