Search Results - "Hudson, Kathy L"
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The 21st Century Cures Act — A View from the NIH
Published in The New England journal of medicine (12-01-2017)“…The Cures Act that President Obama has signed into law will provide the National Institutes of Health with critical tools and resources to advance biomedical…”
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A Survey of U.S Adults' Opinions about Conduct of a Nationwide Precision Medicine Initiative® Cohort Study of Genes and Environment
Published in PloS one (17-08-2016)“…A survey of a population-based sample of U.S adults was conducted to measure their attitudes about, and inform the design of the Precision Medicine…”
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Public Opinion about the Importance of Privacy in Biobank Research
Published in American journal of human genetics (13-11-2009)“…Concerns about privacy may deter people from participating in genetic research. Recruitment and retention of biobank participants requires understanding the…”
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Genetic testing of embryos: practices and perspectives of US in vitro fertilization clinics
Published in Fertility and sterility (01-05-2008)“…Objective To better understand the current practices of IVF clinics regarding preimplantation genetic diagnosis (PGD) and explore the attitudes and opinions of…”
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Ten simple rules for open human health research
Published in PLoS computational biology (03-09-2020)“…About the Authors: Aïda Bafeta Affiliation: Center for Research and Interdisciplinarity (CRI), Université de Paris, INSERM U1284, Paris, France ORCID logo…”
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Genomics, Health Care, and Society
Published in The New England journal of medicine (15-09-2011)“…Advances in genomic approaches have affected biomedical research, clinical practice, and areas outside medicine. This article reviews societal issues raised by…”
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Toward a New Era of Trust and Transparency in Clinical Trials
Published in JAMA : the journal of the American Medical Association (04-10-2016)“…Clinical trials are the most publicly visible component of the biomedical research enterprise, from the potential human application of novel laboratory…”
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Sharing and Reporting the Results of Clinical Trials
Published in JAMA : the journal of the American Medical Association (27-01-2015)“…The principle of data sharing dates to the dawn of scientific discovery--it is how researchers from different disciplines and countries form collaborations,…”
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Bringing the Common Rule into the 21st Century
Published in The New England journal of medicine (10-12-2015)“…Proposed revisions to the rules governing the ethical conduct of research involving humans aim to enhance respect and safeguards for research participants and…”
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Undermining Genetic Privacy? Employee Wellness Programs and the Law
Published in The New England journal of medicine (06-07-2017)“…A bill in the House of Representatives would substantially change legal protections related to the collection and treatment of genetic and other personal…”
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PCORnet: turning a dream into reality
Published in Journal of the American Medical Informatics Association : JAMIA (01-07-2014)Get full text
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The BRAIN Initiative: developing technology to catalyse neuroscience discovery
Published in Philosophical transactions of the Royal Society of London. Series B. Biological sciences (19-05-2015)“…The evolution of the field of neuroscience has been propelled by the advent of novel technological capabilities, and the pace at which these capabilities are…”
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Keeping Pace with the Times — The Genetic Information Nondiscrimination Act of 2008
Published in The New England journal of medicine (19-06-2008)“…On May 21, President George Bush signed the Genetic Information Nondiscrimination Act (GINA). Kathy Hudson, M.K. Holohan, and Dr. Francis Collins write that at…”
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Biospecimen policy: Family matters
Published in Nature (London) (08-08-2013)Get full text
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In Support of SUPPORT — A View from the NIH
Published in The New England journal of medicine (20-06-2013)“…Debate over informed consent in SUPPORT (a study meant to identify oxygen-saturation levels for premature infants that minimize the risk of retinopathy) could…”
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Prohibiting Genetic Discrimination
Published in The New England journal of medicine (17-05-2007)“…This year, the reintroduced Genetic Information Nondiscrimination Act has been winding through three House committees and one Senate committee. Kathy Hudson…”
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Preimplantation genetic diagnosis: public policy and public attitudes
Published in Fertility and sterility (01-06-2006)“…This paper summarizes the regulatory framework surrounding preimplantation genetic diagnosis (PGD) in the United States. In addition, the author reports…”
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Genetic testing oversight
Published in Science (American Association for the Advancement of Science) (29-09-2006)“…A major impact of sequencing the human genome has been the ability to detect disease and the risk of disease through genetic testing. However, no one in the US…”
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Genomics, Health Care, and Society
Published in Obstetrical & gynecological survey (01-01-2012)“…Genetic tests are growing in number and in clinical relevance as a result of rapid advances in genomic technologies. The widespread availability of genomic…”
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Ethics. The ISSCR guidelines for human embryonic stem cell research
Published in Science (American Association for the Advancement of Science) (02-02-2007)Get full text
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