Evidence map›Paper›PMID 42238800›Full record

ArticleBreast cancer : basic and clinical research2026

Low Frequency of Pathogenic Variants in BRCA1 Exons 11/20 and BRCA2 Exon 11 Suggests Divergent Mutational Hotspots in Sudanese Breast Cancer Patients: A Case-Control Study.

Hadia Abass Eltaib Ahmed, Babbiker Mohammed Taher Gorish, Ghanem Mohammed Mahjaf, Waha Ismail Yahia Abdelmula, Alsmawal A Elimam, Hisham N Altayb, Mona Dawood, Asma Al-Ameer M Zeen, Tibyan Abd Almajed Altaher, Emad Bakri Abass Ahmed and 1 more

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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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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Hadia Abass Eltaib AhmedDepartment of Medical Microbiology, Faculty of Medical Laboratory Sciences, Shendi University, Shendi, Sudan.ORCID https://orcid.org/0009-0006-0675-6337
Babbiker Mohammed Taher GorishDepartment of Medical Microbiology, Faculty of Medical Laboratory Sciences, Omdurman Islamic University, Omdurman, Sudan.
Ghanem Mohammed MahjafDepartment of Medical Microbiology, Faculty of Medical Laboratory Sciences, Shendi University, Shendi, Sudan.
Waha Ismail Yahia AbdelmulaInternational Joint Laboratory on Synthetic Biology and Biomass Biorefinery, Biofuels Institute, Jiangsu University, Zhenjiang, PR China.
Alsmawal A ElimamDepartment of Histopathology and Cytology, Faculty of Medical Laboratory Sciences, AL-Neelain University, Khartoum, Sudan.
Hisham N AltaybDepartment of Biochemistry, Faculty of Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Mona DawoodDepartment of Molecular Biology, Faculty of Medical Laboratory Sciences, AL-Neelain University, Khartoum, Sudan.
Asma Al-Ameer M ZeenDepartment of Histopathology and Cytopathology, Faculty of Medical Laboratory Sciences, Shendi University, Shendi, Sudan.
Tibyan Abd Almajed AltaherDepartment of Clinical Chemistry, Faculty of Medical Laboratory Sciences, Shendi University, Shendi, Wad Medani, Gezira state, Sudan.
Emad Bakri Abass AhmedDepartment of Biotechnology, Faculty of Science, University of Gezera.
Rashid Eltayeb AbdallaDepartment of Biochemistry, Faculty of Medicine and Surgery, Shendi University, Shendi, Sudan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Breast cancers represent a heterogeneous group of diseases; approximately 7% may be attributed to inherited pathogenic variants in Objectives: This study aimed to investigate the frequency and nature of sequence variants in Design: This was a case-control study conducted at Shendi's Tumor Treatment and Cancer Research Center in Northern Sudan. Methods: The study included fifty-two female breast cancer patients and thirty healthy female controls aged at least 18 years. Demographic data and blood samples were collected for genomic DNA extraction. Polymerase Chain Reaction (PCR) and Sanger sequencing were performed for Results: Invasive ductal carcinoma was the predominant histological type, significantly associated with grade II tumors (P = 0.0001). Non-hereditary breast cancers were more prevalent (55.8%), with second-degree relatives most commonly affected in hereditary cases (69.6%). Three Conclusion: No pathogenic variants were identified in

Indexed as

BRCA1BRCA2breast cancerhereditary predispositionsequence variants

Identifiers

PMID42238800
PMCPMC13227026

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.