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MARC Record from Library of Congress

Record ID marc_loc_updates/v40.i27.records.utf8:12212212:5164
Source Library of Congress
Download Link /show-records/marc_loc_updates/v40.i27.records.utf8:12212212:5164?format=raw

LEADER: 05164cam a2200493 a 4500
001 2012405309
003 DLC
005 20120702091319.0
008 120523s2011 dcu b 100 0 eng c
010 $a 2012405309
016 7 $a101561808$2DNLM
016 7 $a015843725$2Uk
020 $a9780309162166
020 $a0309162165
035 $a(OCoLC)ocn698376202
040 $aIWA$beng$cIWA$dNRZ$dNDD$dUPM$dYDXCP$dUBY$dOCLCA$dNLM$dBTCTA$dOCLCQ$dUKMGB$dOCLCQ$dDLC
042 $apcc
050 00 $aRB155.65$b.D57 2011
082 00 $a616/.042$223
060 00 $a2011 F-678
060 10 $aQZ 52
245 00 $aDirect-to-consumer genetic testing :$bsummary of a workshop /$cMary Fraker and Anne-Marie Mazza, rapporteurs ; Committee on Science, Technology, and Law Policy and Global Affairs ; Board on Life Sciences, Division on Earth and Life Studies ; Forum on Drug Discovery, Development and Translation, Board on Health Sciences Policy ; Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy ; National Cancer Policy Forum, Board on Health Care Services ; Institute of Medicine and National Research Council of the National Academies.
260 $aWashington, D.C. :$bNational Academies Press,$cc2011.
300 $axii, 93 p. ;$c23 cm.
504 $aIncludes bibliographical references.
530 $aAlso available in Open Book format via the National Academies Press home page.
505 0 $aIntroduction -- Scientific foundations for direct-to-consumer genetic testing -- Personal and social issues -- Research and medical issues -- Impact on health care and public health -- Current legislative and regulatory framework in the United States -- Areas for further study.
520 $a"Today, scores of companies, primarily in the United States and Europe, are offering whole genome scanning services directly to the public. The proliferation of these companies and the services they offer demonstrate a public appetite for this information and where the future of genetics may be headed; they also demonstrate the need for serious discussion about the regulatory environment, patient privacy, and other policy implications of direct-to-consumer (DTC) genetic testing. Rapid advances in genetic research already have begun to transform clinical practice and our understanding of disease progression. Existing research has revealed a genetic basis or component for numerous diseases, including Parkinson's disease, Alzheimer's disease, diabetes, heart disease, and several forms of cancer. The availability of the human genome sequence and the HapMap, plummeting costs of high-throughput screening, and increasingly sophisticated computational analyses have led to an explosion of discoveries of linkages between patterns of genetic variation and disease susceptibility. While this research is by no means a straight path toward better public health, improved knowledge of the genetic linkages has the potential to change fundamentally the way health professionals and public health practitioners approach the prevention and treatment of disease. Realizing this potential will require greater sophistication in the interpretation of genetic tests, new training for physicians and other diagnosticians, and new approaches to communicating findings to the public. As this rapidly growing field matures, all of these questions require attention from a variety of perspectives. To discuss some of the foregoing issues, several units of the National Academies held a workshop on August 31 and September 1, 2009, to bring together a still-developing community of professionals from a variety of relevant disciplines, to educate the public and policy-makers about this emerging field, and to identify issues for future study. The meeting featured several invited presentations and discussions on the many technical, legal, policy, and ethical questions that such DTC testing raises, including: (1) overview of the current state of knowledge and the future research trajectory; (2) shared genes and emerging issues in privacy; (3) the regulatory framework; and (4) education of the public and the medical community."--Publisher's description.
650 0 $aHuman chromosome abnormalities$xDiagnosis$vCongresses.
650 0 $aSelf-examination, Medical$vCongresses.
650 12 $aGenetic Testing$vCongresses.
650 22 $aGenetic Predisposition to Disease$vCongresses.
650 22 $aMarketing of Health Services$vCongresses.
650 22 $aSelf Care$vCongresses.
655 4 $aElectronic books.
700 1 $aFraker, Mary.
700 1 $aMazza, Anne-Marie.
710 2 $aNational Research Council (U.S.).$bCommittee on Science, Technology, and Law.
710 2 $aNational Research Council (U.S.).$bBoard on Life Sciences.
710 2 $aInstitute of Medicine (U.S.).$bForum on Drug Discovery, Development, and Translation.
710 2 $aInstitute of Medicine (U.S.).$bRoundtable on Translating Genomic-Based Research for Health.
710 2 $aNational Cancer Policy Forum (U.S.)
710 2 $aNational Academies Press (U.S.)
856 41 $3National Academies Press$uhttp://www.nap.edu/catalog.php?record_id=13021