Matthew Zawistowski

Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross‐disease analyses

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants

Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests

An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People