Associate Professor Veronica Wiley

Clinical Associate Professor
Genetic Medicine, Children's Hospital, Westmead

Telephone +61 2 9845 3256
Fax +61 2 9845 3800

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Selected grants

2013

  • Infant thyroid hormone levels and long-term child educational outcomes; Nassar N, Roberts C, Wilcken B, Martin A, Jack M, Wiley V, Algert C; National Health and Medical Research Council (NHMRC)/Project Grants.

Selected publications

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Book Chapters

  • Alodaib, A., Carpenter, K., Wiley, V., Wotton, T., Christodoulou, J., Wilcken, B. (2012). Homocysteine Measurement in Dried Blood Spot for Neonatal Detection of Homocystinurias. In Society for the Study of Inborn Errors of Metabolism (Eds.), JIMD Reports - Case and Research Reports, 2012/2, (pp. 1-6). Heidelberg: Springer.

Journals

  • Christie, L., Wotton, T., Bennetts, B., Wiley, V., Wilcken, B., Rogers, C., Boyle, J., Turner, C., Hansen, J., Hunter, M., et al (2013). Maternal attitudes to newborn screening for fragile X syndrome. American Journal of Medical Genetics. Part A, 161A (2), 301-311. [More Information]
  • Alodaib, A., Carpenter, K., Wiley, V., Wotton, T., Christodoulou, J., Wilcken, B. (2012). Homocysteine Measurement in Dried Blood Spot for Neonatal Detection of Homocystinurias. JIMD Reports - Case and Research Reports, 5, 1-6.
  • Mullins, R., Clark, S., Wiley, V., Eyles, D., Camargo, C. (2012). Neonatal vitamin D status and childhood peanut allergy: a pilot study. Annals of Allergy, Asthma, and Immunology, 109(5), 324-328. [More Information]
  • Alodaib, A., Carpenter, K., Wiley, V., Sim, K., Christodoulou, J., Wilcken, B. (2011). An improved ultra performance liquid chromatography-tandem mass spectrometry method for the determination of alloisoleucine and branched chain amino acids in dried blood samples. Annals of clinical biochemistry, 48(5), 468-470. [More Information]
  • McHugh, D., Cameron, C., Abdenur, J., Abdulrahman, M., Adair, O., Nuaimi, S., Ahlman, H., Allen, J., Antonozzi, I., Archer, S., Wilcken, B., Wiley, V., et al (2011). Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project. Genetics in Medicine, 13(3), 230-254. [More Information]
  • Wilcken, B., Wiley, V. (2011). Increased iodine deficiency in Victoria, Australia: analysis of neonatal thyroid-stimulating hormone data, 2001 to 2006. Medical Journal of Australia, 194(4), 209-210. [More Information]
  • Bijarnia, S., Wilcken, B., Wiley, V. (2011). Newborn screening for congenital hypothyroidism in very-low-birth-weight babies: the need for a second test. Journal of Inherited Metabolic Disease (JIMD), 34(3), 827-833. [More Information]
  • Khalid, J., Oerton, J., Besley, G., Dalton, N., Downing, M., Green, A., Henderson, M., Krywawych, S., Wiley, V., Wilcken, B., et al (2010). Relationship of Octanoylcarnitine Concentrations to Age at Sampling in Unaffected Newborns Screened for Medium-Chain Acyl-CoA Dehydrogenase Deficiency. Clinical Chemistry (Washington, DC), 56(6), 1015-1021. [More Information]
  • Wilcken, B., Haas, M., Joy, P., Wiley, V., Bowling, F., Carpenter, K., Christodoulou, J., Cowley, D., Ellaway, C., Fletcher, J., et al (2009). Expanded Newborn Screening: Outcome in Screened and Unscreened Patients at Age 6 Years. Pediatrics (English Edition), 124(2), e241-e248. [More Information]
  • Bijarnia, S., Wiley, V., Carpenter, K., Christodoulou, J., Ellaway, C., Wilcken, B. (2008). Glutaric aciduria type I: outcome following detection by newborn screening. Journal of Inherited Metabolic Disease (JIMD), 31(4), 503-507. [More Information]
  • Wilcken, B., Wiley, V. (2008). Newborn screening. Pathology, 40(2), 104-115. [More Information]
  • Gleeson, H., Wiley, V., Wilcken, B., Elliott, E., Cowell, C., Thonsett, M., Byrne, G., Ambler, G. (2008). Two-year pilot study of newborn screening for congenital adrenal hyperlasia in New South Wales compared with nationwide case surveillance in Australia. Journal of Paediatrics and Child Health, 44(10), 554-559. [More Information]
  • Wilcken, B., Haas, M., Joy, P., Wiley, V., Chaplin, M., Black, C., Fletcher, J., McGill, J., Boneh, A. (2007). Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study. The Lancet, 369(9555), 37-42. [More Information]
  • Travers, C., Guttikonda, K., Norton, C., Lewis, P., Mollart, L., Wiley, V., Wilcken, B., Eastman, C., Boyages, S. (2006). Iodine status in pregnant women and their newborns: are our babies at risk of iodine deficiency? Medical Journal of Australia, 184(12), 617-620. [More Information]
  • Waddell, L., Wiley, V., Carpenter, K., Bennetts, B., Angel, L., Andresen, B., Wilcken, B. (2006). Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. Molecular Genetics and Metabolism, 87(1), 32-39. [More Information]
  • Bayliss, U., Cowell, C., Hong, J., Wiley, V., Wilcken, B. (2005). Acute presentation of childhood hypothyroidism. Medical Journal of Australia, 182(4), 200-200. [More Information]
  • Mitchell, J., Wilcken, B., Alexander, I., Ellaway, C., O'Grady, H., Wiley, V., Earl, J., Christodoulou, J. (2005). Tetrahydrobiopterin-responsive phenylketonuria: The New South Wales experience. Molecular Genetics and Metabolism, 86(Suppl 1), S81-S85. [More Information]
  • Wiley, V., Carpenter, K., Bennetts, B., Wilcken, B. (2003). Information overload - new technologies, can we store the data? Southeast Asian Journal of Tropical Medicine and Public Health, 34(S3), 59-62.
  • Wiley, V., Carpenter, K., Bayliss, U., Wilcken, B. (2003). Newborn screening - is it really that simple? Southeast Asian Journal of Tropical Medicine and Public Health, 34(S3), 107-110.
  • Wilcken, B., Wiley, V. (2003). Newborn screening methods for cystic fibrosis. Paediatric Respiratory Reviews, 11, 272-277.
  • Wilcken, B., Wiley, V., Hammond, J., Carpenter, K. (2003). Screening newborns for inborn errors of metabolism by tandem mass spectrometry. New England Journal of Medicine, 348(5), 2304-2312.
  • Wilcken, B., Carpenter, K., Wiley, V. (2002). Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency. The Lancet (North American Edition), 359(9306), 627-628.
  • McElduff, A., McElduff, P., Gunton, J., Hams, G., Wiley, V., Wilcken, B. (2002). Neonatal thyroid-stimulating hormone concentrations in northern Sydney: further indications of mild iodine deficiency. Medical Journal of Australia, 176(7), 317-320.
  • Massie, J., Wilcken, B., Van Asperen, P., Dorney, S., Gruca, M., Wiley, V., Gaskin, K. (2000). Pancreatic function and extended mutation analysis in ?F508 heterozygous infants with ane levated immunoreactive trypsinogen but normal sweat electrolyte levels. The Journal of Pediatrics, 137(2), 214-220.

2013

  • Christie, L., Wotton, T., Bennetts, B., Wiley, V., Wilcken, B., Rogers, C., Boyle, J., Turner, C., Hansen, J., Hunter, M., et al (2013). Maternal attitudes to newborn screening for fragile X syndrome. American Journal of Medical Genetics. Part A, 161A (2), 301-311. [More Information]

2012

  • Alodaib, A., Carpenter, K., Wiley, V., Wotton, T., Christodoulou, J., Wilcken, B. (2012). Homocysteine Measurement in Dried Blood Spot for Neonatal Detection of Homocystinurias. JIMD Reports - Case and Research Reports, 5, 1-6.
  • Alodaib, A., Carpenter, K., Wiley, V., Wotton, T., Christodoulou, J., Wilcken, B. (2012). Homocysteine Measurement in Dried Blood Spot for Neonatal Detection of Homocystinurias. In Society for the Study of Inborn Errors of Metabolism (Eds.), JIMD Reports - Case and Research Reports, 2012/2, (pp. 1-6). Heidelberg: Springer.
  • Mullins, R., Clark, S., Wiley, V., Eyles, D., Camargo, C. (2012). Neonatal vitamin D status and childhood peanut allergy: a pilot study. Annals of Allergy, Asthma, and Immunology, 109(5), 324-328. [More Information]

2011

  • Alodaib, A., Carpenter, K., Wiley, V., Sim, K., Christodoulou, J., Wilcken, B. (2011). An improved ultra performance liquid chromatography-tandem mass spectrometry method for the determination of alloisoleucine and branched chain amino acids in dried blood samples. Annals of clinical biochemistry, 48(5), 468-470. [More Information]
  • McHugh, D., Cameron, C., Abdenur, J., Abdulrahman, M., Adair, O., Nuaimi, S., Ahlman, H., Allen, J., Antonozzi, I., Archer, S., Wilcken, B., Wiley, V., et al (2011). Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project. Genetics in Medicine, 13(3), 230-254. [More Information]
  • Wilcken, B., Wiley, V. (2011). Increased iodine deficiency in Victoria, Australia: analysis of neonatal thyroid-stimulating hormone data, 2001 to 2006. Medical Journal of Australia, 194(4), 209-210. [More Information]
  • Bijarnia, S., Wilcken, B., Wiley, V. (2011). Newborn screening for congenital hypothyroidism in very-low-birth-weight babies: the need for a second test. Journal of Inherited Metabolic Disease (JIMD), 34(3), 827-833. [More Information]

2010

  • Khalid, J., Oerton, J., Besley, G., Dalton, N., Downing, M., Green, A., Henderson, M., Krywawych, S., Wiley, V., Wilcken, B., et al (2010). Relationship of Octanoylcarnitine Concentrations to Age at Sampling in Unaffected Newborns Screened for Medium-Chain Acyl-CoA Dehydrogenase Deficiency. Clinical Chemistry (Washington, DC), 56(6), 1015-1021. [More Information]

2009

  • Wilcken, B., Haas, M., Joy, P., Wiley, V., Bowling, F., Carpenter, K., Christodoulou, J., Cowley, D., Ellaway, C., Fletcher, J., et al (2009). Expanded Newborn Screening: Outcome in Screened and Unscreened Patients at Age 6 Years. Pediatrics (English Edition), 124(2), e241-e248. [More Information]

2008

  • Bijarnia, S., Wiley, V., Carpenter, K., Christodoulou, J., Ellaway, C., Wilcken, B. (2008). Glutaric aciduria type I: outcome following detection by newborn screening. Journal of Inherited Metabolic Disease (JIMD), 31(4), 503-507. [More Information]
  • Wilcken, B., Wiley, V. (2008). Newborn screening. Pathology, 40(2), 104-115. [More Information]
  • Gleeson, H., Wiley, V., Wilcken, B., Elliott, E., Cowell, C., Thonsett, M., Byrne, G., Ambler, G. (2008). Two-year pilot study of newborn screening for congenital adrenal hyperlasia in New South Wales compared with nationwide case surveillance in Australia. Journal of Paediatrics and Child Health, 44(10), 554-559. [More Information]

2007

  • Wilcken, B., Haas, M., Joy, P., Wiley, V., Chaplin, M., Black, C., Fletcher, J., McGill, J., Boneh, A. (2007). Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study. The Lancet, 369(9555), 37-42. [More Information]

2006

  • Travers, C., Guttikonda, K., Norton, C., Lewis, P., Mollart, L., Wiley, V., Wilcken, B., Eastman, C., Boyages, S. (2006). Iodine status in pregnant women and their newborns: are our babies at risk of iodine deficiency? Medical Journal of Australia, 184(12), 617-620. [More Information]
  • Waddell, L., Wiley, V., Carpenter, K., Bennetts, B., Angel, L., Andresen, B., Wilcken, B. (2006). Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. Molecular Genetics and Metabolism, 87(1), 32-39. [More Information]

2005

  • Bayliss, U., Cowell, C., Hong, J., Wiley, V., Wilcken, B. (2005). Acute presentation of childhood hypothyroidism. Medical Journal of Australia, 182(4), 200-200. [More Information]
  • Mitchell, J., Wilcken, B., Alexander, I., Ellaway, C., O'Grady, H., Wiley, V., Earl, J., Christodoulou, J. (2005). Tetrahydrobiopterin-responsive phenylketonuria: The New South Wales experience. Molecular Genetics and Metabolism, 86(Suppl 1), S81-S85. [More Information]

2003

  • Wiley, V., Carpenter, K., Bennetts, B., Wilcken, B. (2003). Information overload - new technologies, can we store the data? Southeast Asian Journal of Tropical Medicine and Public Health, 34(S3), 59-62.
  • Wiley, V., Carpenter, K., Bayliss, U., Wilcken, B. (2003). Newborn screening - is it really that simple? Southeast Asian Journal of Tropical Medicine and Public Health, 34(S3), 107-110.
  • Wilcken, B., Wiley, V. (2003). Newborn screening methods for cystic fibrosis. Paediatric Respiratory Reviews, 11, 272-277.
  • Wilcken, B., Wiley, V., Hammond, J., Carpenter, K. (2003). Screening newborns for inborn errors of metabolism by tandem mass spectrometry. New England Journal of Medicine, 348(5), 2304-2312.

2002

  • Wilcken, B., Carpenter, K., Wiley, V. (2002). Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency. The Lancet (North American Edition), 359(9306), 627-628.
  • McElduff, A., McElduff, P., Gunton, J., Hams, G., Wiley, V., Wilcken, B. (2002). Neonatal thyroid-stimulating hormone concentrations in northern Sydney: further indications of mild iodine deficiency. Medical Journal of Australia, 176(7), 317-320.

2000

  • Massie, J., Wilcken, B., Van Asperen, P., Dorney, S., Gruca, M., Wiley, V., Gaskin, K. (2000). Pancreatic function and extended mutation analysis in ?F508 heterozygous infants with ane levated immunoreactive trypsinogen but normal sweat electrolyte levels. The Journal of Pediatrics, 137(2), 214-220.

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