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A general framework for detecting disease associations with rare variants in sequencing studies.

  • Read more about A general framework for detecting disease associations with rare variants in sequencing studies.

Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.

  • Read more about Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.

Multiple testing for gene sets from microarray experiments.

  • Read more about Multiple testing for gene sets from microarray experiments.

Identification of predictive pathways for non-hodgkin lymphoma prognosis.

  • Read more about Identification of predictive pathways for non-hodgkin lymphoma prognosis.

Incorporating higher-order representative features improves prediction in network-based cancer prognosis analysis.

  • Read more about Incorporating higher-order representative features improves prediction in network-based cancer prognosis analysis.

Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis?

  • Read more about Evaluating haplotype effects in case-control studies via penalized-likelihood approaches: prospective or retrospective analysis?

Analysis of untyped SNPs: maximum likelihood and imputation methods.

  • Read more about Analysis of untyped SNPs: maximum likelihood and imputation methods.

Robust test method for time-course microarray experiments.

  • Read more about Robust test method for time-course microarray experiments.

permGPU: Using graphics processing units in RNA microarray association studies.

  • Read more about permGPU: Using graphics processing units in RNA microarray association studies.

Meta-analysis of genome-wide association studies: no efficiency gain in using individual participant data.

  • Read more about Meta-analysis of genome-wide association studies: no efficiency gain in using individual participant data.

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