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1. Full Text Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine
by Green, Robert C and Goddard, Katrina A.B and Jarvik, Gail P and Amendola, Laura M and Appelbaum, Paul S and Berg, Jonathan S and Bernhardt, Barbara A and Biesecker, Leslie G and Biswas, Sawona and Blout, Carrie L and Bowling, Kevin M and Brothers, Kyle B and Burke, Wylie and Caga-anan, Charlisse F and Chinnaiyan, Arul M and Chung, Wendy K and Clayton, Ellen W and Cooper, Gregory M and East, Kelly and Evans, James P and Fullerton, Stephanie M and Garraway, Levi A and Garrett, Jeremy R and Gray, Stacy W and Henderson, Gail E and Hindorff, Lucia A and Holm, Ingrid A and Lewis, Michelle Huckaby and Hutter, Carolyn M and Janne, Pasi A and Joffe, Steven and Kaufman, David and Knoppers, Bartha M and Koenig, Barbara A and Krantz, Ian D and Manolio, Teri A and McCullough, Laurence and McEwen, Jean and McGuire, Amy and Muzny, Donna and Myers, Richard M and Nickerson, Deborah A and Ou, Jeffrey and Parsons, Donald W and Petersen, Gloria M and Plon, Sharon E and Rehm, Heidi L and Roberts, J. Scott and Robinson, Dan and Salama, Joseph S and Scollon, Sarah and Sharp, Richard R and Shirts, Brian and Spinner, Nancy B and Tabor, Holly K and Tarczy-Hornoch, Peter and Veenstra, David L and Wagle, Nikhil and Weck, Karen and Wilfond, Benjamin S and Wilhelmsen, Kirk and Wolf, Susan M and Wynn, Julia and Yu, Joon-Ho and Amaral, Michelle and Amendola, Laura and Appelbaum, Paul S and Aronson, Samuel J and Arora, Shubhangi and Azzariti, Danielle R and Barsh, Greg S and Bebin, E.M and Biesecker, Barbara B and Biesecker, Leslie G and Biswas, Sawona and Blout, Carrie L and Bowling, Kevin M and Brothers, Kyle B and Brown, Brian L and Burt, Amber A and Byers, Peter H and Caga-anan, Charlisse F and Calikoglu, Muge G and Carlson, Sara J and Chahin, Nizar and Chinnaiyan, Arul M and Christensen, Kurt D and Chung, Wendy and Cirino, Allison L and Clayton, Ellen and Conlin, Laura K and Cooper, Greg M and Crosslin, David R and Davis, James V and Davis, Kelly and Deardorff, Matthew A and Devkota, Batsal and De Vries, Raymond and Diamond, Pamela and Dorschner, Michael O and ... and the CSER Consortium and CSER Consortium
American journal of human genetics, ISSN 0002-9297, 06/2016, Volume 98, Issue 6, pp. 1051 - 1066
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Evidence-Based Practice | United States | Humans | Clinical Trials as Topic | Cardiovascular Diseases - genetics | Exome - genetics | National Human Genome Research Institute (U.S.) | Polymorphism, Single Nucleotide - genetics | Adult | Biomedical Research | Population Groups | Software | Genome, Human | Genomics - methods | High-Throughput Nucleotide Sequencing - methods | Child | Genetic research | Nucleotide sequencing | Methods | DNA sequencing | Medical diagnosis | Electronic health records | Genomics | Genes | Children & youth | Index Medicus
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2. Full Text A taxonomy of medical uncertainties in clinical genome sequencing
by Han, Paul K.J and Umstead, Kendall L and Bernhardt, Barbara A and Green, Robert C and Joffe, Steven and Koenig, Barbara and Krantz, Ian and Waterston, Leo B and Biesecker, Leslie G and Biesecker, Barbara B
Genetics in medicine, ISSN 1098-3600, 08/2017, Volume 19, Issue 8, pp. 918 - 925
Uncertainty | Next-generation sequencing | Genome sequencing | Taxonomy | Exome sequencing | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Predictive Value of Tests | Genetic Predisposition to Disease | Molecular Diagnostic Techniques | Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects | Humans | Adult | Male | Muscular Diseases - chemically induced | Muscular Diseases - genetics | Whole Genome Sequencing | Index Medicus | genome sequencing | exome sequencing | taxonomy | uncertainty | next-generation sequencing
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3. Full Text Ethics and Genomic Incidental Findings
by Amy L. McGuire and Steven Joffe and Barbara A. Koenig and Barbara B. Biesecker and Laurence B. McCullough and Jennifer S. Blumenthal-Barby and Timothy Caulfield and Sharon F. Terry and Robert C. Green
Science (American Association for the Advancement of Science), ISSN 0036-8075, 5/2013, Volume 340, Issue 6136, pp. 1047 - 1048
Recommendations | Youths at risk | Medical practice | Genomics | Incidental findings | Genetics | Informed consent | Child psychology | Children | Sequencing | POLICY FORUM | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Ethics | Ethical standards | Communities | Lists | Genes | Evolution
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4. Full Text Clinical Genome Sequencing
: Psychological Considerations
by Tibben, Aad and Biesecker, Barbara B
2019, ISBN 012813335X, 259
Gene mapping | Human gene mapping
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5. Full Text Predictive genetic testing of minors: Evidence and experience with families
by Biesecker, Barbara B
Genetics in medicine, ISSN 1098-3600, 08/2016, Volume 18, Issue 8, pp. 763 - 764
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Index Medicus
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6. Full Text Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
by Hart, M. Ragan and Biesecker, Barbara B and Blout, Carrie L and Christensen, Kurt D and Amendola, Laura M and Bergstrom, Katie L and Biswas, Sawona and Bowling, Kevin M and Brothers, Kyle B and Conlin, Laura K and Cooper, Greg M and Dulik, Matthew C and East, Kelly M and Everett, Jessica N and Finnila, Candice R and Ghazani, Arezou A and Gilmore, Marian J and Goddard, Katrina A. B and Jarvik, Gail P and Johnston, Jennifer J and Kauffman, Tia L and Kelley, Whitley V and Krier, Joel B and Lewis, Katie L and McGuire, Amy L and McMullen, Carmit and Ou, Jeffrey and Plon, Sharon E and Rehm, Heidi L and Richards, C. Sue and Romasko, Edward J and Miren Sagardia, Ane and Spinner, Nancy B and Thompson, Michelle L and Turbitt, Erin and Vassy, Jason L and Wilfond, Benjamin S and Veenstra, David L and Berg, Jonathan S and Green, Robert C and Biesecker, Leslie G and Hindorff, Lucia A
Genetics in medicine, ISSN 1098-3600, 05/2019, Volume 21, Issue 5, pp. 1100 - 1110
genomic sequencing | health-care resource utilization | secondary findings | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Prevalence | Genetic Testing - standards | Humans | Incidental Findings | Male | Genetic Testing - ethics | Disclosure | Health Knowledge, Attitudes, Practice | Patients | High-Throughput Nucleotide Sequencing - ethics | Exome | Health Care Costs | Decision Making - ethics | Health Personnel | Adult | Female | Intention | Whole Genome Sequencing - economics | Genetic Testing - economics | Genomics - methods | Whole Genome Sequencing - ethics | Consortia | Index Medicus
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7. Full Text Personal utility in genomic testing: A systematic literature review
by Kohler, Jennefer N and Turbitt, Erin and Biesecker, Barbara B
European journal of human genetics : EJHG, ISSN 1018-4813, 03/2017, Volume 25, Issue 6, pp. 662 - 668
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genetic Counseling - psychology | Attitude | Social Behavior | Humans | Cognition | Genetic Testing - ethics | Emotions | Literature reviews | Population studies | Cognitive ability | Index Medicus | Review
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8. Full Text Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine
by Green, Robert C and Goddard, Katrina A.B and Jarvik, Gail P and Amendola, Laura M and Appelbaum, Paul S and Berg, Jonathan S and Bernhardt, Barbara A and Biesecker, Leslie G and Biswas, Sawona and Blout, Carrie L and Bowling, Kevin M and Brothers, Kyle B and Burke, Wylie and Caga-anan, Charlisse F and Chinnaiyan, Arul M and Chung, Wendy K and Clayton, Ellen W and Cooper, Gregory M and East, Kelly and Evans, James P and Fullerton, Stephanie M and Garraway, Levi A and Garrett, Jeremy R and Gray, Stacy W and Henderson, Gail E and Hindorff, Lucia A and Holm, Ingrid A and Lewis, Michelle Huckaby and Hutter, Carolyn M and Janne, Pasi A and Joffe, Steven and Kaufman, David and Knoppers, Bartha M and Koenig, Barbara A and Krantz, Ian D and Manolio, Teri A and McCullough, Laurence and McEwen, Jean and McGuire, Amy and Muzny, Donna and Myers, Richard M and Nickerson, Deborah A and Ou, Jeffrey and Parsons, Donald W and Petersen, Gloria M and Plon, Sharon E and Rehm, Heidi L and Roberts, J. Scott and Robinson, Dan and Salama, Joseph S and Scollon, Sarah and Sharp, Richard R and Shirts, Brian and Spinner, Nancy B and Tabor, Holly K and Tarczy-Hornoch, Peter and Veenstra, David L and Wagle, Nikhil and Weck, Karen and Wilfond, Benjamin S and Wilhelmsen, Kirk and Wolf, Susan M and Wynn, Julia and Yu, Joon-Ho and Amaral, Michelle and Amendola, Laura and Aronson, Samuel J and Arora, Shubhangi and Azzariti, Danielle R and Barsh, Greg S and Bebin, E.M and Biesecker, Barbara B and Brown, Brian L and Burt, Amber A and Byers, Peter H and Calikoglu, Muge G and Carlson, Sara J and Chahin, Nizar and Christensen, Kurt D and Chung, Wendy and Cirino, Allison L and Clayton, Ellen and Conlin, Laura K and Cooper, Greg M and Crosslin, David R and Davis, James V and Davis, Kelly and Deardorff, Matthew A and Devkota, Batsal and De Vries, Raymond and Diamond, Pamela and Dorschner, Michael O and Dugan, Noreen P and Dukhovny, Dmitry and Dulik, Matthew C and East, Kelly M and Rivera-Munoz, Edgar A and Evans, Barbara and Everett, Jessica and Exe, Nicole and ... and the CSER Consortium
American journal of human genetics, ISSN 0002-9297, 07/2016, Volume 99, Issue 1, pp. 246 - 246
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9. Full Text A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling
by Athens, Barbara A and Caldwell, Samantha L and Umstead, Kendall L and Connors, Philip D and Brenna, Ethan and Biesecker, Barbara B
Journal of genetic counseling, ISSN 1059-7700, 10/2017, Volume 26, Issue 5, pp. 902 - 933
Human Genetics | Public Health | Gynecology | Patient outcomes | Evidence-based practice | Genetic counseling outcomes | Psychological wellbeing | Clinical Psychology | Risk perception | Genetics knowledge | Randomized controlled trials | Ethics | Biomedicine | Genetic counseling | Patient satisfaction | Evidence‐based practice | Social Sciences | Life Sciences & Biomedicine | Social Sciences, Biomedical | Health Care Sciences & Services | Health Policy & Services | Genetics & Heredity | Biomedical Social Sciences | Science & Technology | Genetic Counseling - statistics & numerical data | Outcome Assessment (Health Care) | Patient Satisfaction - statistics & numerical data | Humans | Randomized Controlled Trials as Topic | Health care reform | Medical genetics | Health care | Evidence based research | Publications | Bias | Health care policy | Clinical trials | Population studies | Systematic review | Clinical practice | Clinical outcomes | Precision medicine | Counseling | Genetic counselling | Cancer | Psychological well being | Index Medicus
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10. Full Text Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children
by Sapp, J.C and Dong, D and Stark, C and Ivey, L.E and Hooker, G and Biesecker, L.G and Biesecker, B.B
Clinical genetics, ISSN 0009-9163, 02/2014, Volume 85, Issue 2, pp. 120 - 126
genome sequencing | incidental findings | patient preferences | theory of reasoned action | Patient preferences | Genome sequencing | Theory of reasoned action | Incidental findings | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease - genetics | Genetic Testing | Social Values | Attitude | Humans | Incidental Findings | Male | Disclosure | Sequence Analysis, DNA | Exome - genetics | Parents - psychology | Adult | Female | Interviews as Topic | Child | Culture | Genomics | Children | Studies | Genetic research | Values | Genetic markers | Childrens health | Index Medicus | Theory of Reasoned Action
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