Dinusha Gamage

Parkville, VIC, Australia

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 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

Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow.

Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow.

Journal: JAMA network open
Published: January 04, 2022

Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX.

Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX.

Journal: Genes
Published: April 08, 2021

Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.

Fragile X syndrome full mutation in cognitively normal male identified as part of an Australian reproductive carrier screening program.

Journal: American journal of medical genetics. Part A
Published: September 18, 2020

DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome.

DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome.

Journal: International journal of molecular sciences
Published: September 10, 2020

Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders.

Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders.

Journal: Translational psychiatry
Published: April 18, 2020
Showing 1-8 of 8

Last Updated: 09/26/2026