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

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: suggestive linkage to 10q23.32-q25.3.

Genes, chromosomes & cancer - 1 Mar 2007

Bergman Annika, Karlsson Per, Berggren Jonna, Martinsson Tommy, Björck Karin, Nilsson Staffan, Wahlström Jan, Wallgren Arne, Nordling Margareta

Abstract excerpt

The two breast cancer genes BRCA1 and BRCA2 were identified more than 10 years ago and, depending on population, mutations in these genes are responsible for a varying percentage of familial breast cancer. In more than half the families, the increased risk of breast cancer cannot be explained by mutations in these genes, and the goal of this study was to locate novel susceptibility genes. One of the main...

Read the complete abstract on PubMed

Topics

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

Share to Breast Neoplasms
Share to Chromosomes, Human, Pair 10

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

Share to Genes, BRCA1

Share to Genes, BRCA2

Share to Genetic Linkage

Share to Genome, Human

Share to Polymorphism, Single Nucleotide

Share to White People

Source

Identifiers

PMID: 17171685
DOI: 10.1002/gcc.20405

Genes

BRCA1
BRCA2

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: suggestive linkage to 10q23.32-q25.3.PMID 17171685Read ↗

Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer.Semantic proximity Read ↗

Genome-wide linkage analysis of Swedish families to identify putative susceptibility loci for cutaneous malignant melanoma.Semantic proximity Read ↗

Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus.Semantic proximity Read ↗

A Swedish Familial Genome-Wide Haplotype Analysis Identified Five Novel Breast Cancer Susceptibility Loci on 9p24.3, 11q22.3, 15q11.2, 16q24.1 and Xq21.31.Semantic proximity Read ↗

A genome wide linkage search for breast cancer susceptibility genes.Semantic proximity Read ↗

Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.Semantic proximity Read ↗

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

An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found.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 ↗

Association study confirms two susceptibility loci for breast cancer in Chinese Han women.Semantic proximity Read ↗

Linkage analysis with markers on 17q in 29 Swedish breast cancer families.Semantic proximity Read ↗

Swedish Genome-Wide Haplotype Association Analysis Suggests Breast Cancer Loci with Varying Risk-Modifying Effects.Semantic proximity Read ↗

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