| Small molecule targets TMED9 and promotes lysosomal degradation to reverse proteinopathy M Dvela-Levitt, M Kost-Alimova, M Emani, E Kohnert, R Thompson, ... Cell 178 (3), 521-535. e23, 2019 | 145 | 2019 |
| Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1 E Olinger, P Hofmann, K Kidd, I Dufour, H Belge, C Schaeffer, A Kipp, ... Kidney international 98 (3), 717-731, 2020 | 88 | 2020 |
| 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 |
| New miRNA profiles accurately distinguish renal cell carcinomas and upper tract urothelial carcinomas from the normal kidney A Zaravinos, GI Lambrou, N Mourmouras, P Katafygiotis, ... PloS one 9 (3), e91646, 2014 | 58 | 2014 |
| Noninvasive immunohistochemical diagnosis and novel MUC1 mutations causing autosomal dominant tubulointerstitial kidney disease M Živná, K Kidd, A Přistoupilová, V Barešová, M DeFelice, B Blumenstiel, ... Journal of the American Society of Nephrology 29 (9), 2418-2431, 2018 | 57 | 2018 |
| 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 |
| Cystic diseases of the kidney: molecular biology and genetics C Deltas, G Papagregoriou Archives of pathology & laboratory medicine 134 (4), 569-582, 2010 | 48 | 2010 |
| 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 |
| 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 |
| COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect? K Voskarides, G Papagregoriou, D Hadjipanagi, I Petrou, I Savva, A Elia, ... BMC nephrology 19, 1-8, 2018 | 40 | 2018 |
| An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes M Živná, K Kidd, M Zaidan, P Vyleťal, V Barešová, K Hodaňová, J Sovová, ... Kidney international 98 (6), 1589-1604, 2020 | 39 | 2020 |
| Omega-3 fatty acids protect retinal neurons in the DBA/2J hereditary glaucoma mouse model M Kalogerou, P Kolovos, E Prokopiou, G Papagregoriou, C Deltas, ... Experimental eye research 167, 128-139, 2018 | 35 | 2018 |
| Therapeutic potential of omega-3 fatty acids supplementation in a mouse model of dry macular degeneration E Prokopiou, P Kolovos, M Kalogerou, A Neokleous, G Papagregoriou, ... BMJ open ophthalmology 1 (1), e000056, 2017 | 19 | 2017 |
| Haploinsufficiency of the miR-873/miR-876 microRNA cluster is associated with craniofacial abnormalities C Koufaris, G Papagregoriou, L Kousoulidou, M Moutafi, M Tauber, ... Gene 561 (1), 95-100, 2015 | 17 | 2015 |
| NPHS2 screening with SURVEYOR in Hellenic children with steroid-resistant nephrotic syndrome K Voskarides, C Makariou, G Papagregoriou, N Stergiou, N Printza, ... Pediatric Nephrology 23, 1373-1375, 2008 | 13 | 2008 |
| Rampant introgressive hybridization in Pogoniulus tinkerbirds (Piciformes: Lybiidae) despite millions of years of divergence EC Nwankwo, KG Mortega, A Karageorgos, BO Ogolowa, ... Biological Journal of the Linnean Society 127 (1), 125-142, 2019 | 12 | 2019 |
| Evidence for miR-548c-5p regulation of FOXC2 transcription through a distal genomic target site in human podocytes A Christofides, G Papagregoriou, H Dweep, N Makrides, N Gretz, ... Cellular and Molecular Life Sciences 77, 2441-2459, 2020 | 8 | 2020 |
| Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance M Nagara, G Papagregoriou, RB Abdallah, Z Landoulsi, Y Bouyacoub, ... European Journal of Medical Genetics 61 (1), 1-7, 2018 | 8 | 2018 |
| Renal graft outcome in autosomal dominant medullary cystic kidney disease type 1 AP Soloukides, DAD Moutzouris, GN Papagregoriou, CV Stavrou, ... J Nephrol 26 (4), 793-8, 2013 | 8 | 2013 |
| A glycine substitution in the collagenous domain of Col4a3 in mice recapitulates late onset Alport syndrome C Odiatis, I Savva, M Pieri, P Ioannou, P Petrou, G Papagregoriou, ... Matrix biology plus 9, 100053, 2021 | 6 | 2021 |
