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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 Genetics, 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 Genetics, 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

The data shown below were compiled from readership statistics for 56 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 2%
South Africa 1 2%
Unknown 54 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 13 23%
Student > Ph. D. Student 9 16%
Student > Bachelor 8 14%
Student > Master 6 11%
Student > Postgraduate 5 9%
Other 12 21%
Unknown 3 5%
Readers by discipline Count As %
Medicine and Dentistry 12 21%
Biochemistry, Genetics and Molecular Biology 11 20%
Agricultural and Biological Sciences 11 20%
Psychology 5 9%
Neuroscience 4 7%
Other 8 14%
Unknown 5 9%