Ouzounis, Christos

Are splicing mutations the most frequent cause of hereditary disease?

López-Bigas, N., Audit, B., Ouzounis, C., Parra, G., & Guigó, R. (2005) · FEBS Letters

RNA Research and SplicingGenomics and Rare Diseases

Cited by 412

Critical assessment of protein intrinsic disorder prediction

Necci, M., Piovesan, D., Predictors, C., Hoque, M. T., Walsh, I., Iqbal, S., Vendruscolo, M., Sormanni, P., Wang, C., Raimondi, D., et al. (2021) · Nature Methods

Protein Structure and DynamicsMachine Learning in Bioinformatics

Cited by 343

No wisdom in the crowd: genome annotation in the era of big data – current status and future prospects

Danchin, A., Ouzounis, C., Tokuyasu, T., & Zucker, J. (2018) · Microbial Biotechnology

Genomics and Phylogenetic StudiesBioinformatics and Genomic Networks

Cited by 56

Annotation inconsistencies beyond sequence similarity-based function prediction – phylogeny and genome structure

Promponas, V. J., Iliopoulos, I., & Ouzounis, C. A. (2015) · Standards in Genomic Sciences

Genomics and Phylogenetic StudiesBioinformatics and Genomic Networks

Cited by 43

The grammar of the pangenome: terms, concepts, methods, and emerging patterns—a general framework for comparative genomics and genome biology

Chasapi, A., Michailidis, A., Schriml, L. M., Donati, C., Kyrpides, N. C., & Ouzounis, C. A. (2026) · Microbiology and Molecular Biology Reviews

Genomics and Phylogenetic StudiesChromosomal and Genetic Variations

Cited by 0