Melanie Y. Chan - Publications

KDIGO 2025 Clinical Practice Guideline for ADPKD: a commentary on intracranial aneurysms and other vascular manifestations from the ERA Working Group Genes & Kidney.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: May 01, 2026

Letter to the Editor re: "Genomic testing in pediatric urology: Implications for diagnosis and management".

Journal: Journal of pediatric urology

Published: February 04, 2026

Genetic kidney disease in adults-the pathologists' perspective.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: November 11, 2025

The Genomic Infinity Loop.

Journal: Journal of the American Society of Nephrology : JASN

Published: October 21, 2025

Genomic testing in pediatric urology: Implications for diagnosis and management.

Journal: Journal of pediatric urology

Published: October 08, 2025

Fifty Shades of Risk: Population Studies and the Genetic Architecture of Kidney Diseases.

Journal: Journal of the American Society of Nephrology : JASN

Published: September 11, 2025

The biology of congenital urinary bladder outflow obstruction.

Journal: Trends in molecular medicine

Published: July 01, 2025

FLNA ROD1 and ROD2 Domains are Implicated in Congenital Lower Urinary Tract Obstruction.

Journal: Kidney international reports

Published: December 13, 2024

Commentary: Tolvaptan for Autosomal Dominant Polycystic Kidney Disease (ADPKD) - an update.

Journal: BMC nephrology

Published: November 05, 2024

Quantifying APOL1, Human Leukocyte Antigen, and Other Genetic Contributions to Unexplained Kidney Failure.

Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation

Published: October 23, 2024

Using genomics to understand severe COVID-19.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: October 04, 2023

Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease.

Journal: Kidney international

Published: December 04, 2022