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Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2014
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29 Mendeley
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Title
Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features
Published in
Orphanet Journal of Rare Diseases, April 2014
DOI 10.1186/1750-1172-9-60
Pubmed ID
Authors

Ahmet Arman, Abdullah Bereket, Ajda Coker, Pelin Özlem Şimşek Kiper, Tülay Güran, Behzat Özkan, Zeynep Atay, Teoman Akçay, Belma Haliloglu, Koray Boduroglu, Yasemin Alanay, Serap Turan

Abstract

To characterize cathepsin K (CTSK) mutations in a group of patients with pycnodysostosis, who presented with either short stature or atypical fractures to pediatric endocrinology or dysmorphic features to pediatric genetics clinics.

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%
Student > Bachelor 4 14%
Student > Doctoral Student 3 10%
Other 3 10%
Researcher 3 10%
Other 6 21%
Unknown 5 17%
Readers by discipline Count As %
Medicine and Dentistry 11 38%
Agricultural and Biological Sciences 5 17%
Biochemistry, Genetics and Molecular Biology 3 10%
Social Sciences 1 3%
Neuroscience 1 3%
Other 1 3%
Unknown 7 24%
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 30 April 2014.
All research outputs
#15,299,919
of 22,754,104 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,784
of 2,610 outputs
Outputs of similar age
#133,717
of 226,896 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#22
of 29 outputs
Altmetric has tracked 22,754,104 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,610 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.5. This one is in the 23rd percentile – i.e., 23% 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 226,896 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 31st percentile – i.e., 31% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 29 others from the same source and published within six weeks on either side of this one. This one is in the 17th percentile – i.e., 17% of its contemporaries scored the same or lower than it.