Discover Community Create You

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

Article

Critical Analysis of Genome-Wide Association Studies: Triple Negative Breast Cancer Quae Exempli Causa.

International journal of molecular sciences - 14 Aug 2020

Jurj Maria-Ancuta, Buse Mihail, Zimta Alina-Andreea, Paradiso Angelo, Korban Schuyler S, Pop Laura-Ancuta, Berindan-Neagoe Ioana

Abstract excerpt

Genome-wide association studies (GWAS) are useful in assessing and analyzing either differences or variations in DNA sequences across the human genome to detect genetic risk factors of diseases prevalent within a target population under study. The ultimate goal of GWAS is to predict either disease risk or disease progression by identifying genetic risk factors. These risk factors will define the biological basis...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome-Wide Association Study

Share to MicroRNAs

Share to Polymorphism, Single Nucleotide

Share to Triple Negative Breast Neoplasms

Source

Open in PubMed Open full text

Identifiers

PMID: 32823908
DOI: 10.3390/ijms21165835
PMCID: PMC7461549

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Critical Analysis of Genome-Wide Association Studies: Triple Negative Breast Cancer Quae Exempli Causa.PMID 32823908Read ↗

A Review of the Hereditary Component of Triple Negative Breast Cancer: High- and Moderate-Penetrance Breast Cancer Genes, Low-Penetrance Loci, and the Role of Nontraditional Genetic ElementsSemantic proximity Read ↗

Common Genetic Variation and Breast Cancer Risk-Past, Present, and Future.Semantic proximity Read ↗

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

Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction.Semantic proximity Read ↗

Breast cancer susceptibility: an integrative analysis of genomic dataSemantic proximity Read ↗

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

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

Microarray-based SNP genotyping to identify genetic risk factors of triple-negative breast cancer (TNBC) in South Indian population.Semantic proximity Read ↗

Genome-wide association study identifies novel breast cancer susceptibility loci.Semantic proximity Read ↗

Dissecting the heritable risk of breast cancer: From statistical methods to susceptibility genes.Semantic proximity Read ↗

Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer.Semantic proximity Read ↗

Association Study Confirmed Three Breast Cancer-Specific Molecular Subtype-Associated Susceptibility Loci in Chinese Han Women.Semantic proximity Read ↗

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