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1. The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease

2. Phenotypic outcomes of PKD1 compared with non-PKD1 genetically confirmed autosomal dominant polycystic kidney disease

3. Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational study

4. Donor genetic burden for cerebrovascular risk and kidney transplant outcome

6. A Novel Monoallelic ALG5 Variant Causing Late-Onset ADPKD and Tubulointerstitial Fibrosis

7. Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease

9. An intermediate-effect size variant in UMOD confers risk for chronic kidney disease

10. High frequency and mortality of head and neck malignancy in organ transplant recipients in Ireland – A national cohort study

12. The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project

13. Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype

15. Adult presentation of a rare mitochondrial tRNA Val gene mutation—an expanding clinical phenotype.

16. Pilot Randomized Controlled Trial of a Standard Versus a Modified Low-Phosphorus Diet in Hemodialysis Patients

17. Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations

18. #1196 C3G and ic-MPGN across the life span: findings from the European Rare Kidney Disease Registry

21. The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population

22. Monogenic causes of chronic kidney disease in adults

24. Familial Variability of Disease Severity in Adult Patients With ADPKD

31. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

32. Genome-Wide Association Meta-Analysis for Acute Rejection of Kidney Transplants

36. An intermediate-effect size variant in UMOD confers risk for chronic kidney disease

39. A population-based comparison of organ transplant recipients in whom cutaneous squamous cell develops versus those in whom basal cell carcinoma develops

40. Genome-Wide Association Meta-Analysis Identifies Novel Loci for Kidney Failure

41. An intermediate-effect size variant in UMOD confers risk for chronic kidney disease

46. Is Bigger Better? Living Donor Kidney Volume as Measured by the Donor CT Angiogram in Predicting Donor and Recipient eGFR after Living Donor Kidney Transplantation

47. A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

48. A population-based comparison of organ transplant recipients in whom cutaneous squamous cell develops versus those in whom basal cell carcinoma develops

50. Contributors

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