John A. Sayer
Central Parkway
Newcastle Upon Tyne, ENG, United Kingdom
Newcastle Upon Tyne, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 220 publications
Role and relevance of genetic testing in patients with kidney stones: a review from EAU Section of Endourology.
Journal: Current opinion in urology
Published: June 17, 2026
A Whole Exome Sequencing and Targeted Gene Panel Approach to Identify Rare Etiologies of Pediatric Nephrotic Syndrome in Oman.
Journal: Kidney international reports
Published: June 17, 2026
Genetic Evaluation Practices in Living Kidney Donor Candidates.
Journal: Kidney international reports
Published: May 19, 2026
Genetic testing and personalized treatment for kidney stone formers.
Journal: Current opinion in urology
Published: March 14, 2026
Identification of Pathogenic PKHD1 Variants in Infants with Autosomal Recessive Polycystic Kidney Disease from the Dhofar Region, Oman.
Journal: F1000Research
Published: February 02, 2026
Anti-Glomerular Basement Membrane Nephritis Post-Renal Transplant in Alport Syndrome Patients.
Journal: Kidney360
Published: January 14, 2026
Primary hyperoxaluria type 1-current practice in the siRNA era: an ERA Genes & Kidney Working Group survey.
Journal: Clinical kidney journal
Published: December 05, 2025
Lipocalin-2 Is Induced by Uromodulin Aggregates without Affecting Kidney Disease Progression in Autosomal Dominant Tubulointerstitial Kidney Disease- UMOD.
Journal: Journal of the American Society of Nephrology : JASN
Published: November 28, 2025
Editorial: Distinct phenotype but same genotype: hints for the diversity of phenotypes in ciliopathies.
Journal: Frontiers in molecular biosciences
Published: November 24, 2025
The UK kidney association 2025 academic census: a national survey to identify workforce improvements.
Journal: BMC medical education
Published: November 23, 2025
Tackling ciliary specialization to understand phenotypic variability in human primary ciliopathies.
Journal: Journal of cell science
Published: October 27, 2025
Landscape of parental postzygotic mutations across >11,000 rare disease trios.
Journal: American journal of human genetics
Published: September 16, 2025
Last Updated: 09/26/2026