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Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11

Overview of attention for article published in Molecular Cytogenetics, April 2014
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Title
Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11
Published in
Molecular Cytogenetics, April 2014
DOI 10.1186/1755-8166-7-28
Pubmed ID
Authors

Jin-Lan Chen, Xin Zhu, Tian-Li Zhao, Jian Wang, Yi-Feng Yang, Zhi-Ping Tan

Abstract

RASopathies are a group of disorders related to Noonan syndrome that with dysregulated RAS-mitogen-activated protein kinase (MAPK) signaling pathway. Noonan syndrome (NS, OMIM# 163950) is a both phenotypically and genotypically variable disorder. We and other researchers have demonstrated that copy number variations underlie a small percentage of patients with RASopathies.

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X Demographics

The data shown below were collected from the profile of 1 X user 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 34 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
South Africa 1 3%
Unknown 33 97%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 7 21%
Other 5 15%
Researcher 5 15%
Student > Ph. D. Student 4 12%
Student > Bachelor 3 9%
Other 4 12%
Unknown 6 18%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 8 24%
Medicine and Dentistry 8 24%
Agricultural and Biological Sciences 4 12%
Nursing and Health Professions 2 6%
Chemistry 2 6%
Other 4 12%
Unknown 6 18%
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 16 April 2014.
All research outputs
#20,228,193
of 22,753,345 outputs
Outputs from Molecular Cytogenetics
#297
of 400 outputs
Outputs of similar age
#173,170
of 203,744 outputs
Outputs of similar age from Molecular Cytogenetics
#5
of 7 outputs
Altmetric has tracked 22,753,345 research outputs across all sources so far. This one is in the 1st percentile – i.e., 1% of other outputs scored the same or lower than it.
So far Altmetric has tracked 400 research outputs from this source. They receive a mean Attention Score of 2.4. This one is in the 1st percentile – i.e., 1% 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 203,744 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 7 others from the same source and published within six weeks on either side of this one. This one has scored higher than 2 of them.