Population-Based Newborn Screening for Genetic Disorders When Multiple Mutation DNA Testing Is Incorporated: A Cystic Fibrosis Newborn Screening Model Demonstrating Increased Sensitivity but More Carrier DetectionsAnne Marie Comeau, Roger B. Eaton, Richard B. Parad et al.|PEDIATRICS|2004Cited by 154
Sweat Testing Infants Detected by Cystic Fibrosis Newborn ScreeningRichard B. Parad, Brian O’Sullivan, Mark Dovey et al.|The Journal of Pediatrics|2005Cited by 56
Vitamin D metabolites in adolescents and young adults with cystic fibrosis: Effects of sun and seasonEdward O. Reiter, Lynn M. Taussig, J. Wesley Pike et al.|The Journal of Pediatrics|1985Cited by 51
Cystic fibrosis newborn screening: using experience to optimize the screening algorithmJaime E. Hale, Anne Marie Comeau, Richard B. Parad et al.|Journal of Inherited Metabolic Disease|2010Cited by 21
Communications Systems and their Models: Massachusetts Parent Compliance with Recommended Specialty Care after Positive Cystic Fibrosis Newborn Screening ResultAnne Marie Comeau, Roger B. Eaton, Richard B. Parad et al.|The Journal of Pediatrics|2005Cited by 16