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Nathan A Ellis

  1. "Population Sciences Research Program"
Formats
  1. Journal Article (28)
  2. Meeting Abstract (14)
Groups
  1. Population Sciences Research Program (42)
  2. Department of Medicine (41)
  3. Survivorship Research (41)
  4. Clinical Genetics Service (40)
  5. GSK Faculty (40)
  6. Solid Tumor Oncology Division (40)

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People
  1. Kenneth Offit (40)
  2. Khedoudja Nafa (28)
  3. Mark Robson (13)
  4. Arnold Markowitz (12)
  5. Helen Huang (10)
  6. Jinru Shia (9)

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Years
  1. 2007 (1)
  2. 2006 (1)
  3. 2005 (5)
  4. 2004 (10)
  5. 2003 (10)
  6. 2002 (7)

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Publications
  1. American Journal of Human Genetics (9)
  2. Clinical Cancer Research (3)
  3. Journal of Clinical Oncology (3)
  4. American Journal of Surgical Pathology (2)
  5. Cancer Research (2)
  6. Familial Cancer (2)

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Publishers
  1. Cell Press (9)
  2. American Association for Cancer Research (6)
  3. American Society of Clinical Oncology (3)
  4. Lippincott Williams & Wilkins (3)
  5. Oxford University Press (3)
  6. Biomed Central Ltd (2)

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Results (42)

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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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  • Increased occurrence of non-Hodgkin's lymphoma (NHL) and Hodgkin's disease (HD) in families with hereditary nonpolyposis colorectal cancer, HNPCC (Lynch syndrome)
    Meeting Abstract

    Teruya-Feldstein, J.; Cohen, L.; Ellis, N.; Greene, J.; Offit, K.
    Modern Pathology (2001)

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  • Increased occurrence of non-Hodgkin's lymphoma (NHL) and Hodgkin's disease (HD) in families with hereditary nonpolyposis colorectal cancer, HNPCC (Lynch syndrome)
    Meeting Abstract

    Teruya-Feldstein, J.; Cohen, L.; Ellis, N.; Greene, J.; Offit, K.
    Laboratory Investigation (2001)

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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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  • A founder mutation in MSH2 in the Ashkenazim
    Meeting Abstract

    Foulkes, W. D.; Thiffault, I.; Farber, D.; Gruber, S. B.; Tomsho, L.; Horwitz, M.; Walsh, T.; King, M. C.; Ellis, N.; Offit, K.; more...
    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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