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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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Mentioned by

twitter
2 tweeters

Citations

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16 Dimensions

Readers on

mendeley
26 Mendeley
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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

Postma AV, Alders M, Sylva M, Bilardo CM, Pajkrt E, van Rijn RR, Schulte-Merker S, Bulk S, Stefanovic S, Ilgun A, Barnett P, Mannens MM, Moorman AF, Oostra RJ, van Maarle MC, 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.

Twitter Demographics

The data shown below were collected from the profiles of 2 tweeters who shared this research output. Click here to find out more about how the information was compiled.

Mendeley readers

The data shown below were compiled from readership statistics for 26 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Sweden 1 4%
Unknown 25 96%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 31%
Professor 4 15%
Student > Master 3 12%
Researcher 3 12%
Professor > Associate Professor 3 12%
Other 5 19%
Readers by discipline Count As %
Agricultural and Biological Sciences 10 38%
Biochemistry, Genetics and Molecular Biology 7 27%
Medicine and Dentistry 6 23%
Unspecified 1 4%
Neuroscience 1 4%
Other 1 4%

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
#2,927,091
of 6,230,238 outputs
Outputs from Journal of Medical Genetics
#1,143
of 1,369 outputs
Outputs of similar age
#67,309
of 133,366 outputs
Outputs of similar age from Journal of Medical Genetics
#23
of 26 outputs
Altmetric has tracked 6,230,238 research outputs across all sources so far. This one is in the 29th percentile – i.e., 29% of other outputs scored the same or lower than it.
So far Altmetric has tracked 1,369 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 5.2. This one is in the 9th percentile – i.e., 9% 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 133,366 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 36th percentile – i.e., 36% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 26 others from the same source and published within six weeks on either side of this one. This one is in the 7th percentile – i.e., 7% of its contemporaries scored the same or lower than it.