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 | 254 | 2012 |
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 | 194 | 2019 |
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 | 171 | 2007 |
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 | 148 | 2013 |
A prospective multi-center quality improvement initiative (NINJA) indicates a reduction in nephrotoxic acute kidney injury in hospitalized children SL Goldstein, D Dahale, ES Kirkendall, T Mottes, H Kaplan, S Muething, ... Kidney international 97 (3), 580-588, 2020 | 136 | 2020 |
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 | 95 | 2011 |
Angiotensin II Type 1 receptor antibodies are associated with inflammatory cytokines and poor clinical outcomes in pediatric kidney transplantation MH Pearl, Q Zhang, MFP Diaz, J Grotts, M Rossetti, D Elashoff, ... Kidney international 93 (1), 260-269, 2018 | 70 | 2018 |
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 | 55 | 2009 |
Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33 S Sanna-Cherchi, G Caridi, PL Weng, M Dagnino, M Seri, A Konka, ... The American Journal of Human Genetics 80 (3), 539-549, 2007 | 50 | 2007 |
COVID‐19 in pediatric kidney transplantation: the improving renal outcomes collaborative C Varnell Jr, LA Harshman, L Smith, C Liu, S Chen, S Al‐Akash, ... American journal of transplantation 21 (8), 2740-2748, 2021 | 46 | 2021 |
Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings JH Pelletier, KR Kumar, R Engen, A Bensimhon, JD Varner, MN Rheault, ... Pediatric Nephrology 33, 1773-1780, 2018 | 41 | 2018 |
Endothelin type A receptor antibodies are associated with angiotensin II type 1 receptor antibodies, vascular inflammation, and decline in renal function in pediatric kidney … MH Pearl, L Chen, R ElChaki, D Elashoff, DW Gjertson, M Rossetti, ... Kidney international reports 5 (11), 1925-1936, 2020 | 31 | 2020 |
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 | 30 | 2023 |
State M, Scolari F, Ravazzolo R, Kiryluk K, Al-Awqati Q, D’Agati VD, Drummond IA, Tasic V, Lifton RP, Ghiggeri GM, Gharavi AG: Mutations in DSTYK and dominant urinary tract … S Sanna-Cherchi, RV Sampogna, N Papeta, KE Burgess, SN Nees, ... N Engl J Med 369 (7), 621-629, 2013 | 30 | 2013 |
Endotoxin-neutralizing capacity of serum from cardiac surgical patients E Bennett-Guerrero, GR Barclay, PL Weng, CA Bodian, DE Feierman, ... Journal of cardiothoracic and vascular anesthesia 15 (4), 451-454, 2001 | 28 | 2001 |
An automated histological classification system for precision diagnostics of kidney allografts D Yoo, V Goutaudier, G Divard, J Gueguen, BC Astor, O Aubert, ... Nature medicine 29 (5), 1211-1220, 2023 | 23 | 2023 |
Diagnosis, treatment, and outcomes in children with congenital nephrogenic diabetes insipidus: a pediatric nephrology research consortium study C D'Alessandri-Silva, M Carpenter, R Ayoob, J Barcia, A Chishti, ... Frontiers in pediatrics 7, 550, 2020 | 22 | 2020 |
Cytokine profiles associated with angiotensin II type 1 receptor antibodies MH Pearl, J Grotts, M Rossetti, Q Zhang, DW Gjertson, P Weng, D Elashoff, ... Kidney international reports 4 (4), 541-550, 2019 | 22 | 2019 |
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis PL Weng, AJ Majmundar, K Khan, TY Lim, S Shril, G Jin, J Musgrove, ... The American Journal of Human Genetics 108 (2), 357-367, 2021 | 18 | 2021 |
Copy number variant analysis and genome-wide association study identify loci with large effect for vesicoureteral reflux M Verbitsky, P Krithivasan, E Batourina, A Khan, SE Graham, M Marasà, ... Journal of the American Society of Nephrology 32 (4), 805-820, 2021 | 17 | 2021 |