Yvonne J. Hort
Sydney, NSW, Australia
Last Updated: 09/26/2026
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Found 10 publications
Targeted sequencing and iterative assembly of near-complete genomes.
Journal: Nature communications
Published: May 28, 2025
PKD1 5'UTR variants are a rare cause of disease in ADPKD and suggest a new focus for therapeutic development.
Journal: European journal of human genetics : EJHG
Published: March 30, 2025
Somatic mutation in autosomal dominant polycystic kidney disease revealed by deep sequencing human kidney cysts.
Journal: NPJ genomic medicine
Published: December 19, 2023
Atypical splicing variants in PKD1 explain most undiagnosed typical familial ADPKD.
Journal: NPJ genomic medicine
Published: December 20, 2022
Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing.
Journal: European journal of human genetics : EJHG
Published: March 31, 2020
Role of neuropeptide Y (NPY) in the differentiation of Trpm-5-positive olfactory microvillar cells.
Journal: Neuropeptides
Published: November 21, 2017
Whole-genome sequencing overcomes pseudogene homology to diagnose autosomal dominant polycystic kidney disease.
Journal: European journal of human genetics : EJHG
Published: December 16, 2015
Neuropeptide Y and peptide YY have distinct roles in adult mouse olfactory neurogenesis.
Journal: Journal of neuroscience research
Published: September 25, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026