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Journal of Neurodevelopmental Disorders|August 7, 2014
Associated features in females with an FMR1 premutationAnne C Wheeler, Donald B Bailey, Elizabeth Berry-Kravis, et al.
Trials|June 29, 2018
Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocolLaura V Milko, Christine Rini, Megan A Lewis, et al.
Pediatrics|November 7, 2012
Newborn, carrier, and early childhood screening recommendations for fragile XLiane Abrams, Amy Cronister, William T Brown, et al.
Pediatrics|April 29, 2021
Emergence of Developmental Delay in Infants and Toddlers With an FMR1 MutationAnne C Wheeler, Angela Gwaltney, Melissa Raspa, et al.
Frontiers in Genetics|June 1, 2022
Education and Consent for Population-Based DNA Screening: A Mixed-Methods Evaluation of the Early Check Newborn Screening Pilot StudyHolly L Peay, Angela You Gwaltney, Rebecca Moultrie, et al.
Clinical and Translational Science|December 31, 2020
Outreach to new mothers through direct mail and email: recruitment in the Early Check research studyRyan S Paquin, Megan A Lewis, Blake A Harper, et al.
JAMA Network Open|February 1, 2020
Evaluation of X-Linked Adrenoleukodystrophy Newborn Screening in North CarolinaStacey Lee, Kristin Clinard, Sarah P Young, et al.
Developmental Psychology|January 23, 2014
"My Baby & Me": effects of an early, comprehensive parenting intervention on at-risk mothers and their childrenCathy L Guttentag, Susan H Landry, Jeffrey M Williams, et al.
The Journal of Pediatrics|May 29, 2019
The North Carolina Experience with Mucopolysaccharidosis Type I Newborn ScreeningJennifer L Taylor, Kristin Clinard, Cynthia M Powell, et al.
International Journal of Neonatal Screening|April 3, 2021
A Voluntary Statewide Newborn Screening Pilot for Spinal Muscular Atrophy: Results from Early CheckKaterina S Kucera, Jennifer L Taylor, Veronica R Robles, et al.
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