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Mark E Robson

  1. "Vignesh Ravichandran"
Formats
  1. Journal Article (11)
  2. Meeting Abstract (6)
Groups
  1. Breast Medicine Service (17)
  2. Clinical Genetics Service (17)
  3. Department of Medicine (17)
  4. GSK Faculty (17)
  5. Population Sciences Research Program (17)
  6. Solid Tumor Oncology Division (17)

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People
  1. Kenneth Offit (17)
  2. Vignesh Ravichandran (17)
  3. Vijai Joseph (17)
  4. Zsofia Stadler (13)
  5. Michael Walsh (11)
  6. Yelena Kemel (11)

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Years
  1. 2023 (2)
  2. 2022 (1)
  3. 2020 (4)
  4. 2019 (3)
  5. 2018 (2)
  6. 2017 (2)

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Publications
  1. Journal of Clinical Oncology (7)
  2. JCO Precision Oncology (2)
  3. American Journal of Human Genetics (1)
  4. Cancer Discovery (1)
  5. Cancer Epidemiology Biomarkers and Prevention (1)
  6. Cancer Research (1)

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Publishers
  1. American Society of Clinical Oncology (9)
  2. American Association for Cancer Research (4)
  3. Nature Publishing Group (2)
  4. American Medical Association (1)
  5. Cell Press (1)

Results (17)

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  • Frequency of actionable cancer predisposing germline mutations in patients with lung cancers
    Meeting Abstract

    Mukherjee, S.; Zauderer, M. G.; Ravichandran, V.; Kemel, Y.; Mandelker, D.; Pradhan, N.; Zehir, A.; Lipkin, S. M.; Srinivasan, P.; Bandlamudi, C.; more...
    Journal of Clinical Oncology (2018)

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  • Detection of germline homologous recombination deficiency (HRD) in patients with metastatic esophagogastric (EG) cancer using clinical next generation sequencing (NGS)
    Meeting Abstract

    Janjigian, Y. Y.; Jonsson, P.; Kemel, Y.; Joseph, V.; Tuvy, Y.; Shameer, Z.; Ravichandran, V.; Zhang, L. Y.; Mandelker, D.; Ku, G. Y.; more...
    Journal of Clinical Oncology (2018)

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  • The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk
    Journal Article

    Slavin, T. P.; Maxwell, K. N.; Lilyquist, J.; Vijai, J.; Neuhausen, S. L.; Hart, S. N.; Ravichandran, V.; Thomas, T.; Maria, A.; Villano, D.; more...
    npj Breast Cancer (2017)

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  • Mutation detection in patients with advanced cancer by universal sequencing of cancer-related genes in tumor and normal DNA vs guideline-based germline testing
    Journal Article

    Mandelker, D.; Zhang, L.; Kemel, Y.; Stadler, Z. K.; Joseph, V.; Zehir, A.; Pradhan, N.; Arnold, A.; Walsh, M. F.; Li, Y.; more...
    JAMA - Journal of the American Medical Association (2017)

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  • Cancer susceptibility mutations in individuals with breast and ovarian cancer using next-generation sequencing
    Meeting Abstract

    Offit, K.; Schrader, K. A.; Maxwell, K. N.; Vijai, J.; Hart, S.; Thomas, T.; Wubbenhorst, B.; Ravichandran, V.; Moore, R.; Hu, C.; more...
    Journal of Clinical Oncology (2016)

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  • A recurrent ERCC3 truncating mutation confers moderate risk for breast cancer
    Journal Article

    Vijai, J.; Topka, S.; Villano, D.; Ravichandran, V.; Maxwell, K. N.; Maria, A.; Thomas, T.; Gaddam, P.; Lincoln, A.; Kazzaz, S.; more...
    Cancer Discovery (2016)

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  • Evaluation of ACMG-guideline-based variant classification of cancer susceptibility and non-cancer-associated genes in families affected by breast cancer
    Journal Article

    Maxwell, K. N.; Hart, S. N.; Vijai, J.; Schrader, K. A.; Slavin, T. P.; Thomas, T.; Wubbenhorst, B.; Ravichandran, V.; Moore, R. M.; Hu, C.; more...
    American Journal of Human Genetics (2016)

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