Evidence map›Paper›PMID 41783385›Full record

ArticleBreast cancer : basic and clinical research2026

Identification of Genetic Variants Among Breast Cancer Patients and At-Risk Individuals: A Cohort Study in Sri Lanka.

Lalani Yatawara, Badra Hewavithana, Ashansa P Ramanayake, Susiji Wickramasinghe, Malithi Amarasiri

Abstract read
In one paragraph

Article in Breast cancer : basic and clinical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Lalani YatawaraDepartment of Medical Laboratory Science, Faculty of Allied Health Sciences, University of Peradeniya, Peradeniya, Sri Lanka.ORCID https://orcid.org/0000-0003-2231-6586
Badra HewavithanaDepartment of Radiology, Faculty of Medicine, University of Peradeniya, Peradeniya, Sri Lanka.
Ashansa P RamanayakeDepartment of Medical Laboratory Science, Faculty of Allied Health Sciences, University of Peradeniya, Peradeniya, Sri Lanka.
Susiji WickramasingheDepartment of Parasitology, Faculty of Medicine, University of Peradeniya, Peradeniya, Sri Lanka.
Malithi AmarasiriDepartment of Medical Laboratory Science, Faculty of Allied Health Sciences, University of Peradeniya, Peradeniya, Sri Lanka.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Breast cancer remains a major global health challenge, as it is the most commonly diagnosed malignancy worldwide, particularly among women. Germline variants in cancer-predisposing genes play a critical role in breast cancers with familial origin. Objectives: To identify genetic variants in cancer-predisposing genes among breast cancer patients and individuals at risk in a selected cohort from two imaging facilities in the Central Province of Sri Lanka. Design: A genetic association study involving breast cancer confirmed patients, at-risk individuals, and healthy controls. Methods: Blood samples were collected from consenting patients, and genomic DNA was extracted from the samples and subjected to Next Generation Sequencing and Sanger sequencing. The inherited predisposition to breast cancer was evaluated to find genes associated with breast cancer using the Ion Torrent PGM platform followed by bioinformatics analysis. Results: Variants were detected in several high- and moderate-penetrance genes, including

Indexed as

Breast cancercancer-predisposing genesgermline variantsmultigene panel testingpathogenic variants

Identifiers

PMID41783385
PMCPMC12954010

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