Search Results
2. Diagnostic odyssey of patients with mitochondrial disease: Results of a survey
3. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
4. A Simple Test of Class-Level Genetic Association Can Reveal Novel Cardiometabolic Trait Loci
5. A New Estimating Equation Based Approach for Secondary Trait Analyses in Genetic Case-control Studies
6. A dual-clustering framework for association screening with whole genome sequencing data and longitudinal traits
7. A partition-based approach to identify gene-environment interactions in genome wide association studies
8. Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data
9. Considering interactive effects in the identification of influential regions with extremely rare variants via fixed bin approach
10. Discovering pure gene-environment interactions in blood pressure genome-wide association studies data: a two-step approach incorporating new statistics
11. Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism
12. Small sample properties of rare variant analysis methods
13. Association analysis of complex diseases using triads, parent-child dyads and singleton monads
14. Bayesian hierarchical graph-structured model for pathway analysis using gene expression data
15. Haplotype Inference through Sequential Monte Carlo
16. Maximum-parsimony haplotype frequencies inference based on a joint constrained sparse representation of pooled DNA
17. Rare Variant Analysis for Family-Based Design
18. SAVI: a statistical algorithm for variant frequency identification
19. Implications for health and disease in the genetic signature of the Ashkenazi Jewish population
20. APOE Genotype-Function Relationship: Evidence of −491 A/T Promoter Polymorphism Modifying Transcription Control but Not Type 2 Diabetes Risk
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