Search Results - "JOHANSEN TABER, Katherine A"
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Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
Published in Genetics in medicine (01-09-2019)“…Carrier screening identifies couples at high risk for conceiving offspring affected with serious heritable conditions. Minimal guidelines recommend offering…”
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The promise and challenges of next-generation genome sequencing for clinical care
Published in JAMA internal medicine (01-02-2014)“…With increased speed and decreased costs, next-generation gene sequencing has the potential to improve medical care by making possible widespread evaluation of…”
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Strategies for Improving Access to Hereditary Cancer Testing: Recommendations from Stakeholders
Published in Genetics in medicine (01-08-2019)Get full text
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Clinical utility of expanded carrier screening: results-guided actionability and outcomes
Published in Genetics in medicine (01-05-2019)“…Purpose Expanded carrier screening (ECS) informs couples of their risk of having offspring affected by certain genetic conditions. Limited data exists…”
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Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
Published in Genetics in medicine (01-04-2022)Get full text
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Sequencing as a first-line methodology for cystic fibrosis carrier screening
Published in Genetics in medicine (01-11-2019)“…Purpose Medical society guidelines recommend offering genotyping-based cystic fibrosis (CF) carrier screening to pregnant women or women considering pregnancy…”
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Pharmacogenomic knowledge gaps and educational resource needs among physicians in selected specialties
Published in Pharmacogenomics and personalized medicine (01-01-2014)“…The use of pharmacogenomic testing in the clinical setting has the potential to improve the safety and effectiveness of drug therapy, yet studies have revealed…”
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What works in genomics education: outcomes of an evidenced-based instructional model for community-based physicians
Published in Genetics in medicine (01-07-2016)“…Education of practicing health professionals is likely to be one factor that will speed appropriate integration of genomics into routine clinical practice. Yet…”
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Male breast cancer: Risk factors, diagnosis, and management (Review)
Published in Oncology reports (01-11-2010)“…Male breast cancer (MBC) is extremely rare, with an incidence in the general US population of <1%. It tends to be diagnosed at later stages than breast cancer…”
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Challenges and Opportunities for Genomics Education: Insights from an Institute of Medicine Roundtable Activity
Published in The Journal of continuing education in the health professions (2016)“…Despite the growing availability of genomic tools for clinical care, many health care providers experience gaps in genomics knowledge and skills that serve as…”
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Correction: Sequencing as a first-line methodology for cystic fibrosis carrier screening
Published in Genetics in medicine (01-10-2019)“…The original version of this Article contained an error in Figure 3. Specifically, the result “3 (67%) TOP” should read “2 (67%) TOP.” This has now been…”
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Genomic-based tools for the risk assessment, management, and prevention of type 2 diabetes
Published in Application of clinical genetics (01-01-2015)“…Type 2 diabetes (T2D) is a common and serious disorder and is a significant risk factor for the development of cardiovascular disease, neuropathy, nephropathy,…”
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Clinical Utility of Expanded Carrier Screening: Results-Guided Actionability and Outcomes
Published in Obstetrical & gynecological survey (01-10-2019)“…(Abstracted from Genet Med 2019;21(5):1041–1048)One in 300 pregnancies is impacted by a recessive or X-linked condition. Universal screening is recommended by…”
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Sequencing as a first-line methodology for cystic fibrosiscarrier screening
Published in Genetics in medicine (01-11-2019)“…PurposeMedical society guidelines recommend offering genotyping-based cystic fibrosis (CF) carrier screening to pregnant women or women considering pregnancy…”
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