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Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2017
Prenatal exome sequencing in anomalous fetuses: new opportunities and challengesNeeta L Vora, Bradford Powell, Alicia Brandt, et al.
Molecular Genetics & Genomic Medicine|July 19, 2022
Descriptive analysis of seizures and comorbidities associated with fragile X syndromeIgor Albizua, Krista Charen, Lisa Shubeck, et al.
Infant Behavior & Development|April 26, 2025
Evaluating canonical babbling ratios extracted from day-long audio recordings in infants later diagnosed with autism spectrum disorderShoba S Meera, Divya Swaminathan, Rahul Pawar, et al.
BMC Pediatrics|July 19, 2019
Early Check: translational science at the intersection of public health and newborn screeningDonald B Bailey, Lisa M Gehtland, Megan A Lewis, et al.
American Journal of Human Genetics|August 28, 2020
Genomic Sequencing for Newborn Screening: Results of the NC NEXUS ProjectTamara S Roman, Stephanie B Crowley, Myra I Roche, et al.
Nature Medicine|September 5, 2025
Feasibility and clinical utility of expanded genomic newborn screening in the Early Check programHeidi L Cope, Elizabeth R Jalazo, Jonathan S Berg, et al.
Pediatrics|January 19, 2017
Newborn Sequencing in Genomic Medicine and Public HealthJonathan S Berg, Pankaj B Agrawal, Donald B Bailey, et al.
Translational Science of Rare Diseases|July 16, 2021
Opportunities, barriers, and recommendations in down syndrome researchJames A Hendrix, Angelika Amon, Leonard Abbeduto, et al.
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