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A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach

Overview of attention for article published in Molecular Cytogenetics, June 2014
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About this Attention Score

  • Good Attention Score compared to outputs of the same age and source (71st percentile)

Mentioned by

twitter
1 X user
facebook
1 Facebook page

Citations

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8 Dimensions

Readers on

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13 Mendeley
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Title
A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach
Published in
Molecular Cytogenetics, June 2014
DOI 10.1186/1755-8166-7-44
Pubmed ID
Authors

Irene Plaza Pinto, Lysa Bernardes Minasi, Alex Silva da Cruz, Aldaires Vieira de Melo, Damiana Míriam da Cruz e Cunha, Rodrigo Roncato Pereira, Cristiano Luiz Ribeiro, Claudio Carlos da Silva, Daniela de Melo e Silva, Aparecido Divino da Cruz

Abstract

Chromosome abnormalities that segregate with a disease phenotype can facilitate the identification of disease loci and genes. The relationship between chromosome 18 anomalies with severe intellectual disability has attracted the attention of cytogeneticists worldwide. Duplications of the X chromosome can cause intellectual disability in females with variable phenotypic effects, due in part to variations in X-inactivation patterns. Additionally, deletions of the 7qter region are associated with a range of phenotypes.

X Demographics

X Demographics

The data shown below were collected from the profile of 1 X user 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 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Germany 1 8%
Unknown 12 92%

Demographic breakdown

Readers by professional status Count As %
Unspecified 4 31%
Student > Bachelor 3 23%
Student > Postgraduate 2 15%
Researcher 1 8%
Professor > Associate Professor 1 8%
Other 0 0%
Unknown 2 15%
Readers by discipline Count As %
Unspecified 4 31%
Nursing and Health Professions 2 15%
Biochemistry, Genetics and Molecular Biology 1 8%
Agricultural and Biological Sciences 1 8%
Sports and Recreations 1 8%
Other 1 8%
Unknown 3 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 March 2015.
All research outputs
#17,722,431
of 22,757,541 outputs
Outputs from Molecular Cytogenetics
#209
of 400 outputs
Outputs of similar age
#155,294
of 227,675 outputs
Outputs of similar age from Molecular Cytogenetics
#2
of 7 outputs
Altmetric has tracked 22,757,541 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 400 research outputs from this source. They receive a mean Attention Score of 2.4. This one is in the 41st percentile – i.e., 41% 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 227,675 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 28th percentile – i.e., 28% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 7 others from the same source and published within six weeks on either side of this one. This one has scored higher than 5 of them.