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American Journal of Human Genetics|February 3, 2007
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33Simone Sanna-Cherchi, Gianluca Caridi, Patricia L Weng, et al.Frontiers in Immunology|April 28, 2022
Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The "Fil Rouge" of Treg Between IPEX Features and Other Clinical Entities?Micaela Gentile, Maurizio Miano, Paola Terranova, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 8, 2018
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndromeSara Nuovo, Laura Fuiano, Alessia Micalizzi, et al.Journal of the American Society of Nephrology : JASN|May 16, 2009
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13Patricia L Weng, Simone Sanna-Cherchi, Terry Hensle, et al.Kidney International|June 7, 2013
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndromePietro Ravani, Alessandro Ponticelli, Chiara Siciliano, et al.Kidney International|June 24, 2011
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndromeSimone Sanna-Cherchi, Katelyn E Burgess, Shannon N Nees, et al.Kidney International|January 10, 2014
Genotype-phenotype associations in WT1 glomerulopathyBeata S Lipska, Bruno Ranchin, Paraskevas Iatropoulos, et al.Transplantation Direct|January 22, 2026
Combined Anti-CD20/Anti-CD38 Therapy in Posttransplant Focal Segmental Glomerulosclerosis Recurrence: A Retrospective, International, Multicenter StudyPaolo Cravedi, Umberto Maggiore, Gabriele Mortari, et al.Nature Genetics|January 19, 2010
AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisisCarrie M Louie, Gianluca Caridi, Vanda S Lopes, et al.Annals of Internal Medicine|December 6, 2017
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot StudySneh Lata, Maddalena Marasa, Yifu Li, et al.Pageof 11