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JAMA Network Open|July 20, 2021
Principles of Genomic Newborn Screening Programs: A Systematic ReviewLilian Downie, Jane Halliday, Sharon Lewis, et al.The Laryngoscope|December 31, 2020
Exome Sequencing for Isolated Congenital Hearing Loss: A Cost-Effectiveness AnalysisLilian Downie, David J Amor, Jane Halliday, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2020
Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing projectLilian Downie, Jane Halliday, Sharon Lewis, et al.Reproductive Biomedicine Online|February 2, 2021
Child health after preimplantation genetic testingSharon Lewis, David J Amor, Anne Glynn, et al.Human Reproduction (Oxford, England)|August 16, 2008
A review of known imprinting syndromes and their association with assisted reproduction technologiesDavid J Amor, Jane HallidayBMC Pediatrics|October 11, 2021
Study protocol: childhood outcomes of fetal genomic variants: the PrenatAL Microarray (PALM) cohort studyLisa Hui, Cecilia Pynaker, Joanne Kennedy, et al.BMC Pediatrics|August 22, 2024
Perinatal outcomes after a prenatal diagnosis of a fetal copy number variant: a retrospective population-based cohort studyCecilia Pynaker, Jacqui McCoy, Jane Halliday, et al.Reproductive Biomedicine Online|April 24, 2025
Comparing subjective indicators of health in adults aged 27-38 years conceived with and without assisted reproductive technologySharon Lewis, Karin Hammarberg, Joanne Kennedy, et al.American Journal of Medical Genetics. Part A|June 29, 2021
Personal utility of genomic sequencing for infants with congenital deafnessErin Tutty, David J Amor, Anna Jarmolowicz, et al.Journal of Paediatrics and Child Health|December 31, 2013
Implementation of written consent for newborn screening in Victoria, AustraliaTaryn Charles, James Pitt, Jane Halliday, et al.Pageof 45