Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 62
Times Cited: 62
Times Cited
Times Co-cited
Similarity
Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small.
Richard R Sharp. Genet Med 2011
Richard R Sharp. Genet Med 2011
5
Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine.
Janice G Edwards, Gerald Feldman, James Goldberg, Anthony R Gregg, Mary E Norton, Nancy C Rose, Adele Schneider, Katie Stoll, Ronald Wapner, Michael S Watson. Obstet Gynecol 2015
Janice G Edwards, Gerald Feldman, James Goldberg, Anthony R Gregg, Mary E Norton, Nancy C Rose, Adele Schneider, Katie Stoll, Ronald Wapner, Michael S Watson. Obstet Gynecol 2015
4
Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework.
Bernice S Elger, Arthur L Caplan. EMBO Rep 2006
Bernice S Elger, Arthur L Caplan. EMBO Rep 2006
4
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
4
Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
4
Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
6
An index of barriers for the implementation of personalised medicine and pharmacogenomics in Europe.
Denis Horgan, Marleen Jansen, Lada Leyens, Jonathan A Lal, Ralf Sudbrak, Erica Hackenitz, Ulrike Bußhoff, Wolfgang Ballensiefen, Angela Brand. Public Health Genomics 2014
Denis Horgan, Marleen Jansen, Lada Leyens, Jonathan A Lal, Ralf Sudbrak, Erica Hackenitz, Ulrike Bußhoff, Wolfgang Ballensiefen, Angela Brand. Public Health Genomics 2014
5
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
6
Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers.
Christina R Lachance, Lori A H Erby, Beth M Ford, Vincent C Allen, Kimberly A Kaphingst. Genet Med 2010
Christina R Lachance, Lori A H Erby, Beth M Ford, Vincent C Allen, Kimberly A Kaphingst. Genet Med 2010
4
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
. Genet Med 2015
. Genet Med 2015
4
Public viewpoints on new non-invasive prenatal genetic tests.
Hannah R Farrimond, Susan E Kelly. Public Underst Sci 2013
Hannah R Farrimond, Susan E Kelly. Public Underst Sci 2013
9
It's complicated: criteria for policy decisions for the clinical integration of genome-scale sequencing for reproductive decision making.
Benjamin S Wilfond, Katrina Ab Goddard. Mol Genet Genomic Med 2015
Benjamin S Wilfond, Katrina Ab Goddard. Mol Genet Genomic Med 2015
15
Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing.
Peter Benn, Audrey R Chapman, Kristine Erickson, Mark S Defrancesco, Louise Wilkins-Haug, James F X Egan, Jay Schulkin. Prenat Diagn 2014
Peter Benn, Audrey R Chapman, Kristine Erickson, Mark S Defrancesco, Louise Wilkins-Haug, James F X Egan, Jay Schulkin. Prenat Diagn 2014
5
Non-invasive prenatal testing for Down's syndrome: pregnant women's views and likely uptake.
C Lewis, C Silcock, L S Chitty. Public Health Genomics 2013
C Lewis, C Silcock, L S Chitty. Public Health Genomics 2013
4
The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users.
Antina de Jong, Wybo J Dondorp, Anja Krumeich, Julie Boonekamp, Jan M M van Lith, Guido M W R de Wert. J Community Genet 2013
Antina de Jong, Wybo J Dondorp, Anja Krumeich, Julie Boonekamp, Jan M M van Lith, Guido M W R de Wert. J Community Genet 2013
16
Informed consent in the genomics era.
Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
5
Comparison of Informed Consent Preferences for Multiplex Genetic Carrier Screening among a Diverse Population.
Ashley Reeves, Angela Trepanier. J Genet Couns 2016
Ashley Reeves, Angela Trepanier. J Genet Couns 2016
30
Models of consent to return of incidental findings in genomic research.
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
5
From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
4
Should donors be allowed to give broad consent to future biobank research?
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
Mats G Hansson, Joakim Dillner, Claus R Bartram, Joyce A Carlson, Gert Helgesson. Lancet Oncol 2006
4
DNA databanks and consent: a suggested policy option involving an authorization model.
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
Timothy Caulfield, Ross E G Upshur, Abdallah Daar. BMC Med Ethics 2003
4
Broad versus blanket consent for research with human biological samples.
David Wendler. Hastings Cent Rep 2013
David Wendler. Hastings Cent Rep 2013
15
A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and Enhancing the Autonomy of Prospective Parents.
Stephanie C Chen, David T Wasserman. Am J Bioeth 2017
Stephanie C Chen, David T Wasserman. Am J Bioeth 2017
7
The challenge of consent in clinical genome-wide testing.
Katherine Burke, Angus Clarke. Arch Dis Child 2016
Katherine Burke, Angus Clarke. Arch Dis Child 2016
18
Genetic counselling in the era of genomic medicine.
Christine Patch, Anna Middleton. Br Med Bull 2018
Christine Patch, Anna Middleton. Br Med Bull 2018
7
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019
4
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
4
Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
7
Equitable Participation in Biobanks: The Risks and Benefits of a "Dynamic Consent" Approach.
Megan Prictor, Harriet J A Teare, Jane Kaye. Front Public Health 2018
Megan Prictor, Harriet J A Teare, Jane Kaye. Front Public Health 2018
12
Informed Consent in Genome-Scale Research: What Do Prospective Participants Think?
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. AJOB Prim Res 2012
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. AJOB Prim Res 2012
5
Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
3
Patients' understanding of and responses to multiplex genetic susceptibility test results.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2012
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D Baxevanis, Lawrence C Brody. Genet Med 2012
3
Navigating a research partnership between academia and industry to assess the impact of personalized genetic testing.
Lisa Soleymani Lehmann, David J Kaufman, Richard R Sharp, Tanya A Moreno, Joanna L Mountain, J Scott Roberts, Robert C Green. Genet Med 2012
Lisa Soleymani Lehmann, David J Kaufman, Richard R Sharp, Tanya A Moreno, Joanna L Mountain, J Scott Roberts, Robert C Green. Genet Med 2012
10
Impact of direct-to-consumer genomic testing at long term follow-up.
Cinnamon S Bloss, Nathan E Wineinger, Burcu F Darst, Nicholas J Schork, Eric J Topol. J Med Genet 2013
Cinnamon S Bloss, Nathan E Wineinger, Burcu F Darst, Nicholas J Schork, Eric J Topol. J Med Genet 2013
3
Effect of direct-to-consumer genetic tests on health behaviour and anxiety: a survey of consumers and potential consumers.
Corin Egglestone, Anne Morris, Ann O'Brien. J Genet Couns 2013
Corin Egglestone, Anne Morris, Ann O'Brien. J Genet Couns 2013
5
"It's not like judgment day": public understanding of and reactions to personalized genomic risk information.
Erynn S Gordon, Georgia Griffin, Lisa Wawak, Hauchie Pang, Sarah E Gollust, Barbara A Bernhardt. J Genet Couns 2012
Erynn S Gordon, Georgia Griffin, Lisa Wawak, Hauchie Pang, Sarah E Gollust, Barbara A Bernhardt. J Genet Couns 2012
4
Impact of direct-to-consumer predictive genomic testing on risk perception and worry among patients receiving routine care in a preventive health clinic.
Katherine M James, Clayton T Cowl, Jon C Tilburt, Pamela S Sinicrope, Marguerite E Robinson, Katrin R Frimannsdottir, Kristina Tiedje, Barbara A Koenig. Mayo Clin Proc 2011
Katherine M James, Clayton T Cowl, Jon C Tilburt, Pamela S Sinicrope, Marguerite E Robinson, Katrin R Frimannsdottir, Kristina Tiedje, Barbara A Koenig. Mayo Clin Proc 2011
6
Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
3
Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1.
Irmgard Nippert, Hilary J Harris, Claire Julian-Reynier, Ulf Kristoffersson, Leo P Ten Kate, Elizabeth Anionwu, Caroline Benjamin, Kirsty Challen, Jörg Schmidtke, R Peter Nippert,[...]. J Community Genet 2011
Irmgard Nippert, Hilary J Harris, Claire Julian-Reynier, Ulf Kristoffersson, Leo P Ten Kate, Elizabeth Anionwu, Caroline Benjamin, Kirsty Challen, Jörg Schmidtke, R Peter Nippert,[...]. J Community Genet 2011
3
Informed choice in direct-to-consumer genetic testing (DTCGT) websites: a content analysis of benefits, risks, and limitations.
Amanda Singleton, Lori Hamby Erby, Kathryn V Foisie, Kimberly A Kaphingst. J Genet Couns 2012
Amanda Singleton, Lori Hamby Erby, Kathryn V Foisie, Kimberly A Kaphingst. J Genet Couns 2012
4
Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.
S E Gollust, E S Gordon, C Zayac, G Griffin, M F Christman, R E Pyeritz, L Wawak, B A Bernhardt. Public Health Genomics 2012
S E Gollust, E S Gordon, C Zayac, G Griffin, M F Christman, R E Pyeritz, L Wawak, B A Bernhardt. Public Health Genomics 2012
3
Experiences of early users of direct-to-consumer genomics in Switzerland: an exploratory study.
E Vayena, E Gourna, J Streuli, E Hafen, B Prainsack. Public Health Genomics 2012
E Vayena, E Gourna, J Streuli, E Hafen, B Prainsack. Public Health Genomics 2012
5
Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
3
Incidental findings of therapeutic misconception in biobank-based research.
Colin M E Halverson, Lainie Friedman Ross. Genet Med 2012
Colin M E Halverson, Lainie Friedman Ross. Genet Med 2012
6
The debate over research on stored biological samples: what do sources think?
Dave Wendler, Ezekiel Emanuel. Arch Intern Med 2002
Dave Wendler, Ezekiel Emanuel. Arch Intern Med 2002
3
Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project.
Leslie G Biesecker. Genet Med 2012
Leslie G Biesecker. Genet Med 2012
3
Disclosure of individual genetic data to research participants: the debate reconsidered.
Annelien L Bredenoord, Hester Y Kroes, Edwin Cuppen, Michael Parker, Johannes J M van Delden. Trends Genet 2011
Annelien L Bredenoord, Hester Y Kroes, Edwin Cuppen, Michael Parker, Johannes J M van Delden. Trends Genet 2011
3
The evolution of consent forms for research: a quarter century of changes.
Ilene Albala, Margaret Doyle, Paul S Appelbaum. IRB 2010
Ilene Albala, Margaret Doyle, Paul S Appelbaum. IRB 2010
4
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.