Gianluca Caridi
Gianluca Caridi
Istituto Giannina Gaslini IRCCS
Verified email at gaslini.org - Homepage
TitleCited byYear
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, 2000
3652000
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, CN Lo, GM Ghiggeri, ...
Nature genetics 26 (1), 103-105, 2000
3342000
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
2612007
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, 2014
2382014
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
2262009
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
2132001
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
2002003
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
1892003
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, 2010
1572010
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
1572003
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
1212012
NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms
G Caridi, F Perfumo, GM Ghiggeri
Pediatric research 57 (5 Part 2), 54R, 2005
1202005
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
1192004
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
1132009
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 (10), 1675-1684, 2007
1122007
Identification of a new locus for medullary cystic disease, on chromosome 16p12
F Scolari, D Puzzer, A Amoroso, G Caridi, GM Ghiggeri, R Maiorca, ...
The American Journal of Human Genetics 64 (6), 1655-1660, 1999
1061999
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
1022003
Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistantnephrotic syndrome
M Carraro, G Caridi, M Bruschi, M Artero, R Bertelli, C Zennaro, ...
Journal of the American Society of Nephrology 13 (7), 1946-1952, 2002
992002
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
812013
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
812013
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