| Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin J Borg, P Papadopoulos, M Georgitsi, L Gutiérrez, G Grech, P Fanis, ... Nature genetics 42 (9), 801-805, 2010 | 478 | 2010 |
| Impaired immunity and enhanced resistance to endotoxin in the absence of neutrophil elastase and cathepsin G J Tkalcevic, M Novelli, M Phylactides, JP Iredale, AW Segal, J Roes Immunity 12 (2), 201-210, 2000 | 476 | 2000 |
| European contribution to the study of ROS: A summary of the findings and prospects for the future from the COST action BM1203 (EU-ROS) J Egea, I Fabregat, YM Frapart, P Ghezzi, A Görlach, T Kietzmann, ... Redox biology 13, 94-162, 2017 | 338 | 2017 |
| Oxidative stress in β-thalassaemia and sickle cell disease S Voskou, M Aslan, P Fanis, M Phylactides, M Kleanthous Redox biology 6, 226-239, 2015 | 213 | 2015 |
| An element in intron 1 of the CFTR gene augments intestinal expression in vivo RK Rowntree, G Vassaux, TL McDowell, S Howe, A McGuigan, ... Human molecular genetics 10 (14), 1455-1464, 2001 | 73 | 2001 |
| HNF1alpha is involved in tissue-specific regulation of CFTR gene expression N Mouchel, SA Henstra, VA McCARTHY, SH Williams, M Phylactides, ... Biochemical Journal 378 (3), 909-918, 2004 | 71 | 2004 |
| The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study P Kountouris, I Kousiappa, T Papasavva, G Christopoulos, E Pavlou, ... Scientific reports 6 (1), 26371, 2016 | 59 | 2016 |
| Evaluation of potential regulatory elements identified as DNase I hypersensitive sites in the CFTR gene M Phylactides, R Rowntree, H Nuthall, D Ussery, A Wheeler, A Harris European journal of biochemistry 269 (2), 553-559, 2002 | 52 | 2002 |
| KLF10 Gene Expression is Associated with High Fetal Hemoglobin Levels and with Response to Hydroxyurea Treatment in β-Hemoglobinopathy Patients J Borg, M Phylactides, M Bartsakoulia, C Tafrali, C Lederer, AE Felice, ... Pharmacogenomics 13 (13), 1487-1500, 2012 | 46 | 2012 |
| Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approach P Fanis, I Kousiappa, M Phylactides, M Kleanthous BMC genomics 15, 1-12, 2014 | 35 | 2014 |
| The International Hemoglobinopathy Research Network (INHERENT): An international initiative to study the role of genetic modifiers in hemoglobinopathies P Kountouris, C Stephanou, NM Archer, F Bonifazi, V Giannuzzi, ... Blood 138 (Supplement 1), 948-948, 2021 | 34 | 2021 |
| δ-Thalassemia in Cyprus E Pavlou, M Phylactides, A Kyrri, E Kalogerou, C Makariou, I Georgiou, ... Hemoglobin 30 (4), 455-462, 2006 | 33 | 2006 |
| The changing epidemiology of β-thalassemia in the Greek-Cypriot population AR Kyrri, E Kalogerou, D Loizidou, C Ioannou, C Makariou, L Kythreotis, ... Hemoglobin 37 (5), 435-443, 2013 | 29 | 2013 |
| The investigation of resveratrol and analogs as potential inducers of fetal hemoglobin A Theodorou, M Phylactides, L Forti, MR Cramarossa, P Spyrou, ... Blood Cells, Molecules, and Diseases 58, 6-12, 2016 | 25 | 2016 |
| Hemoglobin variants in Cyprus AR Kyrri, X Felekis, E Kalogerou, BJ Wild, L Kythreotis, M Phylactides, ... Hemoglobin 33 (2), 81-94, 2009 | 22 | 2009 |
| Interaction of intestinal and pancreatic transcription factors in the regulation of CFTR gene expression VA McCarthy, CJ Ott, M Phylactides, A Harris Biochimica et Biophysica Acta (BBA)-Gene Regulatory Mechanisms 1789 (11-12 …, 2009 | 18 | 2009 |
| A novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β‐thalassemia major P Fanis, I Kousiappa, M Phylactides, A Kyrri, M Hadjigavriel, S Christou, ... Human mutation 40 (10), 1768-1780, 2019 | 17 | 2019 |
| The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter C Chassanidis, A Kalamaras, M Phylactides, F Pourfarzad, S Likousi, ... Annals of hematology 88, 549-555, 2009 | 12 | 2009 |
| Hb Agrinio [α29(B10)Leu→Pro (α2)] in Combination with – –MED I Results in a Severe Form of Hb H Disease X Felekis, M Phylactides, A Drousiotou, S Christou, A Kyrri, K Kyriakou, ... Hemoglobin 32 (3), 237-246, 2008 | 11 | 2008 |
| Compounds of the anthracycline family of antibiotics elevate human γ-globin expression both in erythroid cultures and in a transgenic mouse model P Spyrou, M Phylactides, CW Lederer, L Kithreotis, A Kirri, S Christou, ... Blood Cells, Molecules, and Diseases 44 (2), 100-106, 2010 | 9 | 2010 |
