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

CDC-Authored Genomics and Precision Health Publications Database


Reproductive and Child Health

Last data update: Jun 28, 2022. (Total: 3910 publications since 2011)
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Records 1-30 (of 34 Records)
Query Trace: Newborn Screening[original query]
Newborn Screen for X-Linked Adrenoleukodystrophy Using Flow Injection Tandem Mass Spectrometry in Negative Ion Mode.
Tarek A Teber, Brian J Conti, Christopher A Haynes, Amy Hietala, and Mei W Baker
International journal of neonatal screening 2022 8(2)
Common Challenges and Identified Solutions for State Newborn Screening Programs during COVID-19 Pandemic.
Dylan Simon, Elizabeth Broadbridge, Mei Baker, Amy Gaviglio, Dorota Gruber, Kimberly Noble Piper, Norma P Tavakoli, Jamie Sullivan, and Annie Kennedy
International journal of neonatal screening 2022 8(1)
Genomics and Newborn Screening: Perspectives of Public Health Programs.
Aaron J Goldenberg, Roselle Ponsaran, Amy Gaviglio, Dalton Simancek, and Beth A Tarini
International journal of neonatal screening 2022 8(1)
Newborn Screening Practices for Beta-Thalassemia in the United States.
Michael A Bender, Mary Hulihan, Mary Christine Dorley, Maria Del Pilar Aguinaga, Jelili Ojodu, and Careema Yusuf
International journal of neonatal screening 2021 7(4)
Detection of Cytomegalovirus in Urine Dried on Filter Paper.
Minal M Amin, Phili Wong, Mark McCann, and Sheila C Dollard
Journal of the Pediatric Infectious Diseases Society 2021 10(10) 958-961
Health and economic outcomes of newborn screening for infantile-onset Pompe disease.
John S Richardson, Alex R Kemper, Scott D Grosse, Wendy K K Lam, Angela M Rose, Ayesha Ahmad, Achamyeleh Gebremariam, and Lisa A Prosser
Genetics in medicine : official journal of the American College of Medical Genetics 2020 Dec
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
Newborn Screening Quality Assurance Program for CFTR Mutation Detection and Gene Sequencing to Identify Cystic Fibrosis.
Miyono M Hendrix, Stephanie L Foster, and Suzanne K Cordovado
Journal of inborn errors of metabolism and screening 4
Ensuring the Life-Span Benefits of Newborn Screening.
Alex R Kemper, Coleen A Boyle, Jeffrey P Brosco, and Scott D Grosse
Pediatrics 2019 Nov
CDC Grand Rounds: Newborn screening and improved outcomes.

MMWR. Morbidity and mortality weekly report 2012 Jun 61(21) 390-3
Showing Value in Newborn Screening: Challenges in Quantifying the Effectiveness and Cost-Effectiveness of Early Detection of Phenylketonuria and Cystic Fibrosis.
Scott D Grosse
Healthcare (Basel, Switzerland) 2015 3(4) 1133-57
The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study.
Maria D Karaceper, Pranesh Chakraborty, Doug Coyle, Kumanan Wilson, Jonathan B Kronick, Steven Hawken, Christine Davies, Marni Brownell, Linda Dodds, Annette Feigenbaum, Deshayne B Fell, Scott D Grosse, Astrid Guttmann, Anne-Marie Laberge, Aizeddin Mhanni, Fiona A Miller, John J Mitchell, Meranda Nakhla, Chitra Prasad, Cheryl Rockman-Greenberg, Rebecca Sparkes, Brenda J Wilson, Beth K Potter, and
Orphanet journal of rare diseases 2016 Feb 1112
Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation.
Alex R Kemper, Jeffrey Brosco, Anne Marie Comeau, Nancy S Green, Scott D Grosse, Elizabeth Jones, Jennifer M Kwon, Wendy K K Lam, Jelili Ojodu, Lisa A Prosser, and Susan Tanksley
Genetics in medicine : official journal of the American College of Medical Genetics 2017 19(1) 121-126
Using Decision Analysis to Support Newborn Screening Policy Decisions: A Case Study for Pompe Disease.
Lisa A Prosser, K K Lam, Scott D Grosse, Mia Casale, and Alex R Kemper
MDM policy & practice 3(1)
Public health action in genomics is now needed beyond newborn screening.
M S Bowen, K Kolor, W D Dotson, R M Ned, and M J Khoury
Public health genomics 2012 15(6) 327-34
Primary Care Provider Management of Congenital Hypothyroidism Identified Through Newborn Screening.
N A Rosenthal, E Bezar, S Mann, L K Bachrach, S Banerjee, M E Geffner, M Gottschalk, S K Shapira, L Hasegawa, and L Feuchtbaum
Annals of thyroid research 2017 3(1) 95-101
Liquid Chromatography-Tandem Mass Spectrometry Assay of Leukocyte Acid a-Glucosidase for Post-Newborn Screening Evaluation of Pompe Disease.
Na Lin, Jingyu Huang, Sara Violante, Joseph J Orsini, Michele Caggana, Erin E Hughes, Colleen Stevens, Lisa DiAntonio, Hsuan Chieh Liao, Xinying Hong, Farideh Ghomashchi, Arun Babu Kumar, Hui Zhou, Ruth Kornreich, Melissa Wasserstein, Michael H Gelb, and Chunli Yu
Clinical chemistry 2017 Feb
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
Cost-Effectiveness/Cost-Benefit Analysis of Newborn Screening for Severe Combined Immune Deficiency in Washington State.
Yao Ding, John D Thompson, Lisa Kobrynski, Jelili Ojodu, Guisou Zarbalian, and Scott D Grosse
The Journal of pediatrics 2016 Feb
Observed and expected frequencies of structural hemoglobin variants in newborn screening surveys in Africa and the Middle East: deviations from Hardy-Weinberg equilibrium.
Frédéric B Piel, Thomas V Adamkiewicz, Djesika Amendah, Thomas N Williams, Sunetra Gupta, and Scott D Grosse
Genetics in medicine : official journal of the American College of Medical Genetics 2015 Dec
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.
Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study.
Mei W Baker, Anne E Atkins, Suzanne K Cordovado, Miyono Hendrix, Marie C Earley, and Philip M Farrell
Genet. Med. 2015 Feb 12.
Mortality of New York children with sickle cell disease identified through newborn screening.
Ying Wang, Gang Liu, Michele Caggana, Joseph Kennedy, Regina Zimmerman, Suzette O Oyeku, Ellen M Werner, Althea M Grant, Nancy S Green, and Scott D Grosse
Genet. Med. 2015 Jun 17(6) 452-9
Succinylacetone as primary marker to detect tyrosinemia type I in newborns and its measurement by newborn screening programs.
Víctor R De Jesús, Barbara W Adam, Daniel Mandel, Carla D Cuthbert, and Dietrich Matern
Mol. Genet. Metab. 113(1-2) 67-75
Universal state newborn screening programs can reduce health disparities.
Jeffrey P Brosco, Scott D Grosse, and Lainie Friedman Ross
JAMA Pediatr 2015 Jan 169(1) 7-8
Reflections on 50 years of newborn screening.
Coleen A Boyle, Joseph A Bocchini, and James Kelly
Pediatrics 2014 Jun 133(6) 961-3
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
Newborn screening: from Guthrie to whole genome sequencing.
Michele Caggana, Elizabeth A Jones, S I Shahied, Susan Tanksley, Cheryl A Hermerath, and Ira M Lubin
Public Health Rep 128 Suppl 214-9
Decision analysis, economic evaluation, and newborn screening: challenges and opportunities.
Lisa A Prosser, Scott D Grosse, Alex R Kemper, Beth A Tarini, and James M Perrin
Genet. Med. 2012 Apr 5.
Evidence-based path to newborn screening for Duchenne muscular dystrophy.
Jerry R Mendell, Chris Shilling, Nancy D Leslie, Kevin M Flanigan, Roula al-Dahhak, Julie Gastier-Foster, Kelley Kneile, Diane M Dunn, Brett Duval, Alexander Aoyagi, Cindy Hamil, Maha Mahmoud, Kandice Roush, Lauren Bird, Chelsea Rankin, Heather Lilly, Natalie Street, Ram Chandrasekar, and Robert B Weiss
Ann. Neurol. 2012 Mar 71(3) 304-13
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