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Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2009
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Mentioned by

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3 Wikipedia pages

Citations

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114 Dimensions

Readers on

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88 Mendeley
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Title
Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports
Published in
Orphanet Journal of Rare Diseases, November 2009
DOI 10.1186/1750-1172-4-25
Pubmed ID
Authors

Laura Bernardini, Stefania Gimelli, Cristina Gervasini, Massimo Carella, Anwar Baban, Giada Frontino, Giancarlo Barbano, Maria Teresa Divizia, Luigi Fedele, Antonio Novelli, Frédérique Béna, Faustina Lalatta, Monica Miozzo, Bruno Dallapiccola

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 88 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 1%
Russia 1 1%
Italy 1 1%
Australia 1 1%
Unknown 84 95%

Demographic breakdown

Readers by professional status Count As %
Researcher 15 17%
Other 13 15%
Student > Ph. D. Student 9 10%
Student > Master 9 10%
Student > Bachelor 8 9%
Other 19 22%
Unknown 15 17%
Readers by discipline Count As %
Medicine and Dentistry 31 35%
Agricultural and Biological Sciences 17 19%
Biochemistry, Genetics and Molecular Biology 13 15%
Psychology 3 3%
Immunology and Microbiology 2 2%
Other 8 9%
Unknown 14 16%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. 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 20 July 2022.
All research outputs
#7,976,256
of 23,994,935 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,164
of 2,800 outputs
Outputs of similar age
#35,492
of 97,505 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#4
of 5 outputs
Altmetric has tracked 23,994,935 research outputs across all sources so far. This one is in the 44th percentile – i.e., 44% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,800 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.0. This one has gotten more attention than average, scoring higher than 54% 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 97,505 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 20th percentile – i.e., 20% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 5 others from the same source and published within six weeks on either side of this one.