Andrew McLennan

17PUBLICATIONS
16CO-AUTHORS
African languagesFoetal development and medicineGene expression (incl. microarray and other genome-wide approaches)Psychosocial aspects of childbirth and perinatal mental healthNeurogenetics
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Publications (17)

|Jun 19, 2025
Patient Preferences and Understanding of Genome-Wide Cell-Free DNA Screening for Foetal Chromosomal Imbalances: A Survey Study.

Yvette Raymond, Shavi Fernando, Ben W Mol

|Apr 16, 2025
Simplified First-Trimester Fetal Cardiac Screening Protocol for Low-Risk Pregnancies: Enhancing Efficiency and Accuracy.

Vanessa Pincham, Andrew McLennan, Jonathan Forsey

|Feb 21, 2025
Strategies to Detect Chromosomal Anomalies Not Identified by NIPT.

Fergus Scott, May Phoo Han, Ana Elizabeth Gomes de Melo Tavares Ferreira

|Jan 18, 2025
Combined first-trimester screening for preterm small-for-gestational-age infants: Australian multicenter clinical feasibility study.

R J Selvaratnam, D L Rolnik, M Setterfield

|Jan 04, 2025
How Useful is Nuchal Translucency in Detecting Chromosomal Abnormalities Missed by Genome-Wide NIPT and What Measurement Threshold Should Be Used?

May Phoo Han, Ana Elizabeth Gomes de Melo Tavares Ferreira, James Elhindi

|Oct 28, 2024
Validation of Fetal Medicine Foundation charts for fetal growth in twins: nationwide Danish cohort study.

S E Kristensen, A Wright, D Wright

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Frequent Collaborators

8 joint publications

Fergus Scott

3 joint publications

Maria-Elisabeth Smet

2 joint publications

Daniel L Rolnik

2 joint publications

Jon Hyett