Clinically significant germline pathogenic variants are missed by tumor genomic sequencing

por Stout, Leigh Anne, Hunter, Cynthia, Schroeder, Courtney, Kassem, Nawal, Schneider, Bryan P.
Publicado 2023

Identification of germline cancer predisposition variants during clinical ctDNA testing

por Stout, Leigh Anne, Kassem, Nawal, Hunter, Cynthia, Philips, Santosh, Radovich, Milan, Schneider, Bryan P.
Publicado 2021

A pharmacogenetics study to predict outcome in patients receiving anti-VEGF therapy in age related macular degeneration

por Kitchens, John W, Kassem, Nawal, Wood, William, Stone, Thomas W, Isernhagen, Rick, Wood, Edward, Hancock, Brad A, Radovich, Milan, Waymire, Josh, Li, Lang, Schneider, Bryan P
Publicado 2013