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Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families

Overview of attention for article published in Orphanet Journal of Rare Diseases, July 2014
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • Good Attention Score compared to outputs of the same age (79th percentile)
  • Good Attention Score compared to outputs of the same age and source (76th percentile)

Mentioned by

blogs
1 blog

Citations

dimensions_citation
23 Dimensions

Readers on

mendeley
28 Mendeley
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Title
Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families
Published in
Orphanet Journal of Rare Diseases, July 2014
DOI 10.1186/s13023-014-0108-6
Pubmed ID
Authors

Naeimeh Tayebi, Aleksander Jamsheer, Ricarda Flöttmann, Anna Sowinska-Seidler, Sandra C Doelken, Barbara Oehl-Jaschkowitz, Wiebke Hülsemann, Rolf Habenicht, Eva Klopocki, Stefan Mundlos, Malte Spielmann

Abstract

A growing number of non-coding regulatory mutations are being identified in congenital disease. Very recently also some exons of protein coding genes have been identified to act as tissue specific enhancer elements and were therefore termed exonic enhancers or "eExons".

Mendeley readers

The data shown below were compiled from readership statistics for 28 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Hong Kong 1 4%
Unknown 27 96%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 11 39%
Researcher 6 21%
Student > Bachelor 3 11%
Student > Master 3 11%
Professor 2 7%
Other 2 7%
Unknown 1 4%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 11 39%
Agricultural and Biological Sciences 9 32%
Medicine and Dentistry 3 11%
Environmental Science 1 4%
Arts and Humanities 1 4%
Other 0 0%
Unknown 3 11%

Attention Score in Context

This research output has an Altmetric Attention Score of 6. 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 19 September 2014.
All research outputs
#855,537
of 5,036,026 outputs
Outputs from Orphanet Journal of Rare Diseases
#140
of 858 outputs
Outputs of similar age
#27,974
of 135,360 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#9
of 39 outputs
Altmetric has tracked 5,036,026 research outputs across all sources so far. Compared to these this one has done well and is in the 82nd percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 858 research outputs from this source. They receive a mean Attention Score of 4.3. This one has done well, scoring higher than 83% 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 135,360 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 79% of its contemporaries.
We're also able to compare this research output to 39 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 76% of its contemporaries.