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A genomic copy number variant analysis implicates the MBD5 and HNRNPUgenes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletion

Overview of attention for article published in BMC Medical Genomics, May 2014
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Title
A genomic copy number variant analysis implicates the MBD5 and HNRNPUgenes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletion
Published in
BMC Medical Genomics, May 2014
DOI 10.1186/1471-2350-15-62
Pubmed ID
Authors

Xiaonan Du, Yu An, Lifei Yu, Renchao Liu, Yanrong Qin, Xiaohong Guo, Daokan Sun, Shuizhen Zhou, Bailin Wu, Yong-hui Jiang, Yi Wang

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 84 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 1%
South Africa 1 1%
Unknown 82 98%

Demographic breakdown

Readers by professional status Count As %
Researcher 15 18%
Student > Ph. D. Student 12 14%
Student > Bachelor 10 12%
Student > Master 8 10%
Student > Postgraduate 7 8%
Other 16 19%
Unknown 16 19%
Readers by discipline Count As %
Medicine and Dentistry 17 20%
Biochemistry, Genetics and Molecular Biology 13 15%
Agricultural and Biological Sciences 13 15%
Neuroscience 6 7%
Psychology 5 6%
Other 10 12%
Unknown 20 24%