Genomic Approaches to Identifying Breast Cancer Susceptibility Factors

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Breast Disease

• Publication date

  2004-10-19

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.3233/BD-2004-19102PMID 15687692
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2002cited by this paper
• HapScope: a software system for automated and visual analysis of functionally annotated haplotypes.

  2002cited by this paper
• A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

  2002influential reference
• Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility

  2002cited by this paper
• Attributable risks of familial cancer from the Family-Cancer Database.

  2002cited by this paper
• Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations

  2002cited by this paper
• The Structure of Haplotype Blocks in the Human Genome

  2002cited by this paper
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  2002cited by this paper
• Properties of linkage disequilibrium (LD) maps

  2002cited by this paper
• A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer.

  2002cited by this paper
• Attributable risks for familial breast cancer by proband status and morphology: A nationwide epidemiologic study from Sweden

  2002cited by this paper
• STI571: a paradigm of new agents for cancer therapeutics.

  2002cited by this paper
• Variants in DNA double-strand break repair genes and breast cancer susceptibility.

  2002cited by this paper
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  2002cited by this paper
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  2002cited by this paper
• Once and again-issues surrounding replication in genetic association studies.

  2002cited by this paper
• The fabric of cancer cell biology-Weaving together the strands.

  2002cited by this paper
• Cancer Molecular Analysis Project: weaving a rich cancer research tapestry.

  2002cited by this paper
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  2001cited by this paper
• The future of genetic case-control studies.

  2001cited by this paper
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  2001cited by this paper
• Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease.

  2001cited by this paper
• Haplotype Variation and Linkage Disequilibrium in 313 Human Genes

  2001cited by this paper
• Gene-expression profiles in hereditary breast cancer.

  2001cited by this paper
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  2001cited by this paper
• Initial sequencing and analysis of the human genome

  2001cited by this paper
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  2001cited by this paper
• The genetic epidemiology of cancer: interpreting family and twin studies and their implications for molecular genetic approaches.

  2001cited by this paper
• Linkage disequilibrium in the human genome

  2001cited by this paper
• Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni Syndrome.

  2001cited by this paper
• Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland.

  2000cited by this paper
• Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.

  1999cited by this paper
• Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.

  1998cited by this paper
• Linkage disequilibrium mapping of complex disease: fantasy or reality?

  1998cited by this paper
• The Future of Genetic Studies of Complex Human Diseases

  1996influential reference
• Localization of the gene for Cowden disease to chromosome 10q22–23

  1996cited by this paper
• Breast cancer among radiologic technologists.

  1996influential reference
• Identification of the breast cancer susceptibility gene BRCA2

  1995cited by this paper
• Breast cancer among radiologic technologists.

  1995cited by this paper
• A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.

  1994cited by this paper
• Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

  1994cited by this paper
• An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.

  1993cited by this paper
• Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms.

  1990influential reference
• Linkage of early-onset familial breast cancer to chromosome 17q21.

  1990cited by this paper

• Next-generation sequencing analysis of lung and colon carcinomas reveals a variety of genetic alterations.

  2014cites this paper
• Comparison of automated literature based gene-disease association using gene set enrichment analysis

  2013cites this paper
• Race and the Molecular Origins of Breast Cancer in Chinese Women

  2012cites this paper
• Study of differential allelic expression in the breast cancer intermediate-risk susceptibility genes CHEK2, ATM and TP53

  2010cites this paper
• The breast cancer polygene and longevity genes : the implications for insurance

  2008cites this paper
• Genetic determinants of breast cancer

  2007cites this paper
• Application of a Polygenic Model of Breast and Ovarian Cancer to Critical Illness Insurance

  2006cites this paper
• Family Systems genetic Illness Model--breast cancer.

  2006cites this paper
• Polyposis and early cancer in a patient with low penetrant mutations in MSH6 and APC: hereditary colorectal cancer as a polygenic trait

  2006cites this paper