Ahram D, Lim T, Ke J, Jin G, Verbitsky M, Bodria M, Kil B, Chatterjee D, Piva S, Marasa M, Zhang J, Cocchi E, Caridi G, Gucev Z, Lozanovski V, Pisani I, Izzi C, Savoldi G, Gnutti B, Capone V, Morello W, Guarino S, Esposito P, Lambert S, Radhakrishnan J, Appel G, Uy N, Rao M, Canetta P, Bomback A, Nestor J, Hays T, Cohen D, Finale C, van Wijk J, La Scola C, Baraldi O, Tondolo F, Di Renzo D, Jamry-Dziurla A, Pezzutto A, Manca V, Mitrotti A, Santoro D, Conti G, Martino M, Giordano M, Gesualdo L, Zibar L, Masnata G, Bonomini M, Alberti D, La Manna G, Caliskan Y, Ranghino A, Marzuillo P, Kiryluk K, Krzemień G, Miklaszewska M, Lin F, Montini G, Scolari F, Fiaccadori E, Arapović A, Saraga M, McKiernan J, Alam S, Zaniew M, Szczepańska M, Szmigielska A, Sikora P, Drożdż D, Mizerska-Wasiak M, Mane S, Lifton R, Tasic V, Latos-Bielenska A, Gharavi A, Ghiggeri G, Materna-Kiryluk A, Westland R, Sanna-Cherchi S. Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis. Journal Of The American Society Of Nephrology 2023, 34: 1105-1119. PMID: 36995132, PMCID: PMC10278788, DOI: 10.1681/asn.0000000000000132.Peer-Reviewed Original Research