DNA Dialogues: Conversations in Genetic Counseling Research
DNA Dialogues is a podcast that explores genetic counseling research by featuring conversations with authors of articles published in the Journal of Genetic Counseling. Each episode examines recent discoveries, ethical debates, and technological developments in medical genetics. The show also covers topics like complex testing decisions and building trust with diverse communities, emphasizing the human side of genetic counseling. It aims to make genetic research accessible through engaging discussions.
Episodes
#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 lived experiences of families.
Segment 1: Defining joy after a genetic diagnosis: A narrative inqu
#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 directly into oncology clinics. In the second half of the episode, Tesla Theoryn discusses research e
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 are included, the findings are not only richer but also more relevant to the community.
Featured A
#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): Experiences of decision-making and engagement with UK genetic counseling services”
In this episode
#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 almost 20 years of experience as a genetic counselor in the Chicagoland area, specializing in cardiovascula
#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 in their lives.
Segment 1: Putting control into parents' hands: Parent experiences with a genomic
#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 Sheffield Institute for Translational Neuroscience (SITraN) at the University of Sheffield. The aim of her re
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 Journal of Genetic Counseling editor-in-chief on why and how to publish research.
- How to choose a journ
#24-Clinical genetic services: Provider retention & telegenetics
Today’s episode is about clinical genetic services. In the first segment, Khalida talks to authors Courtney and Jade about retention of patient-facing genetic counselors and how generational age and work environment influence retention. For the second segment, Khalida chats with Dr. Ba-Jaj about telegenetics in India, reviewing data from 3 years and almost 1000 cases!
Segment 1: Factors influe
#23- Building Systems for Genetic Care: PRS Implementation and EDS Triage
Today we are featuring two articles that relate to moving genetics into mainstream healthcare. In our first segment, we discuss polygenic risk scores and the transition from research to clinical use. Our second segment focuses on hypermobility Ehlers Danlos Syndrome and the triaging of clinical referrals.
Segment 1: Readiness and leadership for the implementation of polygenic risk scores: Genet
#22-Genetic Counselor Appreciation: Professional Identity & Well Being
Earlier this month, we celebrated Genetic Counselor Appreciation Day on November 13! In recognition of this, we are featuring 2 articles that explore professional issues in the field of genetic counseling. In our first segment, we talk to Dr. Rachel Mills about the professional identity of early-career genetic counselors and in the second segment, we speak to Dr. Laura Yeates about self care strat
#21- From Specialty Clinics to Family Medicine: Rethinking Access to Genetics
The case for integrating genetic counselors into primary care:A paradigm shift for our profession
Natasha Berman (she/her) MA, MS, MPH, CGC is a clinical genetic counselor at the UPMC Department of Family Medicine who works within the primary care precision medicine clinic. She provides direct patient care to patients for a variety of indications. She has coauthored multiple textbook chapters co
#20- Revisiting Research: Implementation Science & Retrospective Chart Review
In this episode, we talk with two authors who have papers featured in the special issue of the Journal of Genetic Counseling on Research Methods in Genetic Counseling. In the first segment we explore implementation science and its utilization in bridging the gap between research and clinical practice. In our second segment, we talk to an author about retrospective chart reviews and the benefits an
#19-Shifting Paradigms: APOE in Dyslipidemia & Patient Voices in Neurogenetics
We are discussing perspective changes in neurology genetics with the crossover of the APOE gene in neuro and cardio as well as telehealth for neurology predictive testing.
Segment 1: Is it time for a paradigm shift? Inclusion of APOE on genetic dyslipidemia panels.
Emily Brown is a certified genetic counselor at the Center for Inherited Heart Disease at Johns Hopkins Hospital. She graduated fro
#18-Stats, Stories, and Science: Rethinking Research in Genetic Counseling
In this episode, we talk to two genetic counselors about their recent publications in a special edition of the Journal of Genetic Counseling focused on research methods in genetic counseling. First, Benjamin Helm delves into statistical approaches and discusses how transparency and honesty in research can lead to more meaningful scientific contributions. Then Kennedy Borle explores the challenges
#17-Patient Understanding of Sex and Gender in cell-free DNA Screening
In this episode, we explore the motivations, findings, and clinical implications of a recent study examining patient understanding of the terms “sex” and “gender” in the context of prenatal testing, particularly non-invasive prenatal testing (NIPT).
“Patient understanding of fetal sex versus gender in the context of routine cell-free DNA screening”
Mindy Kolodziejski (she/her) is a Senior Gen
#16-Cancer Care: Surgical Genetic Testing & Pancreatic Cancer Screening
In this episode we are exploring two publications related to cancer care. In our first segment we talk to 2 authors about their research on genetic counselors and identification of patients for high-risk pancreatic cancer screening. In our second segment, Khalida interviews a genetic counselor about their study to evaluate surgical patient perspectives of genetic testing provided by a non-genetics
#15-DNA Day: Unexpected DTC Results & Gender Diverse Care
In this episode we feature 2 articles that explore hot topics in genetics as well as opportunities to improve patient care in honor of DNA Day on April 25. DNA day commemorates the completion of the Human Genome Project and the discovery of DNA’s double helix. Both of these studies utilize qualitative methodologies to highlight people’s experiences and share their stories.
Segment 1: Not Parent Ex
#14- Cardio & Genetics: Exploring Revenue & Best Practices
In this episode, we are discussing 2 articles focused on cardiovascular genetics. In the first segment, Khalida talks to authors Marianne and Erin about their research exploring the opportunities for downstream revenue of cardiac genetic counseling services in a pediatric medical center. In the second segment, Naomi chats with Jodie and Erin about the recent NSGC Practice Resource about genetic te
#13- Rare Disease Day 2025: Digital Tools for Rare Conditions & Navigating Ultra-rare Disorders
In this episode we are exploring rare and ultra-rare disease in honor of Rare Disease Day on February 28 which raises awareness for the 300 million people worldwide living with a rare disease. We are talking with one author about their study on the role of digital tools in rare disease management and another author about their research into experiences of parents who have a child with an emerging-
#12-Genetic Testing in the General Population: Communication and Understanding
On This Episode We Discuss:
In this episode we explore genetic testing in low risk populations, both in direct-to-consumer and clinical settings. We interview authors on two recent JoGC papers related to topics of communication of health risks, understanding of genetic testing, and informed decision-making. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via t
DNA Today: Genetics Wrapped 2024: Top Advances in Genomic Medicine
We’re thrilled to share a special episode drop from one of our producers, Kira Dineen, and her flagship podcast, DNA Today! As a multi award winning genetics podcast with over 12 years of groundbreaking episodes, DNA Today explores the latest in genetics and genomics through expert interviews and engaging discussions.
To celebrate the new year, this episode reflects back on the top genetics and
#11-Dystrophinopathies: A Practice Resource from the National Society of Genetic Counselors
In this episode we discuss the recent National Society of Genetic Counselor’s Practice Resource on Dystrophinopathies, which was recently published in JoGC, with two of the publications’ authors. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.
Segment 1: “Genetic counseling for the dystrophinopathies- P
#10- Family Health History: Communication and Decision Making
In this episode we discuss two papers that highlight the importance of communication around family health history and the influence of family beliefs on genetic testing decisions. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.
Segment 1: ““Family health beliefs and cascade genetic testing in Asian fami
#9 Black Previvor and Survivor Breast Cancer Genetic Testing Experiences
In this episode we discuss a research study that focuses on Black women who tested positive for a pathogenic variant associated with an increased risk for breast cancer. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website. Please note that the terminology used refers to women to reflect the language used in th
#2 Intersection of the Disability Community and Genetic Counseling Training/Practice
In our second episode, we explore two recent articles focusing on the intersection of the disability community and genetic counseling training and practice.
Segment 1: “Disability education and implications for genetic counselor training”
Lauren Douglas (she/her) serves as an oncology genetic counselor and supervisor for graduate student rotations at MHealth Fairview in Minneapolis, MN. She r
#8 Neurogenetics: Predictive Testing for ALS and Dynamic Coping in Pediatric Ataxia-Telangiectasia
In this episode we discuss research on patient and family experiences in neurogenetics. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.
Segment 1: “Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis”
Connolly Steigerwald is a certified genet
#7 Simulation and Leadership Development in Clinical Training for Genetic Counselors
Guests include Megan Cho to discuss her paper, “Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies” as well as Amanda Polanski and Ashley Kuhl to discuss their paper, “Leadership development in genetic counseling graduate programs.”
In this episode we discuss clinical training by exploring papers that discuss clinical simu
#6 Exploring Abortion Care: Reproductive Justice and Healthcare Professional Training in the Face of Changing Legislation
Guests include Gina Sanchez to talk about her paper, “Status of abortion curriculum in genetic counseling: Survey of graduate programs and recent graduates in the United States” and Dr. Holly Rankin to discuss her paper, “Termination counseling among US perinatal genetic counselors in the setting of second trimester fetal anomalies.”
Segment 1:
Gina Sanchez, MS, MB(ASCP), CGC is a genetic counse
#5 Non-Invasive Prenatal Screening (NIPS) and Fetal Sex Prediction
In this episode we discuss navigating non-invasive prenatal screening, also known as non-invasive prenatal testing, by reviewing two articles covering genetic counseling insights, informed consent challenges, and inclusive practices. You can find the Journal of Genetic Counseling webpage via onlinelibrary.wiley.com or via the National Society of Genetic Counselors website.
Segment 1 “Genetic co
#4 Discussing Gender Inclusive Terminology and Gender-Affirming Hereditary Cancer Care
In our fourth episode, we delve into the importance of gender-inclusive language in genetic counseling and the specific challenges transgender and gender-diverse (TGD) individuals face in accessing hereditary cancer care. You can find these articles in a special virtual issue of the Journal of Genetic Counseling which is free and open access for the month of June. You can find the Journal of Genet
#3 Diagnostic Odysseys with Secondary and No Primary Findings
To celebrate DNA Day we are releasing our April episode exploring concepts related to the diagnostic odyssey, whole genome sequencing, and results returned.
Segment 1: A Journey of Hope and Resilience
In our first segment, we delve into the research conducted by Celine Lewis, focusing on the emotional impact of receiving a "no primary finding" (NPF) result from genome sequencing. This recent
#1 Rare Disease Family Experience (Chromosome 18 Conditions and Pediatric Oncology)
Welcome to the first episode of DNA Dialogues! Today is February 29th, 2024. It is a leap year, so today marks an extra special rare disease day.
Rare diseases can impact so many people - from patients themselves, to families, to broader communities. To celebrate rare disease day, we are going to dive into two recent articles from the Journal of Genetic Counseling that showcase the rare disease
Introducing DNA Dialogues
Welcome to DNA Dialogues, where we dive into the intricate world of genetic counseling research. We are excited to announce our pilot episode will be released on Rare Disease Day 2024 (Thursday February 29th).
Listen for a sneak peek at what is coming up on the podcast.
Join us as we peel back the layers of groundbreaking articles from the Journal of Genetic Counseling, bringing you exclusive di
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