Mehta, Bhaven K.
Broad Institute · Boston Children's Hospital · Howard Hughes Medical Institute · Harvard University · Manton Center for Orphan Disease Research
5 papers on CoChatORCID 0000-0003-1077-7895
Most cited papers
- Verified
Somatic mutation in single human neurons tracks developmental and transcriptional history
Lodato, M. A., Woodworth, M. B., Lee, S., Evrony, G. D., Mehta, B. K., Karger, A., Lee, S., Chittenden, T. W., D’Gama, A. M., Cai, X., et al. (2015) · Science
Single-cell and spatial transcriptomicsCancer Genomics and Diagnostics
Cited by 570
- Verified
Somatic mutations in cerebral cortical malformations
Jamuar, S. S., Lam, A.-T. N., Kircher, M., D’Gama, A. M., Wang, J., Barry, B. J., Zhang, X., Hill, R. S., Partlow, J. N., Rozzo, A., et al. (2014) · New England Journal of Medicine
Fetal and Pediatric Neurological DisordersGenomics and Rare Diseases
Cited by 392
- Verified
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain
Cai, X., Evrony, G. D., Lehmann, H. S., Elhosary, P. C., Mehta, B. K., Poduri, A., & Walsh, C. A. (2014) · Cell Reports
Genomic variations and chromosomal abnormalitiesCancer Genomics and Diagnostics
Cited by 318
- Verified
Cell lineage analysis in human brain using endogenous retroelements
Evrony, G. D., Lee, E., Mehta, B. K., Benjamini, Y., Johnson, R. M., Cai, X., Yang, L., Haseley, P., Lehmann, H. S., Park, P. J., et al. (2015) · Neuron
Genomic variations and chromosomal abnormalitiesSingle-cell and spatial transcriptomics
Cited by 269
- Verified
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain
Cai, X., Evrony, G. D., Lehmann, H. S., Elhosary, P. C., Mehta, B. K., Poduri, A., & Walsh, C. A. (2015) · Cell Reports
Genomic variations and chromosomal abnormalitiesCancer Genomics and Diagnostics
Cited by 42
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