Adhikari, Aashish N.
Illumina (United States)
3 papers on CoChatORCID 0000-0003-4305-9494
Most cited papers
- Verified
The landscape of tolerated genetic variation in humans and primates
Gao, H., Hamp, T., Ede, J., Schraiber, J. G., McRae, J., Singer-Berk, M., Yang, Y., Dietrich, A., Fiziev, P., Kuderna, L., et al. (2023) · Science
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 183
- Verified
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
- Verified
VIPdb, a genetic variant impact predictor database
Hu, Z., Yu, C., Furutsuki, M., Andreoletti, G., Ly, M., Hoskins, R., Adhikari, A. N., & Brenner, S. E. (2019) · Human Mutation
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 37
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free