| 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 | 448 | 2010 |
| 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 | 237 | 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 |
| Friend of Prmt1, a novel chromatin target of protein arginine methyltransferases TB van Dijk, N Gillemans, C Stein, P Fanis, J Demmers, M van de Corput, ... Molecular and cellular biology 30 (1), 260-272, 2010 | 77 | 2010 |
| Five friends of methylated chromatin target of protein-arginine-methyltransferase [prmt]-1 (chtop), a complex linking arginine methylation to desumoylation P Fanis, N Gillemans, A Aghajanirefah, F Pourfarzad, J Demmers, ... Molecular & Cellular Proteomics 11 (11), 1263-1273, 2012 | 60 | 2012 |
| 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 |
| 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 | 31 | 2014 |
| GnRH deficient patients with congenital hypogonadotropic hypogonadism: novel genetic findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A genes in a case series and review … V Neocleous, P Fanis, M Toumba, GA Tanteles, M Schiza, F Cinarli, ... Frontiers in endocrinology 11, 550772, 2020 | 27 | 2020 |
| Central precocious puberty caused by novel mutations in the promoter and 5′-UTR region of the imprinted MKRN3 gene P Fanis, N Skordis, M Toumba, N Papaioannou, A Makris, A Kyriakou, ... Frontiers in Endocrinology 10, 460982, 2019 | 26 | 2019 |
| A novel MKRN3 nonsense mutation causing familial central precocious puberty A Christoforidis, N Skordis, P Fanis, M Dimitriadou, M Sevastidou, ... Endocrine 56, 446-449, 2017 | 25 | 2017 |
| The DNA binding factor Hmg20b is a repressor of erythroid differentiation F Esteghamat, TB van Dijk, H Braun, S Dekker, R van der Linden, J Hou, ... Haematologica 96 (9), 1252, 2011 | 22 | 2011 |
| Genotype is associated to the degree of virilization in patients with classic congenital adrenal hyperplasia V Neocleous, P Fanis, LA Phylactou, N Skordis Frontiers in Endocrinology 9, 423157, 2018 | 16 | 2018 |
| Multiple endocrine neoplasia 2 in Cyprus: evidence for a founder effect P Fanis, N Skordis, S Frangos, G Christopoulos, E Spanou-Aristidou, ... Journal of Endocrinological Investigation 41, 1149-1157, 2018 | 16 | 2018 |
| Sequential role of SOXB2 factors in GABAergic neuron specification of the dorsal midbrain N Makrides, E Panayiotou, P Fanis, C Karaiskos, G Lapathitis, S Malas Frontiers in molecular neuroscience 11, 152, 2018 | 16 | 2018 |
| Variations in the 3′ UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia V Neocleous, P Fanis, M Toumba, AAP Phedonos, M Picolos, E Andreou, ... International Journal of Endocrinology 2017, 2017 | 16 | 2017 |
| 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 | 15 | 2019 |
| 46, XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency in an infant of Greek origin A Galli-Tsinopoulou, A Serbis, EP Kotanidou, E Litou, V Dokousli, ... J Clin Res Pediatr Endocrinol 10 (1), 74-78, 2018 | 13 | 2018 |
| Pathogenic and low-frequency variants in children with central precocious puberty V Neocleous, P Fanis, M Toumba, B Gorka, I Kousiappa, GA Tanteles, ... Frontiers in endocrinology 12, 745048, 2021 | 12 | 2021 |
| The spectrum of genetic defects in congenital adrenal hyperplasia in the population of Cyprus: a retrospective analysis V Neocleous, P Fanis, M Toumba, C Stylianou, M Picolos, E Andreou, ... Hormone and Metabolic Research 51 (09), 586-594, 2019 | 11 | 2019 |
| Molecular modelling of novel ADCY3 variant predicts a molecular target for tackling obesity M Toumba, P Fanis, D Vlachakis, V Neocleous, LA Phylactou, N Skordis, ... International Journal of Molecular Medicine 49 (1), 1-11, 2022 | 10 | 2022 |
