Cassandra E. Murcray

Beyond the fourth wave of genome-wide obesity association studies

An integrated map of genetic variation from 1,092 human genomes

A Powerful and Flexible Multilocus Association Test for Quantitative Traits

Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

Rheumatoid arthritis

Fibrosis and Adipose Tissue Dysfunction

Rare-Variant Association Analysis: Study Designs and Statistical Tests

Innate Immunity and Asthma Risk in Amish and Hutterite Farm Children

Gene–environment-wide association studies: emerging approaches

Genetic Risk Factors for Hepatopulmonary Syndrome in Patients With Advanced Liver Disease

Gene-environment interaction for childhood asthma and exposure to farming in Central Europe

10 Years of GWAS Discovery: Biology, Function, and Translation

GATES: A Rapid and Powerful Gene-Based Association Test Using Extended Simes Procedure

DNA methylation mediates genotype and smoking interaction in the development of anti-citrullinated peptide antibody-positive rheumatoid arthritis

Sequencing technologies — the next generation

Genetic Mapping in Human Disease

The Genotype-Tissue Expression (GTEx) project.

The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the American Association for the Study of Liver Diseases

The rs2294918 E434K variant modulates patatin‐like phospholipase domain‐containing 3 expression and liver damage

EASL Clinical Practice Guidelines for the management of patients with decompensated cirrhosis

Accurate proteome-wide missense variant effect prediction with AlphaMissense

Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies

Gene-Environment Interaction in Genome-Wide Association Studies

Testing association between disease and multiple SNPs in a candidate gene