Related references
Note: Only part of the references are listed.Rethinking counselling in prenatal screening: An ethical analysis of informed consent in the context of non-invasive prenatal testing (NIPT)
Adriana Kater-Kuipers et al.
BIOETHICS (2020)
The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study
Kelly Reumkens et al.
FAMILIAL CANCER (2019)
Direct to consumer versus clinical genetic testing
Kenneth Wysocki et al.
JOURNAL OF THE AMERICAN ASSOCIATION OF NURSE PRACTITIONERS (2019)
Predictive Psychiatric Genetic Testing in Minors: An Exploration of the Non-Medical Benefits
Arianna Manzini et al.
JOURNAL OF BIOETHICAL INQUIRY (2018)
Evaluation of the Decisional Fatigue Scale Among Surrogate Decision Makers of the Critically Ill
Ronald L. Hickman et al.
WESTERN JOURNAL OF NURSING RESEARCH (2018)
How is genetic testing evaluated? A systematic review of the literature
Erica Pitini et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2018)
Risk Perception and Psychological Distress in Genetic Counselling for Hereditary Breast and/or Ovarian Cancer
G. Cicero et al.
JOURNAL OF GENETIC COUNSELING (2017)
Toward a Broader Concept of Value: Identifying and Defining Elements for an Expanded Cost-Effectiveness Analysis
Louis P. Garrison et al.
VALUE IN HEALTH (2017)
WHAT CAN WE LEARN FROM PATIENTS' ETHICAL THINKING ABOUT THE RIGHT 'NOT TO KNOW' IN GENOMICS? LESSONS FROM CANCER GENETIC TESTING FOR GENETIC COUNSELLING
Lorraine Cowley
BIOETHICS (2016)
Pros and cons of implementing a carrier genetic test in an infertility practice
Elisa Gil-Arribas et al.
CURRENT OPINION IN OBSTETRICS & GYNECOLOGY (2016)
Is There a Right Time to Know? The Right Not to Know and Genetic Testing in Children
Pascal Borry et al.
JOURNAL OF LAW MEDICINE & ETHICS (2014)
Benefits and burdens of newborn screening: public understanding and decision-making
Stuart G. Nicholls et al.
PERSONALIZED MEDICINE (2014)
Melanoma Genetic Counseling and Test Reporting Improve Screening Adherence Among Unaffected Carriers 2 Years Later
Lisa G. Aspinwall et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2013)
Willingness-to-pay for predictive tests with no immediate treatment implications: a survey of US residents
Peter J. Neumann et al.
HEALTH ECONOMICS (2012)
Effects of genetic risk information on children's psychosocial wellbeing: A systematic review of the literature
Christopher H. Wade et al.
GENETICS IN MEDICINE (2010)
Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences
Chantal R. M. Lammens et al.
JOURNAL OF CLINICAL ONCOLOGY (2010)
Benchmarks for Cystic Fibrosis carrier screening: A European consensus document
Carlo Castellani et al.
JOURNAL OF CYSTIC FIBROSIS (2010)
Subjective interpretation of inconclusive BRCA1/2 cancer genetic test results and transmission of information to the relatives
C. Cypowyj et al.
PSYCHO-ONCOLOGY (2009)
Interactive patient decision aids for women facing genetic testing for familial breast cancer: a systematic web and literature review
Lisa Williams et al.
JOURNAL OF EVALUATION IN CLINICAL PRACTICE (2008)
Ethical issues in predictive genetic testing: a public health perspective
KG Fulda et al.
JOURNAL OF MEDICAL ETHICS (2006)