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Kenneth Offit

  1. "Khedoudja Nafa"
Formats
  1. Journal Article (28)
  2. Meeting Abstract (10)
  3. Research Letter (1)
Groups
  1. Clinical Genetics Service (39)
  2. Department of Medicine (39)
  3. Department of Pathology and Laboratory Medicine (39)
  4. GSK Faculty (39)
  5. Population Sciences Research Program (39)
  6. Solid Tumor Oncology Division (39)

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People
  1. Khedoudja Nafa (39)
  2. Nathan Ellis (28)
  3. Mark Robson (16)
  4. Arnold Markowitz (10)
  5. Helen Huang (9)
  6. Jose Guillem (9)

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Years
  1. 2024 (1)
  2. 2022 (1)
  3. 2017 (2)
  4. 2009 (1)
  5. 2007 (1)
  6. 2006 (3)

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Publications
  1. American Journal of Human Genetics (8)
  2. Clinical Cancer Research (3)
  3. American Journal of Surgical Pathology (2)
  4. Cancer Research (2)
  5. Familial Cancer (2)
  6. Genetics in Medicine (2)

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Publishers
  1. Cell Press (8)
  2. American Association for Cancer Research (5)
  3. Oxford University Press (4)
  4. Lippincott Williams & Wilkins (3)
  5. Nature Publishing Group (3)
  6. Springer (3)

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Results (39)

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  • Universal germline genetic testing in patients with hematologic malignancies using DNA isolated from nail clippings
    Research Letter

    Ceyhan-Birsoy, O.; Fiala, E.; Rana, S.; Sheehan, M.; Kennedy, J.; Yelskaya, Z.; Rai, V.; Li, Y.; Yang, C.; Wong, D.; more...
    Haematologica (2024)

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  • A validation of models for prediction of pathogenic variants in mismatch repair genes
    Journal Article

    Shyr, C.; Blackford, A. L.; Huang, T.; Ke, J.; Ouardaoui, N.; Trippa, L.; Syngal, S.; Ukaegbu, C.; Uno, H.; Nafa, K.; more...
    Genetics in Medicine (2022)

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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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  • Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing
    Journal Article

    Cheng, D. T.; Prasad, M.; Chekaluk, Y.; Benayed, R.; Sadowska, J.; Zehir, A.; Syed, A.; Wang, Y. E.; Somar, J.; Li, Y.; more...
    BMC Medical Genomics (2017)

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  • cDNA analysis demonstrates that the BRCA2 intronic variant IVS4-12del5 is a deleterious mutation
    Journal Article

    Zhang, L.; Bacares, R.; Boyar, S.; Hudis, C.; Nafa, K.; Offit, K.
    Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis (2009)

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  • Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: Role in presurgical management
    Journal Article

    Guillem, J. G.; Glogowski, E.; Moore, H. G.; Nafa, K.; Markowitz, A. J.; Shia, J.; Offit, K.; Ellis, N. A.
    Annals of Surgery (2007)

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  • Increased frequency of disease-causing MYH mutations in colon cancer families
    Journal Article

    Peterlongo, P.; Mitra, N.; de Abajo, A. S.; De la Hoya, M.; Bassi, C.; Bertario, L.; Radice, P.; Glogowski, E.; Nafa, K.; CaldeĢs, T.; more...
    Carcinogenesis (2006)

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  • Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping
    Journal Article

    Ellis, N. A.; Kirchhoff, T.; Mitra, N.; Ye, T. Z.; Chuai, S.; Huang, H.; Nafa, K.; Norton, L.; Neuhausen, S.; Gordon, D.; more...
    Genetic Epidemiology (2006)

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  • Prediction of germline mutations and cancer risk in the lynch syndrome
    Journal Article

    Chen, S.; Wang, W.; Lee, S.; Nafa, K.; Lee, J.; Romans, K.; Watson, P.; Gruber, S. B.; Euhus, D.; Kinzler, K. W.; more...
    JAMA - Journal of the American Medical Association (2006)

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  • Implications of ductal carcinoma in situ in predicting BRCA status in Ashkenazi Jewish women
    Meeting Abstract

    Sukumvanich, P.; Wadsworth, E.; Nafa, K.; Kolachana, P.; Borgen, P. I.; Robson, M. E.; Offit, K.
    Annals of Surgical Oncology (2005)

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