Publications by authors named "Angela Wittenauer"

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Evaluating Georgia's Cystic Fibrosis Newborn Screening Algorithm to Inform Improvement Recommendations.
Brittany Truitt, Eileen Barr, Angela Wittenauer, Andrew Jergel, Shasha Bai

Int J Neonatal Screen· September 2025

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A multinational study of acute and long-term outcomes of Type 1 galactosemia patients who carry the S135L (c.404C > T) variant of GALT.
Quinton S Katler, Karolina M Stepien, Nathan Paull, Sneh Patel, Michael Adams, Angela Wittenauer

J Inherit Metab Dis· November 2022

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Proximal urea cycle defects are challenging to detect with newborn screening: Results of a prospective pilot study using post-analytical tools.
Patricia Liane Hall, Angela Lynn Wittenauer, William Ross Wilcox

Am J Med Genet C Semin Med Genet· June 2022

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Georgia state spinal muscular atrophy newborn screening experience: Screening assay performance and early clinical outcomes.
Kathryn Elkins, Angela Wittenauer, Arthur F Hagar, Rachel Logan, Elizabeth Sekul

Am J Med Genet C Semin Med Genet· June 2022

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Health care practitioners' experience-based opinions on providing care after a positive newborn screen for Pompe disease.
Laura Davids, Yuxian Sun, Reneé H Moore, Emily Lisi, Angela Wittenauer

Mol Genet Metab· February 2022

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Newborn Screening for X-Linked Adrenoleukodystrophy in Georgia: Experiences from a Pilot Study Screening of 51,081 Newborns.
Patricia L Hall, Hong Li, Arthur F Hagar, S Caleb Jerris, Angela Wittenauer

Int J Neonatal Screen· October 2020

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Two-Tiered Newborn Screening with Post-Analytical Tools for Pompe Disease and Mucopolysaccharidosis Type I Results in Performance Improvement and Future Direction.
Patricia L Hall, Rossana Sanchez, Arthur F Hagar, S Caleb Jerris, Angela Wittenauer

Int J Neonatal Screen· March 2020

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Post-Analytical Tools for the Triage of Newborn Screening Results in Follow-up Can Reduce Confirmatory Testing and Guide Performance Improvement.
Patricia L Hall, Angela Wittenauer, Arthur Hagar

Int J Neonatal Screen· March 2020

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Increased parental anxiety and a benign clinical course: Infants identified with short-chain acyl-CoA dehydrogenase deficiency and isobutyryl-CoA dehydrogenase deficiency through newborn screening in Georgia.
Roa Sadat, Patricia L Hall, Angela L Wittenauer, Elizabeth D Vengoechea, Kevin Park

Mol Genet Metab· January 2020

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Developmental outcomes of children with Duarte galactosemia: exploring the bases of an apparent contradiction in the literature.
Judith L Fridovich-Keil, Grace Carlock, Claire D Coles, Mary Ellen Lynch, Molly N Millians, Angela Wittenauer

Genet Med· December 2019

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Newborn screening for medium chain acyl-CoA dehydrogenase deficiency: performance improvement by monitoring a new ratio.
Patricia L Hall, Angela Wittenauer, Arthur Hagar

Mol Genet Metab· December 2014

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An incidental case of dihydropyrimidine dehydrogenase deficiency: One case, multiple challenges.
Hamoud H Al Khallaf, Miao He, Angela Wittenauer, Elizabeth E Woolley, Mariagrazia Cunto

Indian J Hum Genet· October 2013

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