Genome-wide association study and polygenic risk prediction of hypothyroidism
Genome-wide association analysis identifies PLA2G4C as a susceptibility locus for Multiple System Atrophy
Partitioned polygenic risk scores identify distinct types of metabolic dysfunction-associated steatotic liver disease
SEAD: an augmented reference panel with 22,134 haplotypes boosts the rare variants imputation and GWAS analysis in Asian population
Robust Mendelian Randomization Analysis by Automatically Selecting Valid Genetic Instruments with Applications to Identify Plasma Protein Biomarkers for Alzheimer’s Disease
Associations between common genetic variants and income provide insights about the socioeconomic health gradient
Isolating transdiagnostic effects reveals specific genetic profiles in psychiatric disorders.
Identification of Novel Loci and Cross-Disorder Pleiotropy Through Multi-Ancestry Genome-Wide Analysis of Alcohol Use Disorder in Over One Million Individuals
Partitioning and aggregating cross-tissue and tissue-specific genetic effects in identifying gene-trait associations
Rapid and accurate multi-phenotype imputation for millions of individuals