I Had Genetic Testing for Alzheimer’s Disease Without My Consent

Narrative Inquiry in Bioethics 5 (3):214-216 (2015)
  Copy   BIBTEX

Abstract

This article has no associated abstract. (fix it)

Categories

Keywords

Reprint years

DOI

10.1353/nib.2015.0071

Other Versions

No versions found

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 103,449

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

My notes

Similar books and articles

The Impact of My Genetic Testing on My Father.Anonymous One - 2015 - Narrative Inquiry in Bioethics 5 (3):224-226.
My Experience with Direct to Consumer Genetic Testing.Sarah M. Hartz - 2015 - Narrative Inquiry in Bioethics 5 (3):208-210.
Our Journey with Alzheimer's Disease: A Love Story.Scott Weikart - 2020 - Narrative Inquiry in Bioethics 10 (2):E11-E14.
Living With Alzheimer's Disease: A Shared Caregiver's Story.Catherine M. Politi - 2020 - Narrative Inquiry in Bioethics 10 (2):E8-E9.
I Don't Talk to My Wife Anymore: One Couple's Account on Dealing with Alzheimer's.Bernard 'Bernie' Binning - 2020 - Narrative Inquiry in Bioethics 10 (2):96-100.
The Dangers of Direct-to-Consumer Genetic Testing for Alzheimer’s Disease: Comment on “Personal Genomic Testing, Genetic Inheritance, and Uncertainty”.Paul Lacaze, Jane Tiller & Joanne Ryan - 2017 - Journal of Bioethical Inquiry 14 (4):585-587.
Narrative Symposium: Patient and Research Participant experiences with Genetic Testing.Dena Davis, Sarah Foye, Sarah M. Hartz, Carla C. Keirns, Christopher M. Lietz, Anneke Lucassen, Jacqueline Savard, K. A. Strong, Kiri Sunde, Michael J. Young, Anonymous One & Anonymous Two - 2015 - Narrative Inquiry in Bioethics 5 (3):203-228.
A Sister, a Father and a Son: Autism, Genetic Testing, and Impossible Decisions.Anonymous Two - 2015 - Narrative Inquiry in Bioethics 5 (3):226-228.
Losing our minds? direct-to-consumer genetic testing and Alzheimer's disease.Emily Largent - 2021 - In I. Glenn Cohen, Nita A. Farahany, Henry T. Greely & Carmel Shachar, Consumer genetic technologies: ethical and legal considerations. New York, NY: Cambridge University Press.
The question not asked: The challenge of pleiotropic genetic tests.Robert Samuel Wachbroit - 1998 - Kennedy Institute of Ethics Journal 8 (2):131-144.

Analytics

Added to PP
2016-02-04

Downloads
27 (#864,536)

6 months
4 (#864,415)

Historical graph of downloads
How can I increase my downloads?

Citations of this work

Others’ information and my privacy: an ethical discussion.Yuanye Ma - 2023 - Journal of Information, Communication and Ethics in Society 21 (3):259-270.

Add more citations

References found in this work

No references found.

Add more references