2q35-rs13387042 variant and the risk of breast cancer: a case-control study.

doi:10.1007/s11033-022-07195-6

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

2q35-rs13387042 variant and the risk of breast cancer: a case-control study.

Molecular biology reports - 1 May 2022

Nesaei Abolfazl, Naderi Ghale-Noie Zari, Khorshid Shamshiri Asma, Afzaljavan Fahimeh, Rivandi Mahdi, Tajbakhsh Amir, Homaei Shandiz Fatemeh, Pasdar Alireza

Abstract excerpt

BACKGROUND: Breast Cancer is the most frequent neoplasm diagnosed among women worldwide. Genetic background and lifestyle/environment play a significant role in the disease etiology. According to Genome-wide association studies, some single-nucleotide polymorphisms such as 2q35-rs13387042-(G/A) have been introduced to be associated with breast cancer risk and features. In this study, we aimed to evaluate the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Breast Neoplasms

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Share to Genotype

Share to Iran

Share to Polymorphism, Single Nucleotide

Share to Risk Factors

Source

Open in PubMed

Identifiers

PMID: 35445312
DOI: 10.1007/s11033-022-07195-6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

2q35-rs13387042 variant and the risk of breast cancer: a case-control study.PMID 35445312Read ↗

Assessing interactions between common genetic variant on 2q35 and hormone receptor status with breast cancer risk: evidence based on 26 studies.Semantic proximity Read ↗

Quantitative assessment of 2q35-rs13387042 polymorphism and hormone receptor status with breast cancer risk.Semantic proximity Read ↗

Germline DNA variations in breast cancer predisposition and prognosis: a systematic review of the literature.Semantic proximity Read ↗

Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population.Semantic proximity Read ↗

The FGFR2 Variant rs13387042 is Associated With Breast Cancer Risk: A Meta-Analysis and Systematic Review.Semantic proximity Read ↗

Association of 8q24 rs13281615A > G polymorphism with breast cancer risk: evidence from 40,762 cases and 50,380 controls.Semantic proximity Read ↗

Genome-wide association studies and the clinic: a focus on breast cancer.Semantic proximity Read ↗

Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042.Semantic proximity Read ↗

Evaluation of breast cancer susceptibility loci on 2q35, 3p24, 17q23 and FGFR2 genes in Taiwanese women with breast cancer.Semantic proximity Read ↗

Genomic Variants and Worldwide Epidemiology of Breast Cancer: A Genome-Wide Association Studies Correlation Analysis.Semantic proximity Read ↗

Risk of genome-wide association study newly identified genetic variants for breast cancer in Chinese women of Heilongjiang Province.Semantic proximity Read ↗

A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.