Lehmann, Hillel S.
Broad Institute · Boston Children's Hospital · Howard Hughes Medical Institute · Harvard University · Manton Center for Orphan Disease Research
4 papers on CoChatORCID 0000-0003-3446-5394
Most cited papers
- Verified
Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain
Evrony, G. D., Cai, X., Lee, E., Hills, L. B., Elhosary, P. C., Lehmann, H. S., Parker, J. J., Atabay, K. D., Gilmore, E. C., Poduri, A., et al. (2012) · Cell
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 548
- 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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