Shabbir Moochhala

The National Registry of Rare Kidney Diseases (RaDaR): design, recruitment, and cross-sectional analyses of 25,880 adults and children with rare kidney diseases in the UK

Austin Waters, A. Turner, D. Bockenhauer, 2023, medRxiv.

Genetic variants predisposing to increased risk of kidney stone disease

D. Smelser, Shabbir Moochhala, Sarah Howles, 2024, medRxiv.

Rare variants in SLC34A3 explain missing heritability of urinary stone disease

D. Bockenhauer, S. Moochhala, O. Sadeghi-Alavijeh, 2022, medRxiv.

Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort

P. Goggolidou, Leonard Woodward, H. Cockerill, 2024, Kidney international reports.

Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope

B. Knebelmann, J. Bacchetta, J. Groothoff, 2023, Nature Reviews Nephrology.