1. "Clinical Genetics Service"
Formats
  1. Journal Article (708)
  2. Meeting Abstract (340)
  3. Review (20)
  4. Book Section (10)
  5. Guidelines (8)
  6. Editorial (7)
  7. Research Letter (6)
  8. Conference Paper (5)
  9. Correspondence (4)
  10. Book Whole (1)
  11. Miscellaneous (1)
Groups
  1. Clinical Genetics Service (1110)
  2. Department of Medicine (1110)
  3. Population Sciences Research Program (1110)
  4. Solid Tumor Oncology Division (1110)
  5. Survivorship Research (930)
  6. GSK Faculty (897)

More Groups

People
  1. Kenneth Offit (788)
  2. Zsofia Stadler (390)
  3. Mark Robson (297)
  4. Vijai Joseph (211)
  5. Michael Walsh (156)
  6. Jinru Shia (134)

More People

Years
  1. 2025 (13)
  2. 2024 (46)
  3. 2023 (68)
  4. 2022 (69)
  5. 2021 (71)
  6. 2020 (76)

More Years

Publications
  1. Journal of Clinical Oncology (188)
  2. Cancer Research (59)
  3. Blood (42)
  4. American Journal of Human Genetics (32)
  5. Clinical Cancer Research (32)
  6. Genetics in Medicine (28)

More Publications

Publishers
  1. American Society of Clinical Oncology (216)
  2. Nature Publishing Group (140)
  3. American Association for Cancer Research (125)
  4. Elsevier Inc. (64)
  5. Oxford University Press (63)
  6. Springer (60)

More Publishers

Results (1110)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • 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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  • Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers
    Journal Article

    Narod, S. A.; Dubé, M. P.; Klijn, J.; Lubinski, J.; Lynch, H. T.; Ghadirian, P.; Provencher, D.; Heimdal, K.; Möller, P.; Robson, M.; more...
    JNCI: Journal of the National Cancer Institute (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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  • Ovarian cancer with a family history
    Book Section

    Poynor, E. A.; Offit, K.
    In Ledermann, J. A.; Hoskins, W. J.; Kaye, S. B.; Vergote, I. B. (Eds.) Clinical Management of Ovarian Cancer (2001)

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  • Counseling for hereditary cancer risk
    Book Section

    Offit, K.
    In Mendelsohn, J.; Howley, P. M.; Israel, M. A.; Liotta, L. A. (Eds.) The Molecular Basis of Cancer. 2nd ed (2001)

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  • Risk of endometrial carcinoma associated with BRCA mutation
    Meeting Abstract

    Levine, D. A.; Lin, O.; Barakat, R. R.; Robson, M. E.; Offit, K.; McDermott, D.; Cohen, L.; Satagopan, J.; Boyd, J.
    Gynecologic Oncology (2001)

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  • Genetic analysis of ovarian carcinoma histogenesis
    Meeting Abstract

    Pothuri, B.; Leitao, M.; Barakat, R. R.; Akram, M.; Bogomolniy, F.; Olvera, N.; Lin, O.; Soslow, R.; Robson, M. E.; Offit, K.; more...
    Gynecologic Oncology (2001)

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  • Insurance reimbursement for risk-reducing surgeries in BRCA1 and BRCA2 heterozygotes
    Meeting Abstract

    Kauff, N.; Scheuer, L.; Robson, M.; Barakat, R.; Borgen, P.; Heerdt, A.; Hudis, C.; Norton, L.; Davis, J.; Offit, K.
    Genetics in Medicine (2001)

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