Year: 2026
Type: article
Source: Genetics in Medicine
Authors: Nina B. Gold, Britt A. Johnson, Harini Somanchi, Thomas Minten, Stephanie A. Coury, Carrie Blout Zawatsky, Amber Begtrup, Elizabeth Butler, Katherine G. Langley, Rebekah Zimmerman, Heather M. McLaughlin, Tessa Ellefson, Adriann Kern, Heidi L. Rehm, David Bick, Steven E. Brenner, Dalia Kasperaviciute, Roshini S. Abraham, Ivona Aksentijevich, Melanie Babinski, Charles J. Billington, Manish J. Butte, Scott W. Canna, Makena Caron, Yee-Ming Chan, Shanmuganathan Chandrakasan, Samuel C.C. Chiang, Ottavia M. Delmonte, Lisa R. Diller, Lilian Downie, Julie Fleischer, Anne Fulton, Rebecca D. Ganetzky, Jessica Gold, Raphaela Goldbach-Mansky, Eyal Grunebaum, Rebecca C. Hale, Ada Hamosh, Friedhelm Hildebrandt, Alexander M. Holtz, Christina Jacobsen, Matthew J. Kan, Maleewan Kitcharoensakkul, Vilmante Kodyte, Raymond J. Kreienkamp, Belinda S. Lennerz, Angela E. Lin, Adithya V. Madduri, Joseph A. Majzoub, Rebecca A. Marsh, David T. Miller, Joshua D. Milner, Deborah M. Mitchell, Brittney Murray, Luigi D. Notarangelo, Xiao P. Peng, Emily M. Place, Craig D. Platt, Sharon E. Plon, Scott R. Plotkin, Cynthia M. Powell, Jennifer M. Puck, Amy E. Roberts, Vijay G. Sankaran, Daniella M. Schwartz, Christine M. Seroogy, Shreyas Srinath, Alanna Strong, Kathleen E. Sullivan, Weizhen Tan, Teresa K. Tarrant, Jay R. Thiagarajah, Melissa A. Walker, Ari J. Wassner, Hannie Zomer Bolanos, Amy M. Gaviglio, Natasha Bonhomme, Jelili Ojodu, Sikha Singh, Guisou Zarbalian, Stacey Pereira, Aaron J. Goldenberg, Ingrid A. Holm, Melissa P. Wasserstein, Robert C. Green
Institutions: Harvard University, Massachusetts General Hospital, KU Leuven, Brigham and Women's Hospital, Broad Institute, Ariadne Labs, Genomics England, University of California, Berkeley, Nationwide Children's Hospital, The Ohio State University, National Human Genome Research Institute, Boston Children's Hospital, University of Minnesota, University of California, Los Angeles, Children's Hospital of Philadelphia, University of Pennsylvania, Dartmouth–Hitchcock Medical Center, Emory University, Cincinnati Children's Hospital Medical Center, University of Cincinnati, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Dana-Farber Cancer Institute, Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Southern Illinois University Carbondale, SIU Medicine, Northwell Health, Hospital for Sick Children, Johns Hopkins University, University of California, San Francisco, Washington University in St. Louis, Mass General Brigham, Columbia University, Montefiore Health System, Massachusetts Eye and Ear Infirmary, Baylor College of Medicine, University of North Carolina at Chapel Hill, Howard Hughes Medical Institute, University of Pittsburgh, University of Wisconsin–Madison, Duke University, Durham VA Medical Center, The University of Texas Southwestern Medical Center, Association of Public Health Laboratories, Case Western Reserve University, Albert Einstein College of Medicine, Children's Hospital at Montefiore
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
Funders: U.S. Department of Health and Human Services, U.S. Department of Justice, Alex's Lemonade Stand Foundation for Childhood Cancer, Amgen, American Academy of Allergy Asthma and Immunology, Eli Lilly and Company, Sanofi, Biogen, St. Jude Children's Research Hospital, Vertex Pharmaceuticals, American Lebanese Syrian Associated Charities, Innovative Genomics Institute, MannKind Corporation, Chiesi USA, Swedish Orphan Biovitrum, National Institutes of Health, Spark Therapeutics, National Human Genome Research Institute, NIH Clinical Center, Hyundai Hope On Wheels, Common Fund
OpenAlex ID: W7223708564