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Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2011
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About this Attention Score

  • Good Attention Score compared to outputs of the same age (65th percentile)
  • Above-average Attention Score compared to outputs of the same age and source (62nd percentile)

Mentioned by

twitter
1 tweeter
wikipedia
2 Wikipedia pages

Citations

dimensions_citation
127 Dimensions

Readers on

mendeley
95 Mendeley
Title
Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland
Published in
Orphanet Journal of Rare Diseases, June 2011
DOI 10.1186/1750-1172-6-41
Pubmed ID
Authors

Eeva-Maria Laitinen, Kirsi Vaaralahti, Johanna Tommiska, Elina Eklund, Mari Tervaniemi, Leena Valanne, Taneli Raivio

Twitter Demographics

The data shown below were collected from the profile of 1 tweeter who shared this research output. Click here to find out more about how the information was compiled.

Mendeley readers

The data shown below were compiled from readership statistics for 95 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 1%
Spain 1 1%
Italy 1 1%
Unknown 92 97%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 19 20%
Student > Master 12 13%
Student > Postgraduate 11 12%
Other 9 9%
Researcher 8 8%
Other 20 21%
Unknown 16 17%
Readers by discipline Count As %
Medicine and Dentistry 49 52%
Biochemistry, Genetics and Molecular Biology 9 9%
Neuroscience 4 4%
Agricultural and Biological Sciences 4 4%
Veterinary Science and Veterinary Medicine 2 2%
Other 7 7%
Unknown 20 21%

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 05 February 2021.
All research outputs
#6,965,297
of 22,840,638 outputs
Outputs from Orphanet Journal of Rare Diseases
#985
of 2,621 outputs
Outputs of similar age
#38,166
of 114,232 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#3
of 8 outputs
Altmetric has tracked 22,840,638 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 2,621 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 60% 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 114,232 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 65% of its contemporaries.
We're also able to compare this research output to 8 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.