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
Times Co-cited
Similarity
Informed decision making in the context of prenatal screening.
Matthijs van den Berg, Danielle R M Timmermans, Leo P ten Kate, John M G van Vugt, Gerrit van der Wal. Patient Educ Couns 2006
Matthijs van den Berg, Danielle R M Timmermans, Leo P ten Kate, John M G van Vugt, Gerrit van der Wal. Patient Educ Couns 2006
3
Are pregnant Australian women well informed about prenatal genetic screening? A systematic investigation using the Multidimensional Measure of Informed Choice.
Heather J Rowe, Jane R W Fisher, Julie A Quinlivan. Aust N Z J Obstet Gynaecol 2006
Heather J Rowe, Jane R W Fisher, Julie A Quinlivan. Aust N Z J Obstet Gynaecol 2006
3
Assessment of psychosocial outcomes in genetic counseling research: an overview of available measurement scales.
Nadine A Kasparian, Claire E Wakefield, Bettina Meiser. J Genet Couns 2007
Nadine A Kasparian, Claire E Wakefield, Bettina Meiser. J Genet Couns 2007
4
Informed decision making: an annotated bibliography and systematic review.
H Bekker, J G Thornton, C M Airey, J B Connelly, J Hewison, M B Robinson, J Lilleyman, M MacIntosh, A J Maule, S Michie,[...]. Health Technol Assess 1999
H Bekker, J G Thornton, C M Airey, J B Connelly, J Hewison, M B Robinson, J Lilleyman, M MacIntosh, A J Maule, S Michie,[...]. Health Technol Assess 1999
3
Views of genetics health professionals on the return of genomic results.
Megan E Grove, Maya N Wolpert, Mildred K Cho, Sandra Soo-Jin Lee, Kelly E Ormond. J Genet Couns 2014
Megan E Grove, Maya N Wolpert, Mildred K Cho, Sandra Soo-Jin Lee, Kelly E Ormond. J Genet Couns 2014
5
New challenges for informed consent through whole genome array testing.
C Netzer, C Klein, J Kohlhase, C Kubisch. J Med Genet 2009
C Netzer, C Klein, J Kohlhase, C Kubisch. J Med Genet 2009
6
Staged informed consent for a randomized clinical trial in childhood leukemia: impact on the consent process.
A L Angiolillo, C Simon, E Kodish, B Lange, R B Noll, K Ruccione, Y Matloub. Pediatr Blood Cancer 2004
A L Angiolillo, C Simon, E Kodish, B Lange, R B Noll, K Ruccione, Y Matloub. Pediatr Blood Cancer 2004
5
Tiered disclosure options promote the autonomy and well-being of research subjects.
Mark A Rothstein. Am J Bioeth 2006
Mark A Rothstein. Am J Bioeth 2006
5
To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
3
Incidental findings in genetics research using archived DNA.
Ellen Wright Clayton. J Law Med Ethics 2008
Ellen Wright Clayton. J Law Med Ethics 2008
4
5
Anticipate and communicate: Ethical management of incidental and secondary findings in the clinical, research, and direct-to-consumer contexts (December 2013 report of the Presidential Commission for the Study of Bioethical Issues).
Christine Weiner. Am J Epidemiol 2014
Christine Weiner. Am J Epidemiol 2014
3
Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.
Chantal R M Lammens, Neil K Aaronson, Anja Wagner, Rolf H Sijmons, Margreet G E M Ausems, Annette H J T Vriends, Mariëlle W G Ruijs, Theo A M van Os, Liesbeth Spruijt, Encarna B Gómez García,[...]. J Clin Oncol 2010
Chantal R M Lammens, Neil K Aaronson, Anja Wagner, Rolf H Sijmons, Margreet G E M Ausems, Annette H J T Vriends, Mariëlle W G Ruijs, Theo A M van Os, Liesbeth Spruijt, Encarna B Gómez García,[...]. J Clin Oncol 2010
3
Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment.
B A Bernhardt, B B Biesecker, C L Mastromarino. Am J Med Genet 2000
B A Bernhardt, B B Biesecker, C L Mastromarino. Am J Med Genet 2000
3
Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing.
Megan Allyse, Marsha Michie. Trends Biotechnol 2013
Megan Allyse, Marsha Michie. Trends Biotechnol 2013
3
Knowledge and attitudes regarding expanded genetic carrier screening among women's healthcare providers.
Kaylene Ready, Imran S Haque, Balaji S Srinivasan, John R Marshall. Fertil Steril 2012
Kaylene Ready, Imran S Haque, Balaji S Srinivasan, John R Marshall. Fertil Steril 2012
6
A universal carrier test for the long tail of Mendelian disease.
Balaji S Srinivasan, Eric A Evans, Jason Flannick, A Scott Patterson, Christopher C Chang, Tuan Pham, Sharon Young, Amit Kaushal, James Lee, Jessica L Jacobson,[...]. Reprod Biomed Online 2010
Balaji S Srinivasan, Eric A Evans, Jason Flannick, A Scott Patterson, Christopher C Chang, Tuan Pham, Sharon Young, Amit Kaushal, James Lee, Jessica L Jacobson,[...]. Reprod Biomed Online 2010
3
ACMG position statement on prenatal/preconception expanded carrier screening.
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet Med 2013
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet Med 2013
3
ACOG Committee Opinion No. 486: Update on carrier screening for cystic fibrosis.
. Obstet Gynecol 2011
. Obstet Gynecol 2011
3
Carrier testing for severe childhood recessive diseases by next-generation sequencing.
Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey,[...]. Sci Transl Med 2011
Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey,[...]. Sci Transl Med 2011
3
Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience.
Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2012
Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2012
3
Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents.
Nchangwi Syntia Munung, Patricia Marshall, Megan Campbell, Katherine Littler, Francis Masiye, Odile Ouwe-Missi-Oukem-Boyer, Janet Seeley, D J Stein, Paulina Tindana, Jantina de Vries. J Med Ethics 2016
Nchangwi Syntia Munung, Patricia Marshall, Megan Campbell, Katherine Littler, Francis Masiye, Odile Ouwe-Missi-Oukem-Boyer, Janet Seeley, D J Stein, Paulina Tindana, Jantina de Vries. J Med Ethics 2016
6
Scrutinizing the Right Not to Know.
Benjamin E Berkman, Sara Chandros Hull, Leslie G Biesecker. Am J Bioeth 2015
Benjamin E Berkman, Sara Chandros Hull, Leslie G Biesecker. Am J Bioeth 2015
50
Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Marcia Van Riper, Rebecca L Walker, Eric T Juengst. Am J Bioeth 2015
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Marcia Van Riper, Rebecca L Walker, Eric T Juengst. Am J Bioeth 2015
6
Attitudes of non-African American focus group participants toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Michael J Bamshad, Holly K Tabor. Am J Med Genet A 2014
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Michael J Bamshad, Holly K Tabor. Am J Med Genet A 2014
5
Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
3
Genetic counselors' views and experiences with the clinical integration of genome sequencing.
Kalotina Machini, Jessica Douglas, Alicia Braxton, Judith Tsipis, Kate Kramer. J Genet Couns 2014
Kalotina Machini, Jessica Douglas, Alicia Braxton, Judith Tsipis, Kate Kramer. J Genet Couns 2014
5
Informed consent for medical treatment and research: a review.
Marcela G del Carmen, Steven Joffe. Oncologist 2005
Marcela G del Carmen, Steven Joffe. Oncologist 2005
3
Practices and policies of clinical exome sequencing providers: analysis and implications.
Seema M Jamal, Joon-Ho Yu, Jessica X Chong, Karin M Dent, Jessie H Conta, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
Seema M Jamal, Joon-Ho Yu, Jessica X Chong, Karin M Dent, Jessie H Conta, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
3
Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
3
Blurring lines. The research activities of direct-to-consumer genetic testing companies raise questions about consumers as research subjects.
Heidi C Howard, Bartha Maria Knoppers, Pascal Borry. EMBO Rep 2010
Heidi C Howard, Bartha Maria Knoppers, Pascal Borry. EMBO Rep 2010
7
Informed consent in direct-to-consumer personal genome testing: the outline of a model between specific and generic consent.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Bioethics 2014
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Bioethics 2014
11
Genetic testing of embryos: practices and perspectives of US in vitro fertilization clinics.
Susannah Baruch, David Kaufman, Kathy L Hudson. Fertil Steril 2008
Susannah Baruch, David Kaufman, Kathy L Hudson. Fertil Steril 2008
3
Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
3
Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
3
Attitudes of pregnant women regarding termination of pregnancy for fetal abnormality.
A P Souka, V D Michalitsi, H Skentou, H Euripioti, G K Papadopoulos, D Kassanos, I E Messinis, E E Salamalekis. Prenat Diagn 2010
A P Souka, V D Michalitsi, H Skentou, H Euripioti, G K Papadopoulos, D Kassanos, I E Messinis, E E Salamalekis. Prenat Diagn 2010
8
Noninvasive prenatal diagnosis: pregnant women's interest and expected uptake.
Reana Tischler, Louanne Hudgins, Yair J Blumenfeld, Henry T Greely, Kelly E Ormond. Prenat Diagn 2011
Reana Tischler, Louanne Hudgins, Yair J Blumenfeld, Henry T Greely, Kelly E Ormond. Prenat Diagn 2011
3
From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.
Diana W Bianchi. Nat Med 2012
Diana W Bianchi. Nat Med 2012
3
What women want: lead considerations for current and future applications of noninvasive prenatal testing in prenatal care.
Ruth M Farrell, Patricia K Agatisa, Benjamin Nutter. Birth 2014
Ruth M Farrell, Patricia K Agatisa, Benjamin Nutter. Birth 2014
5
Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening.
Shilpa Chetty, Matthew J Garabedian, Mary E Norton. Prenat Diagn 2013
Shilpa Chetty, Matthew J Garabedian, Mary E Norton. Prenat Diagn 2013
3
A new ethical landscape of prenatal testing: individualizing choice to serve autonomy and promote public health: a radical proposal.
Christian Munthe. Bioethics 2015
Christian Munthe. Bioethics 2015
6
Noninvasive whole-genome sequencing of a human fetus.
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
3
Non-invasive prenatal measurement of the fetal genome.
H Christina Fan, Wei Gu, Jianbin Wang, Yair J Blumenfeld, Yasser Y El-Sayed, Stephen R Quake. Nature 2012
H Christina Fan, Wei Gu, Jianbin Wang, Yair J Blumenfeld, Yasser Y El-Sayed, Stephen R Quake. Nature 2012
3
Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
3
Advances in prenatal screening: the ethical dimension.
Antina de Jong, Wybo J Dondorp, Suzanna G M Frints, Christine E M de Die-Smulders, Guido M W R de Wert. Nat Rev Genet 2011
Antina de Jong, Wybo J Dondorp, Suzanna G M Frints, Christine E M de Die-Smulders, Guido M W R de Wert. Nat Rev Genet 2011
3
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.