Genetic Epidemiology
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Publication Venue For
- Methods for large-scale single mediator hypothesis testing: Possible choices and comparisons.. 47:167-184. 2023
- Precisely modeling zero-inflated count phenotype for rare variants.. 46:73-86. 2022
- An exploration of genetic association tests for disease risk and age at onset.. 45:249-279. 2021
- Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analyses.. 44:330-338. 2020
- Estimating the number of potential family members eligible for BRCA1 and BRCA2 mutation testing in a "Traceback" approach.. 42:117-122. 2018
- The more you test, the more you find: The smallest P-values become increasingly enriched with real findings as more tests are conducted.. 41:726-743. 2017
- gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.. 41:297-308. 2017
- Leveraging population information in family-based rare variant association analyses of quantitative traits.. 41:98-107. 2017
- Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.. 40:461-469. 2016
- An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group.. 40:404-415. 2016
- Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk.. 39:689-697. 2015
- Computing a Synthetic Chronic Psychosocial Stress Measurement in Multiple Datasets and its Application in the Replication of G × E Interactions of the EBF1 Gene.. 39:489-497. 2015
- Contemporary Considerations for Constructing a Genetic Risk Score: An Empirical Approach.. 39:439-445. 2015
- Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.. 39:207-216. 2015
- Testing the effect of rare compound-heterozygous and recessive mutations in case--parent sequencing studies.. 39:166-172. 2015
- Complete effect-profile assessment in association studies with multiple genetic and multiple environmental factors.. 39:122-133. 2015
- Genetic simulation tools for post-genome wide association studies of complex diseases.. 39:11-19. 2015
- SeqSIMLA2: simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure.. 39:20-24. 2015
- Semiparametric tests for identifying differentially methylated loci with case-control designs using Illumina arrays.. 38:42-50. 2014
- Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking.. 37:846-859. 2013
- Sample size considerations of prediction-validation methods in high-dimensional data for survival outcomes.. 37:276-282. 2013
- Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies.. 37:222-228. 2013
- Power and sample size calculations for SNP association studies with censored time-to-event outcomes.. 36:538-548. 2012
- Stratification-score matching improves correction for confounding by population stratification in case-control association studies.. 36:195-205. 2012
- Association between PARP-1 V762A polymorphism and cancer susceptibility: a meta-analysis.. 36:56-65. 2012
- Meta-analysis of gene-environment interaction: joint estimation of SNP and SNP × environment regression coefficients.. 35:11-18. 2011
- Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis?. 34:892-911. 2010
- Ordered subset analysis for case-control studies.. 34:407-417. 2010
- Score-based adjustment for confounding by population stratification in genetic association studies.. 34:383-385. 2010
- A novel haplotype-sharing approach for genome-wide case-control association studies implicates the calpastatin gene in Parkinson's disease.. 33:657-667. 2009
- Shrinkage estimation for robust and efficient screening of single-SNP association from case-control genome-wide association studies.. 33:740-750. 2009
- Haplotype-based analysis: a summary of GAW16 Group 4 analysis.. 33 Suppl 1:S24-S28. 2009
- Ordered-subset analysis (OSA) for family-based association mapping of complex traits.. 32:627-637. 2008