Liam W. Scott
Parkville, VIC 3052, Australia
Last Updated: 09/26/2026
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Found 8 publications
G Protein: β-Arrestin Bias Confers Differential Regulation of Gαq Signaling by GPR17 Antagonists.
Journal: ACS chemical neuroscience
Published: November 12, 2025
Genetic Risk of Reticular Pseudodrusen in Age-Related Macular Degeneration: HTRA1 /lncRNA BX842242.1 dominates, with no evidence for Complement Cascade involvement.
Journal: medRxiv : the preprint server for health sciences
Published: October 14, 2024
HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvement.
Journal: Nature communications
Published: October 12, 2024
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
Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone.
Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone.
Journal: Annals of clinical and translational neurology
Published: February 02, 2024
Multi-omic spatial effects on high-resolution AI-derived retinal thickness.
Journal: Nature communications
Published: January 09, 2024
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.
Journal: American journal of human genetics
Published: October 12, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026