# Naomi Wagner
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Top podcast episodes featuring naomi wagner.
Bonus- Questions with the Editor of Journal of Genetic Counseling
We are talking about submitting and publishing manuscripts in the Journal of Genetic Counseling! J9 Austin, the Editor-in-Chief, sits down to explain the process of review, tips for submitting and editing, and answers listener questions.
In this episode we discuss:
- A bonus episode with the J…
#25- Patient Perspectives & Preferences with Risk and Uncertainty
In this episode we are talking about uncertainty and risk along with patient preferences for communication.
Segment 1: The attitudes of individuals with or at risk of adult-onset genetic conditions on reproductive genetic testing: A systematic review
Shanice Allen is a PhD student from the Sheffie…
#26-Patient Support: Results Booklet & Logotherapy
Today’s episode explores two deeply human dimensions of genetic counseling- how we support families as they process complex genomic information over time and how people make meaning in the face of uncertainty. Both segments discuss how we can support people as they make sense of genetic information…
#27- Protecting genetic information: Life insurance and GINA
In this episode we are exploring 2 recent Journal of Genetic Counseling articles on the topic of insurance coverage and concerns about genetic discrimination.
Segment 1: Cardiovascular genetic counselor decision making about discussing life insurance with patients
Guest Bios:
Sara Cherny has almo…
#28-Predictive testing in ALS: How do patients make decisions?
In this episode, we discuss the complexities of predictive genetic testing in Amyotrophic Lateral Sclerosis (ALS) from Dr. Jade Howard's recent study. Learn how it impacts decision-making and what it means for families.
Article: “Predictive genetic testing in amyotrophic lateral sclerosis (ALS)…
Community engagement in research: Intersex individual's perspectives of prenatal screening
Learn the importance of community engagement in intersex research from Louis Canavan and Bria Brown-King. Discover insights into how intersex voices shape prenatal screening conversations. It's crucial that research reflects the realities and needs of those being studied. When intersex perspectives…
#29-Cancer Genetic Testing Access: Lessons from Point-of-Care & Primary Care
In this episode of DNA Dialogues, we explore two innovative approaches to improving access to genetic testing and hereditary cancer care. First, Daniella Kamara and Mariana Niell Swiller discuss UCLA's GENETECA™ program, a point-of-care genetic testing model that integrates cancer genetic services …
#30-Reflecting Real Patient Experiences: Innovative Clinical Research Methods
In this episode, we are exploring innovative research methodologies in genetics, including narrative and visual methods, conversation analysis and body mapping. Our guests highlight using these methods to drive inclusive and diverse research as well as providing a more nuanced understanding of the …
#31-Trust & Timing: Parental Decisions About Secondary Findings
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing
Guest Bios:
Robin Hayeems is a Senior Scientist in Child Health Evaluative Sciences (CHES) at The Hospital for Sick Children (SickKids) and an Associate Professor in th…
#32- Exploring new approaches to service delivery: video tools and consumer experiences
This episode explores genetic service delivery and various ways genetic counseling can be incorporated.
Segment 1: How to Reduce Time to Genetic Testing: A Video-Based Approach in the Inherited Cardiac Conditions Service
Guest Bios
Dr Lisa Bryson is a Clinical Genetics Registrar at the Cen…
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