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

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants

medRxiv(2024)10.1101/2024.05.28.24307502Source: DataRank Database

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants is a research paper published in medRxiv (2024). On theSindex it has a DataRank of 0.165. It has been cited 2 times.

N/A

0.165DataRank · unranked

Scored on demand from live citation data

Open Access2 citations

Download PDF

Cite:

Linked data & code

ensembl omim

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 (8 grants)OA: greenTopics (33)IDs (PubMed, OpenAlex)Annotations (2)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)

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 100%Citation Network 0%

Base Score Contribution

0.165

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.

Learn more about DataRank methodology →

Authors (21)

Megan Holdren,Terra Brannan,Miguel de la Hoya ORCID,Amanda B. Spurdle ORCID,Sean V. Tavtigian ORCID

Live enrichment

PubMed:38854136 OpenAlex:https://openalex.org/W4399118277

National Institute for Health Research (NIHR)

Grant: NIHR203312

National Institutes of Health

Grant: 5U24CA258058-02

BRCA1/2 and Hereditary Breast, Ovarian and Pancreatic (HBOP) Cancer Variant Curation Expert Panels

Canadian Institutes of Health Research

Grant: unidentified

unidentified

National Institutes of Health

Grant: 5R35CA253187-06

Resolving the cancer relevance of predisposition gene mutations

National Institutes of Health

Grant: 5P50CA116201-08

Career Development (Ingle)

NCI NIH HHS

Grant: P50 CA116201

NCI NIH HHS

Grant: R35 CA253187

NCI NIH HHS

Grant: U24 CA258058

greenLicense: cc-by

repositoryhttps://doi.org/10.1101/2024.05.28.24307502

publisherhttps://syndication.highwire.org/content/doi/10.1101/2024.05.28.24307502

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38854136

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/11160822

Fields of Study

BRCA gene mutations in cancerDNA Repair MechanismsGenetic factors in colorectal cancer0303 health sciences03 medical and health sciences

Keywords

Medical geneticsMolecular pathologyComputational biologyAtaxia-telangiectasiaGermlineGeneticsBioinformaticsMedicineComputer scienceGeneBiologyClinGenVariant Curation Expert Panelvariant interpretationGenetic VariationAtaxia Telangiectasia Mutated Proteinsrules specificationsArticlebreast cancerclassificationACMGATMDatabases, GeneticHumansataxia telangiectasiaFemaleGenetic TestingGerm-Line Mutation

Sustainable Development Goals

SDG 0: Good health and well-being

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants

FAIR Checklist

DataRank Breakdown

Authors (21)

Funding (8 grants)

Open Access

Topics

Annotations (Europe PMC)