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Clinical Genetics Service

Formats
  1. Journal Article (712)
  2. Meeting Abstract (342)
  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 (1118)
  2. Population Sciences Research Program (1118)
  3. Solid Tumor Oncology Division (1118)
  4. Survivorship Research (937)
  5. GSK Faculty (901)
  6. Center for Pancreatic Cancer Research (421)

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People
  1. Kenneth Offit (791)
  2. Zsofia Stadler (395)
  3. Mark Robson (297)
  4. Vijai Joseph (213)
  5. Michael Walsh (156)
  6. Jinru Shia (135)

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Years
  1. 2025 (19)
  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. Elsevier Inc. (63)
  5. Oxford University Press (63)
  6. Springer (61)

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Results (1118)


Citation style sort is year ascending, and then by author or title. Author ascending is default.
  • Conflicting interpretation of genetic variants and cancer risk by commercial laboratories as assessed by the prospective registry of multiplex testing
    Journal Article

    Balmaña, J.; Digiovanni, L.; Gaddam, P.; Walsh, M. F.; Joseph, V.; Stadler, Z. K.; Nathanson, K. L.; Garber, J. E.; Couch, F. J.; Offit, K.; more...
    Journal of Clinical Oncology (2016)

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  • A recurrent ERCC3 truncating mutation confers moderate risk for breast cancer
    Journal Article

    Vijai, J.; Topka, S.; Villano, D.; Ravichandran, V.; Maxwell, K. N.; Maria, A.; Thomas, T.; Gaddam, P.; Lincoln, A.; Kazzaz, S.; more...
    Cancer Discovery (2016)

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  • Collaborative science in the next-generation sequencing era: A viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes
    Journal Article

    Hart, S. N.; Maxwell, K. N.; Thomas, T.; Ravichandran, V.; Wubberhorst, B.; Klein, R. J.; Schrader, K.; Szabo, C.; Weitzel, J. N.; Neuhausen, S. L.; more...
    Briefings in Bioinformatics (2016)

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  • Fine-scale mapping at 9p22.2 identifies candidate causal variants that modify ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
    Journal Article

    Vigorito, E.; Kuchenbaecker, K. B.; Beesley, J.; Adlard, J.; Agnarsson, B. A.; Andrulis, I. L.; Arun, B. K.; Barjhoux, L.; Belotti, M.; Benitez, J.; more...
    PLoS ONE (2016)

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  • Recommendations from the EGAPP Working Group: Does the use of Oncotype DX tumor gene expression profiling to guide treatment decisions improve outcomes in patients with breast cancer?
    Journal Article

    Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group
    Genetics in Medicine (2016)

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  • Genomic instability in pancreatic adenocarcinoma: A new step towards precision medicine and novel therapeutic approaches
    Journal Article

    Sahin, I. H.; Lowery, M. A.; Stadler, Z. K.; Salo-Mullen, E.; Iacobuzio-Donahue, C. A.; Kelsen, D. P.; O'Reilly, E. M.
    Expert Review of Gastroenterology and Hepatology (2016)

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  • Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast - Ovarian cancer susceptibility locus
    Journal Article

    Lawrenson, K.; Kar, S.; McCue, K.; Kuchenbaeker, K.; Michailidou, K.; Tyrer, J.; Beesley, J.; Ramus, S. J.; Li, Q.; Delgado, M. K.; more...
    Nature Communications (2016)

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  • Hypermutation and neoantigen formation predict response to immune checkpoint inhibition in childhood biallelic mismatch repair deficient glioblastoma
    Meeting Abstract

    Campbell, B.; Bouffet, E.; Larouche, V.; Mason, G.; Reddy, A.; Osborn, M.; Magimairan, V.; Merico, D.; de Borja, R.; Chung, B.; more...
    Neuro-Oncology (2016)

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  • Counselling framework for moderate-penetrance cancer-susceptibility mutations
    Journal Article

    Tung, N.; Domchek, S. M.; Stadler, Z.; Nathanson, K. L.; Couch, F.; Garber, J. E.; Offit, K.; Robson, M. E.
    Nature Reviews Clinical Oncology (2016)

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  • Inherited DNA-repair gene mutations in men with metastatic prostate cancer
    Journal Article

    Pritchard, C. C.; Mateo, J.; Walsh, M. F.; De Sarkar, N.; Abida, W.; Beltran, H.; Garofalo, A.; Gulati, R.; Carreira, S.; Eeles, R.; more...
    New England Journal of Medicine (2016)

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