Articles with public access mandates - Gianluca CaridiLearn more
Not available anywhere: 5
Mutational Spectrum of CYP24A1 Gene in a Cohort of Italian Patients with Idiopathic Infantile Hypercalcemia
M Gigante, L Santangelo, S Diella, G Caridi, L Argentiero, ...
Nephron 133 (3), 193-204, 2016
Mandates: Government of Italy
Low-dose ofatumumab for multidrug-resistant nephrotic syndrome in children: a randomized placebo-controlled trial
P Ravani, I Pisani, M Bodria, G Caridi, ML Degl’Innocenti, GM Ghiggeri
Pediatric Nephrology 35, 997-1003, 2020
Mandates: Government of Italy
Urine proteome analysis in Dent's disease shows high selective changes potentially involved in chronic renal damage
L Santucci, G Candiano, F Anglani, M Bruschi, E Tosetto, D Cremasco, ...
Journal of Proteomics 130, 26-32, 2016
Mandates: Government of Italy
A novel insertion (c. 1098dupT) in the albumin gene causes analbuminemia in a consanguineous family
G Caridi, F Lugani, B Rigat, P Van den Abeele, V Layet, MS Gavard, ...
European journal of medical genetics 62 (2), 144-148, 2019
Mandates: Government of Italy
Atypical presentation of Dent disease in a patient with interstitial Xp11. 22 deletion
S Drovandi, M Servetti, A Angeletti, A Puliti, P Ronchetto, E Tassano, ...
Journal of nephrology 34 (6), 2111-2115, 2021
Mandates: Government of Italy
Available somewhere: 41
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, UK …
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
Mandates: US National Institutes of Health, Fondazione Telethon, Italy, British Heart …
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
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
Mandates: US National Institutes of Health
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
Mandates: German Research Foundation, Hungarian Academy of Sciences
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
Mandates: US National Institutes of Health, Howard Hughes Medical Institute …
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
Mandates: US National Institutes of Health, Government of Italy
Novel TMEM67 mutations and genotype‐phenotype correlates in meckelin‐related ciliopathies
M Iannicelli, F Brancati, S Mougou‐Zerelli, A Mazzotta, S Thomas, ...
Human mutation 31 (5), E1319-E1331, 2010
Mandates: US National Institutes of Health, National Institute of Health and Medical …
Genetic screening in adolescents with steroid-resistant nephrotic syndrome
BS Lipska, P Iatropoulos, R Maranta, G Caridi, F Ozaltin, A Anarat, A Balat, ...
Kidney international 84 (1), 206-213, 2013
Mandates: German Research Foundation
Anti-CD20 antibodies for idiopathic nephrotic syndrome in children
P Ravani, A Bonanni, R Rossi, G Caridi, GM Ghiggeri
Clinical Journal of the American Society of Nephrology 11 (4), 710-720, 2016
Mandates: Government of Italy
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
K Kiryluk, E Sanchez-Rodriguez, XJ Zhou, F Zanoni, L Liu, N Mladkova, ...
Nature genetics 55 (7), 1091-1105, 2023
Mandates: US National Science Foundation, US National Institutes of Health, US …
Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype
TW Hurd, EA Otto, E Mishima, HY Gee, H Inoue, M Inazu, H Yamada, ...
Journal of the American Society of Nephrology 24 (6), 967-977, 2013
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Doris …
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract
S Gimelli, G Caridi, S Beri, K McCracken, R Bocciardi, P Zordan, ...
Human mutation 31 (12), 1352-1359, 2010
Mandates: Fondazione Telethon, Italy
A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13
PL Weng, S Sanna-Cherchi, T Hensle, E Shapiro, A Werzberger, G Caridi, ...
Journal of the American Society of Nephrology 20 (7), 1633-1640, 2009
Mandates: US National Institutes of Health
COVID-19 in children with nephrotic syndrome on anti-CD20 chronic immunosuppression
A Angeletti, S Drovandi, F Sanguineri, M Santaniello, G Ferrando, ...
Clinical Journal of the American Society of Nephrology 15 (10), 1494-1495, 2020
Mandates: Government of Italy
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