W. Phu

seqr: A web‐based analysis and collaboration tool for rare disease genomics

D. MacArthur, H. Rehm, A. O’Donnell-Luria, 2022, Human mutation.

Variant interpretation using population databases: Lessons from gnomAD

D. MacArthur, H. Rehm, A. O’Donnell-Luria, 2021, Human mutation.

Cell Type-Specific Intralocus Interactions Reveal Oligodendrocyte Mechanisms in MS

Daniel C. Factor, Tyler E. Miller, Drew J. Adams, 2020, Cell.

Developmental Dynamics of RNA Translation in the Human Brain

Alan M. Moses, Eric C. Griffith, Ava C. Carter, 2021, bioRxiv.

A genome-wide mutational constraint map quantified from variation in 76,156 human genomes

Ryan L. Collins, Alicia R. Martin, E. Banks, 2022, bioRxiv.

seqr: A web‐based analysis and collaboration tool for rare disease genomics

H. Rehm, A. O’Donnell-Luria, B. Weisburd, 2021, medRxiv.