Maddalena Gigante
Maddalena Gigante
Verified email at unifg.it
Title
Cited by
Cited by
Year
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
3322014
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis
K Kiryluk, Y Li, S Sanna-Cherchi, M Rohanizadegan, H Suzuki, F Eitner, ...
PLoS Genet 8 (6), e1002765, 2012
2592012
The molecular basis of lecithin: cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families
L Calabresi, L Pisciotta, A Costantin, I Frigerio, I Eberini, P Alessandrini, ...
Arteriosclerosis, thrombosis, and vascular biology 25 (9), 1972-1978, 2005
1642005
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
1572012
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
1252009
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
962013
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome
S Sanna-Cherchi, KE Burgess, SN Nees, G Caridi, PL Weng, M Dagnino, ...
Kidney international 80 (4), 389-396, 2011
812011
TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype
M Gigante, G Caridi, E Montemurno, M Soccio, M d'Apolito, G Cerullo, ...
Clinical Journal of the American Society of Nephrology 6 (7), 1626-1634, 2011
792011
TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype
M Gigante, G Caridi, E Montemurno, M Soccio, M d'Apolito, G Cerullo, ...
Clinical Journal of the American Society of Nephrology 6 (7), 1626-1634, 2011
792011
NPHS2 Mutations in Steroid‐Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum
K Bouchireb, O Boyer, O Gribouval, F Nevo, E Huynh‐Cong, V Morinière, ...
Human mutation 35 (2), 178-186, 2014
632014
Sirolimus and proteinuria in renal transplant patients: evidence for a dose-dependent effect on slit diaphragm-associated proteins
G Stallone, B Infante, P Pontrelli, M Gigante, E Montemurno, A Loverre, ...
Transplantation 91 (9), 997-1004, 2011
632011
WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes
F Aucella, L Bisceglia, P De Bonis, M Gigante, G Caridi, G Barbano, ...
Pediatric nephrology 21 (10), 1393-1398, 2006
632006
Natural history of congenital dyserythropoietic anemia type II
A Iolascon, J Delaunay, SN Wickramasinghe, S Perrotta, M Gigante, ...
Blood, The Journal of the American Society of Hematology 98 (4), 1258-1260, 2001
622001
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations
G Caridi, M Gigante, P Ravani, A Trivelli, G Barbano, F Scolari, ...
Clinical Journal of the American Society of Nephrology 4 (6), 1065-1072, 2009
492009
Complement modulation of anti‐aging factor klotho in ischemia/reperfusion injury and delayed graft function
G Castellano, A Intini, A Stasi, C Divella, M Gigante, P Pontrelli, R Franzin, ...
American Journal of Transplantation 16 (1), 325-333, 2016
482016
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach
M Gigante, F Monno, R Roberto, N Laforgia, MB Assael, S Livolti, ...
Journal of nephrology 15 (6), 696-702, 2002
472002
Acquired lecithin: cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney disease
L Calabresi, S Simonelli, P Conca, G Busnach, M Cabibbe, L Gesualdo, ...
Journal of Internal Medicine 277 (5), 552-561, 2015
452015
DIABETES EXPERIMENTAL
JS Chan, S Abdo, A Ghosh, T Alquier, I Chenier, JG Filep, JR Ingelfinger, ...
Nephrology Dialysis Transplanation 29 (suppl_3), iii168-iii177, 2014
432014
Exome-wide association study identifies GREB1L mutations in congenital kidney malformations
S Sanna-Cherchi, K Khan, R Westland, P Krithivasan, L Fievet, ...
The American Journal of Human Genetics 101 (5), 789-802, 2017
392017
Identification of GLA gene deletions in Fabry patients by Multiplex Ligation-dependent Probe Amplification (MLPA)
A Schirinzi, M Centra, C Prattichizzo, M Gigante, M De Fabritiis, ...
Molecular genetics and metabolism 94 (3), 382-385, 2008
382008
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