Harvey, William T.
University of Washington
12 papers on CoChatORCID 0000-0003-0646-7528
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
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
Byrska-Bishop, M., Evani, U. S., Zhao, X., Basile, A. O., Abel, H. J., Regier, A. A., Corvelo, A., Clarke, W. E., Musunuri, R., Nagulapalli, K., et al. (2022) · Cell
Genetic Associations and EpidemiologyGenomics and Phylogenetic Studies
Cited by 1,094
- Verified
Haplotype-resolved diverse human genomes and integrated analysis of structural variation
Ebert, P., Audano, P. A., Zhu, Q., Rodriguez-Martin, B., Porubsky, D., Bonder, M. J., Sulovari, A., Ebler, J., Zhou, W., Serra Mari, R., et al. (2021) · Science
Genomic variations and chromosomal abnormalitiesGenomics and Phylogenetic Studies
Cited by 702
- 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
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Zhou, X., Feliciano, P., Shu, C., Wang, T., Astrovskaya, I., Hall, J. B., Obiajulu, J. U., Wright, J. R., Murali, S. C., Xu, S. X., et al. (2022) · Nature Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 453
- Verified
Segmental duplications and their variation in a complete human genome
Vollger, M. R., Guitart, X., Dishuck, P. C., Mercuri, L., Harvey, W. T., Gershman, A., Diekhans, M., Sulovari, A., Munson, K. M., Lewis, A. P., et al. (2022) · Science
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 350
- 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
Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads
Human Genome Structural Variation Consortium, Porubsky, D., Ebert, P., Audano, P. A., Vollger, M. R., Harvey, W. T., Marijon, P., Ebler, J., Munson, K. M., Sorensen, M., et al. (2021) · Nature Biotechnology
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 203
- 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
Structurally divergent and recurrently mutated regions of primate genomes
Mao, Y., Harvey, W. T., Porubsky, D., Munson, K. M., Hoekzema, K., Lewis, A. P., Audano, P. A., Rozanski, A., Yang, X., Zhang, S., et al. (2023) · Cell
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 73
- Verified
Gaps and complex structurally variant loci in phased genome assemblies
Porubsky, D., Vollger, M. R., Harvey, W. T., Rozanski, A. N., Ebert, P., Hickey, G., Hasenfeld, P., Sanders, A. D., Stober, C., Human Pangenome Reference Consortium, et al. (2023) · Genome Research
Genomics and Phylogenetic StudiesGenomic variations and chromosomal abnormalities
Cited by 58
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