Attributable risks for familial breast cancer by proband status and morphology: A nationwide epidemiologic study from Sweden

International Journal of Cancer

Volumn 100, Issue 2, 2002, Pages 214-219

  Hemminki, Kari ^a   Granström, Charlotta ^a   Czene, Kamila ^a  

^a KAROLINSKA INSTITUTE   (Sweden)

Author keywords

Ductal cancer; Familial risk; In situ cancer; Lobular cancer; Sibling risk

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; BREAST CANCER; CANCER INCIDENCE; CANCER RISK; CARCINOMA IN SITU; CHILD; DATA BASE; FAMILIAL CANCER; FAMILY HISTORY; FEMALE; GENETIC EPIDEMIOLOGY; HUMAN; MAJOR CLINICAL STUDY; MOLECULAR GENETICS; PRIORITY JOURNAL; SIBLING; SWEDEN;

ADOLESCENT; ADULT; AGED; BREAST NEOPLASMS; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INCIDENCE; INFANT; INFANT, NEWBORN; MIDDLE AGED; NEOPLASM INVASIVENESS; NUCLEAR FAMILY; REGISTRIES; RISK FACTORS; SWEDEN;

EID: 0037054932     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/ijc.10467     Document Type: Article

References (44)

1. Family history and the risk of breast cancer: A systematic review and meta-analysis
2. Familial breast cancer: Collaborative reanalysis of individual data from 52 epidemiological studies including 58 209 women with breast cancer and 101 986 women without the disease
3. Genetic epidemiology of breast cancer
4. Sibling risks in cancer: Clues to recessive or X-linked genes?
5. The genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches
6. After BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer
7. Environmental and heritable factors in the causation of cancer
8. The reliability of recollections of family history: Implications for the medical provider
9. Familial breast cancer in southern Finland: How prevalent are breast cancer families and can we trust the family history reported by patients?
10. The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2
11. Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations
12. Familial breast cancer risks by morphology: A nation-wide epidemiologic study from Sweden
13. Morphological types of breast cancer in family members and multiple primary tumours: Is morphology an inherited trait?
14. Age at onset as an indicator of familial risk of breast cancer
15. Genetic analysis of breast cancer in the cancer and steroid hormone study
16. Effect of family history, body-fat distribution, and reproductive factors on the risk of postmenopausal breast cancer
17. A comprehensive evaluation of family history and breast cancer risk. The Utah Population Database
18. Family history, age, and risk of breast cancer. Prospective data from the Nurses' Health Study
19. Proportion of breast cancer cases in the United States explained by well-established risk factors
20. Familial predisposition to breast cancer in a British population: Implications for prevention
21. Familial breast and ovarian cancer: A Swedish population-based register study
22. The nationwide Swedish Family-Cancer Database: Updated structure and familial rates
23. Genetic epidemiology: Science and ethics on familial cancers
24. Familial carcinoid tumors and subsequent cancers: A nation-wide epidemiological study from Sweden
25. Proportion of disease caused or prevented by a given exposure, trait or intervention
26. Breast carcinoma in situ: Risk factors and screening patterns
27. Profiling familial breast cancer
28. Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications
29. Gene-expression profiles in hereditary breast cancer
30. Cancer risks to spouses and offspring in the Family-Cancer Database
31. Colorectal cancer: Molecules and populations
32. Re: Genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches
33. Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
34. Population-based study of BRCA1 and BRCA2 mutations in 1035 unselected Finnish breast cancer patients
35. Cancer in patients with ataxia-telangiectasia and in their relatives in the Nordic countries
36. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
37. Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium
38. Large upward bias in estimation of locus-specific effects from genomewide scans
39. Risk factors and age-incidence relationships for contralateral breast cancer
40. High constant incidence in twins and other relatives of women with breast cancer