| Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9 O Barel, SA Shalev, R Ofir, A Cohen, J Zlotogora, Z Shorer, G Mazor, ... The American Journal of Human Genetics 83 (2), 193-199, 2008 | 222 | 2008 |
| Pathogenesis of urinary tract infections with normal female anatomy G Finer, D Landau The Lancet infectious diseases 4 (10), 631-635, 2004 | 197 | 2004 |
| Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ O Barel, Z Shorer, H Flusser, R Ofir, G Narkis, G Finer, H Shalev, ... The American Journal of Human Genetics 82 (5), 1211-1216, 2008 | 153 | 2008 |
| Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome G Finer, H Shalev, OS Birk, D Galron, N Jeck, L Sinai-Treiman, D Landau The Journal of pediatrics 142 (3), 318-323, 2003 | 107 | 2003 |
| Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger protein RY Birnbaum, A Zvulunov, D Hallel-Halevy, E Cagnano, G Finer, R Ofir, ... Nature genetics 38 (7), 749-751, 2006 | 94 | 2006 |
| Hyperphosphatemic familial tumoral calcinosis: response to acetazolamide and postulated mechanisms G Finer, HE Price, RM Shore, KE White, CB Langman American Journal of Medical Genetics Part A 164 (6), 1545-1549, 2014 | 55 | 2014 |
| Applicability of estimating glomerular filtration rate equations in pediatric patients: comparison with a measured glomerular filtration rate by iohexol clearance F Deng, G Finer, S Haymond, E Brooks, CB Langman Translational Research 165 (3), 437-445, 2015 | 52 | 2015 |
| Divergent roles of Smad3 and PI3-kinase in murine adriamycin nephropathy indicate distinct mechanisms of proteinuria and fibrogenesis G Finer, HW Schnaper, YS Kanwar, X Liang, HY Lin, T Hayashida Kidney international 82 (5), 525-536, 2012 | 30 | 2012 |
| Conservative treatment of malignant (invasive) external otitis caused by Aspergillus flavus with oral itraconazole solution in a neutropenic patient G Finer, D Greenberg, E Leibovitz, A Leiberman, I Shelef, J Kapelushnik Scandinavian journal of infectious diseases 34 (3), 227-229, 2002 | 26 | 2002 |
| Transcription factor 21 is required for branching morphogenesis and regulates the Gdnf-axis in kidney development S Ide, G Finer, Y Maezawa, T Onay, T Souma, R Scott, K Ide, Y Akimoto, ... Journal of the American Society of Nephrology 29 (12), 2795-2808, 2018 | 24 | 2018 |
| A conceptual framework for the molecular pathogenesis of progressive kidney disease HW Schnaper, SC Hubchak, CE Runyan, JA Browne, G Finer, X Liu, ... Pediatric Nephrology 25, 2223-2230, 2010 | 21 | 2010 |
| Clinical approach to proximal renal tubular acidosis in children G Finer, D Landau Advances in Chronic Kidney Disease 25 (4), 351-357, 2018 | 19 | 2018 |
| Genetic kidney diseases in the pediatric population of southern Israel G Finer, H Shalev, D Landau Pediatric Nephrology 21, 910-916, 2006 | 14 | 2006 |
| Race, obesity, and the renin-angiotensin-aldosterone system: treatment response in children with primary hypertension AM South, L Arguelles, G Finer, CB Langman Pediatric Nephrology 32, 1585-1594, 2017 | 10 | 2017 |
| Stromal transcription factor 21 regulates development of the renal stroma via interaction with Wnt/β-catenin signaling G Finer, Y Maezawa, S Ide, T Onay, T Souma, R Scott, X Liang, X Zhao, ... Kidney360 3 (7), 1228-1241, 2022 | 7 | 2022 |
| Fluid management: pharmacologic and renal replacement therapies EL Wald, G Finer, ME McBride, N Nguyen, JM Costello, CL Epting Pediatric Critical Care Medicine 17 (8), S257-S265, 2016 | 6 | 2016 |
| Does History of Prematurity Prompt Blood Pressure Evaluations at Primary Care Visits? BD Kornfeld, G Finer, LE Banks, L Bolanos, AJ Ariza Global Pediatric Health 6, 2333794X19828314, 2019 | 5 | 2019 |
| Urinary Tract Infections: Review: Pathogenesis of Urinary Tract Infections With Normal Female Anatomy G Finer, D Landau The Lancet Infectious Diseases, 631-635, 0 | 5 | |
| Genetic and phenotypic aspects of autosomal recessive polycystic kidney disease in southern Israel G Finer, O Birk, D Landau Harefuah 143 (7), 466-70, 552, 2004 | 2 | 2004 |
| The transcription factor Tcf21 is required for specifying Foxd1 cells to the juxtaglomerular cell lineage H Anjum, GS Yacu, S Medrano, RA Gomez, MLS Sequeira-Lopez, ... bioRxiv, 2024.03. 25.586641, 2024 | | 2024 |
