A collaborative linkage study of breast cancer families that are not segregating mutations at either the BRCA1 or BRCA2 loci is ongoing. Collaborators in Finland, Sweden and Iceland are working together with NHGRI to add more families to the data set. Genotyping of several candidate regions and a genome wide scan have been performed on these samples. Linkage analysis is ongoing and a paper is in preparation. Fine mapping of positive regions is also ongoing. - breast cancer, linkage, genetics, mapping, susceptibility - Human Subjects

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Intramural Research (Z01)
Project #
1Z01HG000111-03
Application #
6290321
Study Section
Special Emphasis Panel (IDRB)
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
Name
National Human Genome Research Institute
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Huusko, Pia; Juo, Suh-Hang Hank; Gillanders, Elizabeth et al. (2004) Genome-wide scanning for linkage in Finnish breast cancer families. Eur J Hum Genet 12:98-104
Marroni, F; Aretini, P; D'Andrea, E et al. (2004) Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations. J Med Genet 41:278-85
Rozenblum, Ester; Vahteristo, Pia; Sandberg, Therese et al. (2002) A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes. Hum Genet 110:111-21
Baffoe-Bonnie, A B; Beaty, T H; Bailey-Wilson, J E et al. (2000) Genetic epidemiology of breast cancer: segregation analysis of 389 Icelandic pedigrees. Genet Epidemiol 18:81-94
Kainu, T; Juo, S H; Desper, R et al. (2000) Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus. Proc Natl Acad Sci U S A 97:9603-8