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Practical issues in imputation-based association mapping.
Genome-wide association of lipid-lowering response to statins in combined study populations.
Interactions between glucocorticoid treatment and cis-regulatory polymorphisms contribute to cellular response phenotypes.
Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13).
Mapping gene-environment interactions at regulatory polymorphisms: insights into mechanisms of phenotypic variation.
Next generation analytic tools for large scale genetic epidemiology studies of complex diseases.
Variation in human recombination rates and its genetic determinants.
DNase?I sensitivity QTLs are a major determinant of human expression variation.
A unified framework for association analysis with multiple related phenotypes.
Imputation-based analysis of association studies: candidate regions and quantitative traits.
A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians.
WAVELET-BASED GENETIC ASSOCIATION ANALYSIS OF FUNCTIONAL PHENOTYPES ARISING FROM HIGH-THROUGHPUT SEQUENCING ASSAYS.
Large-scale genome-wide enrichment analyses identify new trait-associated genes and pathways across 31 human phenotypes.
Accurate genomic prediction of Coffea canephora in multiple environments using whole-genome statistical models.
Correction: A Unified Framework for Association Analysis with Multiple Related Phenotypes.
Discovery and characterization of variance QTLs in human induced pluripotent stem cells.
Genetic analyses support the contribution of mRNA N6-methyladenosine (m6A) modification to human disease heritability.
Multipoint and significance methods for genome-wide association studies
A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes.