Search Results - "Burke, Wylie"
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Offering individual genetic research results: context matters
Published in Science translational medicine (30-06-2010)“…The disclosure of individual genetic research results to study participants continues to be the subject of vigorous debate, centered primarily on the nature of…”
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Closing the gap between knowledge and clinical application: challenges for genomic translation
Published in PLoS genetics (01-02-2015)“…Despite early predictions and rapid progress in research, the introduction of personal genomics into clinical practice has been slow. Several factors…”
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The cost-effectiveness of returning incidental findings from next-generation genomic sequencing
Published in Genetics in medicine (01-07-2015)“…Purpose: The American College of Medical Genetics and Genomics (ACMG) recommended that clinical laboratories performing next-generation sequencing analyze and…”
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ASHG Statement on Direct-to-Consumer Genetic Testing in the United States
Published in American journal of human genetics (01-09-2007)Get full text
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Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis
Published in Journal of clinical oncology (20-06-2015)“…To evaluate the cost effectiveness of next-generation sequencing (NGS) panels for the diagnosis of colorectal cancer and polyposis (CRCP) syndromes in patients…”
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Whole-Genome Sequencing in Healthy People
Published in Mayo Clinic proceedings (01-01-2017)“…Abstract Recent technological advances have radically changed genetic testing from an expensive and burdensome undertaking to a rapid and less costly option…”
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ASHG Statement on Direct-to-Consumer Genetic Testing in the United States
Published in Obstetrics and gynecology (New York. 1953) (01-12-2007)Get full text
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Genetic counseling and testing for Alzheimer disease: Joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors
Published in Genetics in medicine (01-06-2011)“…Alzheimer disease is the most common cause of dementia. It occurs worldwide and affects all ethnic groups. The incidence of Alzheimer disease is increasing…”
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Explaining the Black-White Disparity in Preterm Birth: A Consensus Statement From a Multi-Disciplinary Scientific Work Group Convened by the March of Dimes
Published in Frontiers in reproductive health (02-09-2021)“…In 2017-2019, the March of Dimes convened a workgroup with biomedical, clinical, and epidemiologic expertise to review knowledge of the causes of the…”
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Genomic research and wide data sharing: Views of prospective participants
Published in Genetics in medicine (01-08-2010)“…Sharing study data within the research community generates tension between two important goods: promoting scientific goals and protecting the privacy interests…”
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Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial
Published in Circulation (New York, N.Y.) (25-04-2023)“…Managing disease risk among first-degree relatives of probands diagnosed with a heritable disease is central to precision medicine. A critical component is…”
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African immigrants' favorable preterm birth rates challenge genetic etiology of the Black-White disparity in preterm birth
Published in Frontiers in public health (04-01-2024)“…We examined over a million California birth records for 2010 through 2021 to investigate whether disparities in preterm birth (PTB) by nativity and race…”
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Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium
Published in Genetics in medicine (01-11-2013)“…As genomic and exomic testing expands in both the research and clinical arenas, determining whether, how, and which incidental findings to return to the…”
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Data Management in Health-Related Research Involving Indigenous Communities in the United States and Canada: A Scoping Review
Published in Frontiers in genetics (10-10-2019)“…Multiple factors, including experiences with unethical research practices, have made some Indigenous groups in the United States and Canada reticent to…”
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Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance
Published in The Journal of law, medicine & ethics (01-03-2018)“…Neither the range of potential results from genomic research that might be returned to participants nor future uses of stored data and biospecimens can be…”
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Carnitine palmitoyltransferase 1A P479L and infant death: policy implications of emerging data
Published in Genetics in medicine (01-08-2017)“…Carnitine palmitoyltransferase 1 isoform A (CPT1A) is a crucial enzyme for the transport of long-chain fatty acids into the mitochondria. The CPT1A p.P479L…”
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The path from genome-based research to population health: development of an international public health genomics network
Published in Genetics in medicine (01-07-2006)Get full text
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Essential elements of personalized medicine
Published in Urologic oncology (01-02-2014)“…Summary Objectives Genomic information has been promoted as the basis for “personalized” health care. We considered the benefits provided by genomic testing in…”
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Current Priorities for Public Health Practice in Addressing the Role of Human Genomics in Improving Population Health
Published in American journal of preventive medicine (01-04-2011)“…Abstract In spite of accelerating human genome discoveries in a wide variety of diseases of public health significance, the promise of personalized health care…”
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Genetic testing in primary care
Published in Annual review of genomics and human genetics (01-01-2004)“…Rapid advances in genetic research are leading to an expanding array of genetic tests. Primary care providers will increasingly be challenged to identify…”
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