| JAK2 V617F hematopoietic clones are present several years prior to MPN diagnosis and follow different expansion kinetics T McKerrell, N Park, J Chi, G Collord, T Moreno, H Ponstingl, J Dias, ... Blood Advances 1 (14), 968-971, 2017 | 55 | 2017 |
| HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus EC Castelli, P Gerasimou, MA Paz, J Ramalho, IOP Porto, THA Lima, ... Molecular immunology 83, 115-126, 2017 | 41 | 2017 |
| C5aR agonist enhances phagocytosis of fibrillar and non-fibrillar Aβ amyloid and preserves memory in a mouse model of familial Alzheimer’s disease E Panayiotou, E Fella, S Andreou, R Papacharalambous, P Gerasimou, ... PLoS One 14 (12), e0225417, 2019 | 20 | 2019 |
| HLA‐G 14‐bp polymorphism affects the age of onset in Type I Diabetes Mellitus P Gerasimou, N Skordis, M Picolos, A Spyridonidis, P Costeas International journal of immunogenetics 43 (3), 135-142, 2016 | 18 | 2016 |
| Combined effect of glutamine at position 70 of HLA-DRB1 and alanine at position 57 of HLA-DQB1 in type 1 diabetes: An epitope analysis P Gerasimou, V Nicolaidou, N Skordis, M Picolos, D Monos, PA Costeas PLoS One 13 (3), e0193684, 2018 | 13 | 2018 |
| A sensitive detection method for MPLW515L or MPLW515K mutation in myeloproliferative disorders J Chi, P Ch, A Mitsidou Euro. J. Exp. Biol 4, 33-36, 2014 | 7 | 2014 |
| cDNA synthesis for BCR-ABL1 detection at the MMR level: the importance of using the appropriate kit J Chi, C Pierides, A Mitsidou, A Miltiadou, P Gerasimou, P Costeas Biological Procedures Online 17, 1-4, 2015 | 6 | 2015 |
| The rare DNA ligase IV syndrome: A case report P Gerasimou, L Koumas, A Miltiadous, I Kyprianou, J Chi, R Gavrielidou, ... Human Pathology: Case Reports 22, 200442, 2020 | 3 | 2020 |
| Pharmacological activation of the C5a receptor leads to stimulation of the β-adrenergic receptor and alleviates cognitive impairment in a murine model of familial Alzheimer’s … E Fella, R Papacharalambous, D Kynigopoulos, M Ioannou, R Derua, ... Frontiers in Immunology 13, 947071, 2022 | 2 | 2022 |
| A de novo SFMBT1 pathogenic variant identified in a boy with Poland syndrome A Miltiadous, P Demetriou, M Kyriakou, P Gerasimou, G Herodotou, ... Molecular Case Studies 8 (3), a006168, 2022 | 1 | 2022 |
| A mosaic PDGFRB variant in a patient with Kosaki overgrowth syndrome A Miltiadous, P Gerasimou, G Shianiou, M Johnson, Y Kyprianou, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 141-141, 2024 | | 2024 |
| Novel likely pathogenic variant c. 588_612del (p. Trp196CysfsTer5) in EBP gene in a Cypriot family with Conradi-Hunermann Syndrome E Athanasiou, I Savvidou, S Ourani, A Miltiadous, P Gerasimou, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 137-137, 2024 | | 2024 |
| A pathogenic variant in THRA as the cause of Congenital non-goitrous Hypothyroidism in a pair of monozygotic twins V Anastasiadou, A Miltiadous, P Gerasimou, R Metaxa, N Skordis, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 132-132, 2024 | | 2024 |
| Single-cell analysis of bone marrow CD8+ T cells in Myeloid Neoplasms predicts response to treatment with Azacitidine A Tasis, NE Papaioannou, M Grigoriou, N Paschalidis, K Loukogiannaki, ... medRxiv, 2023.12. 30.23300608, 2023 | | 2023 |
| Seminoma in 46, XY Gonadal Dysgenesis: Rare Presentation and Review of the Literature. M Adra, H Nakanishi, E Papachristodoulou, E Karaoli, P Gerasimou, ... Journal of Clinical Research in Pediatric Endocrinology, 2023 | | 2023 |
| Rare KMT2A-USP2 Fusion Using RNA Next-Generation Sequencing in a Pediatric Mixed Phenotype Acute Leukemia P Gerasimou, P Costeas, L Koumas, J Chi, K Nicolaou, A Mitsidou, ... JOURNAL OF MOLECULAR DIAGNOSTICS 24 (10), S31-S31, 2022 | | 2022 |
| Molecular Landscape of different RASopathies in the Cypriot population O Anastasiou, A Miltiadous, P Gerasimou, J Chi, Y Kyprianou, A Mitsidou, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 536-537, 2022 | | 2022 |
| A novel frameshift variant in PIEZO1 responsible for hydrops fetalis in a Cypriot family A Miltiadous, P Gerasimou, I Kyprianou, J Chi, C Sismani, P Evangelidou, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 343-343, 2022 | | 2022 |
| Unraveling the genetic thread of rare disorders by exome sequencing P Gerasimou, A Miltiadous, I Kyprianou, J Chi, V Anastasiadou, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 468-469, 2022 | | 2022 |
| The Rare LIG4 Syndrome: A case report J Chi, P Gerasimou, A Miltiadous, I Kyprianou, L Koumas, L Loizou, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 920-920, 2020 | | 2020 |
