Gianluca Caridi

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Gian Marco GhiggeriU.O.C. Nefrologia, Dialisi e Trapianto, Istituto Giannina GasliniEmail verificata su ospedale-gaslini.ge.it
Francesco Scolaricattedra di nefrologia università di bresciaEmail verificata su unibs.it
Simone Sanna-CherchiDivision of Nephrology, Columbia UniversityEmail verificata su columbia.edu
R RavazzoloProfessore di Genetica, Università di Genova, Istituto G. GasliniEmail verificata su unige.it
Monica GallianoFull Professor of Biochemistry, Department of Molecular Medicine, University of Pavia, ItalyEmail verificata su unipv.it
Ali G. GharaviProfessor of Medicine & Chair, Department of Medicine, Columbia UniversityEmail verificata su columbia.edu
Giovanni CandianoIstituto Giannina Gaslini IRCCS - GenovaEmail verificata su ospedale-gaslini.ge.it
Antonio AmorosoProfessor of Medical Genetics, University of TurinEmail verificata su immunogenetica.net
Lorenzo MinchiottiProfessore di Biochimica Università di PaviaEmail verificata su unipv.it
Pietro Ravani, MD, PhD, Professor of...Cumming School of Medicine, University of CalgaryEmail verificata su ucalgary.ca
Giorgio CasariVita-Salute San Raffaele University and San Raffaele Scientific InstituteEmail verificata su hsr.it
Maddalena GiganteBiologist, University of Foggia, University of BariEmail verificata su asl.bari.it
Andrea AngelettiMount Sinai NephrologyEmail verificata su studio.unibo.it
Loreto GesualdoProfessore Ordinario di NefrologiaEmail verificata su uniba.it
Marco SeriProfessore di Genetica Medica, Università di BolognaEmail verificata su unibo.it
Fabrizio GinevriIstituto G Gaslini, UOC Nefrologia, dialisi e trapiantoEmail verificata su ospedale-gaslini.ge.it
Luca MusanteAssistant Professor of Research, University of Virginia, Charlottesville, VAEmail verificata su hscmail.mcc.virginia.edu
Enrico VerrinaIstituto Giannina Gaslini IRCCSEmail verificata su gaslini.org
Elisa BenettiPediatric Nephrology, Padua University HospitalEmail verificata su aopd.veneto.it
Giovanni MontiniUOC Nefrologia, Dialisi e Trapianto Pediatrico - Università delgi Studi di Milano - FondazioneEmail verificata su unimi.it

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Gianluca Caridi

Istituto Giannina Gaslini IRCCS

Email verificata su gaslini.org - Home page

Genetics of Kidney Disease


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens K Kiryluk, Y Li, F Scolari, S Sanna-Cherchi, M Choi, M Verbitsky, D Fasel, ... Nature genetics 46 (11), 1187-1196, 2014	657	2014
Renal outcome in patients with congenital anomalies of the kidney and urinary tract S Sanna-Cherchi, P Ravani, V Corbani, S Parodi, R Haupt, G Piaggio, ... Kidney international 76 (5), 528-533, 2009	464	2009
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23 AG Gharavi, Y Yan, F Scolari, FP Schena, GM Frasca, GM Ghiggeri, ... Nature genetics 26 (3), 354-357, 2000	445	2000
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. M Seri, R Cusano, S Gangarossa, G Caridi, D Bordo, L Nigro, ... Nature genetics 26 (1), 103-105, 2000	401	2000
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement F Diomedi-Camassei, S Di Giandomenico, FM Santorelli, G Caridi, ... Journal of the American Society of Nephrology 18 (10), 2773-2780, 2007	376	2007
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics L Rampoldi, G Caridi, D Santon, F Boaretto, I Bernascone, G Lamorte, ... Human molecular genetics 12 (24), 3369-3384, 2003	276	2003
Copy-number disorders are a common cause of congenital kidney malformations S Sanna-Cherchi, K Kiryluk, KE Burgess, M Bodria, MG Sampson, ... The American Journal of Human Genetics 91 (6), 987-997, 2012	253	2012
Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis G Caridi, R Bertelli, A Carrea, M Di Duca, P Catarsi, M Artero, M Carraro, ... Journal of the American Society of Nephrology 12 (12), 2742-2746, 2001	252	2001
Broadening the spectrum of diseases related to podocin mutations G Caridi, R Bertelli, M Di Duca, M Dagnino, F Emma, AO Muda, F Scolari, ... Journal of the American Society of Nephrology 14 (5), 1278-1286, 2003	233	2003
AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis CM Louie, G Caridi, VS Lopes, F Brancati, A Kispert, MA Lancaster, ... Nature genetics 42 (2), 175-180, 2010	209	2010
Whole-exome sequencing in adults with chronic kidney disease: a pilot study S Lata, M Marasa, Y Li, DA Fasel, E Groopman, V Jobanputra, H Rasouly, ... Annals of internal medicine 168 (2), 100-109, 2018	199	2018
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin R Bertelli, F Ginevri, G Caridi, M Dagnino, S Sandrini, M Di Duca, F Emma, ... American Journal of Kidney Diseases 41 (6), 1314-1321, 2003	195	2003
Genetic approaches to human renal agenesis/hypoplasia and dysplasia S Sanna-Cherchi, G Caridi, PL Weng, F Scolari, F Perfumo, AG Gharavi, ... Pediatric nephrology 22, 1675-1684, 2007	185	2007
Genotype–phenotype associations in WT1 glomerulopathy BS Lipska, B Ranchin, P Iatropoulos, J Gellermann, A Melk, F Ozaltin, ... Kidney international 85 (5), 1169-1178, 2014	164	2014
Uromodulin storage diseases: clinical aspects and mechanisms F Scolari, G Caridi, L Rampoldi, R Tardanico, C Izzi, D Pirulli, A Amoroso, ... American journal of kidney diseases 44 (6), 987-999, 2004	164	2004
CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS) M Gigante, P Pontrelli, E Montemurno, L Roca, F Aucella, R Penza, ... Nephrology Dialysis Transplantation 24 (6), 1858-1864, 2009	155	2009
NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms G Caridi, F Perfumo, GM Ghiggeri Pediatric research 57 (7), 54-61, 2005	155	2005
Mutations in DSTYK and Dominant Urinary Tract Malformations S Sanna-Cherchi, RV Sampogna, N Papeta, KE Burgess, SN Nees, ... New England Journal of Medicine 369 (7), 621-629, 2013	151	2013
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor–dependent idiopathic nephrotic syndrome P Ravani, A Ponticelli, C Siciliano, A Fornoni, A Magnasco, F Sica, ... Kidney international 84 (5), 1025-1033, 2013	142	2013
Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome) GM Ghiggeri, G Caridi, U Magrini, A Sessa, A Savoia, M Seri, A Pecci, ... American Journal of Kidney Diseases 41 (1), 95-104, 2003	130	2003

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