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Next-generation sequencing reveals novel variants and large deletion in FANCA gene in Polish family with Fanconi anemia

Overview of attention for article published in Orphanet Journal of Rare Diseases, July 2022
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About this Attention Score

  • Good Attention Score compared to outputs of the same age (70th percentile)
  • High Attention Score compared to outputs of the same age and source (80th percentile)

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10 X users

Citations

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5 Dimensions

Readers on

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13 Mendeley
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Title
Next-generation sequencing reveals novel variants and large deletion in FANCA gene in Polish family with Fanconi anemia
Published in
Orphanet Journal of Rare Diseases, July 2022
DOI 10.1186/s13023-022-02424-4
Pubmed ID
Authors

Anna Repczynska, Katarzyna Julga, Jolanta Skalska-Sadowska, Magdalena M. Kacprzak, Alicja Bartoszewska-Kubiak, Ewelina Lazarczyk, Damian Loska, Malgorzata Drozniewska, Kamila Czerska, Jacek Wachowiak, Olga Haus

X Demographics

X Demographics

The data shown below were collected from the profiles of 10 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 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 4 31%
Student > Master 3 23%
Student > Bachelor 2 15%
Researcher 1 8%
Student > Ph. D. Student 1 8%
Other 0 0%
Unknown 2 15%
Readers by discipline Count As %
Unspecified 4 31%
Biochemistry, Genetics and Molecular Biology 3 23%
Pharmacology, Toxicology and Pharmaceutical Science 1 8%
Medicine and Dentistry 1 8%
Neuroscience 1 8%
Other 1 8%
Unknown 2 15%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 5. 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 22 July 2022.
All research outputs
#6,963,946
of 24,878,531 outputs
Outputs from Orphanet Journal of Rare Diseases
#954
of 2,991 outputs
Outputs of similar age
#125,549
of 426,839 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#22
of 110 outputs
Altmetric has tracked 24,878,531 research outputs across all sources so far. This one has received more attention than most of these and is in the 71st percentile.
So far Altmetric has tracked 2,991 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.1. This one has gotten more attention than average, scoring higher than 67% 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 426,839 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 70% of its contemporaries.
We're also able to compare this research output to 110 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 80% of its contemporaries.