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Workshop report: the clinical application of data from multiplex assays of variant effect (MAVEs), 12 July 2023

European Journal of Human Genetics(2024)10.1038/s41431-024-01566-2Source: DataRank Database

Workshop report: the clinical application of data from multiplex assays of variant effect (MAVEs), 12 July 2023 is a research paper published in European Journal of Human Genetics (2024). On theSindex it has a DataRank of 0. It has been cited 22 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access22 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (21 grants)Impact (FWCI 8.33)OA: hybridTopics (19)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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Authors (12)

Alice Garrett ORCID,Lara A. Muffley ORCID,Shawn Fayer ORCID,Julia Foreman ORCID,David J. Adams ORCID

Live enrichment

PubMed:38433264 OpenAlex:https://openalex.org/W4392371883

Cancer Research UK

Grant: EDDPGM-Nov22/100004

Cancer Research UK

Grant: C61296/A27223

U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute

Grant: RM1 HG01046

U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute

Grant: R01 HG013025

Wellcome Trust

Grant: WT223718/Z/21/Z

U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute

Grant: R01 HL164675

Gouvernement du Canada | Canadian Institutes of Health Research

Grant: FDN159926

U.S. Department of Health & Human Services | National Institutes of Health

Grant: HG200328-18

U.S. Department of Health & Human Services | National Institutes of Health

Grant: HG200359-15

Wellcome Trust

Grant: unidentified

unidentified

National Institutes of Health

Grant: 5RM1HG010461-05

Center for the Multiplexed Assessment of Phenotype

National Institutes of Health

Grant: 1R01HG013025-01

Advancing the implementation of variant-level functional data into clinical databases and clinical practice

National Institutes of Health

Grant: 1UM1HG011969-01

The Center for Actionable Variant Analysis; measuring variant function at scale

National Institutes of Health

Grant: 1ZIAHG200359-11

ClinSeq(c) - Molecular and Genetic Aspects

National Institutes of Health

Grant: 5UM1HG011989-02

Molecular phenotyping of ~100,000 coding variants across Mendelian disease genes

Wellcome Trust

Grant: 223718

DECIPHER

National Institutes of Health

Grant: 1R01HL164675-01

Systematically mapping variant effects for cardiovascular genes

National Institutes of Health

Grant: 1ZIAHG200328-13

Molecular Studies of Malformations

Wellcome Trust

Grant: 220540

Wellcome Sanger Institute Quinquennial Review 2021-2026

NHGRI NIH HHS

Grant: RM1 HG010461

Wellcome Trust

FWCI

8.33

Citation Percentile

1.0%

Citation Trend

2024

2025

2026

hybridLicense: cc-by

journalhttps://www.nature.com/articles/s41431-024-01566-2.pdf

publisherhttps://www.nature.com/articles/s41431-024-01566-2.pdf

publisherhttps://www.nature.com/articles/s41431-024-01566-2

journalhttps://doi.org/10.1038/s41431-024-01566-2

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38433264

Fields of Study

Genomics and Rare DiseasesCancer Genomics and DiagnosticsGenetic Associations and EpidemiologyHumansGenetic Testing

MeSH Terms

Genetic TestingHumans

Keywords

Data scienceMultiplexComputational biologyComputer scienceMedical physicsBioinformaticsMedicineBiology610HumansGenetic TestingMeeting Report

Sustainable Development Goals

SDG 0: Partnerships for the goals

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