Greenblatt, Marc S.

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

Plon, S. E., Eccles, D. M., Easton, D., Foulkes, W. D., Genuardi, M., Greenblatt, M. S., Hogervorst, F. B. L., Hoogerbrugge, N., Spurdle, A. B., Tavtigian, S. V., et al. (2008) · Human Mutation

BRCA gene mutations in cancerGenomics and Rare Diseases

Cited by 912

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

In silico analysis of missense substitutions using sequence-alignment based methods

Tavtigian, S. V., Greenblatt, M. S., Lesueur, F., Byrnes, G. B., & for the IARC Unclassified Genetic Variants Working Group (2008) · Human Mutation

Genomics and Rare DiseasesBRCA gene mutations in cancer

Cited by 199

Evolutionary conservation and somatic mutation hotspot maps of p53: correlation with p53 protein structural and functional features

Walker, D. R., Bond, J. P., Tarone, R. E., Harris, C. C., Makalowski, W., Boguski, M. S., & Greenblatt, M. S. (1999) · Oncogene

Cancer-related Molecular PathwaysCancer Genomics and Diagnostics

Cited by 198

Calibration of Multiple In Silico Tools for Predicting Pathogenicity of Mismatch Repair Gene Missense Substitutions

Thompson, B. A., Greenblatt, M. S., Vallee, M. P., Herkert, J. C., Tessereau, C., Young, E. L., Adzhubey, I. A., Li, B., Bell, R., Feng, B., et al. (2013) · Human Mutation

Genomics and Rare DiseasesGenetic factors in colorectal cancer

Cited by 95