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American Journal of Epidemiology|February 17, 2018
Invited Commentary: Male Reproductive System Congenital Malformations and the Risk of Autism Spectrum DisorderLaura A Schieve, Stuart K ShapiraPediatrics|May 4, 2010
Future research directions to identify causes of the increasing incidence rate of congenital hypothyroidism in the United StatesStuart K Shapira, Michele A Lloyd-Puryear, Coleen BoyleBirth Defects Research|April 12, 2017
Survival Disparities Associated with Congenital Diaphragmatic HerniaCynthia F Hinton, Csaba Siffel, Adolfo Correa, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|December 11, 2008
Maternal vasoactive exposures, amniotic bands, and terminal transverse limb defectsMartha M Werler, Jaclyn L F Bosco, Stuart K Shapira, et al.The Journal of Pediatrics|June 7, 2011
Birth prevalence rates of newborn screening disorders in relation to screening practices in the United StatesVicki S Hertzberg, Cynthia F Hinton, Bradford L Therrell, et al.American Journal on Intellectual and Developmental Disabilities|August 7, 2010
Use of special education services among children with and without congenital gastrointestinal anomaliesShannon E G Hamrick, Matthew J Strickland, Stuart K Shapira, et al.MMWR. Morbidity and Mortality Weekly Report|July 20, 2018
Identification of Primary Congenital Hypothyroidism Based on Two Newborn Screens - Utah, 2010-2016David E Jones, Kim Hart, Stuart K Shapira, et al.American Journal of Medical Genetics|May 7, 2002
Familial complex chromosomal rearrangement resulting in a recombinant chromosomeSue Ann Berend, Olaf A F Bodamer, Stuart K Shapira, et al.Molecular Genetics and Metabolism|August 23, 2015
Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen statesPatrice K Held, Stuart K Shapira, Cynthia F Hinton, et al.Molecular Genetics and Metabolism|August 22, 2015
Single newborn screen or routine second screening for primary congenital hypothyroidismStuart K Shapira, Cynthia F Hinton, Patrice K Held, et al.Pageof 4