| Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism MI Stamou, NA Georgopoulos Metabolism 86, 124-134, 2018 | 183 | 2018 |
| Discovering genes essential to the hypothalamic regulation of human reproduction using a human disease model: adjusting to life in the “-omics” era MI Stamou, KH Cox, WF Crowley Jr Endocrine reviews 36 (6), 603-621, 2015 | 116 | 2015 |
| Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations T Ge, MR Irvin, A Patki, V Srinivasasainagendra, YF Lin, HK Tiwari, ... Genome Medicine 14 (1), 70, 2022 | 104 | 2022 |
| Sex differentiation with regard to coronary artery disease NA Papakonstantinou, MI Stamou, NG Baikoussis, J Goudevenos, ... Journal of cardiology 62 (1), 4-11, 2013 | 74 | 2013 |
| Newly diagnosed diabetes vs. pre-existing diabetes upon admission for COVID-19: Associated factors, short-term outcomes, and long-term glycemic phenotypes SJ Cromer, C Colling, D Schatoff, M Leary, MI Stamou, DJ Selen, ... Journal of diabetes and its complications 36 (4), 108145, 2022 | 72 | 2022 |
| Pain management of chronic wounds: Diabetic ulcers and beyond. JE Paschou SA, Stamou M, Vuagnat H, Tentolouris N Maturitas, 2018 | 50 | 2018 |
| A balanced translocation in Kallmann syndrome implicates a long noncoding RNA, RMST, as a GnRH neuronal regulator M Stamou, SY Ng, H Brand, H Wang, L Plummer, L Best, S Havlicek, ... The Journal of Clinical Endocrinology & Metabolism 105 (3), e231-e244, 2020 | 37 | 2020 |
| Adrenal aging and its effects on the stress response and immunosenescence MI Stamou, C Colling, LE Dichtel Maturitas 168, 13-19, 2023 | 31 | 2023 |
| Impaired sexual function in young women with PCOS: the detrimental effect of anovulation D Mantzou, MI Stamou, AK Armeni, ND Roupas, K Assimakopoulos, ... The journal of sexual medicine 18 (11), 1872-1879, 2021 | 22 | 2021 |
| Prevalence and phenotypic effects of copy number variants in isolated hypogonadotropic hypogonadism MI Stamou, H Brand, M Wang, I Wong, MF Lippincott, L Plummer, ... The Journal of Clinical Endocrinology & Metabolism 107 (8), 2228-2242, 2022 | 18 | 2022 |
| Isolated GNRH deficiency: genotypic and phenotypic characteristics of the genetically heterogeneous Greek population MI Stamou, P Varnavas, M Kentrou, F Adamidou, A Voutetakis, J Jing, ... European Journal of Endocrinology 176 (3), L1-L5, 2017 | 14 | 2017 |
| Phenotypic continuum between Waardenburg syndrome and idiopathic hypogonadotropic hypogonadism in humans with SOX10 variants RA Rojas, AA Kutateladze, L Plummer, M Stamou, DL Keefe Jr, ... Genetics in Medicine 23 (4), 629-636, 2021 | 13 | 2021 |
| Next-generation sequencing refines the genetic architecture of Greek GnRH-deficient patients MI Stamou, P Varnavas, L Plummer, V Koika, NA Georgopoulos Endocrine Connections 8 (5), 468-480, 2019 | 12 | 2019 |
| Reproductive phenotypes and genotypes in men with IHH AA Dwyer, MI Stamou, E Anghel, S Hornstein, D Chen, KB Salnikov, ... The Journal of Clinical Endocrinology & Metabolism 108 (4), 897-908, 2023 | 8 | 2023 |
| Gonadotropin-releasing hormone (GnRH) deficiency under treatment: psychological and sexual functioning impacts NA Georgopoulos, AK Armeni, M Stamou, A Kentrou, EE Tsermpini, ... Hormones 17, 383-390, 2018 | 8 | 2018 |
| The p190 RhoGAPs, ARHGAP35, and ARHGAP5 are implicated in GnRH neuronal development: evidence from patients with idiopathic hypogonadotropic hypogonadism, zebrafish, and in … MF Lippincott, W Xu, AA Smith, X Miao, A Lafont, O Shennib, GJ Farley, ... Genetics in Medicine 24 (12), 2501-2515, 2022 | 7 | 2022 |
| Polycystic ovary syndrome physiologic pathways implicated through clustering of genetic loci MI Stamou, KT Smith, H Kim, R Balasubramanian, KJ Gray, MS Udler The Journal of Clinical Endocrinology & Metabolism 109 (4), 968-977, 2024 | 6 | 2024 |
| Reversible hypogonadotropic hypogonadism in men with the fertile eunuch/Pasqualini syndrome: A single-center natural history study AA Dwyer, M Stamou, IR McDonald, E Anghel, KH Cox, KB Salnikov, ... Frontiers in Endocrinology 13, 1054447, 2022 | 5 | 2022 |
| POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression HJ Cho, F Gurbuz, M Stamou, LD Kotan, SM Farmer, S Can, MF Tompkins, ... Frontiers in Endocrinology 14, 1203542, 2023 | 4 | 2023 |
| Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanisms J Cassin, MI Stamou, KW Keefe, KE Sung, CC Bojo, KJ Tonsfeldt, ... JCI insight 8 (3), e164324, 2023 | 4 | 2023 |
Neoklis GeorgopoulosProfessor Of Endocrinology, Reproductive Endocrinology, University of PatrasVerifierad e-postadress på upatras.gr
