Search Results - "Blazer, Kathleen R."
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Reflex Immunohistochemistry and Microsatellite Instability Testing of Colorectal Tumors for Lynch Syndrome Among US Cancer Programs and Follow-Up of Abnormal Results
Published in Journal of clinical oncology (01-04-2012)“…Immunohistochemistry (IHC) for MLH1, MSH2, MSH6, and PMS2 protein expression and microsatellite instability (MSI) are well-established tools to screen for…”
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2
Somatic TP53 variants frequently confound germ-line testing results
Published in Genetics in medicine (01-08-2018)“…Purpose Blood/saliva DNA is thought to represent the germ line in genetic cancer-risk assessment. Cases with pathogenic TP53 variants detected by multigene…”
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3
Significant clinical impact of recurrent BRCA1 and BRCA2 mutations in Mexico
Published in Cancer (01-02-2015)“…BACKGROUND Frequent recurrent mutations in the breast and ovarian cancer susceptibility (BRCA) genes BRCA1 and BRCA2 among Hispanics, including a large…”
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4
Prevalence of BRCA Mutations and Founder Effect in High-Risk Hispanic Families
Published in Cancer epidemiology, biomarkers & prevention (01-07-2005)“…Approximately 12% of the U.S. population is Hispanic, with the majority residing in urban centers such as Los Angeles. The prevalence of BRCA mutations among…”
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5
Uptake of Risk-Reducing Surgeries in an International Real-World Cohort of Hispanic Women
Published in JCO global oncology (01-10-2024)“…Women with pathogenic variants (PVs) in breast cancer (BC) and ovarian cancer (OC) associated genes are candidates for cancer risk-reducing strategies. Limited…”
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Development and Pilot Implementation of the Genomic Risk Assessment for Cancer Implementation and Sustainment (GRACIAS) Intervention in Mexico
Published in JCO global oncology (01-06-2021)“…Genomic cancer risk assessment (GCRA) is standard-of-care practice that uses genomic tools to identify individuals with increased cancer risk, enabling…”
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Evidence for Common Ancestral Origin of a Recurring BRCA1 Genomic Rearrangement Identified in High-Risk Hispanic Families
Published in Cancer epidemiology, biomarkers & prevention (01-08-2007)“…Background: Large rearrangements account for 8% to 15% of deleterious BRCA mutations, although none have been characterized previously in individuals of…”
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Corrigendum: Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management
Published in Frontiers in oncology (02-12-2015)“…[This corrects the article on p. 208 in vol. 5, PMID: 26484312.]…”
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Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine
Published in CA: a cancer journal for clinicians (01-09-2011)“…Scientific and technologic advances are revolutionizing our approach to genetic cancer risk assessment, cancer screening and prevention, and targeted therapy,…”
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10
Social-cognitive aspects of underserved Latinas preparing to undergo genetic cancer risk assessment for hereditary breast and ovarian cancer
Published in Psycho-oncology (Chichester, England) (01-08-2008)“…Objectives: As Latinos are a growing ethnic group in the United States, it is important to understand the socio‐cultural factors that may be associated with…”
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Genetic counselors' and community clinicians' implementation and perceived barriers to informed consent during pre-test counseling for hereditary cancer risk
Published in Journal of genetic counseling (13-03-2024)“…As demand for genetic cancer risk assessment (GCRA) continues to increase, so does the sense of urgency to scale up efforts to triage patients, facilitate…”
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Prospective Study of Cancer Genetic Variants: Variation in Rate of Reclassification by Ancestry
Published in JNCI : Journal of the National Cancer Institute (01-10-2018)“…In germline genetic testing, variants from understudied ancestries have been disproportionately classified as being of uncertain significance. We hypothesized…”
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13
Reduced Mammographic Density with Use of a Gonadotropin-Releasing Hormone Agonist–Based Chemoprevention Regimen in BRCA1 Carriers
Published in Clinical cancer research (15-01-2007)“…Purpose: Women with a BRCA1 mutation ( BRCA1 mut ) need risk reduction options beyond mastectomy and oophorectomy. We evaluated the efficacy, safety, and…”
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14
Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management
Published in Frontiers in oncology (29-09-2015)“…Multigene panels can be a cost- and time-effective alternative to sequentially testing multiple genes, especially with a mixed family cancer phenotype…”
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Multigene assessment of genetic risk for women for two or more breast cancers
Published in Breast cancer research and treatment (01-08-2021)“…Purpose The prevalence, penetrance, and spectrum of pathogenic variants that predispose women to two or more breast cancers is largely unknown. Methods We…”
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When Clinical Care Depends on the Answer: The Challenges of Assessing Germline Cancer Gene Variants
Published in Journal of clinical oncology (01-12-2016)Get full text
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The Burden of Breast Cancer Predisposition Variants Across The Age Spectrum Among 10 000 Patients
Published in Journal of the American Geriatrics Society (JAGS) (01-05-2019)“…BACKGROUND/OBJECTIVES Women diagnosed with breast cancer (BC) at an older age are less likely to undergo genetic cancer risk assessment and genetic testing…”
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18
Limited Family Structure and BRCA Gene Mutation Status in Single Cases of Breast Cancer
Published in JAMA : the journal of the American Medical Association (20-06-2007)“…CONTEXT An autosomal dominant pattern of hereditary breast cancer may be masked by small family size or transmission through males given sex-limited…”
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Next-Generation Testing for Cancer Risk: Perceptions, Experiences, and Needs Among Early Adopters in Community Healthcare Settings
Published in Genetic testing and molecular biomarkers (01-12-2015)“…Advances in next-generation sequencing (NGS) technologies are driving a shift from single-gene to multigene panel testing for clinical genetic cancer risk…”
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Cross‐sectional clinical cancer genomics community of practice survey analysis of provider attitudes and beliefs regarding the use of deceased family member tissue to guide living family member genetic cancer risk assessment
Published in Journal of genetic counseling (01-10-2022)“…Next‐generation tumor tissue sequencing techniques may result in the detection of putative germline pathogenic variants (PVs), raising the possibility that…”
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