1. "Kenneth Offit"
Formats
  1. Journal Article (544)
  2. Meeting Abstract (216)
  3. Review (9)
  4. Book Section (7)
  5. Conference Paper (3)
  6. Guidelines (3)
  7. Research Letter (3)
  8. Correspondence (2)
  9. Book Whole (1)
Groups
  1. Clinical Genetics Service (788)
  2. Department of Medicine (788)
  3. GSK Faculty (788)
  4. Population Sciences Research Program (788)
  5. Solid Tumor Oncology Division (788)
  6. Survivorship Research (788)

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People
  1. Kenneth Offit (788)
  2. Mark Robson (280)
  3. Vijai Joseph (193)
  4. Zsofia Stadler (165)
  5. Diana Mandelker (86)
  6. Michael Walsh (81)

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Years
  1. 2025 (4)
  2. 2024 (18)
  3. 2023 (40)
  4. 2022 (35)
  5. 2021 (39)
  6. 2020 (48)

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Publications
  1. Journal of Clinical Oncology (138)
  2. Cancer Research (46)
  3. Blood (34)
  4. American Journal of Human Genetics (32)
  5. Genetics in Medicine (25)
  6. Nature Genetics (25)

More Publications

Publishers
  1. American Society of Clinical Oncology (153)
  2. Nature Publishing Group (109)
  3. American Association for Cancer Research (84)
  4. Springer (44)
  5. Elsevier Inc. (37)
  6. Oxford University Press (37)

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Results (788)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
    Journal Article

    Antoniou, A. C.; Kuchenbaecker, K. B.; Soucy, P.; Beesley, J.; Chen, X.; McGuffog, L.; Lee, A.; Barrowdale, D.; Healey, S.; Sinilnikova, O. M.; more...
    Breast Cancer Research (2012)

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  • The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers
    Journal Article

    Laitman, Y.; Kuchenbaecker, K. B.; Rantala, J.; Hogervorst, F.; Peock, S.; Godwin, A. K.; Arason, A.; Kirchhoff, T.; Offit, K.; Isaacs, C.; more...
    Breast Cancer Research and Treatment (2012)

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  • Incorporating information regarding preimplantation genetic diagnosis into discussions concerning testing and risk management for BRCA1/2 mutations: A qualitative study of patient preferences
    Journal Article

    Hurley, K.; Rubin, L. R.; Werner-Lin, A.; Sagi, M.; Kemel, Y.; Stern, R.; Phillips, A.; Cholst, I.; Kauff, N.; Offit, K.
    Cancer (2012)

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  • Rare variants in XRCC2 as breast cancer susceptibility alleles
    Journal Article

    Hilbers, F. S.; Wijnen, J. T.; Hoogerbrugge, N.; Oosterwijk, J. C.; Collee, M. J.; Peterlongo, P.; Radice, P.; Manoukian, S.; Feroce, I.; Capra, F.; more...
    Journal of Medical Genetics (2012)

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  • Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers
    Journal Article

    Stevens, K. N.; Wang, X.; Fredericksen, Z.; Pankratz, V. S.; Greene, M. H.; Andrulis, I. L.; Thomassen, M.; Caligo, M.; Nathanson, K. L.; Jakubowska, A.; more...
    Breast Cancer Research and Treatment (2012)

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  • Heterozygous mutations in DNA repair genes and hereditary breast cancer: A question of power
    Journal Article

    Ellis, N. A.; Offit, K.
    PLoS Genetics (2012)

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  • Juvenile polyposis syndrome presenting with familial gastric cancer and massive gastric polyposis
    Journal Article

    Stadler, Z. K.; Salo-Mullen, E.; Zhang, L.; Shia, J.; Bacares, R.; Power, D. G.; Weiser, M.; Coit, D.; Robson, M. E.; Offit, K.; more...
    Journal of Clinical Oncology (2012)

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  • Risks to relatives in genomic research: A duty to warn?
    Journal Article

    Bombard, Y.; Offit, K.; Robson, M. E.
    American Journal of Bioethics (2012)

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  • Rare de novo germline copy-number variation in testicular cancer
    Journal Article

    Stadler, Z. K.; Esposito, D.; Shah, S.; Vijai, J.; Yamrom, B.; Levy, D.; Lee, Y. H.; Kendall, J.; Leotta, A.; Ronemus, M.; more...
    American Journal of Human Genetics (2012)

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  • Genetic testing in gastrointestinal cancers: A case-based approach
    Journal Article

    Schrader, K.; Offit, K.; Stadler, Z. K.
    Oncology (Norwalk) (2012)

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