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TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia

Overview of attention for article published in Orphanet Journal of Rare Diseases, August 2013
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  • Average Attention Score compared to outputs of the same age
  • Above-average Attention Score compared to outputs of the same age and source (62nd percentile)

Mentioned by

wikipedia
1 Wikipedia page

Citations

dimensions_citation
83 Dimensions

Readers on

mendeley
54 Mendeley
citeulike
1 CiteULike
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Title
TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia
Published in
Orphanet Journal of Rare Diseases, August 2013
DOI 10.1186/1750-1172-8-125
Pubmed ID
Authors

Maria Sandbacka, Hannele Laivuori, Érika Freitas, Mervi Halttunen, Varpu Jokimaa, Laure Morin-Papunen, Carla Rosenberg, Kristiina Aittomäki

Abstract

Müllerian aplasia (MA) is a congenital disorder of the female reproductive tract with absence of uterus and vagina with paramount impact on a woman's life. Despite intense research, no major genes have been found to explain the complex genetic etiology.

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 %
Finland 1 2%
Unknown 53 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 15%
Student > Master 8 15%
Student > Bachelor 8 15%
Researcher 5 9%
Student > Postgraduate 4 7%
Other 10 19%
Unknown 11 20%
Readers by discipline Count As %
Medicine and Dentistry 18 33%
Biochemistry, Genetics and Molecular Biology 14 26%
Agricultural and Biological Sciences 5 9%
Neuroscience 2 4%
Nursing and Health Professions 1 2%
Other 5 9%
Unknown 9 17%
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 14 July 2018.
All research outputs
#7,432,894
of 22,723,682 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,075
of 2,604 outputs
Outputs of similar age
#58,545
of 175,535 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#14
of 40 outputs
Altmetric has tracked 22,723,682 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 2,604 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.5. 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 175,535 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 50% of its contemporaries.
We're also able to compare this research output to 40 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 62% of its contemporaries.