Emilia Niemiec, Pascal Borry, Wim Pinxten, Heidi Carmen Howard. Hum. Mutat. 2016
Times Cited: 5
Times Cited: 5
Times Cited
Times Co-cited
Similarity
Ethical issues raised by whole genome sequencing.
Wim Pinxten, Heidi Carmen Howard. Best Pract Res Clin Gastroenterol 2014
Wim Pinxten, Heidi Carmen Howard. Best Pract Res Clin Gastroenterol 2014
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Ethical issues in consumer genome sequencing: Use of consumers' samples and data.
Emilia Niemiec, Heidi Carmen Howard. 2016
Emilia Niemiec, Heidi Carmen Howard. 2016
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Informed choice in direct-to-consumer genetic testing (DTCGT) websites: a content analysis of benefits, risks, and limitations.
Amanda Singleton, Lori Hamby Erby, Kathryn V Foisie, Kimberly A Kaphingst. J Genet Couns 2012
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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
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The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues.
Stuart Hogarth, Gail Javitt, David Melzer. Annu Rev Genomics Hum Genet 2008
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Presence of fetal DNA in maternal plasma and serum.
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Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection.
Antina de Jong, Wybo J Dondorp, Merryn V E Macville, Christine E M de Die-Smulders, Jan M M van Lith, Guido M W R de Wert. Hum. Genet. 2014
Antina de Jong, Wybo J Dondorp, Merryn V E Macville, Christine E M de Die-Smulders, Jan M M van Lith, Guido M W R de Wert. Hum. Genet. 2014
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An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
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Letting the genome out of the bottle--will we get our wish?
David J Hunter, Muin J Khoury, Jeffrey M Drazen. N. Engl. J. Med. 2008
David J Hunter, Muin J Khoury, Jeffrey M Drazen. N. Engl. J. Med. 2008
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Criteria for fairly allocating scarce health-care resources to genetic tests: which matter most?
Wolf H Rogowski, Scott D Grosse, Jörg Schmidtke, Georg Marckmann. Eur. J. Hum. Genet. 2014
Wolf H Rogowski, Scott D Grosse, Jörg Schmidtke, Georg Marckmann. Eur. J. Hum. Genet. 2014
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Prenatal whole-genome sequencing--is the quest to know a fetus's future ethical?
Ilana R Yurkiewicz, Bruce R Korf, Lisa Soleymani Lehmann. N. Engl. J. Med. 2014
Ilana R Yurkiewicz, Bruce R Korf, Lisa Soleymani Lehmann. N. Engl. J. Med. 2014
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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
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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
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Public perspectives on returning genetics and genomics research results.
J O'Daniel, S B Haga. Public Health Genomics 2011
J O'Daniel, S B Haga. Public Health Genomics 2011
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The new genetics and informed consent: differentiating choice to preserve autonomy.
Eline M Bunnik, Antina de Jong, Niels Nijsingh, Guido M W R de Wert. Bioethics 2013
Eline M Bunnik, Antina de Jong, Niels Nijsingh, Guido M W R de Wert. Bioethics 2013
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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
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An old problem in a new age: Revisiting the clinical dilemma of misattributed paternity.
Laura Hercher, Leila Jamal. 2016
Laura Hercher, Leila Jamal. 2016
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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
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Managing the ethical challenges of next-generation sequencing in genomic medicine.
Angus J Clarke. Br. Med. Bull. 2014
Angus J Clarke. Br. Med. Bull. 2014
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Prenatal exome sequencing for fetuses with structural abnormalities: the next step.
S C Hillman, D Willams, K J Carss, D J McMullan, M E Hurles, M D Kilby. Ultrasound Obstet Gynecol 2015
S C Hillman, D Willams, K J Carss, D J McMullan, M E Hurles, M D Kilby. Ultrasound Obstet Gynecol 2015
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Disability equality and prenatal testing: contradictory or compatible?
Adrienne Asch. Fla State Univ Law Rev 2003
Adrienne Asch. Fla State Univ Law Rev 2003
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Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, Stephen Clayton, Jeremy F McRae, Margriet van Kogelenberg, Daniel A King, Kirsty Ambridge, Daniel M Barrett, Tanya Bayzetinova,[...]. Lancet 2015
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The routine and the traumatic in prenatal genetic diagnosis: does clinical information inform patient decision-making?
Linda M Hunt, Katherine B de Voogd, Heide Castañeda. Patient Educ Couns 2005
Linda M Hunt, Katherine B de Voogd, Heide Castañeda. Patient Educ Couns 2005
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Pregnancy Loss Following Amniocentesis or CVS Sampling-Time for a Reassessment of Risk.
Caroline Ogilvie, Ranjit Akolekar. 2014
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Noninvasive whole-genome sequencing of a human fetus.
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20
Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.
Marian Reiff, Ellen Giarelli, Barbara A Bernhardt, Ebony Easley, Nancy B Spinner, Pamela L Sankar, Surabhi Mulchandani. J Autism Dev Disord 2015
Marian Reiff, Ellen Giarelli, Barbara A Bernhardt, Ebony Easley, Nancy B Spinner, Pamela L Sankar, Surabhi Mulchandani. J Autism Dev Disord 2015
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Cell-free fetal DNA: the new tool in fetal medicine.
T R Everett, L S Chitty. Ultrasound Obstet Gynecol 2015
T R Everett, L S Chitty. Ultrasound Obstet Gynecol 2015
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Revealing the results of whole-genome sequencing and whole-exome sequencing in research and clinical investigations: some ethical issues.
Nina Hallowell, Alison Hall, Corinna Alberg, Ron Zimmern. J Med Ethics 2015
Nina Hallowell, Alison Hall, Corinna Alberg, Ron Zimmern. J Med Ethics 2015
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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
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Evolving applications of microarray analysis in prenatal diagnosis.
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Melissa S Savage, Mirella J Mourad, Ronald J Wapner. Curr. Opin. Obstet. Gynecol. 2011
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An offer you can't refuse? Ethical implications of non-invasive prenatal diagnosis.
Dagmar Schmitz, Christian Netzer, Wolfram Henn. Nat. Rev. Genet. 2009
Dagmar Schmitz, Christian Netzer, Wolfram Henn. Nat. Rev. Genet. 2009
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The search for clarity in communicating research results to study participants.
D I Shalowitz, F G Miller. J Med Ethics 2008
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The disability rights critique of prenatal genetic testing. Reflections and Recommendations.
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Genome sequencing: a systematic review of health economic evidence.
Martin Frank, Anne Prenzler, Roland Eils, J-Matthias Graf von der Schulenburg. 2013
Martin Frank, Anne Prenzler, Roland Eils, J-Matthias Graf von der Schulenburg. 2013
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Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units.
Lyn S Chitty, David Wright, Melissa Hill, Talitha I Verhoef, Rebecca Daley, Celine Lewis, Sarah Mason, Fiona McKay, Lucy Jenkins, Abigail Howarth,[...]. BMJ 2016
Lyn S Chitty, David Wright, Melissa Hill, Talitha I Verhoef, Rebecca Daley, Celine Lewis, Sarah Mason, Fiona McKay, Lucy Jenkins, Abigail Howarth,[...]. BMJ 2016
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Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time.
Jonathan S Berg, Muin J Khoury, James P Evans. Genet. Med. 2011
Jonathan S Berg, Muin J Khoury, James P Evans. Genet. Med. 2011
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Contracting with private providers for primary care services: evidence from urban China.
Yan Wang, Karen Eggleston, Zhenjie Yu, Qiong Zhang. 2013
Yan Wang, Karen Eggleston, Zhenjie Yu, Qiong Zhang. 2013
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Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am. J. Hum. Genet. 2014
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Non-invasive prenatal testing for single gene disorders: exploring the ethics.
Zuzana Deans, Melissa Hill, Lyn S Chitty, Celine Lewis. Eur. J. Hum. Genet. 2013
Zuzana Deans, Melissa Hill, Lyn S Chitty, Celine Lewis. Eur. J. Hum. Genet. 2013
20
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.