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2022: “Rare Diseases “diagnostic odysseys”: the road to the end through new scientific discoveries and the hope of personalized medicine” funded by 3Billion.

2022: “Study of complex structural chromosomal rearrangements in patients with neurodevelopmental disorders using Optical Genome Mapping (OGM) and evaluation of the diagnostic yield”.  Pilot study in collaboration with the Genotypos and Bionano Genomics. 

2020-2021: ”Exploring the genetics of Familial Intellectual Disability (ID) towards personalized therapeutic options“, 1st Open Access Call for the provision of research services (pMedGR).

2018-2022: iStemTheOS- Επαγόμενα Πολυδύναμα Βλαστοκύτταρα για την κυτταρική Θεραπεία της οστεοαρθρίτιδας, ΕΥΔ ΕΠΑνΕΚ 2014-2020: Επιχειρησιακό Πρόγραμμα, Ανταγωνιστικότητα-Επιχειρηματικότητα-Καινοτομία. ΔΡΑΣΗ ΕΘΙΚΗΣ ΕΜΒΕΛΕΙΑΣ: ΕΡΕΥΝΩ-ΔΗΜΙΟΥΡΓΩ-ΚΑΙΝΟΤΟΜΩ

2017-2021: ERASMUS+: N-GeneS - Connecting Genes to Rare Diseases through Next Generation Sequencingand Advanced Teaching Methods, This module aims at enhancing the quality of student’s knowledge and skills through open and innovative practices in the field of modern genetics, Project number: 2017-1-EL01-KA203-036361