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Impact of Integrated Translational Research on Clinical Exome Sequencing

Eric W. Klee,Margot A. Cousin,Filippo Pinto e Vairo,Joel A. Morales-Rosado,Erica L. Macke,W. Garrett Jenkinson,Alejandro Ferrer,Laura E. Schultz-Rogers,Rory J. Olson,Gavin R. Oliver,Ashley N. Sigafoos,Tanya L. Schwab,Michael T. Zimmermann,Raul A. Urrutia,Charu Kaiwar,Aditi Gupta,Patrick R. Blackburn,Nicole J. Boczek,Carri A. Prochnow, Rebecca J. Lowy,Lindsay A. Mulvihill,Tammy M. McAllister,Stacy L. Aoudia,Teresa M. Kruisselbrink,Lauren B. Gunderson,Jennifer L. Kemppainen, Laura J. Fisher,Jessica M. Tarnowski,Megan M. Hager,Sarah A. Kroc,Nicole L. Bertsch,Katherine E. Agre,Jessica L. Jackson,Sarah K. Macklin-Mantia,Marine Murphree,Laura M. Rust, Jolene M. Summer Bolster,Scott A. Beck,Paldeep S. Atwal,Marissa S. Ellingson,Sarah S. Barnett,Kristen J. Rasmussen,Carrie A. Lahner,Zhiyv Niu,Linda Hasadsri,Matthew J. Ferber,Cherisse A. Marcou,Karl J. Clark,Pavel N. Pichurin,David R. Deyle,Eva Morava-Kozicz,Ralitza H. Gavrilova,Radhika Dhamija,Klaas J. Wierenga,Brendan C. Lanpher,Dusica Babovic-Vuksanovic,Gianrico Farrugia,Lisa A. Schimmenti,A. Keith Stewart,Konstantinos N. Lazaridis

Genetics in medicine（2023）

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diagnostic odyssey,undiagnosed disease,variants of uncertain significance,clinical practice,genomics
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