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Mutation in MEOX1gene causes a recessive Klippel-Feil syndrome subtype

Overview of attention for article published in BMC Genomic Data, September 2013
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3 Facebook pages

Citations

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53 Dimensions

Readers on

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43 Mendeley
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1 CiteULike
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Title
Mutation in MEOX1gene causes a recessive Klippel-Feil syndrome subtype
Published in
BMC Genomic Data, September 2013
DOI 10.1186/1471-2156-14-95
Pubmed ID
Authors

Fatih Bayrakli, Bulent Guclu, Cengiz Yakicier, Hatice Balaban, Ugur Kartal, Bekir Erguner, Mahmut Samil Sagiroglu, Sirin Yuksel, Ahmet Rasit Ozturk, Burak Kazanci, Unal Ozum, Hamit Zafer Kars

Abstract

Klippel-Feil syndrome (KFS) is characterized by the developmental failure of the cervical spine and has two dominantly inherited subtypes. Affected individuals who are the children of a consanguineous marriage are extremely rare in the medical literature, but the gene responsible for this recessive trait subtype of KFS has recently been reported.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 43 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 43 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 7 16%
Student > Doctoral Student 6 14%
Researcher 5 12%
Other 4 9%
Student > Bachelor 4 9%
Other 9 21%
Unknown 8 19%
Readers by discipline Count As %
Medicine and Dentistry 12 28%
Biochemistry, Genetics and Molecular Biology 10 23%
Nursing and Health Professions 2 5%
Agricultural and Biological Sciences 2 5%
Neuroscience 2 5%
Other 5 12%
Unknown 10 23%
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 12 December 2014.
All research outputs
#19,945,185
of 25,374,917 outputs
Outputs from BMC Genomic Data
#786
of 1,204 outputs
Outputs of similar age
#156,946
of 217,316 outputs
Outputs of similar age from BMC Genomic Data
#12
of 19 outputs
Altmetric has tracked 25,374,917 research outputs across all sources so far. This one is in the 18th percentile – i.e., 18% of other outputs scored the same or lower than it.
So far Altmetric has tracked 1,204 research outputs from this source. They receive a mean Attention Score of 4.3. This one is in the 28th percentile – i.e., 28% 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 217,316 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 24th percentile – i.e., 24% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 19 others from the same source and published within six weeks on either side of this one. This one is in the 36th percentile – i.e., 36% of its contemporaries scored the same or lower than it.