Molecular Analysis of the <i>CYP11B2</i> Gene in 62 Patients with Hypoaldosteronism Due to Aldosterone Synthase DeficiencyChristina Merakou, Christina Kanaka‐Gantenbein, Dionisios Chrysis et al.|The Journal of Clinical Endocrinology & Metabolism|2020Cited by 16
Whole Exome Sequencing Points towards a Multi-Gene Synergistic Action in the Pathogenesis of Congenital Combined Pituitary Hormone DeficiencyAmalia Sertedaki, Christina Kanaka‐Gantenbein, Elizabeth‐Barbara Tatsi et al.|Cells|2022Cited by 13
Estimating at-risk couple rates across 1000 exome sequencing data cohort for 176 genes and its importance relevance for health policiesNikolaos M. Marinakis, Periklis Makrythanasis, Faidon‐Nikolaos Tilemis et al.|European Journal of Human Genetics|2024Cited by 2
Genetics of 21-OH Deficiency and Genotype–Phenotype Correlation: Experience of the Hellenic National Referral CenterIrene Fylaktou, Amalia Sertedaki, Anny Mertzanian et al.|Current Issues in Molecular Biology|2024Cited by 2
Whole Exome Sequencing (WES) Reveals Oligogenic Gene Mutations in a Case of Combined Pituitary Hormone Deficiency (CPHD)Amalia Sertedaki, Christina Kanaka‐Gantenbein, Elizabeth‐Barbara Tatsi et al.|58th Annual ESPE Meeting (ESPE 2019)|2019Cited by 0