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Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study

Circulation(2021)10.1161/circulationaha.121.055562Source: DataRank Database

Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study is a research paper published in Circulation (2021). On theSindex it has a DataRank of 1.2. It has been cited 49 times, with 30 citing works in its 1-hop citation network.

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1.2DataRank · unranked

Scored on demand from live citation data

Deposits data Open Access49 citations · 30 citing works in its network

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Data availability

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

ClinicalTrials.govNCT03394859

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (45 grants)OA: bronzeTopics (32)IDs (PubMed)SDGs (2)

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 50%Citation Network 50%

Base Score Contribution

0.587

From this paper's citation signal

Citation Network Contribution

0.581

From 17 citing papers with measurable signal

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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 30 citers.

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Scientific Reports202256 citations55 referencesContributes 0.074
First Steps of Population Genomic Medicine in the Arrhythmia World: Pros and Cons
Circulation20222 citations15 referencesContributes 0.073
Genetic Testing for Inherited Heart Disease in the Era of Next-Generation Sequencing: Now, Next, and Beyond
Circulation Genomic and Precision Medicine20222 citations15 referencesContributes 0.073
Postmortem investigation of fatalities following vaccination with COVID-19 vaccines
International Journal of Legal Medicine202156 citations63 referencesContributes 0.064
Variant reclassification and clinical implications
Journal of Medical Genetics202461 citations78 referencesContributes 0.053

Authors (51)

Giovanni Davogustto ORCID,Christian M. Shaffer,Carlos G. Vanoye ORCID,Reshma R. Desai ORCID,Eric Farber‐Eger ORCID

Live enrichment

PubMed:34930020

National Institutes of Health

Grant: 3U01HG008672-03S1

VGER, the Vanderbilt Genome-Electronic Records Project

National Institutes of Health

Grant: 5U01HG008657-10

eMERGE IV Northwest: A partnership to evaluate the use of genomic information in the health care of diverse participants

National Institutes of Health

Grant: 7R01HL122010-12

Decrypting Variants of Uncertain Significance in Long-QT Syndrome

National Institutes of Health

Grant: 5U01HG008679-04

EMR-Linked Biobank for Translational Genomics

National Institutes of Health

Grant: 5U01HG008680-03

Columbia GENIE (GENomic Integration with Ehr)

National Institutes of Health

Grant: 3U01HG008676-04S2

EMERGE III CENTRAL SEQUENCING, GENOTYPING AND INTERPRETATION FACILITY

National Institutes of Health

Grant: 6UL1TR000445-11

The Vanderbilt Institute for Clinical and Translational Research (VICTR)

National Institutes of Health

Grant: 3U01HG008684-04S1

The Future of Genomics Medicine in Patient Care: Contributions from CHOP

National Institutes of Health

Grant: 6U01HG008701-02

The Electronic Medical Records and Genomics (eMERGE) Network Phase III - Coordinating Center (U01)

National Institutes of Health

Grant: 5U01HG008666-03

Better Outcomes for Children: Promoting Excellence in Healthcare Genomics to Inform Policy

National Institutes of Health

Grant: 5U01HG008673-03

Genomic Medicine at Northwestern: Discovery and Implementation

National Institutes of Health

Grant: 1S10OD025281-01

Nanion SynchroPatch 384 for Automated, High-throughput Electrophysiology

National Institutes of Health

Grant: 1K99HG010904-01

A pipeline for identifying disease-causing variants in transmembrane proteins

National Institutes of Health

Grant: 5R01HL128075-06

Cardiomyopathy Genomes Project

National Institutes of Health

Grant: 5R01HL122010-08

Decrypting Variants of Uncertain Significance in Long-QT Syndrome

National Institutes of Health

Grant: 1U01HG008664-01

DNA Sequencing Support for the eMERGE Network

National Institutes of Health

Grant: 3U01HG006379-12S3

EHR-based Genomic Discovery and Implementation (Supplement)

National Institutes of Health

Grant: 1U01HG008685-01

EMERGE PHASE III CLINICAL CENTER AT PARTNERS HEALTHCARE

National Institutes of Health

Grant: 5R01HL149826-04

Functional Genomics of Cardiac Sodium Channel Variants

NHGRI NIH HHS

Grant: T32 HG008341

NHGRI NIH HHS

Grant: U01 HG008657

NHGRI NIH HHS

Grant: U01 HG008666

NHGRI NIH HHS

Grant: R00 HG010904

NHGRI NIH HHS

Grant: U01 HG008685

NHGRI NIH HHS

Grant: U01 HG006379

NIH HHS

Grant: S10 OD025281

NHGRI NIH HHS

Grant: U01 HG008676

NCATS NIH HHS

Grant: UL1 TR000445

NHGRI NIH HHS

Grant: U01 HG008672

NCATS NIH HHS

Grant: UL1 TR001422

NHGRI NIH HHS

Grant: U01 HG008684

NHGRI NIH HHS

Grant: K99 HG010904

NHGRI NIH HHS

Grant: U01 HG008679

NHLBI NIH HHS

Grant: R01 HL128075

NHLBI NIH HHS

Grant: R01 HL122010

NIGMS NIH HHS

Grant: T32 GM007347

NHLBI NIH HHS

Grant: R00 HL135442

NHGRI NIH HHS

Grant: U01 HG008680

NIGMS NIH HHS

Grant: T32 GM152284

NIDDK NIH HHS

Grant: P30 DK114857

NHGRI NIH HHS

Grant: U01 HG008673

NHGRI NIH HHS

Grant: U01 HG008664

NHGRI NIH HHS

Grant: U01 HG011181

NHGRI NIH HHS

Grant: U01 HG008701

NHLBI NIH HHS

Grant: R01 HL149826

bronzeLicense: CC BY NC ND

publisherhttps://www.ahajournals.org/doi/pdf/10.1161/CIRCULATIONAHA.121.055562

publisherhttps://www.ahajournals.org/doi/full/10.1161/CIRCULATIONAHA.121.055562

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8940719

https://doi.org/10.1101/2021.03.30.21254549

https://www.medrxiv.org/content/medrxiv/early/2021/04/06/2021.03.30.21254549.full.pdf

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciencesArrhythmias, CardiacGenetic Predisposition to DiseaseGenetic TestingGenomicsHEK293 CellsHumansPhenotypeProspective Studies

MeSH Terms

Arrhythmias, CardiacGenetic Predisposition to DiseaseGenetic TestingGenomicsHEK293 CellsHumansPhenotypeProspective Studies

Keywords

HEK293 CellsPhenotypeHumansArrhythmias, CardiacGenetic Predisposition to DiseaseGenetic TestingGenomicsProspective Studiesarrhythmiascardiacelectronic health recordselectrophysiologylong QT syndrome

Sustainable Development Goals

SDG 3: 3. Good healthSDG 16: 16. Peace & justice