Elsevier Science, Inc.

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People

  1. Offit
    Offit
  2. Stadler
    Stadler
  3. Robson
    Robson
  4. Mandelker
    Mandelker
  5. Birsoy
    Birsoy
  6. Joseph
    Joseph
  7. Carlo
    Carlo
  8. Salo-Mullen
    Salo-Mullen
  9. Kemel
    Kemel
  10. Ladanyi
    Ladanyi

Groups

  1. Clinical Genetics Service (34)
  2. Department of Medicine (34)
  3. Population Sciences Research Program (34)
  4. Solid Tumor Oncology Division (34)
  5. Survivorship Research (29)
  6. GSK Faculty (23)
  7. Center for Pancreatic Cancer Research (17)
  8. Department of Pathology and Laboratory Medicine (16)
  9. Breast Medicine Service (11)
  10. Surgery (10)
Search Within
  1. "Clinical Genetics Service"
Formats
  1. Journal Article (18)
  2. Meeting Abstract (13)
  3. Conference Paper (1)
  4. Guidelines (1)
  5. Review (1)
Groups
  1. Clinical Genetics Service (34)
  2. Department of Medicine (34)
  3. Population Sciences Research Program (34)
  4. Solid Tumor Oncology Division (34)
  5. Survivorship Research (29)
  6. GSK Faculty (23)

More Groups

People
  1. Kenneth Offit (21)
  2. Zsofia Stadler (17)
  3. Mark Robson (9)
  4. Diana Mandelker (8)
  5. Liying Zhang (7)
  6. Michael Walsh (7)

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Years
  1. 2024 (2)
  2. 2023 (4)
  3. 2022 (2)
  4. 2020 (5)
  5. 2019 (4)
  6. 2017 (1)

More Years

Publications
  1. Journal of Molecular Diagnostics (12)
  2. European Urology (5)
  3. Journal of the American College of Surgeons (4)
  4. Lancet (3)
  5. Cancer Genetics and Cytogenetics (2)
  6. Clinical Gastroenterology and Hepatology (2)

More Publications

Results (34)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Does tumor mutation burden explain tumor infiltrating lymphocytes in microsatellite instable (MSI), microsatellite stable (MSS) and POLE or POLD1 (POLE/D1) mutant colon cancer?
    Meeting Abstract

    Keshinro, A.; Vanderbilt, C.; Shia, J.; Stadler, Z.; Chen, C. T.; Weiser, M. R.
    Journal of the American College of Surgeons (2020)

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  • Recommendations for long-term follow-up of adults with heritable retinoblastoma
    Journal Article

    Tonorezos, E. S.; Friedman, D. N.; Barnea, D.; Bosscha, M. I.; Chantada, G.; Dommering, C. J.; de Graaf, P.; Dunkel, I. J.; Fabius, A. W. M.; Francis, J. H.; more...
    Ophthalmology (2020)

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  • Risk of metachronous colorectal neoplasm after a segmental colectomy in lynch syndrome patients according to mismatch repair gene status
    Conference Paper

    Quezada-Diaz, F. F.; Hameed, I.; von Mueffling, A.; Salo-Mullen, E. E.; Catalano, J. D.; Smith, J. J.; Weiser, M. R.; Garcia-Aguilar, J.; Stadler, Z. K.; Guillem, J. G.
    Elsevier Science, Inc. (2020)

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  • False retained mismatch repair protein expression in microsatellite instability-high cancers is associated with missense mutations in mismatch repair genes
    Meeting Abstract

    Rana, S.; Stadler, Z.; Schwark, A.; Yaeger, R.; Middha, S.; Shia, J.; Zehir, A.; Hechtman, J.
    Journal of Molecular Diagnostics (2019)

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  • Integrated germline and somatic analysis identifies actionable cancer predisposing germline mutations in 9,734 patients with advanced cancers
    Meeting Abstract

    Jayakumaran, G.; Mandelker, D.; Birsoy, O.; Jairam, S.; Li, Y.; Yang, C.; Somar, J.; Rai, V.; Syed, A.; Benayed, R.; more...
    Journal of Molecular Diagnostics (2019)

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  • Germline RAD51B loss-of-function variants confer susceptibility to hereditary breast and ovarian cancers and result in homologous recombination deficient tumors
    Meeting Abstract

    Mandelker, D.; Mukherjee, S.; Setton, J.; Cadoo, K.; Selenica, P.; Kemel, Y.; Ceyhan-Birsoy, O.; Sheehan, M.; Tkachuk, K.; Brown, D.; more...
    Journal of Molecular Diagnostics (2019)

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  • Familial kidney cancer: Implications of new syndromes and molecular insights
    Review

    Carlo, M. I.; Hakimi, A. A.; Stewart, G. D.; Bratslavsky, G.; Brugarolas, J.; Chen, Y. B.; Linehan, W. M.; Maher, E. R.; Merino, M. J.; Offit, K.; more...
    European Urology (2019)

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  • Improved screening for cancer predisposition mutations in patients with advanced solid tumors enabled by tumor-normal sequencing
    Meeting Abstract

    Mandelker, D.; Zhang, L.; Kemel, Y.; Stadler, Z.; Joseph, V.; Zehir, A.; Pradhan, N.; Arnold, A. G.; Walsh, M.; Birsoy, O.; more...
    Journal of Molecular Diagnostics (2017)

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  • CDH1 splice site variant c.387+1G>a emphasizes the importance of functional studies
    Meeting Abstract

    Yelskaya, Z.; Somar, J.; Bacares, R.; Salo-Mullen, E. E.; Yang, C.; Ahmed, S.; Stadler, Z. K.; Zhang, L.
    Journal of Molecular Diagnostics (2016)

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  • A two-for-one deal: Detecting germline cancer predisposition variants concurrently with tumor somatic mutations in 777 patients analyzed by MSK-IMPACT
    Meeting Abstract

    Mandelker, D.; Li, Y.; Prasad, M.; Syed, A.; Balakrishnan, A. R.; Chandramohan, R.; Delair, D.; Argueta, S.; Yang, C.; Arnold, A.; more...
    Journal of Molecular Diagnostics (2016)

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