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Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2012
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Mentioned by

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2 X users

Citations

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28 Dimensions

Readers on

mendeley
38 Mendeley
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Title
Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population
Published in
Orphanet Journal of Rare Diseases, June 2012
DOI 10.1186/1750-1172-7-44
Pubmed ID
Authors

Thomas J Jaworek, Tasleem Kausar, Shannon M Bell, Nabeela Tariq, Muhammad Imran Maqsood, Asma Sohail, Muhmmmad Ali, Furhan Iqbal, Shafqat Rasool, Saima Riazuddin, Rehan S Shaikh, Zubair M Ahmed

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 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 38 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 38 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 5 13%
Student > Ph. D. Student 4 11%
Other 3 8%
Student > Master 3 8%
Student > Doctoral Student 2 5%
Other 9 24%
Unknown 12 32%
Readers by discipline Count As %
Medicine and Dentistry 8 21%
Biochemistry, Genetics and Molecular Biology 6 16%
Unspecified 2 5%
Agricultural and Biological Sciences 2 5%
Mathematics 1 3%
Other 5 13%
Unknown 14 37%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. 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 29 July 2020.
All research outputs
#13,454,350
of 22,840,638 outputs
Outputs from Orphanet Journal of Rare Diseases
#1,394
of 2,621 outputs
Outputs of similar age
#91,209
of 164,555 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#9
of 16 outputs
Altmetric has tracked 22,840,638 research outputs across all sources so far. This one is in the 39th percentile – i.e., 39% of other outputs scored the same or lower than it.
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 is in the 43rd percentile – i.e., 43% of its peers scored the same or lower than it.
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 164,555 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 43rd percentile – i.e., 43% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 16 others from the same source and published within six weeks on either side of this one. This one is in the 25th percentile – i.e., 25% of its contemporaries scored the same or lower than it.