| The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom K Schwarze, J Buchanan, JM Fermont, H Dreau, MW Tilley, JM Taylor, ... Genetics in Medicine 22 (1), 85-94, 2020 | 213 | 2020 |
| Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project P Robbe, N Popitsch, SJL Knight, P Antoniou, J Becq, M He, A Kanapin, ... Genetics in Medicine 20 (10), 1196-1205, 2018 | 145 | 2018 |
| A comprehensive survey of congestion control protocols in wireless sensor networks C Sergiou, P Antoniou, V Vassiliou IEEE Communications Surveys & Tutorials 16 (4), 1839-1859, 2014 | 143 | 2014 |
| KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data GAT Sacomoto, J Kielbassa, R Chikhi, R Uricaru, P Antoniou, MF Sagot, ... BMC bioinformatics 13, 1-12, 2012 | 129 | 2012 |
| Congestion control in wireless sensor networks based on bird flocking behavior P Antoniou, A Pitsillides, T Blackwell, A Engelbrecht, L Michael Computer Networks 57 (5), 1167-1191, 2013 | 128 | 2013 |
| Bisulfite conversion of DNA: performance comparison of different kits and methylation quantitation of epigenetic biomarkers that have the potential to be used in non-invasive … CA Leontiou, MD Hadjidaniel, P Mina, P Antoniou, M Ioannides, ... PloS one 10 (8), e0135058, 2015 | 97 | 2015 |
| Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature P Evangelidou, A Alexandrou, M Moutafi, M Ioannides, P Antoniou, ... BioMed research international 2013, 2013 | 77 | 2013 |
| Targeted deep sequencing reveals clinically relevant subclonal IgHV rearrangements in chronic lymphocytic leukemia B Stamatopoulos, A Timbs, D Bruce, T Smith, R Clifford, P Robbe, A Burns, ... Leukemia 31 (4), 837-845, 2017 | 70 | 2017 |
| Complex systems: A communication networks perspective towards 6G C Sergiou, M Lestas, P Antoniou, C Liaskos, A Pitsillides IEEE Access 8, 89007-89030, 2020 | 64 | 2020 |
| Clinical significance of TP53, BIRC3, ATM and MAPK-ERK genes in chronic lymphocytic leukaemia: data from the randomised UK LRF CLL4 trial SJ Blakemore, R Clifford, H Parker, P Antoniou, E Stec-Dziedzic, ... Leukemia 34 (7), 1760-1774, 2020 | 48 | 2020 |
| FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation G Koumbaris, H Hatzisevastou-Loukidou, A Alexandrou, M Ioannides, ... Human molecular genetics 20 (10), 1925-1936, 2011 | 43 | 2011 |
| Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features P Robbe, KE Ridout, DV Vavoulis, H Dréau, B Kinnersley, N Denny, ... Nature genetics 54 (11), 1675-1689, 2022 | 30 | 2022 |
| Conservative String Covering of Indeterminate Strings. P Antoniou, M Crochemore, CS Iliopoulos, I Jayasekera, GM Landau Stringology, 108-115, 2008 | 25 | 2008 |
| Finding common motifs with gaps using finite automata P Antoniou, J Holub, CS Iliopoulos, B Melichar, P Peterlongo Implementation and Application of Automata: 11th International Conference …, 2006 | 24 | 2006 |
| Classical and non-classical presentations of complement factor I deficiency: two contrasting cases diagnosed via genetic and genomic methods AM Shields, AT Pagnamenta, AJ Pollard, OxClinWGS, JC Taylor, ... Frontiers in immunology 10, 1150, 2019 | 23 | 2019 |
| Vibrational control of electron-transfer reactions: a feasibility study for the fast coherent transfer regime P Antoniou, Z Ma, P Zhang, DN Beratan, SS Skourtis Physical Chemistry Chemical Physics 17 (46), 30854-30866, 2015 | 22 | 2015 |
| Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL J Klintman, K Barmpouti, SJL Knight, P Robbe, H Dreau, R Clifford, ... British journal of haematology 182 (3), 412-417, 2018 | 21 | 2018 |
| Mapping uniquely occurring short sequences derived from high throughput technologies to a reference genome P Antoniou, JW Daykin, CS Iliopoulos, D Kourie, L Mouchard, SP Pissis 2009 9th International Conference on Information Technology and Applications …, 2009 | 20 | 2009 |
| Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencing A Schuh, H Dreau, SJL Knight, K Ridout, T Mizani, D Vavoulis, R Colling, ... Molecular Case Studies 4 (2), a002279, 2018 | 19 | 2018 |
| Whole-genome fetal and maternal DNA methylation analysis using MeDIP-NGS for the identification of differentially methylated regions A Keravnou, M Ioannides, K Tsangaras, C Loizides, MD Hadjidaniel, ... Genetics research 98, e15, 2016 | 15 | 2016 |
