Harrison Brand

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.

Robert C. Green, Keith Marsolo, Casey Overby Taylor, 2019, American journal of human genetics.

CNView: a visualization and annotation tool for copy number variation from whole-genome sequencing

Ryan L. Collins, Harrison Brand, Joseph T. Glessner, 2016, bioRxiv.

A structural variation reference for medical and population genetics

Tariq Ahmad, Patrick F. Sullivan, Mark I. McCarthy, 2020, Nature.