Justin L. Read

Melbourne, VIC 3004, Australia

Last Updated: 09/26/2026

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Found 16 publications

Increased Ih Current Is Associated with Reduced Hippocampal CA1 Excitability in a Mouse Model of Multiple Sclerosis.

Increased Ih Current Is Associated with Reduced Hippocampal CA1 Excitability in a Mouse Model of Multiple Sclerosis.

Journal: eNeuro

Published: May 20, 2026

DNA Repair Pathway Variants Are Enriched in Individuals with Biallelic AAGGG CANVAS and RFC1-Related Disease.

DNA Repair Pathway Variants Are Enriched in Individuals with Biallelic AAGGG CANVAS and RFC1-Related Disease.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: February 19, 2026

Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Journal: Nature communications

Published: October 17, 2024

A prospective trial comparing programmable targeted long-read sequencing and short-read genome sequencing for genetic diagnosis of cerebellar ataxia.

A prospective trial comparing programmable targeted long-read sequencing and short-read genome sequencing for genetic diagnosis of cerebellar ataxia.

Journal: Genome research

Published: June 11, 2024

Novel Insights into Changes in Gene Expression within the Hypothalamus in Two Asthma Mouse Models: A Transcriptomic Lung-Brain Axis Study.

Novel Insights into Changes in Gene Expression within the Hypothalamus in Two Asthma Mouse Models: A Transcriptomic Lung-Brain Axis Study.

Journal: International journal of molecular sciences

Published: May 02, 2024

Neuroanatomical distribution of fluorophores within adult RXFP3 Cre-tdTomato/YFP mouse brain.

Neuroanatomical distribution of fluorophores within adult RXFP3 Cre-tdTomato/YFP mouse brain.

Journal: Biochemical pharmacology

Published: January 14, 2024

A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Journal: Nature communications

Published: September 29, 2023

Challenges facing repeat expansion identification, characterisation, and the pathway to discovery.

Challenges facing repeat expansion identification, characterisation, and the pathway to discovery.

Journal: Emerging topics in life sciences

Published: July 31, 2023

An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14.

An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14.

Journal: American journal of human genetics

Published: June 02, 2023

An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14.

An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14.

Journal: American journal of human genetics

Published: October 12, 2022

Characterization of microglial transcriptomes in the brain and spinal cord of mice in early and late experimental autoimmune encephalomyelitis using a RiboTag strategy.

Characterization of microglial transcriptomes in the brain and spinal cord of mice in early and late experimental autoimmune encephalomyelitis using a RiboTag strategy.

Journal: Scientific reports

Published: November 09, 2020

Increased Excitatory Synaptic Transmission Associated with Adult Seizure Vulnerability Induced by Early-Life Inflammation in Mice.

Increased Excitatory Synaptic Transmission Associated with Adult Seizure Vulnerability Induced by Early-Life Inflammation in Mice.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: October 04, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026