Last data update: Jul 01, 2020. (Total: 2837 publications since 2011)
|Query Trace: all>>Stuart K Shapira[CDC Author]|
| Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.
Mary M Jenkins, Lynn M Almli, Faith Pangilinan, Jessica X Chong, Elizabeth E Blue, Stuart K Shapira, Janson White, Daniel McGoldrick, Joshua D Smith, James C Mullikin, Christopher J Bean, Wendy N Nembhard, Xiang-Yang Lou, Gary M Shaw, Paul A Romitti, Kim Keppler-Noreuil, Mahsa M Yazdy, Denise M Kay, Tonia C Carter, Andrew F Olshan, Kristin J Moore, Nanette Nascone-Yoder, Richard H Finnell, Philip J Lupo, Marcia L Feldkamp, , Deborah A Nickerson, Michael J Bamshad, Lawrence C Brody, Jennita Reefhuis,
Birth defects research 2019 Jul
| A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early Development.
Stuart K Shapira, Lin H Tian, Arthur S Aylsworth, Ellen R Elias, Julie E Hoover-Fong, Naomi J L Meeks, Margaret C Souders, Anne C-H Tsai, Elaine H Zackai, Aimee A Alexander, Marshalyn Yeargin-Allsopp, and Laura A Schieve
Journal of autism and developmental disorders 2019 Feb
| Congenital adrenal hyperplasia cases identified by newborn screening in one- and two-screen states.
Patrice K Held, Stuart K Shapira, Cynthia F Hinton, Elizabeth Jones, W Harry Hannon, and Jelili Ojodu
Mol. Genet. Metab. 2015 Aug 12.
| Birth prevalence rates of newborn screening disorders in relation to screening practices in the United States.
Vicki S Hertzberg, Cynthia F Hinton, Bradford L Therrell, and Stuart K Shapira
J. Pediatr. 2011 Oct 159(4) 555-60