David E. Godler

50 Flemington Rd
Parkville, VIC 3052, Australia

Last Updated: 09/26/2026

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Found 62 publications

Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndrome.

Transcriptomic signatures in brain and blood related to cognitive and psychiatric phenotypes of Prader-Willi syndrome.

Journal: Scientific reports

Published: August 29, 2025

High-throughput assessment of FMR1 and SNRPN methylation-based newborn screening using IsoPure and QIAcube HT systems.

High-throughput assessment of FMR1 and SNRPN methylation-based newborn screening using IsoPure and QIAcube HT systems.

Journal: Epigenomics

Published: August 13, 2025

Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infants.

Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infants.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 29, 2025

Genomic Screening Consortium for Australian Newborns (GenSCAN).

Genomic Screening Consortium for Australian Newborns (GenSCAN).

Journal: Journal of paediatrics and child health

Published: March 19, 2025

Genetics of Prader-Willi and Angelman syndromes: 2024 update.

Genetics of Prader-Willi and Angelman syndromes: 2024 update.

Journal: Current opinion in psychiatry

Published: January 13, 2025

Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns.

Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns.

Journal: Epigenomics

Published: October 04, 2024

Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023.

Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023.

Journal: Genes

Published: May 15, 2023

Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome.

Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome.

Journal: International journal of molecular sciences

Published: May 01, 2023

Estimating the impact of Angelman syndrome on parental productivity in Australia using productivity-adjusted life years.

Estimating the impact of Angelman syndrome on parental productivity in Australia using productivity-adjusted life years.

Journal: Disability and health journal

Published: August 17, 2022

Umbilical Cord Blood Cell Clearance Post-Infusion in Immune-Competent Children with Cerebral Palsy.

Umbilical Cord Blood Cell Clearance Post-Infusion in Immune-Competent Children with Cerebral Palsy.

Journal: Cells, tissues, organs

Published: July 19, 2022

Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.

Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.

Journal: American journal of medical genetics. Part A

Published: June 15, 2022

Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders.

Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders.

Journal: Research in developmental disabilities

Published: February 09, 2022

Showing 1-12 of 62

Last Updated: 09/26/2026