Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Ginsberg, Marc
2014.
Informed Consent and the Differential Diagnosis: How the Law Overestimates Patient Autonomy and Compromises Health Care.
SSRN Electronic Journal,
Lázaro-Muñoz, Gabriel
Conley, John M.
Davis, Arlene M.
Van Riper, Marcia
Walker, Rebecca L.
and
Juengst, Eric T.
2015.
Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.
The American Journal of Bioethics,
Vol. 15,
Issue. 7,
p.
3.
Boers, Sarah N.
van Delden, Johannes J.M.
Knoers, Nine V.
and
Bredenoord, Annelien L.
2015.
Postmortem disclosure of genetic information to family members: active or passive?.
Trends in Molecular Medicine,
Vol. 21,
Issue. 3,
p.
148.
Cutas, Daniela
and
Hens, Kristien
2015.
Preserving children’s fertility: two tales about children’s right to an open future and the margins of parental obligations.
Medicine, Health Care and Philosophy,
Vol. 18,
Issue. 2,
p.
253.
Pont‐Sunyer, Claustre
Bressman, Susan
Raymond, Deborah
Glickman, Amanda
Tolosa, Eduardo
and
Saunders‐Pullman, Rachel
2015.
Disclosure of research results in genetic studies of Parkinson's disease caused byLRRK2mutations.
Movement Disorders,
Vol. 30,
Issue. 7,
p.
904.
Bullock, Emma C.
2016.
Mandatory Disclosure and Medical Paternalism.
Ethical Theory and Moral Practice,
Vol. 19,
Issue. 2,
p.
409.
Youngs, Jonathan
and
Simmonds, Joshua
2016.
HIV and the right not to know.
Journal of Medical Ethics,
Vol. 42,
Issue. 2,
p.
95.
Long, Christopher R
Stewart, M Kathryn
Cunningham, Thomas V
Warmack, T Scott
and
McElfish, Pearl A
2016.
Health research participants’ preferences for receiving research results.
Clinical Trials,
Vol. 13,
Issue. 6,
p.
582.
Ost, Suzanne
2016.
A new paradigm of reparation for victims of child pornography.
Legal Studies,
Vol. 36,
Issue. 4,
p.
613.
Long, Christopher R.
Stewart, M. Kathryn
and
McElfish, Pearl A.
2017.
Health research participants are not receiving research results: a collaborative solution is needed.
Trials,
Vol. 18,
Issue. 1,
Stevens, Yvonne A
Senner, Grant D
and
Marchant, Gary E
2017.
Physicians’ Duty to Recontact and Update Genetic Advice.
Personalized Medicine,
Vol. 14,
Issue. 4,
p.
367.
Buchbinder, Mara
2017.
Aid-in-dying laws and the physician's duty to inform.
Journal of Medical Ethics,
Vol. 43,
Issue. 10,
p.
666.
Ienca, Marcello
Wangmo, Tenzin
Jotterand, Fabrice
Kressig, Reto W.
and
Elger, Bernice
2018.
Ethical Design of Intelligent Assistive Technologies for Dementia: A Descriptive Review.
Science and Engineering Ethics,
Vol. 24,
Issue. 4,
p.
1035.
Darling, Katherine Weatherford
2018.
Solidarity in biomedicine and beyond.
New Genetics and Society,
Vol. 37,
Issue. 4,
p.
439.
Morrissey, Clair
and
Walker, Rebecca L
2018.
The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice.
The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine,
Vol. 43,
Issue. 1,
p.
22.
Prainsack, Barbara
2018.
The “We” in the “Me”.
Science, Technology, & Human Values,
Vol. 43,
Issue. 1,
p.
21.
Dove, Edward S
Chico, Vicky
Fay, Michael
Laurie, Graeme
Lucassen, Anneke M
and
Postan, Emily
2019.
Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?.
Journal of Medical Ethics,
Vol. 45,
Issue. 8,
p.
504.
Ost, Suzanne
and
Gillespie, Alisdair A
2019.
To know or not to know: Should crimes regarding photographs of their child sexual abuse be disclosed to now-adult, unknowing victims?.
International Review of Victimology,
Vol. 25,
Issue. 2,
p.
223.
Palm
,
Willy
Nys
,
Herman
Townend
,
David
Shaw
,
David
Clemens
,
Timo
and
Brand
,
Helmut
2020.
Achieving Person-Centred Health Systems.
p.
347.
Frith, Lucy
2020.
Contacting gamete donors to facilitate diagnostic genetic testing for the donor-conceived child: what are the rights and obligations of gamete donors in these cases? A response to Hortonet al.
Journal of Medical Ethics,
Vol. 46,
Issue. 3,
p.
220.