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NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree

Overview of attention for article published in Journal of Ovarian Research, April 2020
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Title
NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree
Published in
Journal of Ovarian Research, April 2020
DOI 10.1186/s13048-020-00645-4
Pubmed ID
Authors

Lin Li, Fan Feng, Minying Zhao, Tengyan Li, Wentao Yue, Xu Ma, Binbin Wang, Chenghong Yin

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 14 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 2 14%
Student > Postgraduate 2 14%
Student > Bachelor 1 7%
Lecturer 1 7%
Researcher 1 7%
Other 1 7%
Unknown 6 43%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 21%
Psychology 2 14%
Nursing and Health Professions 1 7%
Medicine and Dentistry 1 7%
Unknown 7 50%