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Essays in Biochemistry|November 8, 2019
DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disordersDavid E Godler, David J AmorDevelopmental Medicine and Child Neurology|August 8, 2018
Epigenetics of fragile X syndrome and fragile X-related disordersClaudine M Kraan, David E Godler, David J AmorGenetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2026
Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infantsDavid E Godler, Ling Ling, Dinusha Gamage, et al.International Journal of Molecular Sciences|July 14, 2023
Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X SyndromeDavid E Godler, Yoshimi Inaba, Minh Q Bui, et al.Journal of Neurodevelopmental Disorders|August 8, 2018
Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromesEmma K Baker, David E Godler, Minh Bui, et al.Genes|July 8, 2020
Growth Trajectories in Genetic Subtypes of Prader-Willi SyndromeDaisy A Shepherd, Niels Vos, Susan M Reid, et al.Genes|September 28, 2021
Special Issue: Genetics of Prader-Willi SyndromeDavid E Godler, Merlin G ButlerGenes|June 28, 2023
Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023David E Godler, William T BrownThe Journal of Molecular Diagnostics : JMD|July 5, 2011
FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 allelesDavid E Godler, Howard R Slater, Quang M Bui, et al.Current Opinion in Psychiatry|January 13, 2025
Genetics of Prader-Willi and Angelman syndromes: 2024 updateDavid E Godler, Deepan Singh, Merlin G ButlerPageof 27