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Array comparative genomic hybridization based identification of key genetic alterations at 2p21-p16.3 (MSH2, MSH6, EPCAM), 3p23-p14.2 (MLH1), 7p22.1 (PMS2) and 1p34.1-p33 (MUTYH) regions in hereditary non polyposis colorectal cancer (Lynch syndrome) in the Kingdom of Saudi Arabia

Saudi Journal of Biological Sciences(2020)10.1016/j.sjbs.2019.06.012Source: DataRank Database

Array comparative genomic hybridization based identification of key genetic alterations at 2p21-p16.3 (MSH2, MSH6, EPCAM), 3p23-p14.2 (MLH1), 7p22.1 (PMS2) and 1p34.1-p33 (MUTYH) regions in hereditary non polyposis colorectal cancer (Lynch syndrome) in the Kingdom of Saudi Arabia is a research paper published in Saudi Journal of Biological Sciences (2020). On theSindex it has a DataRank of 0.292. It has been cited 6 times.

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0.292DataRank · unranked

Scored on demand from live citation data

6 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (1 grants)Impact (FWCI 0.14)OA: hybridTopics (25)IDs (PubMed, PMC, OpenAlex)Annotations (1)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

0.292

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 (11)

Peter Natesan Pushparaj,Zeenat Mirza,Muhammad Imran Naseer,Heba Abusamra,Maha Alquaiti

Live enrichment

PubMed:31889830 PMC:PMC6933242 OpenAlex:https://openalex.org/W2951968626

NSTIP strategic technologies program in the Kingdom of Saudi Arabia

Grant: 12-MED3078-03

FWCI

0.14

Citation Percentile

0.5%

Citation Trend

2021

2023

2024

2025

hybridLicense: cc-by-nc-nd

journalhttps://www.sciencedirect.com/science/article/pii/S1319562X19301093/pdf

publisherhttps://www.sciencedirect.com/science/article/pii/S1319562X19301093/pdf

publisherhttps://api.elsevier.com/content/article/PII:S1319562X19301093?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1319562X19301093?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.sjbs.2019.06.012

Fields of Study

Genetic factors in colorectal cancerColorectal Cancer Screening and DetectionCancer Genomics and Diagnostics

Keywords

Lynch syndromePMS2MSH6MLH1MUTYHMSH2Comparative genomic hybridizationGeneticsBiologyPopulationCancer researchDNA mismatch repairMutationGermline mutationMedicineCancerGeneGenomeColorectal cancerMismatch repair genesArraycghFamilial Colorectal Cancer

Sustainable Development Goals

SDG 0: Good health and well-being

Array comparative genomic hybridization based identification of key genetic alterations at 2p21-p16.3 (MSH2, MSH6, EPCAM), 3p23-p14.2 (MLH1), 7p22.1 (PMS2) and 1p34.1-p33 (MUTYH) regions in hereditary non polyposis colorectal cancer (Lynch syndrome) in the Kingdom of Saudi Arabia

FAIR Checklist

DataRank Breakdown

Authors (11)

Funding (1 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)