A recurrent de novo variant in NUSAP1 escapes nonsense‐mediated decay and leads to microcephaly, epilepsy, and developmental delay is a research paper published in Clinical Genetics (2023). On theSindex it has a DataRank of 0.396. It has been cited 13 times.
Scored on demand from live citation data
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
0.396
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 →National Heart, Lung, and Blood Institute
Grant: UM1 HG008900
National Human Genome Research Institute
Grant: R01 HG009141
National Institute of Neurological Disorders and Stroke
Grant: R01NS035129
National Institutes of Health
Grant: 5R01NS035129-13
Human Epilepsy Genetics - Neuronal Migration Disorders
National Institutes of Health
Grant: 5UM1HG008900-04
Joint Center for Mendelian Genomics
National Institutes of Health
Grant: 3R25NS070682-04S1
CH/BIDMC/Harvard Medical School Neurology Resident Research Education Program
National Institutes of Health
Grant: 5R01HG009141-02
A powerful web-based discovery platform for rare disease genetics
FWCI
1.70
Citation Percentile
0.8%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals