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Expanding the clinical and genetic spectrum of Heimler syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, December 2019
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Title
Expanding the clinical and genetic spectrum of Heimler syndrome
Published in
Orphanet Journal of Rare Diseases, December 2019
DOI 10.1186/s13023-019-1243-x
Pubmed ID
Authors

Feng-Juan Gao, Fang-Yuan Hu, Ping Xu, Yu-He Qi, Jian-Kang Li, Yong-Jin Zhang, Fang Chen, Qing Chang, Fang Song, Si-Mai Shen, Ge-Zhi Xu, Ji-Hong Wu

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 49 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 49 100%

Demographic breakdown

Readers by professional status Count As %
Other 5 10%
Student > Doctoral Student 5 10%
Student > Bachelor 5 10%
Student > Master 4 8%
Professor 2 4%
Other 8 16%
Unknown 20 41%
Readers by discipline Count As %
Medicine and Dentistry 13 27%
Biochemistry, Genetics and Molecular Biology 7 14%
Agricultural and Biological Sciences 2 4%
Psychology 2 4%
Computer Science 1 2%
Other 2 4%
Unknown 22 45%