The following pages link to Genetic Epidemiology (Q60939):
Displaying 25 items.
- Rare variant association testing for multicategory phenotype (Q60950) (← links)
- A small-sample multivariate kernel machine test for microbiome association studies (Q75165) (← links)
- Identifying genetic risk variants associated with brain volumetric phenotypes via K‐sample Ball Divergence method (Q76135) (← links)
- Evolutionary-based grouping of haplotypes in association analysis (Q80042) (← links)
- Identifying interacting SNPs using Monte Carlo logic regression (Q91329) (← links)
- Functional Linear Models for Association Analysis of Quantitative Traits (Q93060) (← links)
- Bayesian variable selection using partially observed categorical prior information in fine‐mapping association studies (Q96481) (← links)
- Efficient gene–environment interaction tests for large biobank‐scale sequencing studies (Q98984) (← links)
- Robust network-based regularization and variable selection for high-dimensional genomic data in cancer prognosis (Q99807) (← links)
- Accommodating missingness in environmental measurements in gene-environment interaction analysis (Q108193) (← links)
- Simple estimates of haplotype relative risks in case-control data (Q110169) (← links)
- locStra: Fast analysis of regional/global stratification in whole‐genome sequencing studies (Q111356) (← links)
- Ridge Regression in Prediction Problems: Automatic Choice of the Ridge Parameter (Q111500) (← links)
- TWO‐SIGMA: A novel two‐component single cell model‐based association method for single‐cell RNA‐seq data (Q117515) (← links)
- FastSKAT: Sequence kernel association tests for very large sets of markers (Q118469) (← links)
- Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data (Q120807) (← links)
- The X factor: A robust and powerful approach to X‐chromosome‐inclusive whole‐genome association studies (Q120927) (← links)
- Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure (Q120936) (← links)
- Bayes factors for genome-wide association studies: comparison withP-values (Q142076) (← links)
- A unified partial likelihood approach for X-chromosome association on time-to-event outcomes (Q143884) (← links)
- A meta-analysis approach with filtering for identifying gene-level gene-environment interactions (Q149551) (← links)
- Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations (Q151286) (← links)
- Combining Family- and Population-Based Imputation Data for Association Analysis of Rare and Common Variants in Large Pedigrees (Q152615) (← links)
- Adaptive testing for multiple traits in a proportional odds model with applications to detect SNP-brain network associations (Q153876) (← links)
- Gene-based segregation method for identifying rare variants in family-based sequencing studies (Q154104) (← links)
