Stephanie C Chen, David T Wasserman. Am J Bioeth 2017
Times Cited: 25
Times Cited: 25
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
24
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
16
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
100
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
19
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
16
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
12
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
20
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
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
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
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
12
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
12
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
12
8
'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
8
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
8
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
8
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
8
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
8
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
18
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
8
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. 2016
Jean Gekas, Sylvie Langlois, Vardit Ravitsky, François Audibert, David Gradus van den Berg, Hazar Haidar, François Rousseau. 2016
14
8
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
10
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
8
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
8
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
8
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
8
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
16
8
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
8
8
Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. 2014
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. 2014
9
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
8
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
8
"Is It Worth Knowing?" Focus Group Participants' Perceived Utility of Genomic Preconception Carrier Screening.
Jennifer L Schneider, Katrina A B Goddard, James Davis, Benjamin Wilfond, Tia L Kauffman, Jacob A Reiss, Marian Gilmore, Patricia Himes, Frances L Lynch, Michael C Leo,[...]. J Genet Couns 2016
Jennifer L Schneider, Katrina A B Goddard, James Davis, Benjamin Wilfond, Tia L Kauffman, Jacob A Reiss, Marian Gilmore, Patricia Himes, Frances L Lynch, Michael C Leo,[...]. J Genet Couns 2016
8
Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
Michael C Leo, Carmit McMullen, Benjamin S Wilfond, Frances L Lynch, Jacob A Reiss, Marian J Gilmore, Patricia Himes, Tia L Kauffman, James V Davis, Gail P Jarvik,[...]. Am. J. Med. Genet. A 2016
Michael C Leo, Carmit McMullen, Benjamin S Wilfond, Frances L Lynch, Jacob A Reiss, Marian J Gilmore, Patricia Himes, Tia L Kauffman, James V Davis, Gail P Jarvik,[...]. Am. J. Med. Genet. A 2016
13
Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet. Med. 2016
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet. Med. 2016
8
Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial.
Ronald J Wapner, Deborah A Driscoll, Joe Leigh Simpson. Prenat. Diagn. 2012
Ronald J Wapner, Deborah A Driscoll, Joe Leigh Simpson. Prenat. Diagn. 2012
8
Risks, values, and decision making surrounding pregnancy.
Anne Drapkin Lyerly, Lisa M Mitchell, Elizabeth M Armstrong, Lisa H Harris, Rebecca Kukla, Miriam Kuppermann, Margaret Olivia Little. Obstet Gynecol 2007
Anne Drapkin Lyerly, Lisa M Mitchell, Elizabeth M Armstrong, Lisa H Harris, Rebecca Kukla, Miriam Kuppermann, Margaret Olivia Little. Obstet Gynecol 2007
8
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.