Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions
Year: 2025
Type: article
Authors: Alban Ziegler, Carrie Koval-Burt, Denise M. Kay, Sharon F. Suchy, Amber Begtrup, Katherine G. Langley, Rebecca Hernan, Laura M. Amendola, Brenna M. Boyd, Jennifer Bradley, Tracy Brandt, Lilian L. Cohen, Alison J. Coffey, Joseph M. Devaney, Beata Dygulska, Bethany Friedman, Ramsay L. Fuleihan, Awura Gyimah, Sihoun Hahn, Sean Hofherr, Kathleen S. Hruska, Zhanzhi Hu, Médéric Jeanne, Guanjun Jin, D. Aaron Johnson, Haluk Kavus, Rudolph L. Leibel, Steven J. Lobritto, Stephen McGee, Joshua D. Milner, Kirsty McWalter, Kristin G. Monaghan, Jordan S. Orange, Nicole Pimentel Soler, Yeyson Quevedo, Samantha Ratner, Kyle Retterer, Ankur Shah, Natasha Shapiro, Robert J. Sicko, Eric S. Silver, Samuel Strom, Rebecca I. Torene, Olatundun Williams, Vincent D. Ustach, Ryan J. Taft, Paul Kruszka, Michele Caggana, Wendy K. Chung
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4411972829