| Foxp3 expression in human cancer cells V Karanikas, M Speletas, M Zamanakou, F Kalala, G Loules, T Kerenidi, ... Journal of translational medicine 6, 1-8, 2008 | 271 | 2008 |
| International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency H Farkas, I Martinez‐Saguer, K Bork, T Bowen, T Craig, M Frank, ... Allergy 72 (2), 300-313, 2017 | 214 | 2017 |
| Activated murine B lymphocytes and dendritic cells produce a novel CC chemokine which acts selectively on activated T cells C Schaniel, E Pardali, F Sallusto, M Speletas, C Ruedl, T Shimizu, T Seidl, ... The Journal of experimental medicine 188 (3), 451-463, 1998 | 187 | 1998 |
| Regulation of the autophagic machinery in human neutrophils I Mitroulis, I Kourtzelis, K Kambas, S Rafail, A Chrysanthopoulou, ... European journal of immunology 40 (5), 1461-1472, 2010 | 158 | 2010 |
| Activation of bone morphogenetic protein/Smad signaling in bronchial epithelial cells during airway inflammation A Rosendahl, E Pardali, M Speletas, P Ten Dijke, CH Heldin, P Sideras American journal of respiratory cell and molecular biology 27 (2), 160-169, 2002 | 154 | 2002 |
| Genetics of hereditary angioedema revisited AE Germenis, M Speletas Clinical reviews in allergy & immunology 51, 170-182, 2016 | 140 | 2016 |
| MEFV alterations and population genetics analysis in a large cohort of Greek patients with familial Mediterranean fever S Giaglis, V Papadopoulos, K Kambas, M Doumas, V Tsironidou, S Rafail, ... Clinical genetics 71 (5), 458-467, 2007 | 139 | 2007 |
| Hereditary angioedema: molecular and clinical differences among European populations M Speletas, A Szilagyi, F Psarros, D Moldovan, M Magerl, M Kompoti, ... Journal of Allergy and Clinical Immunology 135 (2), 570-573. e10, 2015 | 93 | 2015 |
| Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations J Thalhammer, G Kindle, A Nieters, S Rusch, MRJ Seppänen, A Fischer, ... Journal of Allergy and Clinical Immunology 148 (5), 1332-1341. e5, 2021 | 92 | 2021 |
| Correlations of JAK2–V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders M Speletas, E Katodritou, C Daiou, E Mandala, E Papadakis, A Kioumi, ... Leukemia research 31 (8), 1053-1062, 2007 | 91 | 2007 |
| A novel mutation in TREM2 gene causing Nasu-Hakola disease and review of the literature E Dardiotis, V Siokas, E Pantazi, M Dardioti, D Rikos, G Xiromerisiou, ... Neurobiology of aging 53, 194. e13-194. e22, 2017 | 81 | 2017 |
| Successful response in a case of severe pustular psoriasis after interleukin‐1β inhibition P Skendros, C Papagoras, I Lefaki, A Giatromanolaki, I Kotsianidis, ... British Journal of Dermatology 176 (1), 212-215, 2017 | 76 | 2017 |
| Repeated leftover serosurvey of SARS-CoV-2 IgG antibodies, Greece, march and april 2020 Z Bogogiannidou, A Vontas, K Dadouli, MA Kyritsi, S Soteriades, ... Eurosurveillance 25 (31), 2001369, 2020 | 71 | 2020 |
| Toll-like receptor 4 gene (TLR4), but not TLR2, polymorphisms modify the risk of tonsillar disease due to Streptococcus pyogenes and Haemophilus influenzae K Liadaki, E Petinaki, C Skoulakis, P Tsirevelou, D Klapsa, AE Germenis, ... Clinical and vaccine immunology 18 (2), 217-222, 2011 | 71 | 2011 |
| Leptin induces the expression of functional tissue factor in human neutrophils and peripheral blood mononuclear cells through JAK2-dependent mechanisms and TNFα involvement S Rafail, K Ritis, K Schaefer, I Kourtzelis, M Speletas, M Doumas, ... Thrombosis research 122 (3), 366-375, 2008 | 68 | 2008 |
| International consensus on the use of genetics in the management of hereditary angioedema AE Germenis, M Margaglione, JB Pesquero, H Farkas, S Cichon, D Csuka, ... The Journal of Allergy and Clinical Immunology: In Practice 8 (3), 901-911, 2020 | 67 | 2020 |
| A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency K Pieper, M Rizzi, M Speletas, CR Smulski, H Sic, H Kraus, U Salzer, ... Journal of allergy and clinical immunology 133 (4), 1222-1225. e10, 2014 | 64 | 2014 |
| F12‐46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema M Speletas, Á Szilágyi, D Csuka, N Koutsostathis, F Psarros, D Moldovan, ... Allergy 70 (12), 1661-1664, 2015 | 58 | 2015 |
| Fabry disease due to D313Y and novel GLA mutations K Koulousios, K Stylianou, P Pateinakis, M Zamanakou, G Loules, ... BMJ open 7 (10), e017098, 2017 | 57 | 2017 |
| Association of TLR4-T399I polymorphism with chronic obstructive pulmonary disease in smokers M Speletas, V Merentiti, K Kostikas, K Liadaki, M Minas, K Gourgoulianis, ... Journal of Immunology Research 2009, 2009 | 56 | 2009 |
