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Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome

Gastroenterology(2020)10.1053/j.gastro.2019.12.032Source: DataRank Database

Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome is a research paper published in Gastroenterology (2020). On theSindex it has a DataRank of 0.700. It has been cited 105 times.

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0.700DataRank · unranked

Scored on demand from live citation data

105 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (5 grants)Impact (FWCI 7.70)OA: bronzeTopics (64)IDs (PubMed, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (0/2)

Interoperable (0/2)

Reusable (0/3)

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DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.700

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.

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Authors (40)

Aysel Ahadova ORCID,Toni T. Seppälä ORCID,Stefan Aretz ORCID,Marloes Bigirwamungu-Bargeman,Hendrik Bläker ORCID

Live enrichment

PubMed:31926173 OpenAlex:https://openalex.org/W3000182726

Cancer Foundation Finland sr

Grant: 170128

Cancer Foundation Finland sr

Grant: 190144

Cancer Foundation Finland sr

Grant: 190136Y

Deutsche Krebshilfe

Wilhelm Sander-Stiftung

FWCI

7.70

Citation Percentile

1.0%

Citation Trend

2020

2021

2022

2023

2024

2025

2026

bronzeLicense: cc-by

journalhttp://www.gastrojournal.org/article/S0016508520300147/pdf

publisherhttp://www.gastrojournal.org/article/S0016508520300147/pdf

publisherhttps://api.elsevier.com/content/article/PII:S0016508520300147?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S0016508520300147?httpAccept=text/plain

journalhttps://doi.org/10.1053/j.gastro.2019.12.032

Fields of Study

Genetic factors in colorectal cancerMultiple and Secondary Primary CancersColorectal Cancer Screening and DetectionAdenomaAdenomatous Polyposis Coli ProteinAdultColonoscopyColorectal Neoplasms, Hereditary NonpolyposisDNA Mismatch RepairDNA Mutational AnalysisDNA-Binding ProteinsFemaleFinlandGermanyHumansMaleMiddle AgedMutL Protein Homolog 1MutS Homolog 2 ProteinMutationNetherlandsProspective Studiesbeta Catenin

MeSH Terms

MutL Protein Homolog 1AdenomaAdultColonoscopyColorectal Neoplasms, Hereditary NonpolyposisDNA Mutational AnalysisDNA-Binding ProteinsFemaleFinlandGermanyHumansMaleMiddle AgedMutationNetherlandsProspective StudiesAdenomatous Polyposis Coli Proteinbeta CateninMutS Homolog 2 ProteinDNA Mismatch Repair

Keywords

MSH6Lynch syndromeMLH1MSH2Somatic cellGermline mutationMedicineColorectal cancerInternal medicineOncologyMutationCancer researchDNA mismatch repairGeneticsBiologyGeneCancerGenetic analysisPrognostic factorOutcomeCancer Risk

Sustainable Development Goals

SDG 0: Good health and well-being

Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome

FAIR Checklist

DataRank Breakdown

Authors (40)

Funding (5 grants)

Impact

Open Access

Topics