Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 52
Times Cited: 52
Times Cited
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Similarity
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
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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
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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
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ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
. Genet Med 2015
. Genet Med 2015
5
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
10
Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
5
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
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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
5
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
33
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
5
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
5
Broad versus blanket consent for research with human biological samples.
David Wendler. Hastings Cent Rep 2013
David Wendler. Hastings Cent Rep 2013
18
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
10
Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach.
Gabrielle Natalie Samuel, Sandi Dheensa, Bobbie Farsides, Angela Fenwick, Anneke Lucassen. BMC Med Ethics 2017
Gabrielle Natalie Samuel, Sandi Dheensa, Bobbie Farsides, Angela Fenwick, Anneke Lucassen. BMC Med Ethics 2017
13
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
20
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
6
"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
5
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
Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).
Ebony B Bookman, Corina Din-Lovinescu, Bradford B Worrall, Teri A Manolio, Siiri N Bennett, Cathy Laurie, Daniel B Mirel, Kimberly F Doheny, Garnet L Anderson, Kate Wehr,[...]. Genome Med 2013
Ebony B Bookman, Corina Din-Lovinescu, Bradford B Worrall, Teri A Manolio, Siiri N Bennett, Cathy Laurie, Daniel B Mirel, Kimberly F Doheny, Garnet L Anderson, Kate Wehr,[...]. Genome Med 2013
20
Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
3
"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
3
Assessment of the content and process of genetic counseling: a critical review of empirical studies.
Bettina Meiser, Jennifer Irle, Elizabeth Lobb, Kristine Barlow-Stewart. J Genet Couns 2008
Bettina Meiser, Jennifer Irle, Elizabeth Lobb, Kristine Barlow-Stewart. J Genet Couns 2008
3
What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
3
Computerized prenatal genetic testing decision-assisting tool: a randomized controlled trial.
Miriam Kuppermann, Mary E Norton, Elena Gates, Steven E Gregorich, Lee A Learman, Sanae Nakagawa, Vickie A Feldstein, James Lewis, A Eugene Washington, Robert F Nease. Obstet Gynecol 2009
Miriam Kuppermann, Mary E Norton, Elena Gates, Steven E Gregorich, Lee A Learman, Sanae Nakagawa, Vickie A Feldstein, James Lewis, A Eugene Washington, Robert F Nease. Obstet Gynecol 2009
3
The multi-dimensional measure of informed choice: a validation study.
Susan Michie, Elizabeth Dormandy, Theresa M Marteau. Patient Educ Couns 2002
Susan Michie, Elizabeth Dormandy, Theresa M Marteau. Patient Educ Couns 2002
3
Knowledge of prenatal screening and psychological management of test decisions.
K Dahl, L Hvidman, F S Jørgensen, U S Kesmodel. Ultrasound Obstet Gynecol 2011
K Dahl, L Hvidman, F S Jørgensen, U S Kesmodel. Ultrasound Obstet Gynecol 2011
5
Development of a measure of informed choice suitable for use in low literacy populations.
Elizabeth Dormandy, Elaine Y L Tsui, Theresa M Marteau. Patient Educ Couns 2007
Elizabeth Dormandy, Elaine Y L Tsui, Theresa M Marteau. Patient Educ Couns 2007
7
Risk and uncertainty: shifting decision making for aneuploidy screening to the first trimester of pregnancy.
Ruth M Farrell, Natasha Dolgin, Susan A Flocke, Victoria Winbush, Mary Beth Mercer, Christian Simon. Genet Med 2011
Ruth M Farrell, Natasha Dolgin, Susan A Flocke, Victoria Winbush, Mary Beth Mercer, Christian Simon. Genet Med 2011
10
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.