Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects is a research paper published in Brain (2020). On theSindex it has a DataRank of 0.661. It has been cited 81 times.
Scored on demand from live citation data
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?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
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Base Score Contribution
0.661
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 →NHGRI
Grant: UM1 HG008895
Medical Research Council
Grant: G0800637
NHGRI NIH HHS
Grant: T32 HG009495
National Institute for Health Research (NIHR)
Grant: 09/144/09
NICHD NIH HHS
Grant: U54 HD090255
National Institutes of Health
Grant: 5UM1HG008895-04
Center for Common Disease Genetics
National Institutes of Health
NHGRI
NHLBI
National Human Genome Research Institute
National Heart, Lung, and Blood Institute
CCDG
Centers for Common Disease Genomics
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals