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Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2020
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Title
Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population
Published in
Orphanet Journal of Rare Diseases, January 2020
DOI 10.1186/s13023-020-1294-z
Pubmed ID
Authors

Farjana Akther Noor, Nusrat Sultana, Golam Sarower Bhuyan, Md Tarikul Islam, Mohabbat Hossain, Suprovath Kumar Sarker, Khaleda Islam, Waqar Ahmed Khan, Mujahida Rahman, Syeda Kashfi Qadri, Hossain Uddin Shekhar, Firdausi Qadri, Syed Saleheen Qadri, Kaiissar Mannoor

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The data shown below were collected from the profile of 1 X user 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 80 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 80 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 14 18%
Student > Master 7 9%
Researcher 6 8%
Student > Postgraduate 5 6%
Student > Ph. D. Student 3 4%
Other 8 10%
Unknown 37 46%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 14 18%
Medicine and Dentistry 11 14%
Nursing and Health Professions 4 5%
Immunology and Microbiology 4 5%
Economics, Econometrics and Finance 2 3%
Other 7 9%
Unknown 38 48%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. 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 17 January 2020.
All research outputs
#20,599,981
of 23,186,937 outputs
Outputs from Orphanet Journal of Rare Diseases
#2,505
of 2,661 outputs
Outputs of similar age
#382,048
of 456,917 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#44
of 52 outputs
Altmetric has tracked 23,186,937 research outputs across all sources so far. This one is in the 1st percentile – i.e., 1% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,661 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.7. This one is in the 1st percentile – i.e., 1% 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 456,917 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 52 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.