A harmonized public resource of deeply sequenced diverse human genomes is a dataset published in Genome Research (2024). On theSindex it has a DataRank of 2.6, placing it in the top 8.3% of the data-sharing corpus. It has been cited 130 times, with 100 citing works in its 1-hop citation network.
Ranks in the top 8% 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
0.731
From this paper's citation signal
Citation Network Contribution
1.9
From 70 citing papers with measurable signal
Ranked by each citer's contribution to N(p) — log1p(Cq) divided by its reference count — out of 100 citers.
National Institutes of Health
Grant: K99/R00MH117229
National Institute of Dental and Craniofacial Research
Grant: R01DE031261
National Institute of Mental Health [NIMH]
Grant: R01MH115957
National Institute of Mental Health [NIMH]
Grant: R37MH107649
Novo Nordisk Foundation
Grant: NNF21SA0072102
NIMH NIH HHS
Grant: R00 MH117229
National Institutes of Health
Grant: 1R01MH115957-01A1
Scalable tool and comprehensive maps to interpret structural variation across the neuropsychiatric spectrum
National Institutes of Health
Grant: 1R01DE031261-01
Integration of polygenic risk and facial morphometrics to decipher the genetic susceptibility of orofacial clefting
National Institutes of Health
Grant: 4R00MH117229-03
Generalizing polygenic risk prediction methods across populations for insights into psychiatric disease
Novo Nordisk Foundation
Grant: unidentified
unidentified
National Institutes of Health
Grant: 5R37MH107649-07
Statistical methods to localize disease heritability and identify biological mechanisms
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