Whole Exome Sequencing Points towards a Multi-Gene Synergistic Action in the Pathogenesis of Congenital Combined Pituitary Hormone DeficiencyAmalia Sertedaki, Christina Kanaka‐Gantenbein, Tania Siahanidou et al.|Cells|2022Cited by 13
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, Soultana Siahanidou et al.|58th Annual ESPE Meeting (ESPE 2019)|2019Cited by 0