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Detailed analysis of phenotypes and genotypes in megalencephaly-capillary malformation-polymicrogyria syndrome caused by somatic mosaicism of PIK3CA mutations

Overview of attention for article published in Orphanet Journal of Rare Diseases, August 2020
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About this Attention Score

  • Above-average Attention Score compared to outputs of the same age (61st percentile)
  • Above-average Attention Score compared to outputs of the same age and source (60th percentile)

Mentioned by

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5 X users

Citations

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17 Dimensions

Readers on

mendeley
24 Mendeley
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Title
Detailed analysis of phenotypes and genotypes in megalencephaly-capillary malformation-polymicrogyria syndrome caused by somatic mosaicism of PIK3CA mutations
Published in
Orphanet Journal of Rare Diseases, August 2020
DOI 10.1186/s13023-020-01480-y
Pubmed ID
Authors

Hyun Jin Park, Chang Ho Shin, Won Joon Yoo, Tae-Joon Cho, Man Jin Kim, Moon-Woo Seong, Sung Sup Park, Jeong Ho Lee, Nam Suk Sim, Jung Min Ko

X Demographics

X Demographics

The data shown below were collected from the profiles of 5 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 24 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 24 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 4 17%
Other 3 13%
Researcher 3 13%
Student > Master 2 8%
Student > Ph. D. Student 1 4%
Other 3 13%
Unknown 8 33%
Readers by discipline Count As %
Medicine and Dentistry 7 29%
Veterinary Science and Veterinary Medicine 1 4%
Chemical Engineering 1 4%
Biochemistry, Genetics and Molecular Biology 1 4%
Unspecified 1 4%
Other 2 8%
Unknown 11 46%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 4. 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 13 August 2020.
All research outputs
#7,280,182
of 23,230,825 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,063
of 2,665 outputs
Outputs of similar age
#154,570
of 398,702 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#18
of 45 outputs
Altmetric has tracked 23,230,825 research outputs across all sources so far. This one has received more attention than most of these and is in the 68th percentile.
So far Altmetric has tracked 2,665 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.7. This one has gotten more attention than average, scoring higher than 59% 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 398,702 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 61% of its contemporaries.
We're also able to compare this research output to 45 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 60% of its contemporaries.