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Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss

Overview of attention for article published in BMC Medical Genomics, January 2024
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Title
Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss
Published in
BMC Medical Genomics, January 2024
DOI 10.1186/s12920-023-01777-4
Pubmed ID
Authors

Kaifeng Zheng, Sheng Lin, Jian Gao, Shiguo Chen, Jindi Su, Zhiqiang Liu, Shan Duan

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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 04 January 2024.
All research outputs
#20,424,061
of 25,101,232 outputs
Outputs from BMC Medical Genomics
#980
of 1,380 outputs
Outputs of similar age
#110,731
of 163,280 outputs
Outputs of similar age from BMC Medical Genomics
#15
of 20 outputs
Altmetric has tracked 25,101,232 research outputs across all sources so far. This one is in the 10th percentile – i.e., 10% of other outputs scored the same or lower than it.
So far Altmetric has tracked 1,380 research outputs from this source. They receive a mean Attention Score of 4.6. This one is in the 18th percentile – i.e., 18% of its peers scored the same or lower than it.
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We're also able to compare this research output to 20 others from the same source and published within six weeks on either side of this one. This one is in the 20th percentile – i.e., 20% of its contemporaries scored the same or lower than it.