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Points to consider for the next-generation-sequencing-based detection of copy-number abnormalities (CNAs) and balanced chromosomal rearrangements in neoplastic disorders: A statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2026)10.1016/j.gim.2025.101658Source: DataRank Database

Points to consider for the next-generation-sequencing-based detection of copy-number abnormalities (CNAs) and balanced chromosomal rearrangements in neoplastic disorders: A statement of the American College of Medical Genetics and Genomics (ACMG) is a research paper published in Genetics in Medicine (2026). On theSindex it has a DataRank of 0.

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0DataRank · unranked

Scored on demand from live citation data

Open Access0 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Impact (FWCI 11.56)OA: bronzeTopics (15)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 (9)

Cynthia Hawkins ORCID,Nan Jiang ORCID,Ross L. Levine ORCID,Trevor J. Pugh ORCID,Gordana Raca

Live enrichment

PubMed:41615347 OpenAlex:https://openalex.org/W7126156244

FWCI

11.56

Citation Percentile

1.0%

Citation Trend

2026

bronzeLicense: https://www.elsevier.com/legal/tdmrep-license

journalhttps://www.gimjournal.org/article/S1098-3600(25)00305-3/pdf

publisherhttps://www.gimjournal.org/article/S1098-3600(25)00305-3/pdf

publisherhttps://api.elsevier.com/content/article/PII:S1098360025003053?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1098360025003053?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.gim.2025.101658

Fields of Study

Genomic variations and chromosomal abnormalitiesCancer Genomics and DiagnosticsGenetic factors in colorectal cancer

Keywords

GenomicsMedical geneticsMultiplexStatement (logic)Comparative genomic hybridizationFluorescence in situ hybridizationHuman genomeCopy-number variationGenome sequencingSomaticStructural VariationExome Sequencing

Sustainable Development Goals

SDG 0: Life below water