Case–Control and Case‐Only Designs with Genotype and Family History Data: Estimating Relative Risk, Residual Familial Aggregation, and Cumulative Risk
DOI10.1111/J.1541-0420.2005.00442.XzbMATH Open1099.62126OpenAlexW1969592893WikidataQ33236724 ScholiaQ33236724MaRDI QIDQ5473203FDOQ5473203
Authors: Nilanjan Chatterjee, Zeynep Kalaylioglu, Joanna H. Shih, Mitchell H. Gail 
Publication date: 20 June 2006
Published in: Biometrics (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1111/j.1541-0420.2005.00442.x
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Cites Work
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- Combined association and aggregation analysis of data from case-control family studies
- Analysis of survival data from case-control family studies
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Cited In (15)
- Combining isotonic regression and EM algorithm to predict genetic risk under monotonicity constraint
- The Case‐Only Odds Ratio as a Causal Parameter
- Modeling familial association of ages at onset of disease in the presence of competing risk
- Some Biases That May Affect Kin-Cohort Studies for Estimating the Risks from Identified Disease Genes
- Meta-analysis of family-based and case-control genetic association studies that use the same cases
- A Frailty‐Model‐Based Approach to Estimating the Age‐Dependent Penetrance Function of Candidate Genes Using Population‐Based Case‐Control Study Designs: An Application to Data on the BRCA1 Gene
- Missing genetic information in case-control family data with general semi-parametric shared frailty model
- Effects of violations of assumptions on likelihood methods for estimating the penetrance of an autosomal dominant mutation from kin-cohort studies.
- Analysis of secondary failure time responses in studies with response‐dependent sampling schemes
- Estimation and interpretation of models of absolute risk from epidemiologic data, including family-based studies
- Fully nonparametric estimation of the marginal survival function based on case-control clustered data
- On estimation of the hazard function from population-based case-control studies
- Frailty models for familial risk with application to breast cancer
- A copula model for marked point processes
- Statistical inference on the penetrances of rare genetic mutations based on a case-family design
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