Zhou, Weichen
New York Genome Center
4 papers on CoChatORCID 0000-0003-4755-1072
Most cited papers
- 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
A robust benchmark for detection of germline large deletions and insertions
Zook, J. M., Hansen, N. F., Olson, N. D., Chapman, L., Mullikin, J. C., Xiao, C., Sherry, S., Koren, S., Phillippy, A. M., Boutros, P. C., et al. (2020) · Nature Biotechnology
Genomic variations and chromosomal abnormalitiesGenomics and Phylogenetic Studies
Cited by 418
- Verified
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network
McConnell, M. J., Moran, J. V., Abyzov, A., Akbarian, S., Bae, T., Cortes-Ciriano, I., Erwin, J. A., Fasching, L., Flasch, D. A., Freed, D., et al. (2017) · Science
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 262
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