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Metabolic abnormalities in Williams–Beuren syndrome

Overview of attention for article published in Journal of Medical Genetics, February 2015
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3 Facebook pages

Citations

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35 Dimensions

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54 Mendeley
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Title
Metabolic abnormalities in Williams–Beuren syndrome
Published in
Journal of Medical Genetics, February 2015
DOI 10.1136/jmedgenet-2014-102713
Pubmed ID
Authors

María Gabriela Palacios-Verdú, Maria Segura-Puimedon, Cristina Borralleras, Raquel Flores, Miguel Del Campo, Victoria Campuzano, Luis Alberto Pérez-Jurado

Abstract

Williams-Beuren syndrome (WBS, OMIM-194050) is a neurodevelopmental disorder with multisystemic manifestations caused by a 1.55-1.83 Mb deletion at 7q11.23 including 26-28 genes. Reported endocrine and metabolic abnormalities include transient hypercalcaemia of infancy, subclinical hypothyroidism in ∼30% of children and impaired glucose tolerance in ∼75% of adult individuals. The purpose of this study was to further study metabolic alterations in patients with WBS, as well as in several mouse models, to establish potential candidate genes.

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

Geographical breakdown

Country Count As %
Unknown 54 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 9 17%
Student > Master 8 15%
Student > Doctoral Student 5 9%
Student > Bachelor 5 9%
Student > Postgraduate 5 9%
Other 11 20%
Unknown 11 20%
Readers by discipline Count As %
Medicine and Dentistry 14 26%
Biochemistry, Genetics and Molecular Biology 9 17%
Agricultural and Biological Sciences 9 17%
Nursing and Health Professions 2 4%
Neuroscience 2 4%
Other 4 7%
Unknown 14 26%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. 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 February 2015.
All research outputs
#14,214,321
of 22,787,797 outputs
Outputs from Journal of Medical Genetics
#2,533
of 2,918 outputs
Outputs of similar age
#187,248
of 352,111 outputs
Outputs of similar age from Journal of Medical Genetics
#30
of 35 outputs
Altmetric has tracked 22,787,797 research outputs across all sources so far. This one is in the 35th percentile – i.e., 35% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,918 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 11th percentile – i.e., 11% 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 352,111 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 44th percentile – i.e., 44% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 35 others from the same source and published within six weeks on either side of this one. This one is in the 8th percentile – i.e., 8% of its contemporaries scored the same or lower than it.