Journal of Genetic Counseling: Vol 29, No 6

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Journal of Genetic Counseling

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Journal of Genetic Counseling: Volume 29, Issue 6

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ISSUE INFORMATION

Issue Information

PROFESSIONAL ISSUES

Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force

40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice

ORIGINAL ARTICLES

Genetic counselor and proxy patient perceptions of genetic counselor responses to prenatal patient self-disclosure requests: Skillfulness is in the eye of the beholder

Alternative option labeling impacts decision-making in noninvasive prenatal screening

Genetic testing preferences and intentions in patients with clinically diagnosed familial hypercholesterolemia

A survey of U. S. state insurance commissioners concerning genetic testing and life insurance: Redux at 27

Family storytelling about hereditary cancer: Framing shared understandings of risk

Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty

Factors that impact risk management decisions among women with pathogenic variants in moderate penetrance genes associated with hereditary breast cancer

Impact of hereditary pancreatitis on patients and their families

Health knowledge of women with a fragile X premutation: Improving understanding with targeted educational material

Adult patients with undiagnosed conditions and their responses to unresolved uncertainty from exome sequencing

Ethical and professional challenges encountered by Japanese healthcare professionals who provide genetic counseling services

Evaluating a genetic counseling narrative group session for people who have tested positive for the Huntington's disease expansion: An interpretative phenomenological analysis

Social and cultural influences on genetic screening programme acceptability: A mixed-methods study of the views of adults, carriers, and family members living with thalassemia in the UK

Practices in synagogues regarding Jewish genetic disease education

Understanding genetic learning needs of people affected by rare disease

A Systematized review of experiences of individuals in Arnett’s emerging adulthood stage who live with or are at-risk for genetic conditions

Family health history collected by virtual conversational agents: An empirical study to investigate the efficacy of this approach

Psychological reactions to predictive genetic testing for Huntington’s disease: A qualitative study

Patient perspectives on the diagnostic journey to a monogenic diabetes diagnosis: Barriers and facilitators

Assessing transgender and gender non-conforming pedigree nomenclature in current genetic counselors’ practice: The case for geometric inclusivity

Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017

Perspectives from individuals with familial hypercholesterolemia on direct contact in cascade screening

Factors associated with parental knowledge of neurofibromatosis type 1 (NF1): Parental affected status and genetic counseling

Diagnostic uncertainties, ethical tensions, and accounts of role responsibilities in genetic counseling communication

The incidence and carrier frequency of Tay-Sachs disease in the French-Canadian population of Quebec based on retrospective data from 24 years, 1992–2015

Genetic testing costs and compliance with clinical best practices

Use of telephone intake for family history taking at a cancer genetics service in Asia

Feasibility, face validity, and sensitivity of a web-based simulation tool for assessing genetic counseling communication

Impacts of genesurance considerations on genetic counselors' practice and attitudes

How do geneticists and prospective parents interpret and negotiate an uncertain prenatal genetic result? An analysis of clinical interactions

Experiences and lessons learned by genetic counselors in returning secondary genetic findings to patients

Genetic counseling graduate training to address religion and spirituality in clinical practice: A qualitative exploration of programs in North America

Male–female differences in quality of life and coping style in patients with Marfan syndrome and hereditary thoracic aortic diseases

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