Objective: This study aims to assess information needs and information sources and seeks to illustrate what at-risk individuals consider motivators of and barriers to information-seeking before and after genetic testing for cancer predisposition.Methods: Semi-structured interviews with people seeking genetic counseling in Switzerland were analyzed qualitatively using thematic analysis. Wilson's model of information behavior was the theoretical framework.Results: We identified four themes that illustrate motivators of and barriers to information-seeking: attitudes and emotions; knowledge; social environment; and demographic factors. We also elucidated information needs and collected participants' information sources.Conclusion: This study s ...
OBJECTIVES: Single-gene testing is associated with psycho-social challenges for cancer patients. Gen...
Next-generation sequencing (NGS) can be used to generate information about a patient's tumour and pe...
Recent advancement in genetics testing for late-onset diseases raises fundamental decision dilemmas....
Objective: This study aims to assess information needs and information sources and seeks to illustra...
Increased insight into the information needs of people about cancer genetic predisposition could all...
© 2017 Elsevier B.V. Objective: The aim of the current study was to explore barriers to genetic coun...
Health-related topics are relevant to a diverse array of people, which makes health information seek...
Little is known about the factors that motivate or deter patients from pursuing updated genetic test...
Personalized medicine is a model of healthcare that is predictive, personalized, preventive and part...
Personalized medicine is a model of healthcare that is predictive, personalized, preventive and part...
It can be challenging for individuals to make an informed and reflected decision on whether to take ...
Abstract: Personalized medicine is a model of healthcare that is predictive, personalized, preventiv...
Background Decision-making concerning predictive genetic testing for hereditary cancer syndromes is ...
Objective: To investigate BRCA-positive, unaffected patients’ – referred to as previvors – informati...
Objective. The public has a high interest in seeking personal genetic information, which holds impli...
OBJECTIVES: Single-gene testing is associated with psycho-social challenges for cancer patients. Gen...
Next-generation sequencing (NGS) can be used to generate information about a patient's tumour and pe...
Recent advancement in genetics testing for late-onset diseases raises fundamental decision dilemmas....
Objective: This study aims to assess information needs and information sources and seeks to illustra...
Increased insight into the information needs of people about cancer genetic predisposition could all...
© 2017 Elsevier B.V. Objective: The aim of the current study was to explore barriers to genetic coun...
Health-related topics are relevant to a diverse array of people, which makes health information seek...
Little is known about the factors that motivate or deter patients from pursuing updated genetic test...
Personalized medicine is a model of healthcare that is predictive, personalized, preventive and part...
Personalized medicine is a model of healthcare that is predictive, personalized, preventive and part...
It can be challenging for individuals to make an informed and reflected decision on whether to take ...
Abstract: Personalized medicine is a model of healthcare that is predictive, personalized, preventiv...
Background Decision-making concerning predictive genetic testing for hereditary cancer syndromes is ...
Objective: To investigate BRCA-positive, unaffected patients’ – referred to as previvors – informati...
Objective. The public has a high interest in seeking personal genetic information, which holds impli...
OBJECTIVES: Single-gene testing is associated with psycho-social challenges for cancer patients. Gen...
Next-generation sequencing (NGS) can be used to generate information about a patient's tumour and pe...
Recent advancement in genetics testing for late-onset diseases raises fundamental decision dilemmas....