Susan M Wolf. J Law Med Ethics 2017
Times Cited: 4
Times Cited: 4
Times Cited
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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet. Med. 2017
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet. Med. 2017
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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet. Med. 2013
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet. Med. 2013
75
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am. J. Hum. Genet. 2015
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am. J. Hum. Genet. 2015
50
International Policies on Sharing Genomic Research Results with Relatives: Approaches to Balancing Privacy with Access.
Rebecca Branum, Susan M Wolf. J Law Med Ethics 2015
Rebecca Branum, Susan M Wolf. J Law Med Ethics 2015
50
Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet. Med. 2012
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet. Med. 2012
50
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
. Genet. Med. 2015
. Genet. Med. 2015
50
The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.
Gail E Henderson, Susan M Wolf, Kristine J Kuczynski, Steven Joffe, Richard R Sharp, D Williams Parsons, Bartha M Knoppers, Joon-Ho Yu, Paul S Appelbaum. J Law Med Ethics 2014
Gail E Henderson, Susan M Wolf, Kristine J Kuczynski, Steven Joffe, Richard R Sharp, D Williams Parsons, Bartha M Knoppers, Joon-Ho Yu, Paul S Appelbaum. J Law Med Ethics 2014
50
The law of incidental findings in human subjects research: establishing researchers' duties.
Susan M Wolf, Jordan Paradise, Charlisse Caga-anan. J Law Med Ethics 2008
Susan M Wolf, Jordan Paradise, Charlisse Caga-anan. J Law Med Ethics 2008
50
Return of individual research results and incidental findings: facing the challenges of translational science.
Susan M Wolf. Annu Rev Genomics Hum Genet 2013
Susan M Wolf. Annu Rev Genomics Hum Genet 2013
50
Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.
Susan M Wolf, Laura M Amendola, Jonathan S Berg, Wendy K Chung, Ellen Wright Clayton, Robert C Green, Julie Harris-Wai, Gail E Henderson, Gail P Jarvik, Barbara A Koenig,[...]. Genet. Med. 2018
Susan M Wolf, Laura M Amendola, Jonathan S Berg, Wendy K Chung, Ellen Wright Clayton, Robert C Green, Julie Harris-Wai, Gail E Henderson, Gail P Jarvik, Barbara A Koenig,[...]. Genet. Med. 2018
50
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet. Med. 2015
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet. Med. 2015
50
Comparative Approaches to Biobanks and Privacy.
Mark A Rothstein, Bartha Maria Knoppers, Heather L Harrell. J Law Med Ethics 2016
Mark A Rothstein, Bartha Maria Knoppers, Heather L Harrell. J Law Med Ethics 2016
25
The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J. Med. Genet. 2015
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J. Med. Genet. 2015
25
Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat. Rev. Genet. 2015
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat. Rev. Genet. 2015
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Disclosure of individual pharmacogenomic results in research projects: when and what kind of information to return to research participants.
Sandra Korol, Thierry Hurlimann, Béatrice Godard, Simon de Denus. Pharmacogenomics 2013
Sandra Korol, Thierry Hurlimann, Béatrice Godard, Simon de Denus. Pharmacogenomics 2013
25
Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur. J. Hum. Genet. 2013
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur. J. Hum. Genet. 2013
25
Informed Consent in Translational Genomics: Insufficient Without Trustworthy Governance.
Wylie Burke, Laura M Beskow, Susan Brown Trinidad, Stephanie M Fullerton, Kathleen Brelsford. J Law Med Ethics 2018
Wylie Burke, Laura M Beskow, Susan Brown Trinidad, Stephanie M Fullerton, Kathleen Brelsford. J Law Med Ethics 2018
25
Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur. J. Hum. Genet. 2013
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur. J. Hum. Genet. 2013
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Perceptions of legislation relating to the sharing of genomic biobank results with donors-a survey of BBMRI-ERIC biobanks.
Minna Brunfeldt, Harriet Teare, Sirpa Soini, Helena Kääriäinen. Eur. J. Hum. Genet. 2018
Minna Brunfeldt, Harriet Teare, Sirpa Soini, Helena Kääriäinen. Eur. J. Hum. Genet. 2018
50
Controlled Access under Review: Improving the Governance of Genomic Data Access.
Mahsa Shabani, Stephanie O M Dyke, Yann Joly, Pascal Borry. PLoS Biol. 2015
Mahsa Shabani, Stephanie O M Dyke, Yann Joly, Pascal Borry. PLoS Biol. 2015
25
Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe?
Isabelle Budin-Ljøsne, Deborah Mascalzoni, Sirpa Soini, Helena Machado, Jane Kaye, Heidi Beate Bentzen, Emmanuelle Rial-Sebbag, Flavio D'Abramo, Michał Witt, Geneviève Schamps,[...]. Biopreserv Biobank 2016
Isabelle Budin-Ljøsne, Deborah Mascalzoni, Sirpa Soini, Helena Machado, Jane Kaye, Heidi Beate Bentzen, Emmanuelle Rial-Sebbag, Flavio D'Abramo, Michał Witt, Geneviève Schamps,[...]. Biopreserv Biobank 2016
25
Personal utility in genomic testing: a systematic literature review.
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur. J. Hum. Genet. 2017
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur. J. Hum. Genet. 2017
25
International ethics harmonization and the global alliance for genomics and health.
Bartha M Knoppers. Genome Med 2014
Bartha M Knoppers. Genome Med 2014
25
Guidelines for diagnostic next-generation sequencing.
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur. J. Hum. Genet. 2016
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur. J. Hum. Genet. 2016
25
Medical malpractice in twentieth century United States. The interaction of technology, law and culture.
K De Ville. Int J Technol Assess Health Care 1998
K De Ville. Int J Technol Assess Health Care 1998
25
Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
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Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin. Perinatol. 2015
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin. Perinatol. 2015
25
The Cystic Fibrosis mutation "arms race": when less is more.
Wayne W Grody, Garry R Cutting, Michael S Watson. Genet. Med. 2007
Wayne W Grody, Garry R Cutting, Michael S Watson. Genet. Med. 2007
25
Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.
Joanne Armstrong, Michele Toscano, Nancy Kotchko, Sue Friedman, Marc D Schwartz, Katherine S Virgo, Kristian Lynch, James E Andrews, Claudia X Aguado Loi, Joseph E Bauer,[...]. JAMA Oncol 2015
Joanne Armstrong, Michele Toscano, Nancy Kotchko, Sue Friedman, Marc D Schwartz, Katherine S Virgo, Kristian Lynch, James E Andrews, Claudia X Aguado Loi, Joseph E Bauer,[...]. JAMA Oncol 2015
25
First, do no harm: direct-to-consumer genetic testing.
Jennifer Schleit, Lorraine V Naylor, Fuki M Hisama. Genet. Med. 2019
Jennifer Schleit, Lorraine V Naylor, Fuki M Hisama. Genet. Med. 2019
50
Managing incidental genomic findings: legal obligations of clinicians.
Ellen Wright Clayton, Susanne Haga, Patricia Kuszler, Emily Bane, Krysta Shutske, Wylie Burke. Genet. Med. 2013
Ellen Wright Clayton, Susanne Haga, Patricia Kuszler, Emily Bane, Krysta Shutske, Wylie Burke. Genet. Med. 2013
25
Incidental findings and future testing methodologies: potential application of the ACMG 2013 recommendations.
Anastasia Richardson. 2014
Anastasia Richardson. 2014
25
Recognizing the Right Not to Know: Conceptual, Professional, and Legal Implications.
Graeme Laurie. J Law Med Ethics 2014
Graeme Laurie. J Law Med Ethics 2014
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The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann. Intern. Med. 2017
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann. Intern. Med. 2017
25
Use of panel tests in place of single gene tests in the cancer genetics clinic.
A Yorczyk, L S Robinson, T S Ross. Clin. Genet. 2015
A Yorczyk, L S Robinson, T S Ross. Clin. Genet. 2015
25
The promise of whole-exome sequencing in medical genetics.
Bahareh Rabbani, Mustafa Tekin, Nejat Mahdieh. J. Hum. Genet. 2014
Bahareh Rabbani, Mustafa Tekin, Nejat Mahdieh. J. Hum. Genet. 2014
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Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines.
Wylie Burke, Ellen Wright Clayton, Susan M Wolf, Susan A Berry, Barbara J Evans, James P Evans, Ralph Hall, Diane Korngiebel, Anne-Marie Laberge, Bonnie S LeRoy,[...]. Genet Med 2019
Wylie Burke, Ellen Wright Clayton, Susan M Wolf, Susan A Berry, Barbara J Evans, James P Evans, Ralph Hall, Diane Korngiebel, Anne-Marie Laberge, Bonnie S LeRoy,[...]. Genet Med 2019
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The genetic architecture of long QT syndrome: A critical reappraisal.
John R Giudicessi, Arthur A M Wilde, Michael J Ackerman. Trends Cardiovasc. Med. 2018
John R Giudicessi, Arthur A M Wilde, Michael J Ackerman. Trends Cardiovasc. Med. 2018
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The standard of care: legal history and definitions: the bad and good news.
Peter Moffett, Gregory Moore. West J Emerg Med 2011
Peter Moffett, Gregory Moore. West J Emerg Med 2011
25
HLA-B*5701 screening for hypersensitivity to abacavir.
Simon Mallal, Elizabeth Phillips, Giampiero Carosi, Jean-Michel Molina, Cassy Workman, Janez Tomazic, Eva Jägel-Guedes, Sorin Rugina, Oleg Kozyrev, Juan Flores Cid,[...]. N. Engl. J. Med. 2008
Simon Mallal, Elizabeth Phillips, Giampiero Carosi, Jean-Michel Molina, Cassy Workman, Janez Tomazic, Eva Jägel-Guedes, Sorin Rugina, Oleg Kozyrev, Juan Flores Cid,[...]. N. Engl. J. Med. 2008
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The impact of hereditary cancer gene panels on clinical care and lessons learned.
Volkan Okur, Wendy K Chung. Cold Spring Harb Mol Case Stud 2017
Volkan Okur, Wendy K Chung. Cold Spring Harb Mol Case Stud 2017
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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.
Jonathan S Berg, Laura M Amendola, Christine Eng, Eliezer Van Allen, Stacy W Gray, Nikhil Wagle, Heidi L Rehm, Elizabeth T DeChene, Matthew C Dulik, Fuki M Hisama,[...]. Genet. Med. 2013
Jonathan S Berg, Laura M Amendola, Christine Eng, Eliezer Van Allen, Stacy W Gray, Nikhil Wagle, Heidi L Rehm, Elizabeth T DeChene, Matthew C Dulik, Fuki M Hisama,[...]. Genet. Med. 2013
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A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin,[...]. Genet. Med. 2017
Julianne M O'Daniel, Heather M McLaughlin, Laura M Amendola, Sherri J Bale, Jonathan S Berg, David Bick, Kevin M Bowling, Elizabeth C Chao, Wendy K Chung, Laura K Conlin,[...]. Genet. Med. 2017
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Notifications received by primary care practitioners in electronic health records: a taxonomy and time analysis.
Daniel R Murphy, Brian Reis, Dean F Sittig, Hardeep Singh. Am. J. Med. 2012
Daniel R Murphy, Brian Reis, Dean F Sittig, Hardeep Singh. Am. J. Med. 2012
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ClinGen--the Clinical Genome Resource.
Heidi L Rehm, Jonathan S Berg, Lisa D Brooks, Carlos D Bustamante, James P Evans, Melissa J Landrum, David H Ledbetter, Donna R Maglott, Christa Lese Martin, Robert L Nussbaum,[...]. N. Engl. J. Med. 2015
Heidi L Rehm, Jonathan S Berg, Lisa D Brooks, Carlos D Bustamante, James P Evans, Melissa J Landrum, David H Ledbetter, Donna R Maglott, Christa Lese Martin, Robert L Nussbaum,[...]. N. Engl. J. Med. 2015
25
The nature of adverse events in hospitalized patients. Results of the Harvard Medical Practice Study II.
L L Leape, T A Brennan, N Laird, A G Lawthers, A R Localio, B A Barnes, L Hebert, J P Newhouse, P C Weiler, H Hiatt. N. Engl. J. Med. 1991
L L Leape, T A Brennan, N Laird, A G Lawthers, A R Localio, B A Barnes, L Hebert, J P Newhouse, P C Weiler, H Hiatt. N. Engl. J. Med. 1991
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Self-guided management of exome and whole-genome sequencing results: changing the results return model.
Joon-Ho Yu, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Genet. Med. 2013
Joon-Ho Yu, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Genet. Med. 2013
25
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.