Findlay, Gregory M.

Accurate classification of BRCA1 variants with saturation genome editing

Findlay, G. M., Daza, R. M., Martin, B., Zhang, M. D., Leith, A. P., Gasperini, M., Janizek, J. D., Huang, X., Starita, L. M., & Shendure, J. (2018) · Nature

BRCA gene mutations in cancerGenomics and Rare Diseases

Cited by 843

Whole-organism lineage tracing by combinatorial and cumulative genome editing

McKenna, A., Findlay, G. M., Gagnon, J. A., Horwitz, M. S., Schier, A. F., & Shendure, J. (2016) · Science

CRISPR and Genetic EngineeringSingle-cell and spatial transcriptomics

Cited by 766

Saturation editing of genomic regions by multiplex homology-directed repair

Findlay, G. M., Boyle, E. A., Hause, R. J., Klein, J. C., & Shendure, J. (2014) · Nature

CRISPR and Genetic EngineeringDNA Repair Mechanisms

Cited by 362

CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic Deletions

Gasperini, M., Findlay, G. M., McKenna, A., Milbank, J. H., Lee, C., Zhang, M. D., Cusanovich, D. A., & Shendure, J. (2017) · The American Journal of Human Genetics

CRISPR and Genetic EngineeringGenomics and Chromatin Dynamics

Cited by 143

Saturation Genome Editing Resolves the Functional Spectrum of Pathogenic VHL Alleles

Buckley, M., Kajba, C. M., Forrester, N., Terwagne, C., Sawyer, C., Shepherd, S. T. C., Jonghe, J. D., Dace, P., Turajlic, S., & Findlay, G. M. (2023) · Nature Genetics

Genomics and Rare DiseasesCancer Genomics and Diagnostics

Cited by 62

Saturation genome editing maps the functional spectrum of pathogenic VHL alleles

Buckley, M., Terwagne, C., Ganner, A., Cubitt, L., Brewer, R., Kim, D.-K., Kajba, C. M., Forrester, N., Dace, P., De Jonghe, J., et al. (2024) · Nature Genetics

Genomics and Rare DiseasesCancer Genomics and Diagnostics

Cited by 62