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Kenneth Offit

Formats
  1. Journal Article (546)
  2. Meeting Abstract (217)
  3. Review (9)
  4. Book Section (8)
  5. Conference Paper (3)
  6. Guidelines (3)
  7. Research Letter (3)
  8. Correspondence (2)
  9. Book Whole (1)
Groups
  1. Clinical Genetics Service (792)
  2. Department of Medicine (792)
  3. GSK Faculty (792)
  4. Population Sciences Research Program (792)
  5. Solid Tumor Oncology Division (792)
  6. Survivorship Research (792)

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People
  1. Mark Robson (280)
  2. Vijai Joseph (194)
  3. Zsofia Stadler (168)
  4. Diana Mandelker (89)
  5. Yelena Kemel (82)
  6. Michael Walsh (81)

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Years
  1. 2025 (7)
  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 (139)
  2. Cancer Research (46)
  3. Blood (34)
  4. American Journal of Human Genetics (32)
  5. Nature Genetics (26)
  6. Genetics in Medicine (25)

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Publishers
  1. American Society of Clinical Oncology (154)
  2. Nature Publishing Group (110)
  3. American Association for Cancer Research (84)
  4. Springer (44)
  5. Oxford University Press (37)
  6. American Society of Hematology (35)

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Results (792)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier
    Journal Article

    Alanee, S.; Shah, S.; Murali, R.; Rau-Murthy, R.; Schrader, K. A.; Offit, K.
    Familial Cancer (2013)

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  • Single nucleotide polymorphisms as markers of bacillus Calmette-Guerin intravesical therapy response in non-muscle invasive bladder cancer
    Meeting Abstract

    Alanee, S.; Hamilton, R. J.; Joseph, V.; Ostrovnaya, I.; Garcia-Grossman, I. R.; Gallagher, D. J.; Pendse, D.; Regazzi, A. M.; Przybylo, J. A.; Gaudet, M.; more...
    Journal of Clinical Oncology (2012)

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  • Association of single-nucleotide polymorphisms in BCL2L1 and TACC3 with response to bacillus Calmette-Guerin intravesical therapy in non-muscle-invasive bladder cancer
    Meeting Abstract

    Alanee, S.; Gallagher, D. J.; Vijai, J.; Hamilton, R. J.; Ostrovnaya, I.; Garcia-Grossman, I. R.; Riches, J. C.; Regazzi, A. M.; Przybylo, J. A.; Gaudet, M.; more...
    Journal of Clinical Oncology (2012)

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  • SLX4 mutation in hereditary breast cancer
    Meeting Abstract

    Shah, S.; Lach, F.; Kim, Y.; Sarrel, K.; Rau-Murthy, R.; Hansen, N.; Rendleman, J.; Kirchhoff, T.; Joseph, V.; Offit, K.; more...
    Cancer Research (2012)

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  • 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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