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
60
Ethical issues in consumer genome sequencing: Use of consumers' samples and data.
Emilia Niemiec, Heidi Carmen Howard. Appl Transl Genom 2016
Emilia Niemiec, Heidi Carmen Howard. Appl Transl Genom 2016
40
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
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
40
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
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
20
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
20
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
20
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
20
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
20
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
20
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
20
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
20
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
20
An old problem in a new age: Revisiting the clinical dilemma of misattributed paternity.
Laura Hercher, Leila Jamal. Appl Transl Genom 2016
Laura Hercher, Leila Jamal. Appl Transl Genom 2016
20
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
20
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
20
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
20
Disability equality and prenatal testing: contradictory or compatible?
Adrienne Asch. Fla State Univ Law Rev 2003
Adrienne Asch. Fla State Univ Law Rev 2003
20
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
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
20
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. J Clin Med 2014
Caroline Ogilvie, Ranjit Akolekar. J Clin Med 2014
25
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
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
20
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
20
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
20
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
20
Evolving applications of microarray analysis in prenatal diagnosis.
Melissa S Savage, Mirella J Mourad, Ronald J Wapner. Curr Opin Obstet Gynecol 2011
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
D I Shalowitz, F G Miller. J Med Ethics 2008
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20
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
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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. Health Econ Rev 2013
Martin Frank, Anne Prenzler, Roland Eils, J-Matthias Graf von der Schulenburg. Health Econ Rev 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
20
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
20
Contracting with private providers for primary care services: evidence from urban China.
Yan Wang, Karen Eggleston, Zhenjie Yu, Qiong Zhang. Health Econ Rev 2013
Yan Wang, Karen Eggleston, Zhenjie Yu, Qiong Zhang. Health Econ Rev 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
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
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.