A Note on Penalized Regression Spline Estimation in the Secondary Analysis of Case-Control Data
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Suzan Gazioglu | Jiawei Wei | Elizabeth M. Jennings | Raymond J. Carroll | R. Carroll | Jiawei Wei | Elizabeth M. Jennings | S. Gazioğlu
[1] R. Carroll,et al. Estimation in choice-based sampling with measurement error and bootstrap analysis , 1997 .
[2] D. Ruppert. Selecting the Number of Knots for Penalized Splines , 2002 .
[3] Nilanjan Chatterjee,et al. Cigarette smoking, N-acetyltransferase genes and the risk of advanced colorectal adenoma. , 2006, Pharmacogenomics.
[4] Jack A. Taylor,et al. Non-hierarchical logistic models and case-only designs for assessing susceptibility in population-based case-control studies. , 1994, Statistics in medicine.
[5] D. Zeng,et al. Proper analysis of secondary phenotype data in case‐control association studies , 2009, Genetic epidemiology.
[6] W D Flanders,et al. Sample size requirements in case-only designs to detect gene-environment interaction. , 1997, American journal of epidemiology.
[7] R. Carroll,et al. Haplotype‐Based Regression Analysis and Inference of Case–Control Studies with Unphased Genotypes and Measurement Errors in Environmental Exposures , 2008, Biometrics.
[8] D. Ruppert,et al. Penalized Spline Estimation for Partially Linear Single-Index Models , 2002 .
[9] R. Pyke,et al. Logistic disease incidence models and case-control studies , 1979 .
[10] J. Gohagan,et al. The Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial of the National Cancer Institute: history, organization, and status. , 2000, Controlled clinical trials.
[11] L C Kwee,et al. Simple methods for assessing haplotype‐environment interactions in case‐only and case‐control studies , 2007, Genetic epidemiology.
[12] M. Gail,et al. Using cases to strengthen inference on the association between single nucleotide polymorphisms and a secondary phenotype in genome‐wide association studies , 2010, Genetic epidemiology.
[13] D. Zeng,et al. Likelihood-Based Inference on Haplotype Effects in Genetic Association Studies , 2006 .
[14] Lue Ping Zhao,et al. A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies. , 2003, American journal of human genetics.
[15] S Wacholder,et al. Parity, oral contraceptives, and the risk of ovarian cancer among carriers and noncarriers of a BRCA1 or BRCA2 mutation. , 2001, The New England journal of medicine.
[16] Raymond J Carroll,et al. Retrospective analysis of haplotype-based case control studies under a flexible model for gene environment association. , 2008, Biostatistics.
[17] Arnab Maity,et al. Testing in semiparametric models with interaction, with applications to gene-environment interactions. , 2009, Journal of the Royal Statistical Society. Series B, Statistical methodology.
[18] S. Wood. Generalized Additive Models: An Introduction with R , 2006 .
[19] Raymond J Carroll,et al. Shrinkage Estimators for Robust and Efficient Inference in Haplotype-Based Case-Control Studies , 2009, Journal of the American Statistical Association.
[20] D Zeng,et al. A general framework for studying genetic effects and gene-environment interactions with missing data. , 2010, Biostatistics.
[21] G. Satten,et al. Inference on haplotype effects in case-control studies using unphased genotype data. , 2003, American journal of human genetics.
[22] M. Durbán,et al. Flexible smoothing with P-splines: a unified approach , 2002 .
[23] Raymond J Carroll,et al. Robust estimation for homoscedastic regression in the secondary analysis of case–control data , 2013, Journal of the Royal Statistical Society. Series B, Statistical methodology.
[24] D. Ruppert,et al. On the asymptotics of penalized splines , 2008 .
[25] Nilanjan Chatterjee,et al. Semiparametric maximum likelihood estimation exploiting gene-environment independence in case-control studies , 2005 .