↓ Skip to main content

Case report of intrafamilial variability in autosomal recessive centronuclear myopathy associated to a novel BIN1 stop mutation

Overview of attention for article published in Orphanet Journal of Rare Diseases, December 2010
Altmetric Badge

Mentioned by

patent
1 patent

Citations

dimensions_citation
52 Dimensions

Readers on

mendeley
82 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Title
Case report of intrafamilial variability in autosomal recessive centronuclear myopathy associated to a novel BIN1 stop mutation
Published in
Orphanet Journal of Rare Diseases, December 2010
DOI 10.1186/1750-1172-5-35
Pubmed ID
Authors

Johann Böhm, Uluç Yiş, Ragıp Ortaç, Handan Çakmakçı, Semra Hız Kurul, Eray Dirik, Jocelyn Laporte

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 82 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Denmark 1 1%
Unknown 81 99%

Demographic breakdown

Readers by professional status Count As %
Lecturer 20 24%
Student > Master 12 15%
Student > Ph. D. Student 8 10%
Student > Bachelor 5 6%
Other 5 6%
Other 7 9%
Unknown 25 30%
Readers by discipline Count As %
Nursing and Health Professions 25 30%
Medicine and Dentistry 11 13%
Agricultural and Biological Sciences 7 9%
Biochemistry, Genetics and Molecular Biology 5 6%
Computer Science 3 4%
Other 5 6%
Unknown 26 32%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. 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 May 2019.
All research outputs
#7,610,760
of 23,205,257 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,122
of 2,665 outputs
Outputs of similar age
#54,563
of 181,745 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#25
of 41 outputs
Altmetric has tracked 23,205,257 research outputs across all sources so far. This one is in the 44th percentile – i.e., 44% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,665 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.6. This one has gotten more attention than average, scoring higher than 53% of its peers.
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 181,745 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 27th percentile – i.e., 27% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 41 others from the same source and published within six weeks on either side of this one. This one is in the 12th percentile – i.e., 12% of its contemporaries scored the same or lower than it.