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Alice Elizabeth Schluger

Formats
  1. Journal Article (9)
  2. Meeting Abstract (6)
Groups
  1. Department of Medicine (15)
  2. GSK Faculty (13)
  3. Clinical Genetics Service (12)
  4. Population Sciences Research Program (12)
  5. Solid Tumor Oncology Division (12)
  6. Survivorship Research (12)

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People
  1. Kenneth Offit (12)
  2. Mark Robson (5)
  3. Charlene Schulz (4)
  4. Bayard Clarkson (3)
  5. Khedoudja Nafa (3)
  6. Larry Norton (3)

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Years
  1. 2010 (1)
  2. 2005 (1)
  3. 2002 (2)
  4. 1999 (1)
  5. 1997 (3)
  6. 1996 (3)

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Publications
  1. American Journal of Human Genetics (4)
  2. Blood (2)
  3. Journal of Clinical Oncology (2)
  4. Breast Cancer Research and Treatment (1)
  5. Genetics in Medicine (1)
  6. JAMA - Journal of the American Medical Association (1)

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Publishers
  1. Cell Press (4)
  2. American Society of Clinical Oncology (2)
  3. American Society of Hematology (2)
  4. American Medical Association (1)
  5. BMJ Publishing Group Ltd. (1)
  6. Elsevier Inc. (1)

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Results (15)

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  • Absence of genomic BRCA1 and BRCA2 rearrangements in Ashkenazi breast and ovarian cancer families
    Journal Article

    Stadler, Z. K.; Saloustros, E.; Hansen, N. A. L.; Schluger, A. E.; Kauff, N. D.; Offit, K.; Robson, M. E.
    Breast Cancer Research and Treatment (2010)

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  • Prevalence of BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish (AJ) families with breast cancer (BC) and pancreatic cancer (PC)
    Meeting Abstract

    Marcotrigiano, M. C.; Wadsworth, E.; Balistreri, L.; Schluger, A.; Offit, K.; Robson, M.
    Journal of Clinical Oncology (2005)

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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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  • 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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  • Frequency of BRCA mutations among a series of Ashkenazi Jewish men diagnosed with breast cancer
    Meeting Abstract

    Scheuer, L.; Robson, M.; Hampel, H.; Borgen, P.; Norton, L.; McDermott, D.; Pinto, M.; Hull, J.; Baum, R.; Nafa, K.; more...
    American Journal of Human Genetics (1999)

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  • Effect of patient education on data quality: Implications for assessing hereditary cancer risk in prostate cancer patients
    Meeting Abstract

    Brener, D.; Altwerger, J.; Capasso, M.; Satagopan, J.; Schluger, A.; Schulz, C.; Thayer, J.; Scher, H.; Fair, W.; Offit, K.
    American Journal of Human Genetics (1997)

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  • BRCA 1 sequence analysis in women at high risk for susceptibility mutations: Risk factor analysis and implications for genetic testing
    Journal Article

    Shattuck-Eidens, D.; Oliphant, A.; McClure, M.; McBride, C.; Gupte, J.; Rubano, T.; Pruss, D.; Tavtigian, S. V.; Teng, D. H. F.; Adey, N.; more...
    JAMA - Journal of the American Medical Association (1997)

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  • Familial Hodgkin's and non-Hodgkin's lymphoma: Different patterns in first-degree relatives
    Journal Article

    Siebert, R.; Louie, D.; Lacher, M.; Schluger, A.; Offit, K.
    Leukemia and Lymphoma (1997)

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  • A self-administered Family History Questionnaire (FHQ) utilized in an out-patient setting to assess cancer risk
    Meeting Abstract

    Brener, D.; Schulz, C.; Schluger, A.; Offit, K.
    American Journal of Human Genetics (1996)

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  • The use of optically scannable forms and computerized algorithms for mass family history cancer risk assessment
    Meeting Abstract

    Hampel, H.; Kuhn, T.; Markowitz, A.; Lin, K. H.; Li, S.; Brown, K.; Schulz, C.; Winawer, S. J.; Taylor, F.; McGuire, P.; more...
    American Journal of Human Genetics (1996)

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