Koleske, Megan L.

Opportunities and challenges for the computational interpretation of rare variation in clinically important genes

McInnes, G., Sharo, A. G., Koleske, M. L., Brown, J. E. H., Norstad, M., Adhikari, A. N., Wang, S., Brenner, S. E., Halpern, J., Koenig, B. A., et al. (2021) · The American Journal of Human Genetics

Genomics and Rare DiseasesArtificial Intelligence in Healthcare and Education

Cited by 86

Illuminating the function of the orphan transporter, SLC22A10, in humans and other primates

Yee, S. W., Ferrández-Peral, L., Alentorn-Moron, P., Fontsere, C., Ceylan, M., Koleske, M. L., Handin, N., Artegoitia, V. M., Lara, G., Chien, H.-C., et al. (2024) · Nature Communications

Drug Transport and Resistance MechanismsPharmacogenetics and Drug Metabolism

Cited by 4

Illuminating the Function of the Orphan Transporter, SLC22A10 in Humans and Other Primates

Giacomini, K., Yee, S. W., Ferrández-Peral, L., Alentorn, P., Fontsere, C., Ceylan, M., Koleske, M., Handin, N., Artegoitia, V., Lara, G., et al. (2023) · Research Square

Drug Transport and Resistance MechanismsPharmacogenetics and Drug Metabolism

Cited by 1