David E Godler

14PUBLICATIONS
26CO-AUTHORS
Metabolic medicineEvolutionary computationEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Microelectromechanical systems (MEMS)
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Publications (14)

|Aug 13, 2025
High-throughput assessment of FMR1 and SNRPN methylation-based newborn screening using IsoPure and QIAcube HT systems.

Caleb Cartagena, Mohammed Alshawsh, Minh Q Bui

|Oct 04, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns.

Mohammed Alshawsh, Melissa Wake, Jozef Gecz

|Jul 14, 2023
Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome.

David E Godler, Yoshimi Inaba, Minh Q Bui

|Jun 28, 2023
Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023.

David E Godler, William T Brown

|Nov 09, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.

Emma K Baker, Marta Arpone, Minh Bui

|Sep 28, 2021
Special Issue: Genetics of Prader-Willi Syndrome.

David E Godler, Merlin G Butler

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Frequent Collaborators

8 joint publications

David J Amor

4 joint publications

Minh Q Bui

3 joint publications

Claudine M Kraan

2 joint publications

Emma K Baker