Ioannidis, Nilah M.

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

Ioannidis, N. M., Rothstein, J. H., Pejaver, V., Middha, S., McDonnell, S. K., Baheti, S., Musolf, A., Li, Q., Holzinger, E., Karyadi, D., et al. (2016) · The American Journal of Human Genetics

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 2,908

Personal transcriptome variation is poorly explained by current genomic deep learning models

Huang, C., Shuai, R. W., Baokar, P., Chung, R., Rastogi, R., Kathail, P., & Ioannidis, N. M. (2023) · Nature Genetics

Genetic Associations and EpidemiologyGenomics and Chromatin Dynamics

Cited by 127

Cross-protein transfer learning substantially improves disease variant prediction

Jagota, M., Ye, C., Albors, C., Rastogi, R., Koehl, A., Ioannidis, N., & Song, Y. S. (2022) · Genome biology

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 68