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, Anne Marie Comeau et al.|The Journal of Pediatrics|2005Cited by 56
Genetic counseling after implementation of statewide cystic fibrosis newborn screening: Two years' experience in one medical centerPatricia G. Wheeler, Diana W. Bianchi, Henry L. Dorkin et al.|Genetics in Medicine|2001Cited by 41
Early Pulmonary Manifestation of Cystic Fibrosis in Children With the ΔF508/R117H-7T GenotypeBrian O’Sullivan, Richard B. Parad, Robert G. Zwerdling et al.|PEDIATRICS|2006Cited by 40
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