| Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis DP Gale, EG De Jorge, HT Cook, R Martinez-Barricarte, A Hadjisavvas, ... The Lancet 376 (9743), 794-801, 2010 | 372 | 2010 |
| COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy K Voskarides, L Damianou, V Neocleous, I Zouvani, S Christodoulidou, ... Journal of the American Society of Nephrology 18 (11), 3004-3016, 2007 | 245 | 2007 |
| Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees Y Athanasiou, K Voskarides, DP Gale, L Damianou, C Patsias, M Zavros, ... Clinical Journal of the American Society of Nephrology 6 (6), 1436-1446, 2011 | 170 | 2011 |
| Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes … A Pierides, K Voskarides, Y Athanasiou, K Ioannou, L Damianou, M Arsali, ... Nephrology Dialysis Transplantation 24 (9), 2721-2729, 2009 | 153 | 2009 |
| A European spectrum of pharmacogenomic biomarkers: implications for clinical pharmacogenomics C Mizzi, E Dalabira, J Kumuthini, N Dzimiri, I Balogh, N Başak, R Böhm, ... PloS one 11 (9), e0162866, 2016 | 115 | 2016 |
| Molecular genetics of familial hematuric diseases C Deltas, A Pierides, K Voskarides Nephrology Dialysis Transplantation 28 (12), 2946-2960, 2013 | 109 | 2013 |
| Evidence for activation of the unfolded protein response in collagen IV nephropathies M Pieri, C Stefanou, A Zaravinos, K Erguler, K Stylianou, G Lapathitis, ... Journal of the American Society of Nephrology 25 (2), 260-275, 2014 | 81 | 2014 |
| Carriers of autosomal recessive Alport syndrome with thin basement membrane nephropathy presenting as focal segmental glomerulosclerosis in later life C Deltas, I Savva, K Voskarides, L Papazachariou, A Pierides Nephron 130 (4), 271-280, 2015 | 77 | 2015 |
| Ischemic but not mechanical preconditioning attenuates ischemia/reperfusion induced myocardial apoptosis in anaesthetized rabbits: the role of Bcl-2 family proteins and ERK1/2 A Lazou, EK Iliodromitis, D Cieslak, K Voskarides, S Mousikos, E Bofilis, ... Apoptosis 11, 2195-2204, 2006 | 75 | 2006 |
| Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and … L Papazachariou, P Demosthenous, M Pieri, G Papagregoriou, I Savva, ... PloS one 9 (12), e115015, 2014 | 69 | 2014 |
| The role of molecular genetics in diagnosing familial hematuria (s) C Deltas, A Pierides, K Voskarides Pediatric nephrology 27, 1221-1231, 2012 | 67 | 2012 |
| Evidence that NPHS2-R229Q predisposes to proteinuria and renal failure in familial hematuria K Voskarides, M Arsali, Y Athanasiou, A Elia, A Pierides, C Deltas Pediatric Nephrology 27, 675-679, 2012 | 65 | 2012 |
| Antagonistic pleiotropy in human disease SG Byars, K Voskarides Journal of Molecular Evolution 88 (1), 12-25, 2020 | 58 | 2020 |
| A miR-1207-5p binding site polymorphism abolishes regulation of HBEGF and is associated with disease severity in CFHR5 nephropathy G Papagregoriou, K Erguler, H Dweep, K Voskarides, P Koupepidou, ... Plos one 7 (2), e31021, 2012 | 54 | 2012 |
| X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure A Pierides, K Voskarides, M Kkolou, M Hadjigavriel, C Deltas Hippokratia 17 (3), 207, 2013 | 53 | 2013 |
| X‐linked Alport syndrome in Hellenic families: Phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5 P Demosthenous, K Voskarides, K Stylianou, M Hadjigavriel, M Arsali, ... Clinical Genetics 81 (3), 240-248, 2012 | 47 | 2012 |
| Combination of 247 genome-wide association studies reveals high cancer risk as a result of evolutionary adaptation K Voskarides Molecular Biology and Evolution 35 (2), 473-485, 2018 | 46 | 2018 |
| Frequent COL4 mutations in familial microhematuria accompanied by later‐onset Alport nephropathy due to focal segmental glomerulosclerosis L Papazachariou, G Papagregoriou, D Hadjipanagi, P Demosthenous, ... Clinical Genetics 92 (5), 517-527, 2017 | 46 | 2017 |
| C3 glomerulonephritis/CFHR5 nephropathy is an endemic disease in Cyprus: clinical and molecular findings in 21 families C Deltas, D Gale, T Cook, K Voskarides, Y Athanasiou, A Pierides Complement Therapeutics, 189-196, 2012 | 46 | 2012 |
| SARS-CoV-2: tracing the origin, tracking the evolution K Voskarides BMC Medical Genomics 15 (1), 62, 2022 | 42 | 2022 |
