| Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B. 1.1. 7 B Meng, SA Kemp, G Papa, R Datir, IATM Ferreira, S Marelli, WT Harvey, ... Cell reports 35 (13), 2021 | 424 | 2021 |
| 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 | 315 | 2017 |
| IthaGenes: an interactive database for haemoglobin variations and epidemiology P Kountouris, CW Lederer, P Fanis, X Feleki, J Old, M Kleanthous PloS one 9 (7), e103020, 2014 | 238 | 2014 |
| 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 | 185 | 2015 |
| Recent trends in the gene therapy of β-thalassemia A Finotti, L Breda, CW Lederer, N Bianchi, C Zuccato, M Kleanthous, ... Journal of blood medicine, 69-85, 2015 | 133 | 2015 |
| Newborn screening for sickle cell disease in Europe: recommendations from a Pan‐European Consensus Conference S Lobitz, P Telfer, E Cela, B Allaf, M Angastiniotis, C Backman Johansson, ... British journal of haematology 183 (4), 648-660, 2018 | 114 | 2018 |
| Novel polymorphisms at codons 146 and 151 in the prion protein gene of Cyprus goats, and their association with natural scrapie P Papasavva-Stylianou, M Kleanthous, P Toumazos, P Mavrikiou, ... The Veterinary Journal 173 (2), 459-462, 2007 | 111 | 2007 |
| The European Hematology Association Roadmap for European Hematology Research: a consensus document SJJ Engert A, Balduini C, Brand A, Coiffier B, Cordonnier C, Döhner H, de ... Haematologica 101 (2), 115-208, 2016 | 91 | 2016 |
| α‐Thalassaemia in the population of Cyprus E Baysal, M Kleanthous, G Bozkurt, A Kyrri, E Kalogirou, M Angastiniotis, ... British journal of haematology 89 (3), 496-499, 1995 | 86 | 1995 |
| A multi-center study in order to further define the molecular basis of β-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple … JM Old, SN Khan, I Verma, S Fucharoen, M Kleanthous, P Ioannou, ... Hemoglobin 25 (4), 397-407, 2001 | 77 | 2001 |
| Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia T Papasavva, WFJ Van Ijcken, CEM Kockx, MCGN Van Den Hout, ... European Journal of Human Genetics 21 (12), 1403-1410, 2013 | 69 | 2013 |
| The impact of genotype on endocrine complications in thalassaemia major N Skordis, M Michaelidou, SC Savva, Y Ioannou, A Rousounides, ... European journal of haematology 77 (2), 150-156, 2006 | 69 | 2006 |
| Arrayed primer extension for the noninvasive prenatal diagnosis of β‐thalassemia based on detection of single nucleotide polymorphisms T Papasavva, I Kalikas, A Kyrri, M Kleanthous Annals of the New York Academy of Sciences 1137 (1), 302-308, 2008 | 67 | 2008 |
| Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations IC Verma, M Kleanthous, R Saxena, S Fucharoen, P Winichagoon, ... Hemoglobin 31 (4), 439-452, 2007 | 67 | 2007 |
| Rare opportunities: CRISPR/Cas-based therapy development for rare genetic diseases P Papasavva, M Kleanthous, CW Lederer Molecular diagnosis & therapy 23 (2), 201-222, 2019 | 59 | 2019 |
| Plerixafor+G-CSF–mobilized CD34+ cells represent an optimal graft source for thalassemia gene therapy G Karponi, N Psatha, CW Lederer, JE Adair, F Zervou, N Zogas, ... Blood, The Journal of the American Society of Hematology 126 (5), 616-619, 2015 | 57 | 2015 |
| Prenatal diagnosis of hemoglobin disorders: present and future strategies CL Harteveld, M Kleanthous, J Traeger-Synodinos Clinical biochemistry 42 (18), 1767-1779, 2009 | 56 | 2009 |
| Molecular characterization of β-thalassemia in Syria K Kyriacou, FA Quobaili, E Pavlou, G Christopoulos, P Ioannou, ... Hemoglobin 24 (1), 1-13, 2000 | 56 | 2000 |
| 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 | 53 | 2016 |
| An overview of current microarray-based human globin gene mutation detection methods L Cremonesi, M Ferrari, PC Giordano, CL Harteveld, M Kleanthous, ... Hemoglobin 31 (3), 289-311, 2007 | 52 | 2007 |
Carsten W LedererResearcher, The Cyprus Institute of Neurology and Genetics; Assistant Professor, Cyprus School ofVerified email at cing.ac.cy
