Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis A Daga, AJ Majmundar, DA Braun, HY Gee, JA Lawson, S Shril, ... Kidney international 93 (1), 204-213, 2018 | 167 | 2018 |
TGF-β/Smad3 activates mammalian target of rapamycin complex-1 to promote collagen production by increasing HIF-1α expression B Rozen-Zvi, T Hayashida, SC Hubchak, C Hanna, LC Platanias, ... American Journal of Physiology-Renal Physiology 305 (4), F485-F494, 2013 | 78 | 2013 |
IgA nephropathy presenting as macroscopic hematuria in 2 pediatric patients after receiving the Pfizer COVID-19 vaccine C Hanna, LPH Hernandez, L Bu, S Kizilbash, L Najera, MN Rheault, ... Kidney international 100 (3), 705-706, 2021 | 70 | 2021 |
Hypoxia-inducible factor-2α and TGF-β signaling interact to promote normoxic glomerular fibrogenesis C Hanna, SC Hubchak, X Liang, B Rozen-Zvi, PT Schumacker, ... American Journal of Physiology-Renal Physiology 305 (9), F1323-F1331, 2013 | 62 | 2013 |
Quality of life is improved and kidney function preserved in patients with nephropathic cystinosis treated for 2 years with delayed-release cysteamine bitartrate CB Langman, LA Greenbaum, P Grimm, M Sarwal, P Niaudet, ... The Journal of pediatrics 165 (3), 528-533. e1, 2014 | 59 | 2014 |
Outcomes and risk factors for graft loss: lessons learned from 1,056 pediatric kidney transplants at the University of Minnesota S Chinnakotla, P Verghese, B Chavers, MN Rheault, V Kirchner, T Dunn, ... Journal of the American College of Surgeons 224 (4), 473-486, 2017 | 44 | 2017 |
High prevalence of kidney cysts in patients with CYP24A1 deficiency C Hanna, TA Potretzke, AG Cogal, YG Mkhaimer, PJ Tebben, VE Torres, ... Kidney International Reports 6 (7), 1895-1903, 2021 | 12 | 2021 |
Congenital heart disease in adults with autosomal dominant polycystic kidney disease M Chedid, C Hanna, G Zaatari, Y Mkhaimer, P Reddy, L Rangel, ... American journal of nephrology 53 (4), 316-324, 2022 | 9 | 2022 |
Kidney cysts in hypophosphatemic rickets with hypercalciuria: a case series C Hanna, TA Potretzke, M Chedid, LJ Rangel, J Arroyo, D Zubidat, ... Kidney Medicine 4 (3), 100419, 2022 | 8 | 2022 |
Cardiovascular outcomes in kidney transplant recipients with ADPKD M Chedid, HD Kaidbay, S Wigerinck, Y Mkhaimer, B Smith, D Zubidat, ... Kidney International Reports 7 (9), 1991-2005, 2022 | 6 | 2022 |
De novo PBX1 variant in a patient with glaucoma, kidney anomalies, and developmental delay: An expansion of the CAKUTHED phenotype SL Safgren, RJ Olson, F Pinto e Vairo, ED Bothun, C Hanna, EW Klee, ... American Journal of Medical Genetics Part A 188 (3), 919-925, 2022 | 6 | 2022 |
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease LR Claus, C Chen, J Stallworth, JL Turner, GG Slaats, AL Hawks, ... Kidney International 104 (5), 995-1007, 2023 | 5 | 2023 |
Cytomegalovirus sinusitis in a child with chronic myelogenous leukemia following bone marrow transplantation A Rayes, K Sahni, C Hanna, M Suryadevara, P Goyal, I Cherrick Pediatric blood & cancer 56 (7), 1140-1142, 2011 | 5 | 2011 |
Bone health in autosomal dominant polycystic kidney disease (ADPKD) patients after kidney transplantation D Zubidat, C Hanna, AK Randhawa, BH Smith, M Chedid, DHN Kaidbay, ... Bone Reports 18, 101655, 2023 | 3 | 2023 |
Asymptomatic pyuria as a prognostic biomarker in autosomal dominant polycystic kidney disease BE Jones, YG Mkhaimer, LJ Rangel, M Chedid, PJ Schulte, AK Mohamed, ... Kidney360 3 (3), 465-476, 2022 | 3 | 2022 |
A toddler with severe hypercalcemia and pyelonephritis: answers J Wilbanks, J Hillyer, F Hashim, D Sas, C Hanna Pediatric Nephrology 36, 859-861, 2021 | 3 | 2021 |
State of the science and ethical considerations for preimplantation genetic testing for monogenic cystic kidney diseases and ciliopathies WS Thompson, SN Babayev, ML McGowan, AG Kattah, MJ Wick, ... Journal of the American Society of Nephrology, 10.1681, 2023 | 2 | 2023 |
Copeptin levels in hospitalized infants and children with suspected vasopressin-dependent disorders: a case series A Al Nofal, C Hanna, AN Lteif, ST Pittock, JD Schwartz, JE Brumbaugh, ... Journal of Pediatric Endocrinology and Metabolism 36 (5), 492-499, 2023 | 2 | 2023 |
Genetic etiologies, diagnosis, and management of neonatal cystic kidney disease LS Heidenreich, EM Bendel-Stenzel, PC Harris, C Hanna NeoReviews 23 (3), e175-e188, 2022 | 2 | 2022 |
Refractory rhabdomyolysis responsive to corticosteroid therapy M Hammers, F Hashim, C Hanna, A Farris, S Blasick Baylor University Medical Center Proceedings 34 (2), 314-315, 2021 | 2 | 2021 |