Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements is a dataset published in PLOS Genetics (2019). On theSindex it has a DataRank of 0.590, placing it in the top 33.1% of the data-sharing corpus. It has been cited 50 times.
Ranks in the top 33% for downstream scientific impact
Linked data & code
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
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Base Score Contribution
0.590
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.
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Grant: 2013-2603, 2017-02936
Marianne and Marcus Wallenberg foundation
Grant: 2014-0084
Hjärnfonden
Grant: Ulf Lundahl memory fund
NICHD NIH HHS
Grant: R03 HD092569
Swedish Research Council
Grant: unidentified
unidentified
National Institutes of Health
Grant: 1R03HD092569-01A1
Discovery and functional characterization of genic variants leading to Robinow syndrome and related skeletal dysplasias.
Stockholms Läns Landsting
Science for Life Laboratory
Svenska Sällskapet för Medicinsk Forskning
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 1 of A pipeline for complete characterization of complex germline rearrangements from long DNA reads
Additional file 1 of A pipeline for complete characterization of complex germline rearrangements from long DNA reads
Additional file 1 of Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism
Additional file 1 of Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism