Veronica C. Wiley

Randwick, NSW, Australia

Last Updated: 09/26/2026

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Found 35 publications

Evidence-based multidisciplinary model of care for newborn screening in spinal muscular atrophy.

Evidence-based multidisciplinary model of care for newborn screening in spinal muscular atrophy.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 13, 2025

Genotyping in patients with congenital adrenal hyperplasia by sequencing of newborn bloodspot samples.

Genotyping in patients with congenital adrenal hyperplasia by sequencing of newborn bloodspot samples.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: January 28, 2023

Outcomes of lowered newborn screening thresholds for congenital hypothyroidism.

Outcomes of lowered newborn screening thresholds for congenital hypothyroidism.

Journal: Journal of paediatrics and child health

Published: November 17, 2022

Newborn Screening for the Diagnosis and Treatment of Duchenne Muscular Dystrophy.

Newborn Screening for the Diagnosis and Treatment of Duchenne Muscular Dystrophy.

Journal: Journal of neuromuscular diseases

Published: November 14, 2022

Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?

Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?

Journal: European journal of human genetics : EJHG

Published: September 14, 2022

Newborn screening for spinal muscular atrophy in Australia: a non-randomised cohort study.

Newborn screening for spinal muscular atrophy in Australia: a non-randomised cohort study.

Journal: The Lancet. Child & adolescent health

Published: August 17, 2022

Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation.

Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation.

Journal: Clinical chemistry and laboratory medicine

Published: April 24, 2022

Modelling the Cost-Effectiveness and Budget Impact of a Newborn Screening Program for Spinal Muscular Atrophy and Severe Combined Immunodeficiency.

Modelling the Cost-Effectiveness and Budget Impact of a Newborn Screening Program for Spinal Muscular Atrophy and Severe Combined Immunodeficiency.

Journal: International journal of neonatal screening

Published: March 31, 2022

Economic Evaluation of Newborn Screening for Severe Combined Immunodeficiency.

Economic Evaluation of Newborn Screening for Severe Combined Immunodeficiency.

Journal: International journal of neonatal screening

Published: March 31, 2022

Immunoreactive Trypsinogen and Free Carnitine Changes on Newborn Screening after Birth in Patients Who Develop Type 1 Diabetes.

Immunoreactive Trypsinogen and Free Carnitine Changes on Newborn Screening after Birth in Patients Who Develop Type 1 Diabetes.

Journal: Nutrients

Published: September 05, 2021

Integrating newborn screening for spinal muscular atrophy into health care systems: an Australian pilot programme.

Integrating newborn screening for spinal muscular atrophy into health care systems: an Australian pilot programme.

Journal: Developmental medicine and child neurology

Published: May 04, 2021

Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning.

Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning.

Journal: International journal of neonatal screening

Published: March 27, 2021

Showing 1-12 of 35

Last Updated: 09/26/2026