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Population Sciences Research Program

  1. "2019"
  2. "Kenneth Offit"
  3. "Vijai Joseph"
Formats
  1. Journal Article (11)
  2. Meeting Abstract (3)
Groups
  1. Clinical Genetics Service (14)
  2. Department of Medicine (14)
  3. GSK Faculty (14)
  4. Solid Tumor Oncology Division (14)
  5. Survivorship Research (14)
  6. Center for Pancreatic Cancer Research (7)

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People
  1. Kenneth Offit (14)
  2. Vijai Joseph (14)
  3. Zsofia Stadler (7)
  4. Mark Robson (6)
  5. Diana Mandelker (5)
  6. Liying Zhang (5)

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Years
  1. 2019 (14)
Publications
  1. Cancer Research (2)
  2. American Journal of Human Genetics (1)
  3. Blood Advances (1)
  4. European Journal of Human Genetics (1)
  5. Genetic Epidemiology (1)
  6. Genetics in Medicine (1)

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Publishers
  1. Nature Publishing Group (5)
  2. American Association for Cancer Research (3)
  3. American Society of Clinical Oncology (2)
  4. American Society of Hematology (1)
  5. Cell Press (1)
  6. John Wiley & Sons, Inc. (1)

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Results (14)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Targeting nucleotide excision repair defects in cancer
    Meeting Abstract

    Topka, S.; Steinsnyder, Z.; Tkachuk, K.; Ravichandran, V.; Madsen, M. W.; Furberg-Barnes, H.; Iyer, G.; De Stanchina, E.; Joseph, V.; Offit, K.
    Molecular Cancer Therapeutics (2019)

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  • Understanding inherited risk in unselected newly diagnosed patients with endometrial cancer
    Journal Article

    Cadoo, K. A.; Mandelker, D. L.; Mukherjee, S.; Stewart, C.; DeLair, D.; Ravichandran, V.; Srinivasan, P.; Hurley, D.; Kemel, Y.; Arnold, A. G.; more...
    JCO Precision Oncology (2019)

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  • Toward automation of germline variant curation in clinical cancer genetics
    Journal Article

    Ravichandran, V.; Shameer, Z.; Kemel, Y.; Walsh, M.; Cadoo, K.; Lipkin, S.; Mandelker, D.; Zhang, L.; Stadler, Z.; Robson, M.; more...
    Genetics in Medicine (2019)

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  • Inherited truncating RAD52 variant discovered using integrated germline-somatic analysis predicts clinical outcome in patients with lung cancers
    Meeting Abstract

    Mukherjee, S.; Srinivasan, P.; Bandlamudi, C.; Hellmann, M. D.; Ravichandran, V.; Selvan, M. E.; Kemel, Y.; Mandelker, D.; Zauderer, M.; Walsh, M.; more...
    Cancer Research (2019)

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  • Zygosity, lineage, and penetrance dictate the role of germline pathogenicity in tumorigenesis
    Meeting Abstract

    Bandlamudi, C.; Srinivasan, P.; Jonsson, P.; Kemel, Y. M.; Chavan, S. S.; Richards, A. L.; Penson, A.; Bielski, C. M.; Fong, C.; Syed, A.; more...
    Cancer Research (2019)

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  • Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes
    Journal Article

    Din, L.; Sheikh, M.; Kosaraju, N.; Smedby, K. E.; Bernatsky, S.; Berndt, S. I.; Skibola, C. F.; Nieters, A.; Wang, S.; McKay, J. D.; more...
    Genetic Epidemiology (2019)

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  • Two truncating variants in FANCC and breast cancer risk
    Journal Article

    Dörk, T.; Peterlongo, P.; Mannermaa, A.; Bolla, M. K.; Wang, Q.; Dennis, J.; Ahearn, T.; Andrulis, I. L.; Anton-Culver, H.; Arndt, V.; more...
    Scientific Reports (2019)

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  • Germline deletion of ETV6 in familial acute lymphoblastic leukemia
    Journal Article

    Rampersaud, E.; Ziegler, D. S.; Iacobucci, I.; Payne-Turner, D.; Churchman, M. L.; Schrader, K. A.; Joseph, V.; Offit, K.; Tucker, K.; Sutton, R.; more...
    Blood Advances (2019)

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  • Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes
    Journal Article

    Artomov, M.; Joseph, V.; Tiao, G.; Thomas, T.; Schrader, K.; Klein, R. J.; Kiezun, A.; Gupta, N.; Margolin, L.; Stratigos, A. J.; more...
    European Journal of Human Genetics (2019)

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  • Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
    Journal Article

    Ferreira, M. A.; Gamazon, E. R.; Al-Ejeh, F.; Aittomäki, K.; Andrulis, I. L.; Anton-Culver, H.; Arason, A.; Arndt, V.; Aronson, K. J.; Arun, B. K.; more...
    Nature Communications (2019)

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