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CDC-Authored Genomics and Precision Health Publications Database|Home|PHGKB

CDC-Authored Genomics and Precision Health Publications Database


Last data update: Nov 23, 2021. (Total: 3579 publications since 2011)
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Records 1-8 (of 8 Records)
Query Trace: all>>Cynthia F Hinton[CDC Author]
Infants with Congenital Disorders Identified Through Newborn Screening - United States, 2015-2017.
Marci K Sontag, Careema Yusuf, Scott D Grosse, Sari Edelman, Joshua I Miller, Sarah McKasson, Yvonne Kellar-Guenther, Marcus Gaffney, Cynthia F Hinton, Carla Cuthbert, Sikha Singh, Jelili Ojodu, and Stuart K Shapira
MMWR. Morbidity and mortality weekly report 2020 Sep 69(36) 1265-1268
A framework for assessing outcomes from newborn screening: on the road to measuring its promise.
Cynthia F Hinton, Charles J Homer, Alexis A Thompson, Andrea Williams, Kathryn L Hassell, Lisa Feuchtbaum, Susan A Berry, Anne Marie Comeau, Bradford L Therrell, Amy Brower, Katharine B Harris, Christine Brown, Jana Monaco, Robert J Ostrander, Alan E Zuckerman, Celia Kaye, Denise Dougherty, Carol Greene, Nancy S Green, and
Molecular genetics and metabolism 2016 May
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.
Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings.
Cynthia F Hinton, Cara T Mai, Sarah K Nabukera, Lorenzo D Botto, Lisa Feuchtbaum, Paul A Romitti, Ying Wang, Kimberly Noble Piper, and Richard S Olney
Genet. Med. 2014 Jun 16(6) 484-90
Improving newborn screening follow-up in pediatric practices: quality improvement innovation network.
Cynthia F Hinton, Daniel R Neuspiel, Ruth S Gubernick, Timothy Geleske, Jill Healy, Alex R Kemper, Michele A Lloyd-Puryear, Robert A Saul, Barry H Thompson, and Celia I Kaye
Pediatrics 2012 Sep 130(3) e669-75
Ethical implications and practical considerations of ethnically targeted screening for genetic disorders: the case of hemoglobinopathy screening.
Cynthia F Hinton, Althea M Grant, and Scott D Grosse
Ethn Health 16(4-5) 377-88
What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children.
Cynthia F Hinton, Lisa Feuchtbaum, Christopher A Kus, Alex R Kemper, Susan A Berry, Jill Levy-Fisch, Julie Luedtke, Celia Kaye, and Coleen A Boyle
Genet. Med. 2011 Oct 13(10) 861-5
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
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