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2. New insights into old methods for identifying causal rare variants
3. Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data
4. Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism
5. Small sample properties of rare variant analysis methods
6. On Identifying Rare Variants for Complex Human Traits
7. Statistical correction of the Winner’s Curse explains replication variability in quantitative trait genome-wide association studies
8. Discovery of genetic variants of the kinases that activate tenofovir among individuals in the United States, Thailand, and South Africa: HPTN067
9. Effects of Serotonin Transporter Gene Variation on Impulsivity Mediated by Default Mode Network: A Family Study of Depression
10. Genetic variants influence on the placenta regulatory landscape
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