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Amanda Catchings

  1. "Clinical Genetics Service"
Formats
  1. Journal Article (14)
  2. Meeting Abstract (2)
  3. Review (1)
Groups
  1. Clinical Genetics Service (17)
  2. Department of Medicine (17)
  3. Population Sciences Research Program (17)
  4. Solid Tumor Oncology Division (17)
  5. Center for Pancreatic Cancer Research (16)
  6. GSK Faculty (13)

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People
  1. Zsofia Stadler (15)
  2. Kenneth Offit (11)
  3. Diana Mandelker (9)
  4. Megha Ranganathan (9)
  5. Yelena Kemel (9)
  6. Alicia Latham (8)

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Years
  1. 2024 (3)
  2. 2023 (4)
  3. 2022 (5)
  4. 2021 (3)
  5. 2020 (1)
  6. 2019 (1)
Publications
  1. Genetics in Medicine (3)
  2. JCO Precision Oncology (3)
  3. Breast Cancer Research and Treatment (2)
  4. JNCI: Journal of the National Cancer Institute (2)
  5. Cancer (1)
  6. Clinical Cancer Research (1)

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Publishers
  1. American Society of Clinical Oncology (5)
  2. Nature Publishing Group (3)
  3. Oxford University Press (2)
  4. Springer (2)
  5. American Association for Cancer Research (1)
  6. John Wiley & Sons Ltd. (1)

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Results (17)

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  • Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndrome
    Journal Article

    Liu, Y. L.; Cadoo, K. A.; Maio, A.; Patel, Z.; Kemel, Y.; Salo-Mullen, E.; Catchings, A.; Ranganathan, M.; Kane, S.; Soslow, R.; more...
    Genetics in Medicine (2022)

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  • Risk-reducing bilateral salpingo-oophorectomy for ovarian cancer: A review and clinical guide for hereditary predisposition genes
    Review

    Liu, Y. L.; Breen, K.; Catchings, A.; Ranganathan, M.; Latham, A.; Goldfrank, D. J.; Grisham, R. N.; Long Roche, K.; Frey, M. K.; Chi, D. S.; more...
    JCO Oncology Practice (2022)

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  • Uptake and acceptability of a mainstreaming model of hereditary cancer multigene panel testing among patients with ovarian, pancreatic, and prostate cancer
    Journal Article

    Hamilton, J. G.; Symecko, H.; Spielman, K.; Breen, K.; Mueller, R.; Catchings, A.; Trottier, M.; Salo-Mullen, E. E.; Shah, I.; Arutyunova, A.; more...
    Genetics in Medicine (2021)

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  • Prevalence and characterization of biallelic and monoallelic NTHL1 and MSH3 variant carriers from a pan-cancer patient population
    Journal Article

    Salo-Mullen, E. E.; Maio, A.; Mukherjee, S.; Bandlamudi, C.; Shia, J. R.; Kemel, Y.; Cadoo, K. A.; Liu, Y.; Carlo, M.; Ranganathan, M.; more...
    JCO Precision Oncology (2021)

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  • The RAD51D c.82G>A (p.Val28Met) variant disrupts normal splicing and is associated with hereditary ovarian cancer
    Journal Article

    Yang, C.; Arnold, A. G.; Catchings, A.; Rai, V.; Stadler, Z. K.; Zhang, L.
    Breast Cancer Research and Treatment (2021)

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  • Prevalence and clinical characterization of MMR-D/MSI extra-colonic cancers among germline PMS2 mutation carriers
    Meeting Abstract

    Latham, A.; Salo-Mullen, E. E.; Catchings, A.; Ranganathan, M.; Fiala, E.; Kemel, Y.; Konner, J. A.; Soslow, R. A.; Momeni-Boroujeni, A.; Shia, J.; more...
    Journal of Clinical Oncology (2020)

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  • A synonymous germline variant PALB2 c.18G>T (p.Gly6=) disrupts normal splicing in a family with pancreatic and breast cancers
    Journal Article

    Yang, C.; Ceyhan-Birsoy, O.; Mandelker, D.; Jairam, S.; Catchings, A.; O’Reilly, E. M.; Walsh, M. F.; Zhang, L.
    Breast Cancer Research and Treatment (2019)

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