| A Novel Point Mutation in the KCNJ5 Gene Causing Primary Hyperaldosteronism and Early-Onset Autosomal Dominant Hypertension E Charmandari, A Sertedaki, T Kino, C Merakou, DA Hoffman, MM Hatch, ... The Journal of Clinical Endocrinology & Metabolism 97 (8), E1532-E1539, 2012 | 138 | 2012 |
| Stress-induced aldosterone hyper-secretion in a substantial subset of patients with essential hypertension A Markou, A Sertedaki, G Kaltsas, II Androulakis, C Marakaki, T Pappa, ... The Journal of Clinical Endocrinology & Metabolism 100 (8), 2857-2864, 2015 | 118 | 2015 |
| Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe A Voutetakis, M Argyropoulou, A Sertedaki, S Livadas, P Xekouki, ... The Journal of Clinical Endocrinology & Metabolism 89 (5), 2200-2206, 2004 | 116 | 2004 |
| The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP 21A2 gene S Livadas, M Dracopoulou, A Dastamani, A Sertedaki, M Maniati‐Christidi, ... Clinical endocrinology 82 (4), 543-549, 2015 | 99 | 2015 |
| Pituitary stalk interruption syndrome and isolated pituitary hypoplasia may be caused by mutations in holoprosencephaly-related genes C Tatsi, A Sertedaki, A Voutetakis, E Valavani, MA Magiakou, ... The Journal of Clinical Endocrinology & Metabolism 98 (4), E779-E784, 2013 | 66 | 2013 |
| A novel point mutation of the human glucocorticoid receptor gene causes primary generalized glucocorticoid resistance through impaired interaction with the LXXLL motif of the … NC Nicolaides, ML Roberts, T Kino, G Braatvedt, DE Hurt, E Katsantoni, ... The Journal of Clinical Endocrinology & Metabolism 99 (5), E902-E907, 2014 | 62 | 2014 |
| Glucocorticoid signaling and epigenetic alterations in stress-related disorders N Mourtzi, A Sertedaki, E Charmandari International Journal of Molecular Sciences 22 (11), 5964, 2021 | 58 | 2021 |
| Increased glucocorticoid receptor expression in sepsis is related to heat shock proteins, cytokines, and cortisol and is associated with increased mortality K Vardas, S Ilia, A Sertedaki, E Charmandari, E Briassouli, D Goukos, ... Intensive care medicine experimental 5, 1-17, 2017 | 56 | 2017 |
| Pituitary stalk interruption syndrome: cause, clinical manifestations, diagnosis, and management A Voutetakis, A Sertedaki, C Dacou-Voutetakis Current Opinion in Pediatrics 28 (4), 545-550, 2016 | 51 | 2016 |
| Primary aldosteronism: the next five years JW Funder Hormone and Metabolic Research 49 (12), 977-983, 2017 | 45 | 2017 |
| A novel point mutation in the DNA-binding domain (DBD) of the human glucocorticoid receptor causes primary generalized glucocorticoid resistance by disrupting the hydrophobic … ML Roberts, T Kino, NC Nicolaides, DE Hurt, E Katsantoni, A Sertedaki, ... The Journal of Clinical Endocrinology & Metabolism 98 (4), E790-E795, 2013 | 45 | 2013 |
| Next generation sequencing targeted gene panel in Greek MODY patients increases diagnostic accuracy EB Tatsi, C Kanaka‐Gantenbein, A Scorilas, GP Chrousos, A Sertedaki Pediatric Diabetes 21 (1), 28-39, 2020 | 38 | 2020 |
| Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X) A Voutetakis, M Maniati-Christidi, C Kanaka-Gantenbein, M Dracopoulou, ... European journal of endocrinology 150 (3), 257-264, 2004 | 37 | 2004 |
| A novel mutation of the hGR gene causing Chrousos syndrome NC Nicolaides, EB Geer, D Vlachakis, ML Roberts, AMG Psarra, ... European Journal of Clinical Investigation 45 (8), 782-791, 2015 | 36 | 2015 |
| Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance NC Nicolaides, A Lamprokostopoulou, A Sertedaki, E Charmandari Hormones 15 (1), 23-34, 2016 | 33 | 2016 |
| Conception and pregnancy outcome in a patient with 11-bp deletion of the steroidogenic acute regulatory protein gene A Sertedaki, K Pantos, C Vrettou, G Kokkali, C Christofidou, E Kanavakis, ... Fertility and sterility 91 (3), 934. e15-934. e18, 2009 | 32 | 2009 |
| Low TSH congenital hypothyroidism: identification of a novel mutation of the TSH ß-subunit gene in one sporadic case (C85R) and of mutation Q49stop in two siblings with … A Sertedaki, A Papadimitriou, A Voutetakis, M Dracopoulou, ... Pediatric research 52 (6), 935-940, 2002 | 31 | 2002 |
| Comparative functional analysis of two fibroblast growth factor receptor 1 (FGFR1) mutations affecting the same residue (R254W and R254Q) in isolated hypogonadotropic … V Koika, P Varnavas, H Valavani, Y Sidis, L Plummer, A Dwyer, R Quinton, ... Gene 516 (1), 146-151, 2013 | 26 | 2013 |
| Functional characterization of the hGRαT556I causing Chrousos syndrome NC Nicolaides, E Skyrla, D Vlachakis, AMG Psarra, P Moutsatsou, ... European Journal of Clinical Investigation 46 (1), 42-49, 2016 | 25 | 2016 |
| Insulin dependent diabetes mellitus (IDDM) and autoimmune thyroiditis in a boy with a ring chromosome 18: additional evidence of autoimmunity or IDDM gene (s) on chromosome 18 C Dacou-Voutetakis, A Sertedaki, M Maniatis-Christidis, C Sarri, ... Journal of medical genetics 36 (2), 156-158, 1999 | 24 | 1999 |
