Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease−associated genes is a research paper published in Genetics in Medicine (2023). On theSindex it has a DataRank of 0.561. It has been cited 41 times.
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Base Score Contribution
0.561
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
Learn more about DataRank methodology →Health Research Board
Grant: MRCG-2016-14
Application of Next Generation Sequencing for the Genetic Characterisation of Irish Retinal Degeneration Patients
European Commission
Grant: 779257
Solving the unsolved Rare Diseases
Irish Research Council
Grant: unidentified
unidentified
European Commission
Grant: 825575
European Joint Programme on Rare Diseases
FWCI
6.41
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals