Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur. J. Hum. Genet. 2013
Times Cited: 46
Times Cited: 46
Times Cited
Citation Count
Similarity
Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases.
Mirjam Plantinga, Erwin Birnie, Kristin M Abbott, Richard J Sinke, Anneke M Lucassen, Juliette Schuurmans, Seyma Kaplan, Marian A Verkerk, Adelita V Ranchor, Irene M van Langen. Eur. J. Hum. Genet. 2016
Mirjam Plantinga, Erwin Birnie, Kristin M Abbott, Richard J Sinke, Anneke M Lucassen, Juliette Schuurmans, Seyma Kaplan, Marian A Verkerk, Adelita V Ranchor, Irene M van Langen. Eur. J. Hum. Genet. 2016
6
Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape.
Kim C A Holtkamp, Evelien M Vos, Tessel Rigter, Phillis Lakeman, Lidewij Henneman, Martina C Cornel. BMC Health Serv Res 2017
Kim C A Holtkamp, Evelien M Vos, Tessel Rigter, Phillis Lakeman, Lidewij Henneman, Martina C Cornel. BMC Health Serv Res 2017
22
Comparison of participant information and informed consent forms of five European studies in genetic isolated populations.
Deborah Mascalzoni, A Cecile J W Janssens, Alison Stewart, Peter Pramstaller, Ulf Gyllensten, Igor Rudan, Cornelia M van Duijn, James F Wilson, Harry Campbell, Ruth M C Quillan. Eur. J. Hum. Genet. 2010
Deborah Mascalzoni, A Cecile J W Janssens, Alison Stewart, Peter Pramstaller, Ulf Gyllensten, Igor Rudan, Cornelia M van Duijn, James F Wilson, Harry Campbell, Ruth M C Quillan. Eur. J. Hum. Genet. 2010
8
Informed consent for human genetic and genomic studies: a systematic review.
A Khan, B J Capps, M Y Sum, C N Kuswanto, K Sim. Clin. Genet. 2014
A Khan, B J Capps, M Y Sum, C N Kuswanto, K Sim. Clin. Genet. 2014
10
Defining and managing incidental findings in genetic and genomic practice.
Shiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, Angela Fenwick, Anneke Lucassen. J. Med. Genet. 2014
Shiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, Angela Fenwick, Anneke Lucassen. J. Med. Genet. 2014
6
Should you profit from your genome?
Jessica L Roberts, Stacey Pereira, Amy L McGuire. Nat. Biotechnol. 2017
Jessica L Roberts, Stacey Pereira, Amy L McGuire. Nat. Biotechnol. 2017
20
Mining electronic health records: towards better research applications and clinical care.
Peter B Jensen, Lars J Jensen, Søren Brunak. Nat. Rev. Genet. 2012
Peter B Jensen, Lars J Jensen, Søren Brunak. Nat. Rev. Genet. 2012
4
From consent to institutions: designing adaptive governance for genomic biobanks.
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
Kieran C O'Doherty, Michael M Burgess, Kelly Edwards, Richard P Gallagher, Alice K Hawkins, Jane Kaye, Veronica McCaffrey, David E Winickoff. Soc Sci Med 2011
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
Open sharing of genomic data: Who does it and why?
Tobias Haeusermann, Bastian Greshake, Alessandro Blasimme, Darja Irdam, Martin Richards, Effy Vayena. PLoS ONE 2017
Tobias Haeusermann, Bastian Greshake, Alessandro Blasimme, Darja Irdam, Martin Richards, Effy Vayena. PLoS ONE 2017
8
Becoming partners, retaining autonomy: ethical considerations on the development of precision medicine.
Alessandro Blasimme, Effy Vayena. BMC Med Ethics 2016
Alessandro Blasimme, Effy Vayena. BMC Med Ethics 2016
11
Precision medicine: Beyond the inflection point.
Sam Hawgood, India G Hook-Barnard, Theresa C O'Brien, Keith R Yamamoto. Sci Transl Med 2015
Sam Hawgood, India G Hook-Barnard, Theresa C O'Brien, Keith R Yamamoto. Sci Transl Med 2015
4
Caught in the web: informed consent for online health research.
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
Effy Vayena, Anna Mastroianni, Jeffrey Kahn. Sci Transl Med 2013
9
The digital phenotype.
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat. Biotechnol. 2015
Sachin H Jain, Brian W Powers, Jared B Hawkins, John S Brownstein. Nat. Biotechnol. 2015
4
Dynamic Consent: a potential solution to some of the challenges of modern biomedical research.
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
Isabelle Budin-Ljøsne, Harriet J A Teare, Jane Kaye, Stephan Beck, Heidi Beate Bentzen, Luciana Caenazzo, Clive Collett, Flavio D'Abramo, Heike Felzmann, Teresa Finlay,[...]. BMC Med Ethics 2017
4
Digital drug safety surveillance: monitoring pharmaceutical products in twitter.
Clark C Freifeld, John S Brownstein, Christopher M Menone, Wenjie Bao, Ross Filice, Taha Kass-Hout, Nabarun Dasgupta. Drug Saf 2014
Clark C Freifeld, John S Brownstein, Christopher M Menone, Wenjie Bao, Ross Filice, Taha Kass-Hout, Nabarun Dasgupta. Drug Saf 2014
4
Ethical endgames: broad consent for narrow interests; open consent for closed minds.
Jan Reinert Karlsen, Jan Helge Solbakk, Søren Holm. Camb Q Healthc Ethics 2011
Jan Reinert Karlsen, Jan Helge Solbakk, Søren Holm. Camb Q Healthc Ethics 2011
12
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
8
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives.
Rachèl V van Schendel, G C Lieve Page-Christiaens, Lean Beulen, Catia M Bilardo, Marjon A de Boer, Audrey B C Coumans, Brigitte H Faas, Irene M van Langen, Klaske D Lichtenbelt, Merel C van Maarle,[...]. Prenat. Diagn. 2016
Rachèl V van Schendel, G C Lieve Page-Christiaens, Lean Beulen, Catia M Bilardo, Marjon A de Boer, Audrey B C Coumans, Brigitte H Faas, Irene M van Langen, Klaske D Lichtenbelt, Merel C van Maarle,[...]. Prenat. Diagn. 2016
9
Changing to NIPT as a first-tier screening test and future perspectives: opinions of health professionals.
Saskia Tamminga, Rachèl V van Schendel, Wieke Rommers, Caterina M Bilardo, Eva Pajkrt, Wybo J Dondorp, Merel van Maarle, Martina C Cornel, Lidewij Henneman. Prenat. Diagn. 2015
Saskia Tamminga, Rachèl V van Schendel, Wieke Rommers, Caterina M Bilardo, Eva Pajkrt, Wybo J Dondorp, Merel van Maarle, Martina C Cornel, Lidewij Henneman. Prenat. Diagn. 2015
13
Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet. Med. 2010
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet. Med. 2010
4
Naked bodies, naked genomes: the special (but not exceptional) nature of genomic information.
Daniel P Sulmasy. Genet. Med. 2015
Daniel P Sulmasy. Genet. Med. 2015
28
Integration of genetic and epigenetic markers for risk stratification: opportunities and challenges.
Nora Pashayan, Daniel Reisel, Martin Widschwendter. Per Med 2016
Nora Pashayan, Daniel Reisel, Martin Widschwendter. Per Med 2016
20
Linking Broad Consent to Biobank Governance: Support From a Deliberative Public Engagement in California.
Sarah B Garrett, Daniel Dohan, Barbara A Koenig. Am J Bioeth 2015
Sarah B Garrett, Daniel Dohan, Barbara A Koenig. Am J Bioeth 2015
22
Factors influencing health insurers' decisions to cover new genetic technologies.
M M Schoonmaker, B A Bernhardt, N A Holtzman. Int J Technol Assess Health Care 2000
M M Schoonmaker, B A Bernhardt, N A Holtzman. Int J Technol Assess Health Care 2000
6
Predictive genetic testing in minors for late-onset conditions: a chronological and analytical review of the ethical arguments.
Cara Mand, Lynn Gillam, Martin B Delatycki, Rony E Duncan. J Med Ethics 2012
Cara Mand, Lynn Gillam, Martin B Delatycki, Rony E Duncan. J Med Ethics 2012
3
Billing for medical genetics and genetic counseling services: a national survey.
Tabitha A Harrison, Debra Lochner Doyle, Caroline McGowan, Leslie Cohen, Elizabeth Repass, Ruthann B Pfau, Trish Brown. J Genet Couns 2010
Tabitha A Harrison, Debra Lochner Doyle, Caroline McGowan, Leslie Cohen, Elizabeth Repass, Ruthann B Pfau, Trish Brown. J Genet Couns 2010
6
Population studies: return of research results and incidental findings Policy Statement.
Bartha Maria Knoppers, Mylène Deschênes, Ma'n H Zawati, Anne Marie Tassé. Eur. J. Hum. Genet. 2013
Bartha Maria Knoppers, Mylène Deschênes, Ma'n H Zawati, Anne Marie Tassé. Eur. J. Hum. Genet. 2013
2
Barriers to genetic testing for breast cancer risk among ethnic minority women: an exploratory study.
Beth A Glenn, Neetu Chawla, Roshan Bastani. Ethn Dis 2012
Beth A Glenn, Neetu Chawla, Roshan Bastani. Ethn Dis 2012
3
A brief historical and theoretical perspective on patient autonomy and medical decision making: Part I: The beneficence model.
Jonathan F Will. Chest 2011
Jonathan F Will. Chest 2011
5
Participation in genetic testing research varies by social group.
Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
Sharon Hensley Alford, Colleen M McBride, Robert J Reid, Eric B Larson, Andreas D Baxevanis, Lawrence C Brody. Public Health Genomics 2011
2
Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing.
David J Kaufman, Juli M Bollinger, Rachel L Dvoskin, Joan A Scott. J Genet Couns 2012
David J Kaufman, Juli M Bollinger, Rachel L Dvoskin, Joan A Scott. J Genet Couns 2012
2
Attitudes toward direct-to-consumer advertisements and online genetic testing among high-risk women participating in a hereditary cancer clinic.
Giselle K Perez, Dean G Cruess, Stacy Cruess, Molly Brewer, Jennifer Stroop, Robin Schwartz, Robert Greenstein. J Health Commun 2011
Giselle K Perez, Dean G Cruess, Stacy Cruess, Molly Brewer, Jennifer Stroop, Robin Schwartz, Robert Greenstein. J Health Commun 2011
9
The general public's understanding and perception of direct-to-consumer genetic test results.
J W Leighton, K Valverde, B A Bernhardt. Public Health Genomics 2012
J W Leighton, K Valverde, B A Bernhardt. Public Health Genomics 2012
2
Direct-to-consumer testing: if consumers are not anxious, why are policymakers?
Timothy Caulfield. Hum. Genet. 2011
Timothy Caulfield. Hum. Genet. 2011
6
Association between health-service use and multiplex genetic testing.
Robert J Reid, Colleen M McBride, Sharon Hensley Alford, Cristofer Price, Andreas D Baxevanis, Lawrence C Brody, Eric B Larson. Genet. Med. 2012
Robert J Reid, Colleen M McBride, Sharon Hensley Alford, Cristofer Price, Andreas D Baxevanis, Lawrence C Brody, Eric B Larson. Genet. Med. 2012
3
Psychological consequences of predictive genetic testing: a systematic review.
M Broadstock, S Michie, T Marteau. Eur. J. Hum. Genet. 2000
M Broadstock, S Michie, T Marteau. Eur. J. Hum. Genet. 2000
2
Racial and ethnic differences in direct-to-consumer genetic tests awareness in HINTS 2007: sociodemographic and numeracy correlates.
Aisha T Langford, Ken Resnicow, J Scott Roberts, Brian J Zikmund-Fisher. J Genet Couns 2012
Aisha T Langford, Ken Resnicow, J Scott Roberts, Brian J Zikmund-Fisher. J Genet Couns 2012
4
An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons.
Amy L McGuire, Wylie Burke. JAMA 2008
Amy L McGuire, Wylie Burke. JAMA 2008
2
Psychological distress with direct-to-consumer genetic testing: a case report of an unexpected BRCA positive test result.
Lindsay Dohany, Shanna Gustafson, Whitney Ducaine, Dana Zakalik. J Genet Couns 2012
Lindsay Dohany, Shanna Gustafson, Whitney Ducaine, Dana Zakalik. J Genet Couns 2012
6
Communication about DTC testing: commentary on a 'family experience of personal genomics'.
Anna Middleton. J Genet Couns 2012
Anna Middleton. J Genet Couns 2012
16
The effect of direct-to-consumer genetic tests on anticipated affect and health-seeking behaviors: a pilot survey.
Nick Bansback, Sonia Sizto, Daphne Guh, Aslam H Anis. Genet Test Mol Biomarkers 2012
Nick Bansback, Sonia Sizto, Daphne Guh, Aslam H Anis. Genet Test Mol Biomarkers 2012
16
Direct-to-consumer genetic testing: an assessment of genetic counselors' knowledge and beliefs.
Kathryn T Hock, Kurt D Christensen, Beverly M Yashar, J Scott Roberts, Sarah E Gollust, Wendy R Uhlmann. Genet. Med. 2011
Kathryn T Hock, Kurt D Christensen, Beverly M Yashar, J Scott Roberts, Sarah E Gollust, Wendy R Uhlmann. Genet. Med. 2011
2
Perception of direct-to-consumer genetic testing and direct-to-consumer advertising of genetic tests among members of a large managed care organization.
Alanna Kulchak Rahm, Heather Spencer Feigelson, Nicole Wagner, Anh Quynh Le, Eve Halterman, Nadine Cornish, James W Dearing. J Genet Couns 2012
Alanna Kulchak Rahm, Heather Spencer Feigelson, Nicole Wagner, Anh Quynh Le, Eve Halterman, Nadine Cornish, James W Dearing. J Genet Couns 2012
6
Self diagnosis of Lynch syndrome using direct to consumer genetic testing: a case study.
Maegan E Roberts, Douglas L Riegert-Johnson, Brittany C Thomas. J Genet Couns 2011
Maegan E Roberts, Douglas L Riegert-Johnson, Brittany C Thomas. J Genet Couns 2011
7
ASHG Statement* on direct-to-consumer genetic testing in the United States.
Kathy Hudson, Gail Javitt, Wylie Burke, Peter Byers. Obstet Gynecol 2007
Kathy Hudson, Gail Javitt, Wylie Burke, Peter Byers. Obstet Gynecol 2007
2
Legislation on direct-to-consumer genetic testing in seven European countries.
Pascal Borry, Rachel E van Hellemondt, Dominique Sprumont, Camilla Fittipaldi Duarte Jales, Emmanuelle Rial-Sebbag, Tade Matthias Spranger, Liam Curren, Jane Kaye, Herman Nys, Heidi Howard. Eur. J. Hum. Genet. 2012
Pascal Borry, Rachel E van Hellemondt, Dominique Sprumont, Camilla Fittipaldi Duarte Jales, Emmanuelle Rial-Sebbag, Tade Matthias Spranger, Liam Curren, Jane Kaye, Herman Nys, Heidi Howard. Eur. J. Hum. Genet. 2012
2
Patterns of cancer genetic testing: a randomized survey of Oregon clinicians.
Summer L Cox, Amy I Zlot, Kerry Silvey, Debi Elliott, Tara Horn, Amber Johnson, Richard F Leman. 2012
Summer L Cox, Amy I Zlot, Kerry Silvey, Debi Elliott, Tara Horn, Amber Johnson, Richard F Leman. 2012
5
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.