Harrison, Steven M.

Genomic data in the all of us research program

The All of Us Research Program Genomics Investigators, Manuscript Writing Group, Bick, A. G., Metcalf, G. A., Mayo, K. R., Lichtenstein, L., Rura, S., Carroll, R. J., Musick, A., Linder, J. E., et al. (2024) · Nature

Genetic Associations and EpidemiologyGenomics and Rare Diseases

Cited by 829

Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification framework

Tavtigian, S. V., Greenblatt, M. S., Harrison, S. M., Nussbaum, R. L., Prabhu, S. A., Boucher, K. M., & Biesecker, L. G. (2018) · Genetics in Medicine

Genomics and Rare DiseasesBRCA gene mutations in cancer

Cited by 590

Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar

Harrison, S. M., Dolinsky, J. S., Knight Johnson, A. E., Pesaran, T., Azzariti, D. R., Bale, S., Chao, E. C., Das, S., Vincent, L., & Rehm, H. L. (2017) · Genetics in Medicine

Genomics and Rare DiseasesClinical Laboratory Practices and Quality Control

Cited by 234