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Returning integrated genomic risk and clinical recommendations: The eMERGE study

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

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006Source: DataRank Database

Returning integrated genomic risk and clinical recommendations: The eMERGE study is a research paper published in Genetics in Medicine (2023). On theSindex it has a DataRank of 2.6. It has been cited 121 times, with 79 citing works in its 1-hop citation network.

N/A

2.6DataRank · unranked

Scored on demand from live citation data

Deposits data Open Access121 citations · 79 citing works in its network

Cite:

Linked data & code

doi

Data availability

Repositories this paper deposited data in (declared in PubMed).

ClinicalTrials.govNCT05277116

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 (28 grants)Impact (FWCI 26.22)OA: greenTopics (35)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (1)

FAIR Checklist

Context only (not used in score)

FFindable (1/2)

Has DOI

AAccessible (1/2)

Open Access

IInteroperable (0/2)

RReusable (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.

DataRank Breakdown

Base Score 27%Citation Network 73%

Base Score Contribution

0.721

From this paper's citation signal

Citation Network Contribution

1.9

From 55 citing papers with measurable signal

Learn more about DataRank methodology →

Top 5 citers driving the network score

Ranked by each citer's contribution to N(p) — log1p(C_q) divided by its reference count — out of 79 citers.

Enhancing the Polygenic Score Catalog with tools for score calculation and ancestry normalization
Nature Genetics202496 citations15 referencesContributes 0.305
Performance and Agreement of Coronary Heart Disease Polygenic Risk Scores—Reply
JAMA20252 citations6 referencesContributes 0.183
A polygenic risk score added to a QRISK®2 cardiovascular disease risk calculator demonstrated robust clinical acceptance and clinical utility in the primary care setting
European Journal of Preventive Cardiology202449 citations30 referencesContributes 0.130
Evaluating Performance and Agreement of Coronary Heart Disease Polygenic Risk Scores
JAMA202460 citations38 referencesContributes 0.108
Instability of high polygenic risk classification and mitigation by integrative scoring
Nature Communications202523 citations31 referencesContributes 0.103

Authors (100)

Aimee Allworth,Harris T. Bland ORCID,Pedro J. Caraballo ORCID,Rex L. Chisholm ORCID,Ellen Wright Clayton ORCID

Live enrichment

PubMed:36621880 PMC:PMC10085845 OpenAlex:https://openalex.org/W4313644892

National Human Genome Research Institute

Grant: U01HG006379

National Human Genome Research Institute

Grant: U01HG008657

National Human Genome Research Institute

Grant: U01HG008680

National Human Genome Research Institute

Grant: U01HG008685

National Human Genome Research Institute

Grant: U01HG011166

National Human Genome Research Institute

Grant: U01HG011167

National Human Genome Research Institute

Grant: U01HG011169

National Human Genome Research Institute

Grant: U01HG011172

National Human Genome Research Institute

Grant: U01HG011175

National Human Genome Research Institute

Grant: U01HG011176

National Human Genome Research Institute

Grant: U01HG011181

NIAMS NIH HHS

Grant: K12 AR084232

NICHD NIH HHS

Grant: K12 HD043483

NHLBI NIH HHS

Grant: R01 HL128075

NHLBI NIH HHS

Grant: K24 HL133373

NIH HHS

Grant: S10 OD030463

NIH HHS

Grant: S10 OD026880

NCATS NIH HHS

Grant: UL1 TR001873

NCATS NIH HHS

Grant: UL1 TR002319

NCATS NIH HHS

Grant: UL1 TR004419

Cincinnati Children's Hospital Medical Center

Northwestern University

Children's Hospital of Philadelphia

Columbia University

Icahn School of Medicine at Mount Sinai

University of Washington

Mayo Clinic

Vanderbilt University Medical Center

FWCI

26.22

Citation Percentile

1.0%

Influential Citations

6

Citation Trend

2022

2023

2024

2025

2026

greenLicense: http://creativecommons.org/licenses/by-nc-nd/4.0/

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10085845/pdf/nihms-1875295.pdf

GREENhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10085845

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10085845/pdf/nihms-1875295.pdf

publisherhttps://api.elsevier.com/content/article/PII:S1098360023000023?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1098360023000023?httpAccept=text/plain

Fields of Study

BRCA gene mutations in cancerGenetic Associations and EpidemiologyGenomics and Rare DiseasesMedicineHumansProspective StudiesGenomeGenomicsRisk FactorsRisk Assessment

MeSH Terms

HumansProspective StudiesRisk FactorsGenomeRisk AssessmentGenomics

Keywords

Polygenic risk scoreMedicineRisk assessmentFamily historyRisk managementRisk analysis (engineering)Intensive care medicineGeneticsBusinessBiologyInternal medicineSingle-nucleotide polymorphismComputer scienceGeneGenotypeGenotypingCommon VariantsPolygenic Risk ScoresMonogenic Risks

Sustainable Development Goals

SDG 0: Industry, innovation and infrastructure

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