Zeffie Poulakis

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

A Lindquist, L Hui, A Poulton, E Kluckow, B Hutchinson, MD Pertile, L Bonacquisto, L Gugasyan, A Kulkarni, J Harraway, A Howden, R Mccoy, F Da Silva Costa, M Menezes, R Palma-Dias, D Nisbet, N Martin, M Bethune, Z Poulakis, J Halliday

Journal article  |  2020  |  ULTRASOUND IN OBSTETRICS & GYNECOLOGY

OBJECTIVES: To perform individual record linkage of women undergoing screening with cell-free DNA (cfDNA), combined first-trimeste..

Exome sequencing in infants with congenital hearing impairment: a population-based cohort study

Lilian Downie, Jane Halliday, Rachel Burt, Sebastian Lunke, Elly Lynch, Melissa Martyn, Zeffie Poulakis, Clara Gaff, Valerie Sung, Melissa Wake, Matthew F Hunter, Kerryn Saunders, Elizabeth Rose, Sharon Lewis, Anna Jarmolowicz, Dean Phelan, Heidi L Rehm, David J Amor

Journal article  |  2020  |  EUROPEAN JOURNAL OF HUMAN GENETICS

Congenital hearing impairment (HI) is the most common sensory impairment and can be isolated or part of a syndrome. Diagnosis thro..

Youths with a non-binary gender identity: a review of their sociodemographic and clinical profile

Denise Chew, Michelle A Tollit, Zeffie Poulakis, Sav Zwickl, Ada S Cheung, Ken C Pang

Journal article  |  2020  |  LANCET CHILD & ADOLESCENT HEALTH

Many of the considerable number of young people who identify as transgender or gender diverse do not conform to traditional binary..

A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort

Lisa Hui, Alice Poulton, Eliza Kluckow, Anthea Lindquist, Briohny Hutchinson, Mark D Pertile, Leonard Bonacquisto, Lucy Gugasyan, Abhijit Kulkarni, James Harraway, Amanda Howden, Richard Mccoy, Fabricio Da Silva Costa, Melody Menezes, Ricardo Palma-Dias, Debbie Nisbet, Nicole Martin, Michael Bethune, Zeffie Poulakis, Jane Halliday

Journal article  |  2020  |  HUMAN REPRODUCTION

STUDY QUESTION: What is the frequency of major chromosome abnormalities in a population-based diagnostic data set of genomic tests..

Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016

Eliza Kluckow, Jane Halliday, Alice Poulton, Anthea Lindquist, Briohny Hutchinson, Michael Bethune, Leonard Bonacquisto, Fabricio Da Silva Costa, Lucy Gugasyan, James Harraway, Amanda Howden, Abhijit Kulkarni, Nicole Martin, Richard McCoy, Melody Menezes, Debbie Nisbet, Ricardo Palma-Dias, Mark D Pertile, Zeffie Poulakis, Lisa Hui

Journal article  |  2019  |  PRENATAL DIAGNOSIS

OBJECTIVES: To explore the association between timing of diagnosis of common autosomal trisomies, maternal age, and socio-economic..

Population-Based Prevalence of 22q11 Deletion Syndrome and Other Chromosome Abnormalities in a Combined Prenatal and Postnatal Cohort

L Hui, A Poulton, E Kluckow, A Lindquist, B Hutchinson, M Pertile, L Bonacquisto, L Gugasyan, A Kulkarni, J Harraway, A Howden, R Mccoy, F Da Silva Costa, M Menezes, R Palma-Dias, D Nisbet, N Martin, M Bethune, Z Poulakis, J Halliday

Conference Proceedings  |  2019  |  AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY

Data Resource Profile: The Victorian Childhood Hearing Impairment Longitudinal Databank (VicCHILD)

Valerie Sung, Libby Smith, Zeffie Poulakis, Rachel A Burt, Peter Carew, Sherryn Tobin, Melissa Wake

Journal article  |  2019  |  INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Abstracts of the 29th World Congress on Ultrasound in Obstetrics and Gynecology, 12-16 October 2019, Berlin, Germany.

L Hui, A Lindquist, A Poulton, E Kluckow, B Hutchinson, L Bonacquisto, MD Pertile, L Gugasyan, A Kulkarni, J Harraway, A Howden, R McCoy, F da Silva Costa, R Palma-Dias, D Nisbet, N Martin, M Behune, Z Poulakis, J Halliday

Conference Proceedings  |  2019  |  Ultrasound Obstet Gynecol

Decision-making for additional genomic findings in parents of newborns with congenital deafness

L Downie, M Martyn, A Jarmolowicz, V Sung, A Kanga-Parabia, J Halliday, E Lynch, Z Poulakis, Y Prawer, C Gaff, D Amor

Conference Proceedings  |  2019  |  EUROPEAN JOURNAL OF HUMAN GENETICS

Consider the costs of aiding mild hearing loss in the absence of clear benefits: Response to McCreery and colleagues

Peter Carew, Fiona K Mensah, Gary Rance, Traci Flynn, Zeffie Poulakis, Melissa Wake

Journal article  |  2018  |  CHILD CARE HEALTH AND DEVELOPMENT