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These selected publications highlight the major themes of research at Mercy Perinatal. Further information on individual researchers and Obstetrics and Gynaecology Research at the University of Melbourne can be found here.

Noninvasive prenatal testing for aneuploidy – the vanguard of genomic medicine.

Hui L and Bianchi DW. Annual Review of Medicine 2017; 68(1). DOI: 10.1146/annurev-med-072115-033220.
Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screening.

Cohen PA, Flowers N, Tong S, Hannan N, Pertile MD and Hui L. BMC Medicine 2016; 14:126.
Population-based trends in prenatal screening and diagnosis for aneuploidy: a retrospective analysis of 38 years of state-wide data.

Hui L, Muggli E, Halliday JL. BJOG: An International Journal of Obstetrics & Gynaecology 2016;123(1):90-7.
How to safeguard competency and training in invasive prenatal diagnosis: “The elephant in the room”.

Hui L, Tabor A, Walker SP, Kilby MD. Ultrasound in Obstetrics and Gynecology 2016; 47: 8-13.
The pathway not taken: understanding 'omics data in the perinatal context.

Edlow AG, Slonim DK, Wick HC, Hui L, Bianchi DW. American Journal of Obstetrics and Gynecology. 2015;213(1):59.e1-172
Clinical implementation of cell-free DNA based aneuploidy screening: perspectives from a national audit.

Hui L, Teoh M, da Silva Costa F, Ramsay P, Palma-Dias R, Richmond Z, Piessens S, Walker S. Ultrasound in Obstetrics and ...
Prenatal diagnostic testing and atypical chromosome abnormalities following combined first-trimester screening: implications for contingent models of non-invasive prenatal testing
Population-based trends in ultrasound-indicated prenatal diagnosis from 1994 to 2016: two decades of change.
State‐wide utilization and performance of traditional and cell‐free DNA‐based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study

Noninvasive prenatal testing for aneuploidy – the vanguard of genomic medicine.

Abnormal plasma DNA profiles in early ovarian cancer using a non-invasive prenatal testing platform: implications for cancer screening.

Population-based trends in prenatal screening and diagnosis for aneuploidy: a retrospective analysis of 38 years of state-wide data.

How to safeguard competency and training in invasive prenatal diagnosis: “The elephant in the room”.

The pathway not taken: understanding 'omics data in the perinatal context.

Clinical implementation of cell-free DNA based aneuploidy screening: perspectives from a national audit.

Prenatal diagnostic testing and atypical chromosome abnormalities following combined first-trimester screening: implications for contingent models of non-invasive prenatal testing

Population-based trends in ultrasound-indicated prenatal diagnosis from 1994 to 2016: two decades of change.

State‐wide utilization and performance of traditional and cell‐free DNA‐based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study

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