Jessica Mozersky, Pamela Sankar. Am J Bioeth 2017
Times Cited: 2
Times Cited: 2
Times Cited
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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
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
100
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
100
100
Noninvasive Prenatal Whole-Genome Sequencing: A Solution in Search of a Problem.
Chris Kaposy. Am J Bioeth 2017
Chris Kaposy. Am J Bioeth 2017
100
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
100
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
50
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
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
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
50
Defining and redefining the scope and goals of genetic counseling.
Robert G Resta. Am J Med Genet C Semin Med Genet 2006
Robert G Resta. Am J Med Genet C Semin Med Genet 2006
50
Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease.
Yvonne Bombard, JoAnne Palin, Jan M Friedman, Gerry Veenstra, Susan Creighton, Joan L Bottorff, Michael R Hayden. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2012
Yvonne Bombard, JoAnne Palin, Jan M Friedman, Gerry Veenstra, Susan Creighton, Joan L Bottorff, Michael R Hayden. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2012
50
Naming of syndromes and unethical activities: the case of Hallervorden and Spatz.
P S Harper. Lancet 1996
P S Harper. Lancet 1996
50
'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care.
Angus J Clarke, David N Cooper, Michael Krawczak, Chris Tyler-Smith, Helen M Wallace, Andrew O M Wilkie, Frances Lucy Raymond, Ruth Chadwick, Nick Craddock, Ros John,[...]. Hum. Genomics 2012
Angus J Clarke, David N Cooper, Michael Krawczak, Chris Tyler-Smith, Helen M Wallace, Andrew O M Wilkie, Frances Lucy Raymond, Ruth Chadwick, Nick Craddock, Ros John,[...]. Hum. Genomics 2012
50
50
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
Anita Villani, Uri Tabori, Joshua Schiffman, Adam Shlien, Joseph Beyene, Harriet Druker, Ana Novokmet, Jonathan Finlay, David Malkin. Lancet Oncol. 2011
Anita Villani, Uri Tabori, Joshua Schiffman, Adam Shlien, Joseph Beyene, Harriet Druker, Ana Novokmet, Jonathan Finlay, David Malkin. Lancet Oncol. 2011
50
The expansion of newborn screening: is reproductive benefit an appropriate pursuit?
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, Denise Avard, Bartha M Knoppers, Martina C Cornel, Pascal Borry. Nat. Rev. Genet. 2009
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, Denise Avard, Bartha M Knoppers, Martina C Cornel, Pascal Borry. Nat. Rev. Genet. 2009
50
The Genetic Counseling Outcome Scale: a new patient-reported outcome measure for clinical genetics services.
M McAllister, A M Wood, G Dunn, S Shiloh, C Todd. Clin. Genet. 2011
M McAllister, A M Wood, G Dunn, S Shiloh, C Todd. Clin. Genet. 2011
50
"Testing times, challenging choices": an Australian study of prenatal genetic counseling.
Jan M Hodgson, Lynn H Gillam, Margaret A Sahhar, Sylvia A Metcalfe. J Genet Couns 2010
Jan M Hodgson, Lynn H Gillam, Margaret A Sahhar, Sylvia A Metcalfe. J Genet Couns 2010
50
"It was the missing piece": adolescent experiences of predictive genetic testing for adult-onset conditions.
Cara Mand, Lynn Gillam, Rony E Duncan, Martin B Delatycki. Genet. Med. 2013
Cara Mand, Lynn Gillam, Rony E Duncan, Martin B Delatycki. Genet. Med. 2013
50
'I don't see any point in telling them': attitudes to sharing genetic information in the family and carrier testing of relatives among British Pakistani adults referred to a genetics clinic.
Alison Shaw, Jane A Hurst. Ethn Health 2009
Alison Shaw, Jane A Hurst. Ethn Health 2009
50
Feminist discourse on sex screening and selective abortion of female foetuses.
Farhat Moazam. Bioethics 2004
Farhat Moazam. Bioethics 2004
50
Parental procreative obligation and the categorisation of disease: the case of cystic fibrosis.
Gabriel T Bosslet. J Med Ethics 2011
Gabriel T Bosslet. J Med Ethics 2011
50
Barriers to carrier testing for adult cystic fibrosis sibs: the importance of not knowing.
J H Fanos, J P Johnson. Am. J. Med. Genet. 1995
J H Fanos, J P Johnson. Am. J. Med. Genet. 1995
50
Professional ambivalence: accounts of ethical practice in childhood genetic testing.
Michael Arribas-Ayllon, Srikant Sarangi, Angus Clarke. J Genet Couns 2009
Michael Arribas-Ayllon, Srikant Sarangi, Angus Clarke. J Genet Couns 2009
50
Variations in male-female infant ratios among births to Canadian- and Indian-born mothers, 1990-2011: a population-based register study.
Marcelo L Urquia, Joel G Ray, Susitha Wanigaratne, Rahim Moineddin, Patricia J O'Campo. 2016
Marcelo L Urquia, Joel G Ray, Susitha Wanigaratne, Rahim Moineddin, Patricia J O'Campo. 2016
50
Relational autonomy or undue pressure? Family's role in medical decision-making.
Anita Ho. Scand J Caring Sci 2008
Anita Ho. Scand J Caring Sci 2008
50
Clinician integrity and limits to patient autonomy.
John Lantos, Ann Marie Matlock, David Wendler. JAMA 2011
John Lantos, Ann Marie Matlock, David Wendler. JAMA 2011
50
Individual and family coping with polycystic kidney disease: the harvest of denial.
D M Manjoney, F P McKegney. Int J Psychiatry Med 1978
D M Manjoney, F P McKegney. Int J Psychiatry Med 1978
50
Knowledge is power? The role of experiential knowledge in genetically 'risky' reproductive decisions.
Felicity K Boardman. Sociol Health Illn 2014
Felicity K Boardman. Sociol Health Illn 2014
50
The moral obligation to create children with the best chance of the best life.
Julian Savulescu, Guy Kahane. Bioethics 2009
Julian Savulescu, Guy Kahane. Bioethics 2009
50
Accounts of consent: Orienting to self-other relations regarding motivations to participate in cancer bio-banking.
Hannah Shipman, Angus J Clarke, Srikant Sarang. Commun Med 2014
Hannah Shipman, Angus J Clarke, Srikant Sarang. Commun Med 2014
50
Do parental perceptions and motivations towards genetic testing and prenatal diagnosis for deafness vary in different cultures?
Risha Nahar, Ratna D Puri, Renu Saxena, Ishwar C Verma. Am. J. Med. Genet. A 2013
Risha Nahar, Ratna D Puri, Renu Saxena, Ishwar C Verma. Am. J. Med. Genet. A 2013
50
50
Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat. Rev. Genet. 2015
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat. Rev. Genet. 2015
50
Problems assessing uptake of Huntington disease predictive testing and a proposed solution.
Roslyn J Tassicker, Betty Teltscher, M Kaye Trembath, Veronica Collins, Leslie J Sheffield, Edmond Chiu, Lyle Gurrin, Martin B Delatycki. Eur. J. Hum. Genet. 2009
Roslyn J Tassicker, Betty Teltscher, M Kaye Trembath, Veronica Collins, Leslie J Sheffield, Edmond Chiu, Lyle Gurrin, Martin B Delatycki. Eur. J. Hum. Genet. 2009
50
Parental virtue: a new way of thinking about the morality of reproductive actions.
Rosalind McDougall. Bioethics 2007
Rosalind McDougall. Bioethics 2007
50
Perceptions of reproductive risk and carrier testing among adolescent sisters of males with chronic granulomatous disease.
Cynthia A James, Neil A Holtzman, Donald W Hadley. Am J Med Genet C Semin Med Genet 2003
Cynthia A James, Neil A Holtzman, Donald W Hadley. Am J Med Genet C Semin Med Genet 2003
50
Negotiations, superstitions, and the plight of individuals born with severe birth defects.
R H Kenen. Soc Sci Med Med Psychol Med Sociol 1980
R H Kenen. Soc Sci Med Med Psychol Med Sociol 1980
50
An informatics approach to analyzing the incidentalome.
Jonathan S Berg, Michael Adams, Nassib Nassar, Chris Bizon, Kristy Lee, Charles P Schmitt, Kirk C Wilhelmsen, James P Evans. Genet. Med. 2013
Jonathan S Berg, Michael Adams, Nassib Nassar, Chris Bizon, Kristy Lee, Charles P Schmitt, Kirk C Wilhelmsen, James P Evans. Genet. Med. 2013
50
The behavioral response to personalized genetic information: will genetic risk profiles motivate individuals and families to choose more healthful behaviors?
Colleen M McBride, Laura M Koehly, Saskia C Sanderson, Kimberly A Kaphingst. Annu Rev Public Health 2010
Colleen M McBride, Laura M Koehly, Saskia C Sanderson, Kimberly A Kaphingst. Annu Rev Public Health 2010
50
Currents in contemporary ethics. State run newborn screening in the genomic era, or how to avoid drowning when drinking from a fire hose.
Ellen Wright Clayton. J Law Med Ethics 2010
Ellen Wright Clayton. J Law Med Ethics 2010
50
Living with a child at risk for psychotic illness: the experience of parents coping with 22q11 deletion syndrome: an exploratory study.
Laura Hercher, Georgette Bruenner. Am. J. Med. Genet. A 2008
Laura Hercher, Georgette Bruenner. Am. J. Med. Genet. A 2008
50
Negotiating responsibility: case studies of reproductive decision-making and prenatal genetic testing in families facing Huntington disease.
Claudia Downing. J Genet Couns 2005
Claudia Downing. J Genet Couns 2005
50
Communicating moral reasoning in medicine as an expression of respect for patients and integrity among professionals.
Lauris Christopher Kaldjian. Commun Med 2013
Lauris Christopher Kaldjian. Commun Med 2013
100
Family communication matters: the impact of telling relatives about unclassified variants and uninformative DNA-test results.
Joël Vos, Anna M Jansen, Fred Menko, Christi J van Asperen, Anne M Stiggelbout, Aad Tibben. Genet. Med. 2011
Joël Vos, Anna M Jansen, Fred Menko, Christi J van Asperen, Anne M Stiggelbout, Aad Tibben. Genet. Med. 2011
50
Is nondirectiveness possible within the context of antenatal screening and testing?
Clare Williams, Priscilla Alderson, Bobbie Farsides. Soc Sci Med 2002
Clare Williams, Priscilla Alderson, Bobbie Farsides. Soc Sci Med 2002
50
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.