↓ Skip to main content

Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2011
Altmetric Badge

About this Attention Score

  • Average Attention Score compared to outputs of the same age

Mentioned by

wikipedia
1 Wikipedia page

Citations

dimensions_citation
144 Dimensions

Readers on

mendeley
188 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Title
Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum
Published in
Orphanet Journal of Rare Diseases, June 2011
DOI 10.1186/1750-1172-6-39
Pubmed ID
Authors

Saqib Mahmood, Wasim Ahmad, Muhammad J Hassan

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 188 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 <1%
China 1 <1%
Unknown 186 99%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 34 18%
Researcher 31 16%
Student > Bachelor 30 16%
Student > Master 19 10%
Professor > Associate Professor 11 6%
Other 32 17%
Unknown 31 16%
Readers by discipline Count As %
Medicine and Dentistry 46 24%
Agricultural and Biological Sciences 45 24%
Biochemistry, Genetics and Molecular Biology 35 19%
Neuroscience 13 7%
Social Sciences 4 2%
Other 13 7%
Unknown 32 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 15 December 2015.
All research outputs
#7,469,522
of 22,835,198 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,085
of 2,620 outputs
Outputs of similar age
#41,259
of 113,598 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#4
of 8 outputs
Altmetric has tracked 22,835,198 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 2,620 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 113,598 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 33rd percentile – i.e., 33% of its contemporaries scored the same or lower than it.
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 4 of them.