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  1. Offit
    Offit
  2. Robson
    Robson
  3. Shen
    Shen
  4. Schultz
    Schultz
  5. Ellis
    Ellis
  6. Nafa
    Nafa
  7. Berger
    Berger
  8. Ladanyi
    Ladanyi
  9. Norton
    Norton
  10. Joseph
    Joseph

Groups

  1. Population Sciences Research Program (86)
  2. Department of Medicine (65)
  3. GSK Faculty (62)
  4. Solid Tumor Oncology Division (58)
  5. Survivorship Research (47)
  6. Clinical Genetics Service (41)
  7. Epidemiology and Biostatistics (36)
  8. Department of Pathology and Laboratory Medicine (31)
  9. Biostatistics Service (25)
  10. Sloan Kettering Institute Postdocs (23)
Search Within
  1. "Population Sciences Research Program"
Formats
  1. Journal Article (56)
  2. Meeting Abstract (24)
  3. Editorial (2)
  4. Research Letter (2)
  5. Correspondence (1)
  6. Review (1)
Groups
  1. Population Sciences Research Program (86)
  2. Department of Medicine (65)
  3. GSK Faculty (62)
  4. Solid Tumor Oncology Division (58)
  5. Survivorship Research (47)
  6. Clinical Genetics Service (41)

More Groups

People
  1. Kenneth Offit (35)
  2. Mark Robson (15)
  3. Ronglai Shen (13)
  4. Nikolaus Schultz (10)
  5. Nathan Ellis (9)
  6. Khedoudja Nafa (8)

More People

Years
  1. 2025 (4)
  2. 2024 (4)
  3. 2023 (4)
  4. 2022 (6)
  5. 2021 (8)
  6. 2020 (4)

More Years

Publications
  1. American Journal of Human Genetics (39)
  2. Cancer Cell (15)
  3. Cell (12)
  4. Human Genetics and Genomics Advances (5)
  5. Cell Reports (4)
  6. Cell Stem Cell (2)

More Publications

Results (86)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Unique phenotype associated with biallelic BRCA2 mutations includes high risk of brain tumors, Wilms tumors and early onset acute leukemia in children with Fanconi anemia
    Meeting Abstract

    Auerbach, A. D.; Levran, O.; Mullaney, B.; Kutler, D. I.; Mah, K.; Deffenbaugh, A.; Scholl, T.; Berwick, M.; MacMillan, M. L.; Offit, K.; more...
    American Journal of Human Genetics (2003)

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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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  • Relationship of P gene with human eye color and dysplastic nevi or melanoma
    Meeting Abstract

    Rebbeck, T. R.; Kanetsky, P. A.; Walker, A. H.; Holmes, R.; Halpern, A. C.; Elder, D. E.; Guerry, D.
    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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  • The presence of a germ-line BRCA mutation is an independent poor prognostic marker in breast cancer: A two-center historical cohort study
    Meeting Abstract

    Foulkes, W. D.; Satagopan, J. M.; Chappuis, P. O.; Wong, N.; Begin, L. R.; Boyd, J.; Offit, K.; Robson, M. E.
    American Journal of Human Genetics (2000)

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  • Risk-reducing surgery outcomes among a series of BRCA heterozygotes
    Meeting Abstract

    Scheuer, L. M.; Robson, M.; Baum, R.; Capasso, M.; Duteau-Buck, C.; Hull, J.; Kelly, B.; McDermott, D.; Pierce, H.; Pinto, M.; more...
    American Journal of Human Genetics (2000)

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  • Does genetic counseling for breast cancer predisposition increase knowledge?
    Meeting Abstract

    Brown, K.; Valdimarsdottir, H.; Erblich, J.; Amareld, D.; Scheuer, L.; Hull, J.; McDermott, D.; Bovbjerg, D.; Hurley, K.; Offit, K.
    American Journal of Human Genetics (2000)

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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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