Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Fabsitz, Richard R.
McGuire, Amy
Sharp, Richard R.
Puggal, Mona
Beskow, Laura M.
Biesecker, Leslie G.
Bookman, Ebony
Burke, Wylie
Burchard, Esteban Gonzalez
Church, George
Clayton, Ellen Wright
Eckfeldt, John H.
Fernandez, Conrad V.
Fisher, Rebecca
Fullerton, Stephanie M.
Gabriel, Stacey
Gachupin, Francine
James, Cynthia
Jarvik, Gail P.
Kittles, Rick
Leib, Jennifer R.
O'Donnell, Christopher
O'Rourke, P. Pearl
Rodriguez, Laura Lyman
Schully, Sheri D.
Shuldiner, Alan R.
Sze, Rebecca K.F.
Thakuria, Joseph V.
Wolf, Susan M.
and
Burke, Gregory L.
2010.
Ethical and Practical Guidelines for Reporting Genetic Research Results to Study Participants.
Circulation: Cardiovascular Genetics,
Vol. 3,
Issue. 6,
p.
574.
Stein, Richard A.
2011.
Genomics and Bioethics.
p.
51.
Gray, SW
Hornik, RC
Schwartz, JS
and
Armstrong, K
2012.
The impact of risk information exposure on women's beliefs about direct‐to‐consumer genetic testing for BRCA mutations.
Clinical Genetics,
Vol. 81,
Issue. 1,
p.
29.
Caulfield, Timothy
and
McGuire, Amy L.
2012.
Direct-to-Consumer Genetic Testing: Perceptions, Problems, and Policy Responses.
Annual Review of Medicine,
Vol. 63,
Issue. 1,
p.
23.
Stein, Richard A.
2012.
Direct-to-Consumer Genetic Testing.
Journal of Information Technology Research,
Vol. 5,
Issue. 1,
p.
35.
Germino, Nicole
and
Chan, Kee
2013.
Simulation of Consumer Trends in Direct-to-Consumer (DTC) Genetic Testing.
Journal of Consumer Health On the Internet,
Vol. 17,
Issue. 3,
p.
272.
Jales, Camilla Fittipaldi
and
Borry, Pascal
2013.
Legal and Forensic Medicine.
p.
1583.
Borry, Pascal
Shabani, Mahsa
and
Howard, Heidi Carmen
2013.
Nonpropositional Content in Direct-to-Consumer Genetic Testing Advertisements.
The American Journal of Bioethics,
Vol. 13,
Issue. 5,
p.
14.
Kalokairinou, Louiza
Howard, Heidi C
and
Borry, Pascal
2014.
Encyclopedia of Life Sciences.
Haga, S.B.
Barry, W.T.
Mills, R.
Svetkey, L.
Suchindran, S.
Willard, H.F.
and
Ginsburg, G.S.
2014.
Impact of Delivery Models on Understanding Genomic Risk for Type 2 Diabetes.
Public Health Genomics,
Vol. 17,
Issue. 2,
p.
95.
Juth, Niklas
2014.
The Right Not to Know and the Duty to Tell: The Case of Relatives.
Journal of Law, Medicine & Ethics,
Vol. 42,
Issue. 1,
p.
38.
Borry, Pascal
Chokoshvili, Davit
Niemiec, Emilia
Kalokairinou, Louiza
Vears, Danya F.
and
Howard, Heidi Carmen
2015.
Movement Disorder Genetics.
p.
481.
Minor, Jessica
2015.
Informed Consent in Predictive Genetic Testing.
p.
21.
Minor, Jessica
2015.
Informed Consent in Predictive Genetic Testing.
p.
165.
Minor, Jessica
2015.
Informed Consent in Predictive Genetic Testing.
p.
1.
Minor, Jessica
2015.
Informed Consent in Predictive Genetic Testing.
p.
109.
Kalokairinou, Louiza
Borry, Pascal
and
Howard, Heidi Carmen
2017.
Regulating the advertising of genetic tests in Europe: a balancing act.
Journal of Medical Genetics,
Vol. 54,
Issue. 10,
p.
651.
Gilbert, Mark
Bonnell, Amanda
Farrell, Janine
Haag, Devon
Bondyra, Mark
Unger, David
and
Elliot, Elizabeth
2017.
Click yes to consent: Acceptability of incorporating informed consent into an internet-based testing program for sexually transmitted and blood-borne infections.
International Journal of Medical Informatics,
Vol. 105,
Issue. ,
p.
38.
Badalato, Lauren
Kalokairinou, Louiza
and
Borry, Pascal
2017.
Third party interpretation of raw genetic data: an ethical exploration.
European Journal of Human Genetics,
Vol. 25,
Issue. 11,
p.
1189.
Beckett, Emma L.
Jones, Patrice R.
Veysey, Martin
and
Lucock, Mark
2017.
Nutrigenetics—Personalized Nutrition in the Genetic Age.
Exploratory Research and Hypothesis in Medicine,
Vol. 2,
Issue. 4,
p.
1.