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2. Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

4. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

5. Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

6. Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology

7. Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

8. Mouse and human studies support DSTYKloss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies

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