Koenig, Barbara A.
University of California, San Francisco
9 papers on CoChatORCID 0000-0003-3227-6768
Most cited papers
- Verified
A draft human pangenome reference.
Liao, W.-W., Asri, M., Ebler, J., Doerr, D., Haukness, M., Hickey, G., Lu, S., Lucas, J. K., Monlong, J., Abel, H. J., et al. (2023) · Nature
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 1,129
- Verified
The Human Pangenome Project: a global resource to map genomic diversity
Wang, T., Antonacci-Fulton, L., Howe, K., Lawson, H. A., Lucas, J. K., Phillippy, A. M., Popejoy, A. B., Asri, M., Carson, C., Chaisson, M. J. P., et al. (2022) · Nature
Genomics and Phylogenetic StudiesGenetic Associations and Epidemiology
Cited by 494
- Verified
Pangenome graph construction from genome alignments with Minigraph-Cactus
Hickey, G., Monlong, J., Ebler, J., Novak, A. M., Eizenga, J. M., Gao, Y., Human Pangenome Reference Consortium, Abel, H. J., Antonacci-Fulton, L. L., Asri, M., et al. (2024) · Nature Biotechnology
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 343
- Verified
Ethical issues in stopping randomized trials early because of apparent benefit.
Mueller, P. S., Montori, V. M., Bassler, D., Koenig, B. A., & Guyatt, G. H. (2007) · Annals of Internal Medicine
Ethics in Clinical ResearchStatistical Methods in Clinical Trials
Cited by 202
- Verified
Recombination between heterologous human acrocentric chromosomes
Guarracino, A., Buonaiuto, S., de Lima, L. G., Potapova, T., Rhie, A., Koren, S., Rubinstein, B., Fischer, C., Human Pangenome Reference Consortium, Abel, H. J., et al. (2023) · Nature
Chromosomal and Genetic VariationsGenomic variations and chromosomal abnormalities
Cited by 134
- Verified
Increased mutation and gene conversion within human segmental duplications
Vollger, M. R., Dishuck, P. C., Harvey, W. T., DeWitt, W. S., Guitart, X., Goldberg, M. E., Rozanski, A. N., Lucas, J., Asri, M., Human Pangenome Reference Consortium, et al. (2023) · Nature
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 104
- Verified
Have We Asked Too Much of Consent?
Koenig, B. A. (2014) · Hastings Center Report
Ethics in Clinical ResearchEthics and bioethics in healthcare
Cited by 87
- 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
Fixing Research Subjects Protection in the United States: Moving Beyond Consent
Koenig, B. A. (2013) · Mayo Clinic Proceedings
Ethics in Clinical ResearchEthics and bioethics in healthcare
Cited by 7
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