Angelo Condell is an early-career clinical bioinformatician, genomic variant curator, and 'DNA Detective' predominantly based in Canberra, Australia.
He is passionate about the analysis and interpretation of genetic sequencing data, with a wide range of analytic experience across many phenotypes, including neurodevelopmental disorders (NDDs), inherited cardiac conditions (ICCs), connective tissue disorders (CTDs), and more.
Angelo openly and proudly identifies as a queer+ transman, and is an active member of the QueersInScience ACT branch, advocating for LGBTQIA+ representation in STEMM.
Angelo also lives with the classic mitis subtype of Ehlers-Danlos syndrome (cEDS; OMIM #130010), which sparked his curiosity and passion for diagnostic genomics, bioinformatic technologies, and how the intersection between the two can actively help his fellow patients and families within the rare disease community.