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Clinical Genetics Service

Formats
  1. Journal Article (716)
  2. Meeting Abstract (343)
  3. Review (20)
  4. Book Section (11)
  5. Editorial (8)
  6. Guidelines (8)
  7. Research Letter (6)
  8. Conference Paper (5)
  9. Correspondence (4)
  10. Book Whole (1)
  11. Miscellaneous (1)
Groups
  1. Department of Medicine (1123)
  2. Population Sciences Research Program (1123)
  3. Solid Tumor Oncology Division (1123)
  4. Survivorship Research (941)
  5. GSK Faculty (903)
  6. Center for Pancreatic Cancer Research (425)

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People
  1. Kenneth Offit (792)
  2. Zsofia Stadler (398)
  3. Mark Robson (297)
  4. Vijai Joseph (215)
  5. Michael Walsh (156)
  6. Jinru Shia (135)

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Years
  1. 2025 (24)
  2. 2024 (47)
  3. 2023 (68)
  4. 2022 (69)
  5. 2021 (71)
  6. 2020 (76)

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Publications
  1. Journal of Clinical Oncology (189)
  2. Cancer Research (59)
  3. Blood (43)
  4. American Journal of Human Genetics (32)
  5. Clinical Cancer Research (32)
  6. Genetics in Medicine (28)

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Publishers
  1. American Society of Clinical Oncology (217)
  2. Nature Publishing Group (141)
  3. American Association for Cancer Research (125)
  4. Oxford University Press (63)
  5. Springer (62)
  6. American Society of Hematology (48)

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Results (1123)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
    Journal Article

    Peterlongo, P.; Chang-Claude, J.; Boysich, K. B.; Rudolph, A.; Schmutzler, R. K.; Simard, J.; Soucy, P.; Eeles, R. A.; Easton, D. F.; Hamann, U.; more...
    Cancer Epidemiology Biomarkers and Prevention (2015)

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  • Diagnosis and management of DNA mismatch repair-deficient colorectal cancer
    Journal Article

    Stadler, Z. K.
    Hematology/Oncology Clinics of North America (2015)

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  • Refined histopathological predictors of BRCA1 and BRCA2 mutation status: A large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia
    Journal Article

    Spurdle, A. B.; Couch, F. J.; Parsons, M. T.; McGuffog, L.; Barrowdale, D.; Bolla, M. K.; Wang, Q.; Healey, S.; Schmutzler, R. K.; Wappenschmidt, B.; more...
    Breast Cancer Research (2014)

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  • Genome-wide association studies of cancer predisposition
    Book Section

    Stadler, Z. K.; Shah, S.; Offit, K.
    In Gelmann, E. P.; Sawyers, C. L.; Rauscher, F. J. 3rd (Eds.) Molecular Oncology: Causes of Cancer and Targets for Treatment (2014)

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  • Phase IB trial of cisplatin (C), gemcitabine (G), and veliparib (V) in patients with known or potential BRCA or PALB2-mutated pancreas adenocarcinoma (PC)
    Meeting Abstract

    O'Reilly, E. M.; Lowery, M. A.; Segal, M. F.; Smith, S. C.; Moore, M. J.; Kindler, H. L.; Golan, T.; Segal, A.; Salo-Mullen, E. E.; Hollywood, E.; more...
    Journal of Clinical Oncology (2014)

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  • A genome-wide association study suggests evidence of variants at 6p21.32 associated with marginal zone lymphoma
    Meeting Abstract

    Vijai, J.; Wang, Z. M.; Berndt, S. I.; Slager, S. L.; Cerhan, J. R.; Skibola, C.; Wang, S. S.; Brooks-Wilson, A. R.; De Sanjose, S.; Bracci, P. M.; more...
    Cancer Research (2014)

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  • Harmonization of next generation sequencing data within consortia for gene discovery in familial breast cancer
    Meeting Abstract

    Vijai, J.; Hart, S.; Thomas, T.; Wubbenhorst, B.; Guidugli, L.; Schrader, K.; Maxwell, K.; Jacobs, L.; Villano, D.; Klein, R.; more...
    Cancer Research (2014)

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  • Meta-analysis of genome-wide association studies identifies novel susceptibility loci for follicular lymphoma
    Meeting Abstract

    Skibola, C. F.; Berndt, S. I.; Cerhan, J. R.; Wang, Z. M.; Vijai, J.; Conde, L.; de Bakker, P.; Wang, S. S.; Vajdic, C. M.; Birmann, B. M.; more...
    Cancer Research (2014)

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  • Determination of cancer susceptibility in probands with breast and ovarian cancer
    Meeting Abstract

    Schrader, K. A.; Maxwell, K. N.; Vijai, J.; Hart, S.; Thomas, T.; Wubbenhorst, B.; Guidugli, L.; Klein, R.; Corines, M.; Zhang, L.; more...
    Cancer Research (2014)

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  • High and moderate penetrance germline mutations in a number of genes are responsible for a small proportion of familial breast cancer risk in BRCAx families
    Meeting Abstract

    Maxwell, K. N.; Guidugli, L.; Schrader, K.; Hart, S.; Joseph, V.; Thomas, T.; Wang, X. S.; Wubbenhorst, B.; Klein, R.; Domchek, S. M.; more...
    Cancer Research (2014)

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