Search Results - "Reys, Brian"

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  1. 1

    Distinct NSCLC EGFR Variants in a Family With Li-Fraumeni Syndrome: Case Report by Edmondson, Shelby, von Itzstein, Mitchell S., Reys, Brian, Mayer, Melissa, Gagan, Jeffrey, Gerber, David E.

    Published in JTO clinical and research reports (01-08-2022)
    “…Heritable lung cancer may occur in the context of germline TP53 mutations (Li-Fraumeni syndrome). Limited cases of intrafamily tumor genomic characteristics…”
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    Journal Article
  2. 2

    Family still matters: Counseling patients with complex family histories of colon and endometrial cancers by Gemmell, Amber P., Mauer, Caitlin B., Reys, Brian D., Pirzadeh‐Miller, Sara, Ross, Theodora S.

    Published in Molecular genetics & genomic medicine (01-09-2019)
    “…Background There are no national guidelines for the management of patients with a family history consistent with Lynch syndrome (LS) but a negative genetic…”
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    Journal Article
  3. 3

    Do genetic testing criteria identify individuals with Lynch syndrome prior to cancer diagnoses? by Reys, Brian, Mauer, Caitlin, Pirzadeh-Miller, Sara, Ross, Theodora S.

    Published in Journal of clinical oncology (20-05-2019)
    “…Abstract only e13158 Background: Screening colonoscopies every 1-2 years are estimated to decrease the risk for colorectal cancer (CRC) development in…”
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    Journal Article
  4. 4

    De novo SDHB gene mutation in a family with extra-adrenal paraganglioma by Mauer, Caitlin B., Reys, Brian, Wickiser, Jonathan

    Published in Familial cancer (01-07-2020)
    “…A 14-year-old male presented with abdominal pain. Imaging illustrated a left-sided adrenal mass; he underwent a left nephrectomy, confirming an extra-adrenal…”
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    Journal Article
  5. 5

    Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices by Lahiri, Sayoni, Reys, Brian, Wunder, Julia, Pirzadeh‐Miller, Sara

    Published in Journal of genetic counseling (01-02-2023)
    “…Discordant variant classifications (DVCs) can impact patient care and pose challenges for clinicians. A survey‐based study was conducted to examine genetic…”
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    Journal Article
  6. 6

    Brainstem Glioblastoma Multiforme in a Patient with NF1 by Fortunato, John T, Reys, Brian, Singh, Pawan, Pan, Edward

    Published in Anticancer research (01-08-2018)
    “…This case report presents the first known case of a brainstem glioblastoma multiforme (GBM) in a patient with neurofibromatosis type 1 (NF1). While research…”
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    Journal Article
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    Connecting the Dots From Fever of Unknown Origin to Myelodysplastic Syndrome: GATA2 Haploinsufficiency by Montiel-Esparza, Raúl, Reys, Brian, Rogers, Zora R, Evans, Amanda S, Wysocki, Christian A, Timmons, Charles, Dickerson, Kathryn E

    Published in Journal of pediatric hematology/oncology (01-07-2020)
    “…Leukemia-predisposing conditions, such as GATA2 haploinsufficiency, are known for their high penetrance and expressivity profiles. These disorders pose a…”
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    Journal Article
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  12. 12

    Distinct NSCLC EGFR Variants in a Family With Li-Fraumeni Syndrome: Case Report by Edmondson, Shelby, von Itzstein, Mitchell S, Reys, Brian, Mayer, Melissa, Gagan, Jeffrey, Gerber, David E

    Published in JTO clinical and research reports (01-08-2022)
    “…IntroductionHeritable lung cancer may occur in the context of germline TP53 mutations (Li-Fraumeni syndrome). Limited cases of intrafamily tumor genomic…”
    Get full text
    Report