Stephanie C Chen, David T Wasserman. Am J Bioeth 2017
Times Cited: 26
Times Cited: 26
Times Cited
Times Co-cited
Similarity
The disability rights critique of prenatal genetic testing. Reflections and Recommendations.
E Parens, A Asch. Hastings Cent Rep 1999
E Parens, A Asch. Hastings Cent Rep 1999
23
Concerns About Justification for Fetal Genome Sequencing.
Jeffrey R Botkin, Leslie P Francis, Nancy C Rose. Am J Bioeth 2017
Jeffrey R Botkin, Leslie P Francis, Nancy C Rose. Am J Bioeth 2017
71
Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
15
Serious genetic disorders: can or should they be defined?
Dorothy C Wertz, Bartha Maria Knoppers. Am J Med Genet 2002
Dorothy C Wertz, Bartha Maria Knoppers. Am J Med Genet 2002
15
Prenatal Whole Genome Sequencing: An Argument for Professional Self-Regulation.
Benjamin E Berkman, Michelle Bayefsky. Am J Bioeth 2017
Benjamin E Berkman, Michelle Bayefsky. Am J Bioeth 2017
80
Providing Unrestricted Access to Prenatal Testing Does Not Translate to Enhanced Autonomy.
Vardit Ravitsky, Francois Rousseau, Anne-Marie Laberge. Am J Bioeth 2017
Vardit Ravitsky, Francois Rousseau, Anne-Marie Laberge. Am J Bioeth 2017
50
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
17
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall,[...]. Eur J Hum Genet 2015
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall,[...]. Eur J Hum Genet 2015
15
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
15
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
17
Generating a taxonomy for genetic conditions relevant to reproductive planning.
Diane M Korngiebel, Carmit K McMullen, Laura M Amendola, Jonathan S Berg, James V Davis, Marian J Gilmore, Cary O Harding, Patricia Himes, Gail P Jarvik, Tia L Kauffman,[...]. Am J Med Genet A 2016
Diane M Korngiebel, Carmit K McMullen, Laura M Amendola, Jonathan S Berg, James V Davis, Marian J Gilmore, Cary O Harding, Patricia Himes, Gail P Jarvik, Tia L Kauffman,[...]. Am J Med Genet A 2016
18
Beneficence In Utero: A Framework for Restricted Prenatal Whole-Genome Sequencing to Respect and Enhance the Well-Being of Children.
W Kevin Conley Ii, Douglas C McAdams, G Kevin Donovan, Kevin T FitzGerald. Am J Bioeth 2017
W Kevin Conley Ii, Douglas C McAdams, G Kevin Donovan, Kevin T FitzGerald. Am J Bioeth 2017
75
Dr. Pangloss's Clinic: Prenatal Whole Genome Sequencing and a Return to Reality.
Megan Allyse, James P Evans, Marsha Michie. Am J Bioeth 2017
Megan Allyse, James P Evans, Marsha Michie. Am J Bioeth 2017
75
Noninvasive Prenatal Whole-Genome Sequencing: A Solution in Search of a Problem.
Chris Kaposy. Am J Bioeth 2017
Chris Kaposy. Am J Bioeth 2017
75
Prenatal screening: an ethical agenda for the near future.
Antina de Jong, Guido M W R de Wert. Bioethics 2015
Antina de Jong, Guido M W R de Wert. Bioethics 2015
11
Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues.
Jean Gekas, Sylvie Langlois, Vardit Ravitsky, François Audibert, David Gradus van den Berg, Hazar Haidar, François Rousseau. Appl Clin Genet 2016
Jean Gekas, Sylvie Langlois, Vardit Ravitsky, François Audibert, David Gradus van den Berg, Hazar Haidar, François Rousseau. Appl Clin Genet 2016
16
Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
11
Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social Issues.
Mollie A Minear, Stephanie Alessi, Megan Allyse, Marsha Michie, Subhashini Chandrasekharan. Annu Rev Genomics Hum Genet 2015
Mollie A Minear, Stephanie Alessi, Megan Allyse, Marsha Michie, Subhashini Chandrasekharan. Annu Rev Genomics Hum Genet 2015
11
7
'Collective fictions': similarities in reasons for accepting maternal serum alpha-fetoprotein screening among women of diverse ethnic and social class backgrounds.
Nancy Anne Press, C H Browner. Fetal Diagn Ther 1993
Nancy Anne Press, C H Browner. Fetal Diagn Ther 1993
7
Response to Open Peer Commentaries on "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
100
Racial/ethnic disparities in obstetric outcomes and care: prevalence and determinants.
Allison S Bryant, Ayaba Worjoloh, Aaron B Caughey, A Eugene Washington. Am J Obstet Gynecol 2010
Allison S Bryant, Ayaba Worjoloh, Aaron B Caughey, A Eugene Washington. Am J Obstet Gynecol 2010
7
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.
David N Cooper, Michael Krawczak, Constantin Polychronakos, Chris Tyler-Smith, Hildegard Kehrer-Sawatzki. Hum Genet 2013
David N Cooper, Michael Krawczak, Constantin Polychronakos, Chris Tyler-Smith, Hildegard Kehrer-Sawatzki. Hum Genet 2013
7
Permissibility or Priority? Testing or Screening? Essential Distinctions in the Ethics of Prenatal Testing.
Christian Munthe. Am J Bioeth 2017
Christian Munthe. Am J Bioeth 2017
50
Breaking the Sounds of Silence: Respecting People With Disabilities and Reproductive Decision Making.
Benjamin S Wilfond. Am J Bioeth 2017
Benjamin S Wilfond. Am J Bioeth 2017
100
Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
7
Prenatal whole genome sequencing: just because we can, should we?
Greer Donley, Sara Chandros Hull, Benjamin E Berkman. Hastings Cent Rep 2012
Greer Donley, Sara Chandros Hull, Benjamin E Berkman. Hastings Cent Rep 2012
7
Cell-free fetal DNA testing: who is driving implementation?
Jessica Mozersky, Michael T Mennuti. Genet Med 2013
Jessica Mozersky, Michael T Mennuti. Genet Med 2013
16
Relationships Between Health Literacy and Genomics-Related Knowledge, Self-Efficacy, Perceived Importance, and Communication in a Medically Underserved Population.
Kimberly A Kaphingst, Melvin Blanchard, Laurel Milam, Manusheela Pokharel, Ashley Elrick, Melody S Goodman. J Health Commun 2016
Kimberly A Kaphingst, Melvin Blanchard, Laurel Milam, Manusheela Pokharel, Ashley Elrick, Melody S Goodman. J Health Commun 2016
7
7
Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
9
Known unknowns: building an ethics of uncertainty into genomic medicine.
Ainsley J Newson, Samantha J Leonard, Alison Hall, Clara L Gaff. BMC Med Genomics 2016
Ainsley J Newson, Samantha J Leonard, Alison Hall, Clara L Gaff. BMC Med Genomics 2016
7
Prenatal whole-exome sequencing: parental attitudes.
Eve J Kalynchuk, Andrew Althouse, Lisa S Parker, Devereux N Saller, Aleksandar Rajkovic. Prenat Diagn 2015
Eve J Kalynchuk, Andrew Althouse, Lisa S Parker, Devereux N Saller, Aleksandar Rajkovic. Prenat Diagn 2015
7
A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
7
Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing.
Ruth Horn, Michael Parker. Prenat Diagn 2018
Ruth Horn, Michael Parker. Prenat Diagn 2018
7
Views of American OB/GYNs on the ethics of prenatal whole-genome sequencing.
Michelle J Bayefsky, Amina White, Paul Wakim, Sara Chandros Hull, David Wasserman, Stephanie Chen, Benjamin E Berkman. Prenat Diagn 2016
Michelle J Bayefsky, Amina White, Paul Wakim, Sara Chandros Hull, David Wasserman, Stephanie Chen, Benjamin E Berkman. Prenat Diagn 2016
15
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
7
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
11
7
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
7
Non-invasive prenatal testing: ethics and policy considerations.
Meredith Vanstone, Carol King, Barbra de Vrijer, Jeff Nisker. J Obstet Gynaecol Can 2014
Meredith Vanstone, Carol King, Barbra de Vrijer, Jeff Nisker. J Obstet Gynaecol Can 2014
7
Non-invasive Prenatal Testing and the Unveiling of an Impaired Translation Process.
Blake Murdoch, Vardit Ravitsky, Ubaka Ogbogu, Sarah Ali-Khan, Gabrielle Bertier, Stanislav Birko, Tania Bubela, Jeremy De Beer, Charles Dupras, Meika Ellis,[...]. J Obstet Gynaecol Can 2017
Blake Murdoch, Vardit Ravitsky, Ubaka Ogbogu, Sarah Ali-Khan, Gabrielle Bertier, Stanislav Birko, Tania Bubela, Jeremy De Beer, Charles Dupras, Meika Ellis,[...]. J Obstet Gynaecol Can 2017
15
7
Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. J Community Genet 2014
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. J Community Genet 2014
8
Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
7
Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels.
Gabriel A Lazarin, Felicia Hawthorne, Nicholas S Collins, Elizabeth A Platt, Eric A Evans, Imran S Haque. PLoS One 2014
Gabriel A Lazarin, Felicia Hawthorne, Nicholas S Collins, Elizabeth A Platt, Eric A Evans, Imran S Haque. PLoS One 2014
7
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.