Fionnuala Mone

21PUBLICATIONS
84CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsPsychosocial aspects of childbirth and perinatal mental healthCardiology (incl. cardiovascular diseases)
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Publications (21)

|Jun 12, 2026
A Novel Approach to Interrogating Whole Genome Sequencing Data to Optimise Clinical Utility.

|Jul 08, 2025
Performance of international phenotypic criteria for prenatal exome sequencing: systematic review and comparative diagnostic accuracy study using historical individual participant data.

K Reilly, D L Rolnik, S Allen

|Feb 17, 2025
Incremental yield of exome sequencing over standard prenatal testing in structurally normal fetuses: systematic review and meta-analysis.

A Sotiriadis, E Demertzidou, A Ververi

|Oct 11, 2024
The Challenges of Performing Exome Sequencing in Structurally Normal Fetuses.

Natalie Chandler, Muriel Holder-Espinasse, Fionnuala Mone

|Sep 10, 2024
Development and validation of prediction models for fetal growth restriction and birthweight: an individual participant data meta-analysis.

John Allotey, Lucinda Archer, Dyuti Coomar

|Jul 31, 2024
Pitfalls of systematic reviews and meta-analyses to assess the clinical utility of genomic investigations in prenatal diagnosis.

F Mone, D L Rolnik, A Sotiriadis

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Frequent Collaborators

9 joint publications

Mark D Kilby

3 joint publications

Natalie J Chandler

3 joint publications

Asma Khalil

3 joint publications

A Sotiriadis