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

SNPs in cancer research and treatment.

British journal of cancer - 23 Feb 2004

Erichsen H C, Chanock S J

Abstract excerpt

Genetic variation in the human genome is an emerging resource for studying cancer, a complex set of diseases characterised by both environmental and genetic contributions. The number of common germ-line variants is great, on the order of 10-15 million per person, and represents a remarkable opportunity to investigate the aetiology, interindividual differences in treatment response and outcomes of specific...

Read the complete abstract on PubMed

Topics

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

Share to Polymorphism, Single Nucleotide
Share to Research Design
Share to Biomedical Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cell Transformation, Neoplastic

Share to Genomics

Share to Haplotypes

Share to Neoplasms

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 14970847
DOI: 10.1038/sj.bjc.6601574
PMCID: PMC2410167

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

SNPs in cancer research and treatment.PMID 14970847Read ↗

Challenges of SNP genotyping and genetic variation: its future role in diagnosis and treatment of cancer.Semantic proximity Read ↗

Genome-wide association studies in cancer--current and future directions.Semantic proximity Read ↗

Genetic association studies in cancer: good, bad or no longer ugly?Semantic proximity Read ↗

Single nucleotide polymorphisms in clinics: Fantasy or reality for cancer?Semantic proximity Read ↗

Single-nucleotide polymorphism (SNP) analysis to associate cancer risk.Semantic proximity Read ↗

Role of genomics in identifying new targets for cancer therapy.Semantic proximity Read ↗

Cancer genetics.Semantic proximity Read ↗

Using high-throughput SNP technologies to study cancer.Semantic proximity Read ↗

Current status of genome-wide association studies in cancer.Semantic proximity Read ↗

Using germ-line genetic variation to investigate and treat cancer.Semantic proximity Read ↗

Genetic variants in association studies--review of strengths and weaknesses in study design and current knowledge of impact on cancer risk.Semantic proximity Read ↗

Single-Nucleotide Polymorphism to Associate Cancer Risk.Semantic proximity Read ↗

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