Search Within

Nathan A Ellis

  1. "Mark Robson"
Formats
  1. Journal Article (9)
  2. Meeting Abstract (4)
Groups
  1. Breast Medicine Service (13)
  2. Clinical Genetics Service (13)
  3. Department of Medicine (13)
  4. GSK Faculty (13)
  5. Population Sciences Research Program (13)
  6. Solid Tumor Oncology Division (13)

More Groups

People
  1. Kenneth Offit (13)
  2. Mark Robson (13)
  3. Khedoudja Nafa (12)
  4. Noah Kauff (7)
  5. Lauren Scheuer (6)
  6. Helen Huang (4)

More People

Years
  1. 2005 (1)
  2. 2004 (3)
  3. 2003 (2)
  4. 2002 (4)
  5. 2000 (1)
  6. 1999 (2)
Publications
  1. American Journal of Human Genetics (3)
  2. Clinical Cancer Research (3)
  3. Journal of Clinical Oncology (2)
  4. BMC Medical Genetics (1)
  5. Familial Cancer (1)
  6. JNCI: Journal of the National Cancer Institute (1)

More Publications

Publishers
  1. American Association for Cancer Research (3)
  2. Cell Press (3)
  3. American Society of Clinical Oncology (2)
  4. BMJ Publishing Group Ltd. (1)
  5. Biomed Central Ltd (1)
  6. Massachusetts Medical Society (1)

More Publishers

Results (13)

Export to EndNote / Excel | PubMed

Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li-Fraumeni-like kindreds
    Journal Article

    Siddiqui, R.; Onel, K.; Facio, F.; Nafa, K.; Diaz, L. R.; Kauff, N.; Huang, H.; Robson, M.; Ellis, N.; Offit, K.
    Familial Cancer (2005)

    Fulltext@MSK | Save
  • TP53 and CHEK2*1100delC gene mutation in North American families suggestive Li-Fraumeni syndrome: Memorial Sloan-Kettering experience
    Meeting Abstract

    Siddiqui, R.; Diaz, L. R.; Nafa, K.; Kauff, N.; Facio, F.; Huang, H.; Onel, K.; Robson, M.; Ellis, N.; Offit, K.
    Journal of Clinical Oncology (2004)

    Fulltext@MSK | Save
  • Pleomorphic characteristics of a germ-line KIT mutation in a large kindred with gastrointestinal stromal tumors, hyperpigmentation, and dysphagia
    Journal Article

    Robson, M. E.; Glogowski, E.; Sommer, G.; Antonescu, C. R.; Nafa, K.; Maki, R. G.; Ellis, N.; Besmer, P.; Brennan, M.; Offit, K.
    Clinical Cancer Research (2004)

    Fulltext@MSK | Save
  • BRCA mutations and risk of prostate cancer in Ashkenazi Jews
    Journal Article

    Kirchhoff, T.; Kauff, N. D.; Mitra, N.; Nafa, K.; Huang, H.; Palmer, C.; Gulati, T.; Wadsworth, E.; Donat, S.; Robson, M. E.; more...
    Clinical Cancer Research (2004)

    Fulltext@MSK | Save
  • Frequency of CHEK2*1100delC in New York breast cancer cases and controls
    Journal Article

    Offit, K.; Pierce, H.; Kirchhoff, T.; Kolachana, P.; Rapaport, B.; Gregersen, P.; Johnson, S.; Yossepowitch, O.; Huang, H.; Satagopan, J.; more...
    BMC Medical Genetics (2003)

    Fulltext@MSK | Save
  • 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)

    Fulltext@MSK | Save
  • Outcome of preventive surgery and screening for breast and ovarian cancer in BRCA mutation carriers
    Journal Article

    Scheuer, L.; Kauff, N.; Robson, M.; Kelly, B.; Barakat, R.; Satagopan, J.; Ellis, N.; Hensley, M.; Boyd, J.; Borgen, P.; more...
    Journal of Clinical Oncology (2002)

    Fulltext@MSK | Save
  • 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)

    Fulltext@MSK | Save
  • 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)

    Fulltext@MSK | Save
  • 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)

    Fulltext@MSK | Save