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A 29 Mainland Chinese cohort of patients with Phelan–McDermid syndrome: genotype–phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2020
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2 X users

Citations

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Title
A 29 Mainland Chinese cohort of patients with Phelan–McDermid syndrome: genotype–phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes
Published in
Orphanet Journal of Rare Diseases, November 2020
DOI 10.1186/s13023-020-01592-5
Pubmed ID
Authors

Na Xu, Hui Lv, Tingting Yang, Xiujuan Du, Yu Sun, Bing Xiao, Yanjie Fan, Xiaomei Luo, Yongkun Zhan, Lili Wang, Fei Li, Yongguo Yu

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 29 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 29 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 17%
Other 3 10%
Student > Doctoral Student 3 10%
Librarian 2 7%
Student > Bachelor 2 7%
Other 4 14%
Unknown 10 34%
Readers by discipline Count As %
Medicine and Dentistry 4 14%
Neuroscience 4 14%
Psychology 3 10%
Nursing and Health Professions 2 7%
Social Sciences 2 7%
Other 4 14%
Unknown 10 34%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 05 December 2020.
All research outputs
#18,111,817
of 23,267,128 outputs
Outputs from Orphanet Journal of Rare Diseases
#2,054
of 2,669 outputs
Outputs of similar age
#358,927
of 508,818 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#39
of 53 outputs
Altmetric has tracked 23,267,128 research outputs across all sources so far. This one is in the 19th percentile – i.e., 19% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,669 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.7. This one is in the 18th percentile – i.e., 18% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 508,818 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 25th percentile – i.e., 25% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 53 others from the same source and published within six weeks on either side of this one. This one is in the 24th percentile – i.e., 24% of its contemporaries scored the same or lower than it.