Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses

medRxiv(2020)10.1101/2020.08.28.20180414Source: DataRank Database

Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses is a research paper published in medRxiv (2020). On theSindex it has a DataRank of 0. It has been cited 15 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access15 citations

Download PDF

Cite:

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (5 grants)OA: greenTopics (42)IDs (PubMed, OpenAlex)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (4)

Maxwell A. Sherman ORCID,Ronen E. Mukamel ORCID,Po‐Ru Loh ORCID,Alison R. Barton ORCID

Live enrichment

PubMed:23304386 OpenAlex:https://openalex.org/W3082056204

National Institutes of Health

Grant: 1DP2ES030554-01

Revealing somatic genome alterations and their clinical sequelae: Ultrasensitive computational detection of mosaic structural variants

National Institutes of Health

Grant: 5F31HL154537-02

Investigating the contribution of rare coding variants to cardiovascular diseases

National Science Foundation

Grant: 1939015

Totally Geodesic Subvarieties in the Moduli Space of Riemann Surfaces

National Institutes of Health

Grant: 1K25HL150334-01

Exploring the role of genomic repeats in cardiovascular disease heritability

National Institutes of Health

Grant: 5F31MH124393-02

Exploring the role of genetic structural variation in neuropsychiatric diseases

greenLicense: Springer TDM

repositoryhttps://www.medrxiv.org/content/medrxiv/early/2020/09/01/2020.08.28.20180414.full.pdf

publisherhttps://syndication.highwire.org/content/doi/10.1101/2020.08.28.20180414

repositoryhttps://doi.org/10.1101/2020.08.28.20180414

repositoryhttps://nrs.harvard.edu/URN-3:HUL.INSTREPOS:37374291

Fields of Study

Genetic Associations and EpidemiologyGenomics and Rare DiseasesGenetic Syndromes and Imprinting0301 basic medicine03 medical and health sciences

Keywords

ExomeGeneticsMinor allele frequencyBiologyImputation (statistics)Genetic associationExome sequencingBiobankGenome-wide association studyMissense mutationAllele frequencyLinkage disequilibriumPopulationAlleleGeneHaplotypePhenotypeSingle-nucleotide polymorphismGenotypeMedicineMissing dataGenetic MarkersGenetic and Genomic MedicineModels, Genetic610Chromosome MappingMembrane ProteinsProteinsBlood PressurePolymorphism, Single NucleotideArticleUnited KingdomGene FrequencyHumansAtrial Natriuretic Factor Receptor BReceptors, Atrial Natriuretic FactorBiological Specimen Banks