Genetic epidemiology of multistage carcinogenesis.
Explore this paper's citation graph
Summary
The logarithms of the slopes suggest large differences in the apparent numbers of mutations involved in different cancers, and the number of mutations required appears to be less in familial breast cancer compared to sporadic breast cancer.
- Type
- review
- Published
- 2001-01-25
- Cited by
- 54
- References
- 58
- OpenAlex
- https://openalex.org/W1966367628
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:2924312
Keywords
Penetrance, Breast cancer, Cancer, Heritability, Offspring
References
- Hereditary nonpolyposis colorectal cancer--Lynch syndromes I and II.
- Optimal strategies for mapping complex diseases in the presence of multiple loci.
- Evidence for a prostate cancer susceptibility locus on the X chromosome.
- Creation of human tumour cells with defined genetic elements
- The Genetic Basis of Human Cancer
- Population-based molecular detection of hereditary nonpolyposis colorectal cancer.
- Mutation and cancer: a model for human carcinogenesis.
- Familial risks in in situ cancers from the Family-Cancer Database.
- A population-based study of endometrial cancer and familial risk in younger women. Cancer and Steroid Hormone Study Group.
- The Li-Fraumeni syndrome.
- Cancer mortality in relatives of women with ovarian cancer: The OPCS study
- Population risk and physiological rate parameters for colon cancer. The union of an explicit model for carcinogenesis with the public health records of the United States.
- Familial relationships in thyroid cancer by histo‐pathological type
- Environment and cancer: who are susceptible?
- Familial prostate cancer from the family-cancer database.
- Familial breast cancer in the family‐cancer database
- Male breast cancer: risk to daughters
- Second primary cancer after in situ and invasive cervical cancer.
- Genetic epidemiology of breast cancer
- Familial cancers in a nationwide family cancer database: age distribution and prevalence.
Cited by
- Biomarkers aiming at cancer risk estimation of polycyclic aromatic hydrocarbons
- Familial risks for cancer with reference to lung cancer
- Genome wide in silico SNP-tumor association analysis
- Familial risk of urological cancers: data for clinical counseling
- Transformation Assay in Bhas 42 Cells: A Model Using Initiated Cells to Study Mechanisms of Carcinogenesis and Predict Carcinogenic Potential of Chemicals
- A Mathematical Model for Predicting Malignancy of Solitary Pulmonary Nodules
- Risks for familial and contralateral breast cancer interact multiplicatively and cause a high risk.
- Genetic programming neural networks: A powerful bioinformatics tool for human genetics
- New Frontiers 2001.
- Environmental risk factors for breast cancer among African‐American women
- State-of-the-Art Neural Networks Applications in Biology
- Multilocus inheritance determines predisposition to α‐radiation induced bone tumourigenesis in mice
- High Throughput Genotyping Technologies for Pharmacogenomics
- Use of census data for construction of fertility history for Danish women
- Genetic epidemiology of cancer: From families to heritable genes
- Association of ocular melanoma with breast cancer but not with cutaneous melanoma: Results from the Swedish family‐cancer database
- Effect of multiplicity, laterality, and age at onset of breast cancer on familial risk of breast cancer: a nationwide prospective cohort study
- The effect of reduction in cross‐validation intervals on the performance of multifactor dimensionality reduction
- Molecular Origins of Cancer
- Second primary cancers after sporadic and familial colorectal cancer.
Related papers
- Elements of ‘missing heritability’
- Quantitative genetics: heritability is not always missing.
- Why the missing heritability might not be in the DNA
- The mystery of missing heritability: Genetic interactions create phantom heritability
- Inferring the nature of missing heritability in human traits
- Missing heritability of complex diseases: case solved?
- Revealing the missing heritability via cross-validated genome-wide association studies
- Dissolving the Missing Heritability Problem
- The missing heritability revealed in Arabidopsis thaliana
- Rare genetic variants explain missing heritability in smoking