Tyson L. Ware
Hobart, TAS, Australia
Last Updated: 09/26/2026
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Found 23 publications
Evidence-based multidisciplinary model of care for newborn screening in spinal muscular atrophy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 13, 2025
Development and Adaptive Function in Individuals With SCN2A-Related Disorders.
Journal: Neurology
Published: July 22, 2025
The Australian Genomics Mitochondrial Flagship: A national program delivering mitochondrial diagnoses.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 04, 2024
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformations.
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformations.
Journal: Brain communications
Published: May 29, 2023
Lysosomal alterations and decreased electrophysiological activity in CLN3 disease patient-derived cortical neurons.
Journal: Disease models & mechanisms
Published: May 10, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants.
Journal: Communications biology
Published: October 29, 2021
Novel Missense CACNA1G Mutations Associated with Infantile-Onset Developmental and Epileptic Encephalopathy.
Journal: International journal of molecular sciences
Published: July 24, 2020
Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania.
Journal: Epilepsia open
Published: April 09, 2019
Splice variant in ARX leading to loss of C-terminal region in a boy with intellectual disability and infantile onset developmental and epileptic encephalopathy.
Journal: American journal of medical genetics. Part A
Published: November 21, 2018
Australian Clinical Consensus Guideline: The diagnosis and acute management of childhood stroke.
Journal: International journal of stroke : official journal of the International Stroke Society
Published: October 05, 2018
SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy.
Journal: Neurology
Published: March 05, 2018
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Journal: American journal of human genetics
Published: June 27, 2017
Last Updated: 09/26/2026