Timothy J. Furlong
Darlinghurst, NSW, Australia
Last Updated: 09/26/2026
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Found 22 publications
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
Pylephlebitis of the inferior mesenteric vein: a rare complication of sigmoid diverticulitis.
Journal: ANZ journal of surgery
Published: September 29, 2021
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
Is the use of metformin in patients undergoing dialysis hazardous for life? A systematic review of the safety of metformin in patients undergoing dialysis.
Journal: British journal of clinical pharmacology
Published: June 03, 2019
Population data improves variant interpretation in autosomal dominant polycystic kidney disease.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 13, 2018
Could metformin be used in patients with advanced chronic kidney disease?
Journal: Diabetes, obesity & metabolism
Published: October 06, 2016
Pharmacokinetics of Metformin in Patients Receiving Regular Hemodiafiltration.
Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation
Published: February 28, 2016
Whole-genome sequencing overcomes pseudogene homology to diagnose autosomal dominant polycystic kidney disease.
Journal: European journal of human genetics : EJHG
Published: December 16, 2015
Last Updated: 09/26/2026