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Khedoudja Nafa

  1. "Population Sciences Research Program"
Formats
  1. Journal Article (32)
  2. Meeting Abstract (11)
  3. Research Letter (1)
Groups
  1. Department of Medicine (44)
  2. Department of Pathology and Laboratory Medicine (44)
  3. Population Sciences Research Program (44)
  4. GSK Faculty (43)
  5. Solid Tumor Oncology Division (43)
  6. Survivorship Research (42)

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People
  1. Kenneth Offit (39)
  2. Nathan Ellis (28)
  3. Mark Robson (18)
  4. Arnold Markowitz (10)
  5. Helen Huang (9)
  6. Jose Guillem (9)

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Years
  1. 2024 (2)
  2. 2022 (2)
  3. 2019 (1)
  4. 2017 (3)
  5. 2010 (1)
  6. 2009 (1)

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Publications
  1. American Journal of Human Genetics (8)
  2. Clinical Cancer Research (4)
  3. Cancer Research (3)
  4. American Journal of Surgical Pathology (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 (7)
  3. Nature Publishing Group (4)
  4. Oxford University Press (4)
  5. Elsevier Science, Inc. (3)
  6. Lippincott Williams & Wilkins (3)

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Results (44)

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  • Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia
    Journal Article

    Offit, K.; Levran, O.; Mullaney, B.; Mah, K.; Nafa, K.; Batish, S. D.; Diotti, R.; Scheider, H.; Deffenbaugh, A.; Scholl, T.; more...
    JNCI: Journal of the National Cancer Institute (2003)

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  • A636P is associated with early-onset colon cancer in Ashkenazi Jews
    Journal Article

    Guillem, J. G.; Rapaport, B. S.; Kirchhoff, T.; Kolachana, P.; Nafa, K.; Glogowski, E.; Finch, R.; Huang, H.; Foulkes, W. D.; Markowitz, A.; more...
    Journal of the American College of Surgeons (2003)

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  • Incidence of non-founder BRCA1 and BRCA2 mutations in high-risk Ashkenazi breast and ovarian cancer families
    Meeting Abstract

    Kauff, N. D.; Perez-Segura, P.; Robson, M. E.; Scheuer, L.; Siegel, B.; Schluger, A.; Frank, T. S.; Nafa, K.; Parmigiani, G.; Offit, K.
    Genetics in Medicine (2002)

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  • Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancers
    Journal Article

    Offit, K.; Gilad, S.; Paglin, S.; Kolachana, P.; Roisman, L. C.; Nafa, K.; Yeugelowitz, V.; Gonzales, M.; Robson, M.; McDermott, D.; more...
    Clinical Cancer Research (2002)

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  • Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation
    Journal Article

    Kauff, N. D.; Satagopan, J. M.; Robson, M. E.; Scheuer, L.; Hensley, M.; Hudis, C. A.; Ellis, N. A.; Boyd, J.; Borgen, P. I.; Barakat, R. R.; more...
    New England Journal of Medicine (2002)

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  • Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families
    Journal Article

    Kauff, N. D.; Perez-Segura, P.; Robson, M. E.; Scheuer, L.; Siegel, B.; Schluger, A.; Rapaport, B.; Frank, T. S.; Nafa, K.; Ellis, N. A.; more...
    Journal of Medical Genetics (2002)

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  • The founder mutation MSH2*1906G→C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population
    Journal Article

    Foulkes, W. D.; Thiffault, I.; Gruber, S. B.; Horwitz, M.; Hamel, N.; Lee, C.; Shia, J.; Markowitz, A.; Figer, A.; Friedman, E.; more...
    American Journal of Human Genetics (2002)

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  • Analysis of MSH6 mutations by denaturing high performance liquid chromatography (DHPLC) in HNPCC families
    Meeting Abstract

    Peterlongo, P.; Nafa, K.; Lerman, G.; Pawar, S.; Guillem, J.; Markowitz, A.; Offit, K.; Ellis, N. A.
    American Journal of Human Genetics (2001)

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  • Replication error and mismatch repair gene analyses of families with strong histories of colorectal cancer
    Meeting Abstract

    Nafa, K.; Peterlongo, P.; Glogowski, E.; Guillem, J.; Markowitz, A.; Offit, K.; Ellis, N. A.
    American Journal of Human Genetics (2001)

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  • De novo BRCA2 mutation in a patient with early-onset breast cancer
    Meeting Abstract

    Robson, M.; Scheuer, L.; Baum, R.; Hull, J.; McDermott, D.; Pierce, H.; Nafa, K.; Ellis, N.; Offit, K.
    American Journal of Human Genetics (2000)

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