Matthew Hunter

6PUBLICATIONS
38CO-AUTHORS
Infant and child healthNeurology and neuromuscular diseasesMicroelectromechanical systems (MEMS)Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (6)

|May 04, 2026
KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severity.

|Nov 11, 2022
The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome.

Andrew Paul Fennell, Anne Elizabeth Baxter, Samuel Frank Berkovic

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

Emma K Baker, Marta Arpone, Minh Bui

|Oct 22, 2020
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome.

Claudine M Kraan, Emma K Baker, Marta Arpone

|Jul 12, 2019
The changing face of clinical genetics service delivery in the era of genomics: a framework for monitoring service delivery and data from a comprehensive metropolitan general genetics service.

Andrew Paul Fennell, Matthew Frank Hunter, Gregory Philip Corboy

|Jun 09, 2018
Prenatal Diagnosis of Fragile X Syndrome in a Twin Pregnancy Complicated by a Complete Retraction.

Yael Prawer, Matthew Hunter, Sara Cronin

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Frequent Collaborators

2 joint publications

Marta Arpone

2 joint publications

Minh Bui

2 joint publications

Claudine M Kraan

2 joint publications

David J Amor