| Whole exome sequencing of patients with steroid-resistant nephrotic syndrome JK Warejko, W Tan, A Daga, D Schapiro, JA Lawson, S Shril, S Lovric, ... Clinical Journal of the American Society of Nephrology 13 (1), 53-62, 2018 | 223 | 2018 |
| Lupus nephritis in childhood: a review of 53 patients followed at a single center R Bogdanović, V Nikolić, S Pašić, J Dimitrijević, J Lipkovska-Marković, ... Pediatric Nephrology 19, 36-44, 2004 | 215 | 2004 |
| Innate immune response in kidney ischemia/reperfusion injury: potential target for therapy A Kezić, N Stajic, F Thaiss Journal of immunology research 2017, 2017 | 143 | 2017 |
| Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association P Saisawat, S Kohl, AC Hilger, DY Hwang, HY Gee, GC Dworschak, ... Kidney international 85 (6), 1310-1317, 2014 | 132 | 2014 |
| Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract S Kohl, DY Hwang, GC Dworschak, AC Hilger, P Saisawat, A Vivante, ... Journal of the American Society of Nephrology 25 (9), 1917-1922, 2014 | 120 | 2014 |
| Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment S Ashraf, H Kudo, J Rao, A Kikuchi, E Widmeier, JA Lawson, W Tan, ... Nature communications 9 (1), 1960, 2018 | 118 | 2018 |
| Transient type 1 pseudo-hypoaldosteronism: report on an eight-patient series and literature review R Bogdanović, N Stajić, J Putnik, A Paripović Pediatric nephrology 24 (11), 2167-2175, 2009 | 97 | 2009 |
| Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract DY Hwang, S Kohl, X Fan, A Vivante, S Chan, GC Dworschak, J Schulz, ... Human genetics 134, 905-916, 2015 | 81 | 2015 |
| Schimke immunoosseous dysplasia: suggestions of genetic diversity JM Clewing, H Fryssira, D Goodman, SF Smithson, EA Sloan, S Lou, ... Human mutation 28 (3), 273-283, 2007 | 68 | 2007 |
| Liddle syndrome in a Serbian family and literature review of underlying mutations R Bogdanović, V Kuburović, N Stajić, SS Mughal, A Hilger, S Ninić, ... European journal of pediatrics 171, 471-478, 2012 | 47 | 2012 |
| Dental abnormalities in Schimke immuno-osseous dysplasia M Morimoto, O Kerouredan, M Gendronneau, C Shuen, ... Journal of dental research 91 (7_suppl), S29-S37, 2012 | 44 | 2012 |
| Renal involvement in primary Sjogren syndrome of childhood: case report and literature review R Bogdanović, G Basta-Jovanović, J Putnik, N Stajić, A Paripović Modern rheumatology 23 (1), 182-189, 2013 | 40 | 2013 |
| A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency R Bogdanović, M Draaken, A Toromanović, M Đorđević, N Stajić, ... Pediatric Nephrology 25, 2363-2368, 2010 | 40 | 2010 |
| Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia? M Morimoto, Z Yu, P Stenzel, JM Clewing, B Najafian, C Mayfield, ... Orphanet journal of rare diseases 7 (1), 1-17, 2012 | 39 | 2012 |
| Exome sequencing and identification of phenocopies in patients with clinically presumed hereditary nephropathies KM Riedhammer, MC Braunisch, R Günthner, M Wagner, C Hemmer, ... American journal of kidney diseases 76 (4), 460-470, 2020 | 38 | 2020 |
| Schimke immunoosseous dysplasia: defining skeletal features KB Hunter, T Lücke, J Spranger, SF Smithson, H Alpay, JL André, ... European journal of pediatrics 169, 801-811, 2010 | 30 | 2010 |
| Pulmonary renal syndrome in a child with coexistence of anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane disease: case report and literature review R Bogdanović, P Minić, J Marković-Lipkovski, N Stajić, N Savić, M Rodić BMC nephrology 14, 1-8, 2013 | 24 | 2013 |
| COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans TM Kitzler, R Schneider, S Kohl, CM Kolvenbach, DM Connaughton, ... Human genetics 138, 1105-1115, 2019 | 19 | 2019 |
| Glomerular involvement in myelodysplastic syndromes R Bogdanović, M Kuzmanović, J Marković-Lipkovski, M Ognjanović, ... Pediatric Nephrology 16, 1053-1057, 2001 | 19 | 2001 |
| Acute tubulointerstitial nephritis in children V Nikolić, R Bogdanović, M Ognjanović, N Stajić Srpski Arhiv za Celokupno Lekarstvo 129, 23-27, 2001 | 18 | 2001 |
