Distinct sequence features underlie microdeletions and gross deletions in the human genome is a dataset published in Human Mutation (2021). On theSindex it has a DataRank of 0.421, placing it in the top 44% of the data-sharing corpus. It has been cited 8 times, with 5 citing works in its 1-hop citation network.
Ranks in the top 44% 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?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full — never from an abstract alone.
Base Score Contribution
0.330
From this paper's citation signal
Citation Network Contribution
0.0915
From 4 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 5 citers.
National Natural Science Foundation of China
Grant: 81801132
National Natural Science Foundation of China
Grant: 81971190
National Institutes of Health
Grant: P01 CA092584
National Institutes of Health
Grant: R35 CA220430
National Institutes of Health
Grant: 3P01CA092584-19S1
Structural Cell Biology of DNA Repair Machines
National Institutes of Health
Grant: 5R35CA220430-02
Mesocale And Nanoscale Technologies Integrated by Structures for DNA Repair Complexes (MANTIS-DRC)
FWCI
0.52
Citation Percentile
0.6%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Additional file 1 of A novel large intragenic DPYD deletion causing dihydropyrimidine dehydrogenase deficiency: a case report
Additional file 1 of A novel large intragenic DPYD deletion causing dihydropyrimidine dehydrogenase deficiency: a case report