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Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal

Overview of attention for article published in Journal of Medical Genetics, November 2013
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Title
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal
Published in
Journal of Medical Genetics, November 2013
DOI 10.1136/jmedgenet-2013-102001
Pubmed ID
Authors

A V Postma, M Alders, M Sylva, C M Bilardo, E Pajkrt, R R van Rijn, S Schulte-Merker, S Bulk, S Stefanovic, A Ilgun, P Barnett, M M A M Mannens, A F M Moorman, R J Oostra, M C van Maarle

Abstract

The T gene (brachyury gene) is the founding member of the T-box family of transcription factors and is vital for the formation and differentiation of the mesoderm and the axial development of all vertebrates.

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 50 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Sweden 1 2%
Unknown 49 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 16%
Professor > Associate Professor 6 12%
Professor 6 12%
Researcher 5 10%
Student > Doctoral Student 4 8%
Other 12 24%
Unknown 9 18%
Readers by discipline Count As %
Medicine and Dentistry 12 24%
Agricultural and Biological Sciences 11 22%
Biochemistry, Genetics and Molecular Biology 10 20%
Neuroscience 2 4%
Unspecified 1 2%
Other 2 4%
Unknown 12 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 02 March 2014.
All research outputs
#17,713,929
of 22,745,803 outputs
Outputs from Journal of Medical Genetics
#2,704
of 2,917 outputs
Outputs of similar age
#219,575
of 302,151 outputs
Outputs of similar age from Journal of Medical Genetics
#19
of 21 outputs
Altmetric has tracked 22,745,803 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 2,917 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 7.2. This one is in the 5th percentile – i.e., 5% 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 302,151 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 21 others from the same source and published within six weeks on either side of this one. This one is in the 4th percentile – i.e., 4% of its contemporaries scored the same or lower than it.