Potapova, Tamara
Stowers Institute for Medical Research
6 papers on CoChatORCID 0000-0003-2761-1795
Most cited papers
- Verified
The complete sequence of a human genome
Nurk, S., Koren, S., Rhie, A., Rautiainen, M., Bzikadze, A. V., Mikheenko, A., Vollger, M. R., Altemose, N., Uralsky, L., Gershman, A., et al. (2022) · Science
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 3,136
- Verified
Telomere-to-telomere assembly of a complete human X chromosome
Miga, K. H., Koren, S., Rhie, A., Vollger, M. R., Gershman, A., Bzikadze, A., Brooks, S., Howe, E., Porubsky, D., Logsdon, G. A., et al. (2020) · Nature
Genomics and Phylogenetic StudiesChromosomal and Genetic Variations
Cited by 765
- Verified
Complete genomic and epigenetic maps of human centromeres
Altemose, N., Logsdon, G. A., Bzikadze, A. V., Sidhwani, P., Langley, S. A., Caldas, G. V., Hoyt, S. J., Uralsky, L., Ryabov, F. D., Shew, C. J., et al. (2022) · Science
Chromosomal and Genetic VariationsGenomic variations and chromosomal abnormalities
Cited by 618
- Verified
The complete sequence of a human Y chromosome
Rhie, A., Nurk, S., Cechova, M., Hoyt, S. J., Taylor, D. J., Altemose, N., Hook, P. W., Koren, S., Rautiainen, M., Alexandrov, I. A., et al. (2023) · Nature
Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesGenomics and Phylogenetic Studies
Cited by 471
- Verified
Semi-automated assembly of high-quality diploid human reference genomes
Jarvis, E. D., Formenti, G., Rhie, A., Guarracino, A., Yang, C., Wood, J., Tracey, A., Thibaud-Nissen, F., Vollger, M. R., Porubsky, D., et al. (2022) · Nature
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 209
- 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
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