• 2910 Citations
  • 29 Scopus h-Index
20072019

Research output per year

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Research Output

  • 2910 Citations
  • 29 Scopus h-Index
  • 67 Article
  • 3 Review article
  • 1 Conference contribution
  • 1 Comment/debate

A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients

LaDuca, H., Polley, E., Yussuf, A., Hoang, L., Gutierrez, S., Hart, S., Yadav, S., Hu, C., Na, J., Goldgar, D. E., Fulk, K., Smith, L. P., Horton, C., Profato, J., Pesaran, T., Gau, C. L., Pronold, M., Davis, B. T., Chao, E. C., Couch, F. J. & 1 others, Dolinsky, J. S., Jan 1 2019, (Accepted/In press) In : Genetics in Medicine.

Research output: Contribution to journalArticle

Open Access
  • 3 Scopus citations

    Classification of melanocytic lesions in selected and whole-slide images via convolutional neural networks

    Hart, S., Flotte, W., Norgan, A. P., Shah, K. K., Buchan, Z. R., Mounajjed, T. & Flotte, T. J., Jan 1 2019, In : Journal of Pathology Informatics. 10, 1, 5.

    Research output: Contribution to journalArticle

    Open Access
  • 1 Scopus citations

    Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort

    Li, H., LaDuca, H., Pesaran, T., Chao, E. C., Dolinsky, J. S., Parsons, M., Spurdle, A. B., Polley, E. C., Shimelis, H., Hart, S. N., Hu, C., Couch, F. J. & Goldgar, D. E., Jan 1 2019, (Accepted/In press) In : Genetics in Medicine.

    Research output: Contribution to journalArticle

    Open Access
  • Correction to: Recommendations for performance optimizations when using GATK3.8 and GATK4 (BMC Bioinformatics (2019) 20 (557) DOI: 10.1186/s12859-019-3169-7)

    Heldenbrand, J. R., Baheti, S., Bockol, M. A., Drucker, T. M., Hart, S. N., Hudson, M. E., Iyer, R. K., Kalmbach, M. T., Kendig, K. I., Klee, E. W., Mattson, N. R., Wieben, E. D., Wiepert, M., Wildman, D. E. & Mainzer, L. S., Dec 17 2019, In : BMC bioinformatics. 20, 1, 722.

    Research output: Contribution to journalComment/debate

    Open Access
  • Genome-wide association study of germline variants and breast cancer-specific mortality

    NBCS Collaborators, Mar 19 2019, In : British journal of cancer. 120, 6, p. 647-657 11 p.

    Research output: Contribution to journalArticle

    Open Access
  • 4 Scopus citations