Simone Sanna-Cherchi
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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
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
Diagnostic utility of exome sequencing for kidney disease
EE Groopman, M Marasa, S Cameron-Christie, S Petrovski, VS Aggarwal, ...
New England Journal of Medicine 380 (2), 142-151, 2019
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
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 genetics 8 (6), e1002765, 2012
Scara5 is a ferritin receptor mediating non-transferrin iron delivery
JY Li, N Paragas, RM Ned, A Qiu, M Viltard, T Leete, IR Drexler, X Chen, ...
Developmental cell 16 (1), 35-46, 2009
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
Isolated polycystic liver disease genes define effectors of polycystin-1 function
W Besse, K Dong, J Choi, S Punia, SV Fedeles, M Choi, AR Gallagher, ...
The Journal of clinical investigation 127 (5), 1772-1785, 2017
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ...
Nature genetics 51 (1), 117-127, 2019
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
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
Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract
AT van der Ven, DM Connaughton, H Ityel, N Mann, M Nakayama, J Chen, ...
Journal of the American Society of Nephrology: JASN 29 (9), 2348, 2018
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
α–Intercalated cells defend the urinary system from bacterial infection
N Paragas, R Kulkarni, M Werth, KM Schmidt-Ott, C Forster, R Deng, ...
The Journal of clinical investigation 124 (7), 2963-2976, 2014
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
Genetic drivers of kidney defects in the DiGeorge syndrome
E Lopez-Rivera, YP Liu, M Verbitsky, BR Anderson, VP Capone, EA Otto, ...
New England Journal of Medicine 376 (8), 742-754, 2017
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort
R Thomas, S Sanna-Cherchi, BA Warady, SL Furth, FJ Kaskel, ...
Pediatric nephrology 26, 897-903, 2011
Clinical implications of the solitary functioning kidney
R Westland, MF Schreuder, JB Van Goudoever, S Sanna-Cherchi, ...
Clinical journal of the American Society of Nephrology: CJASN 9 (5), 978, 2014
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
J Xie, L Liu, N Mladkova, Y Li, H Ren, W Wang, Z Cui, L Lin, X Hu, X Yu, ...
Nature communications 11 (1), 1600, 2020
Genetic basis of human congenital anomalies of the kidney and urinary tract
S Sanna-Cherchi, R Westland, GM Ghiggeri, AG Gharavi
The Journal of clinical investigation 128 (1), 4-15, 2018
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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