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Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

EBioMedicine(2021)10.1016/j.ebiom.2020.103157Source: DataRank Database

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium is a research paper published in EBioMedicine (2021). On theSindex it has a DataRank of 0.505. It has been cited 28 times.

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0.505DataRank · unranked

Scored on demand from live citation data

Open Access28 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (22 grants)Impact (FWCI 2.88)OA: goldTopics (84)IDs (PubMed, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.505

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (73)

Kelsey Grinde ORCID,Jennifer A. Brody ORCID,Charles E. Breeze ORCID,Laura M. Raffield ORCID,Josyf C. Mychaleckyj ORCID

Live enrichment

PubMed:33418499 OpenAlex:https://openalex.org/W3118236938

U.S. Department of Health and Human Services

Grant: R01HL131136

National Science Foundation

Grant: DGE-1256082

National Institutes of Health

Grant: K01AG059898

National Institutes of Health

Grant: R01 DK117445

National Institutes of Health

Grant: R01 MD012765

National Institutes of Health

Grant: R21 HL140385

National Institutes of Health

Grant: 5R01MD012765-04

Leveraging ancestry to map kidney loci

National Institutes of Health

Grant: 5R01HL131136-03

Epigenetics of Successful Aging

National Science Foundation

Grant: 1256082

Graduate Research Fellowship Program (GRFP)

National Institutes of Health

Grant: 5R01HL117626-02

Studies of Rare Genetic Variation in the Isolated Population of Sardinia

National Institutes of Health

Grant: 5R01DK117445-02

Genetics of kidney disease in diverse populations

National Institutes of Health

Grant: 5K01AG059898-02

DNA methylation markers of Multimorbidity in Aging Humans and Mice

National Institutes of Health

Grant: 5R01HL120393-03

Rare variants and NHLBI traits in deeply phenotyped cohorts

National Institutes of Health

Grant: 1R21HL140385-01

Phenome-wide association of protein function-altering variants in a family study

NHLBI NIH HHS

Grant: R01 HL120393

NHGRI NIH HHS

Grant: R01 HG010869

NHLBI NIH HHS

Grant: R21 HL123677

NHLBI NIH HHS

Grant: R01 HL117626

NHLBI NIH HHS

Grant: R01 HL149683

NHGRI NIH HHS

Grant: R01 HG009974

NIDDK NIH HHS

Grant: P30 DK072488

NHLBI NIH HHS

Grant: HHSN268201800001C

FWCI

2.88

Citation Percentile

0.9%

Citation Trend

2021

2022

2023

2024

2025

2026

goldLicense: cc-by

journalhttp://www.thelancet.com/article/S2352396420305338/pdf

publisherhttp://www.thelancet.com/article/S2352396420305338/pdf

publisherhttps://api.elsevier.com/content/article/PII:S2352396420305338?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2352396420305338?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.ebiom.2020.103157

Fields of Study

Genetic Associations and EpidemiologyChronic Kidney Disease and DiabetesCancer Genomics and Diagnostics0301 basic medicine03 medical and health sciences0303 health sciencesAllelesGene FrequencyGenetic Predisposition to DiseaseGenome-Wide Association StudyGenomicsGlomerular Filtration RateHumansMaleNational Heart, Lung, and Blood Institute (U.S.)Polymorphism, Single NucleotidePrecision MedicinePublic Health SurveillanceQuantitative Trait, HeritableUnited StatesWhole Genome Sequencing

MeSH Terms

Whole Genome SequencingAllelesGene FrequencyGlomerular Filtration RateHumansMaleUnited StatesQuantitative Trait, HeritableGenetic Predisposition to DiseasePolymorphism, Single NucleotideGenomicsNational Heart, Lung, and Blood Institute (U.S.)Genome-Wide Association StudyPrecision MedicinePublic Health Surveillance

Keywords

Computational biologyPrecision medicineOmicsGenomeWhole genome sequencingGenomicsSequence (biology)BioinformaticsBiologyGeneticsMedicineGeneMaleMedicine (General)EpidemiologyClinical Sciences610Polymorphism, Single NucleotideAncestry-specific variantsQuantitative TraitR5-920Quantitative Trait, HeritableGene FrequencyHealth Sciencesand Blood Institute (U.S.)2.1 Biological and endogenous factorsHumansGenetic Predisposition to DiseasePublic Health SurveillanceAetiologyPolymorphismLungHeritableKidney traitsAllelesHuman GenomeRRare variantsNational HeartSingle NucleotideUnited StatesGood Health and Well BeingPublic Health and Health ServicesNational Heart, Lung, and Blood Institute (U.S.)BiotechnologyResearch PaperGenome-Wide Association StudyGlomerular Filtration Rate

Sustainable Development Goals

SDG 3: 3. Good health