Search Results - "Reys, Brian"
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Distinct NSCLC EGFR Variants in a Family With Li-Fraumeni Syndrome: Case Report
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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Family still matters: Counseling patients with complex family histories of colon and endometrial cancers
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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Do genetic testing criteria identify individuals with Lynch syndrome prior to cancer diagnoses?
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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De novo SDHB gene mutation in a family with extra-adrenal paraganglioma
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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Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices
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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Brainstem Glioblastoma Multiforme in a Patient with NF1
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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Is Malignant Germ-Cell Tumor Associated With Cowden Syndrome?
Published in Clinical genitourinary cancer (01-06-2019)Get full text
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A randomized controlled trial of video-education or in-person genetic counseling for men with prostate cancer (ProGen)
Published in Journal of clinical oncology (20-05-2020)“…Abstract only 1507 Background: Approximately 10% of men with advanced prostate cancer (PC) have pathogenic/likely pathogenic variants (PV) in cancer…”
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Connecting the Dots From Fever of Unknown Origin to Myelodysplastic Syndrome: GATA2 Haploinsufficiency
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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NCCN Guidelines® Insights: Prostate Cancer Early Detection, Version 1.2023
Published in Journal of the National Comprehensive Cancer Network (01-03-2023)“…The NCCN Guidelines for Prostate Cancer Early Detection provide recommendations for individuals with a prostate who opt to participate in an early detection…”
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Pretest Video Education Versus Genetic Counseling for Patients With Prostate Cancer: ProGen, A Multisite Randomized Controlled Trial
Published in JCO oncology practice (01-11-2023)“…Germline genetic testing (GT) is recommended for men with prostate cancer (PC), but testing through traditional models is limited. The ProGen study examined a…”
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Distinct NSCLC EGFR Variants in a Family With Li-Fraumeni Syndrome: Case Report
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…”
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Report