Gian Marco Ghiggeri
Gian Marco Ghiggeri
U.O.C. Nefrologia, Dialisi e Trapianto, Istituto Giannina Gaslini
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Blue silver: a very sensitive colloidal Coomassie G‐250 staining for proteome analysis
G Candiano, M Bruschi, L Musante, L Santucci, GM Ghiggeri, ...
Electrophoresis 25 (9), 1327-1333, 2004
Genome-wide association study identifies susceptibility loci for IgA nephropathy
AG Gharavi, K Kiryluk, M Choi, Y Li, P Hou, J Xie, S Sanna-Cherchi, ...
Nature genetics 43 (4), 321-327, 2011
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
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes
M Seri, R Cusano, S Gangarossa, G Caridi, D Bordo, CL Nigro, ...
Nature genetics 26 (1), 103-105, 2000
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single …
M Seri, A Pecci, F Di Bari, R Cusano, M Savino, E Panza, A Nigro, P Noris, ...
Medicine 82 (3), 203-215, 2003
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
Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study
S Weber, V Moriniere, T Knüppel, M Charbit, J Dusek, GM Ghiggeri, ...
Journal of the American Society of Nephrology 17 (10), 2864-2870, 2006
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
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
Autoimmunity in membranous nephropathy targets aldose reductase and SOD2
M Prunotto, ML Carnevali, G Candiano, C Murtas, M Bruschi, E Corradini, ...
Journal of the American Society of Nephrology 21 (3), 507-519, 2010
The rediscovery of uromodulin (Tamm–Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease
L Rampoldi, F Scolari, A Amoroso, GM Ghiggeri, O Devuyst
Kidney international 80 (4), 338-347, 2011
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
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
Circulating suPAR in two cohorts of primary FSGS
C Wei, H Trachtman, J Li, C Dong, AL Friedman, JJ Gassman, ...
Journal of the American Society of Nephrology 23 (12), 2051-2059, 2012
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
The molecular biology of Rhizobium-legume symbiosis
DPS Verma
Prediction and treatment of recurrent focal segmental glomerulosclerosis after renal transplantation in children
R Dall'Amico, GM Ghiggeri, M Carraro, M Artero, L Ghio, E Zamorani, ...
American Journal of Kidney Diseases 34 (6), 1048-1055, 1999
SIX2 and BMP4 mutations associate with anomalous kidney development
S Weber, JC Taylor, P Winyard, KF Baker, J Sullivan-Brown, R Schild, ...
Journal of the American Society of Nephrology 19 (5), 891-903, 2008
Short-term effects of rituximab in children with steroid-and calcineurin-dependent nephrotic syndrome: a randomized controlled trial
P Ravani, A Magnasco, A Edefonti, L Murer, R Rossi, L Ghio, E Benetti, ...
Clinical Journal of the American Society of Nephrology 6 (6), 1308-1315, 2011
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
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