Emilia Niemiec, Pascal Borry, Wim Pinxten, Heidi Carmen Howard. Hum Mutat 2016
Times Cited: 9
Times Cited: 9
Times Cited
Times Co-cited
Similarity
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
33
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
33
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
33
All your data (effectively) belong to us: data practices among direct-to-consumer genetic testing firms.
Linnea I Laestadius, Jennifer R Rich, Paul L Auer. Genet Med 2017
Linnea I Laestadius, Jennifer R Rich, Paul L Auer. Genet Med 2017
33
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
33
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
22
Should you profit from your genome?
Jessica L Roberts, Stacey Pereira, Amy L McGuire. Nat Biotechnol 2017
Jessica L Roberts, Stacey Pereira, Amy L McGuire. Nat Biotechnol 2017
22
Direct-to-Consumer Genetic Testing and Personal Genomics Services: A Review of Recent Empirical Studies.
J Scott Roberts, Jenny Ostergren. Curr Genet Med Rep 2013
J Scott Roberts, Jenny Ostergren. Curr Genet Med Rep 2013
22
Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature.
Lesley Goldsmith, Leigh Jackson, Anita O'Connor, Heather Skirton. J Community Genet 2013
Lesley Goldsmith, Leigh Jackson, Anita O'Connor, Heather Skirton. J Community Genet 2013
22
Legislation on direct-to-consumer genetic testing in seven European countries.
Pascal Borry, Rachel E van Hellemondt, Dominique Sprumont, Camilla Fittipaldi Duarte Jales, Emmanuelle Rial-Sebbag, Tade Matthias Spranger, Liam Curren, Jane Kaye, Herman Nys, Heidi Howard. Eur J Hum Genet 2012
Pascal Borry, Rachel E van Hellemondt, Dominique Sprumont, Camilla Fittipaldi Duarte Jales, Emmanuelle Rial-Sebbag, Tade Matthias Spranger, Liam Curren, Jane Kaye, Herman Nys, Heidi Howard. Eur J Hum Genet 2012
22
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
22
Is there a doctor in the house? : The presence of physicians in the direct-to-consumer genetic testing context.
Heidi Carmen Howard, Pascal Borry. J Community Genet 2012
Heidi Carmen Howard, Pascal Borry. J Community Genet 2012
22
Direct-to-consumer genetic testing: perceptions, problems, and policy responses.
Timothy Caulfield, Amy L McGuire. Annu Rev Med 2012
Timothy Caulfield, Amy L McGuire. Annu Rev Med 2012
22
Who Knows What, and When?: A Survey of the Privacy Policies Proffered by U.S. Direct-to-Consumer Genetic Testing Companies.
James W Hazel, Christopher Slobogin. Cornell J Law Public Policy 2018
James W Hazel, Christopher Slobogin. Cornell J Law Public Policy 2018
22
Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review.
Loredana Covolo, Sara Rubinelli, Elisabetta Ceretti, Umberto Gelatti. J Med Internet Res 2015
Loredana Covolo, Sara Rubinelli, Elisabetta Ceretti, Umberto Gelatti. J Med Internet Res 2015
22
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
22
Influence of individual differences in disease perception on consumer response to direct-to-consumer genomic testing.
D L Boeldt, N J Schork, E J Topol, C S Bloss. Clin Genet 2015
D L Boeldt, N J Schork, E J Topol, C S Bloss. Clin Genet 2015
22
Presence of fetal DNA in maternal plasma and serum.
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
11
11
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
11
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
11
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
11
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
11
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
11
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
11
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
11
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
11
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
11
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
11
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
11
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
11
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
11
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
11
Disability equality and prenatal testing: contradictory or compatible?
Adrienne Asch. Fla State Univ Law Rev 2003
Adrienne Asch. Fla State Univ Law Rev 2003
11
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
11
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
11
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
20
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
11
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
11
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
11
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
11
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.