Free Daily Podcast Summary
All Access DNA: Daily Summaries Delivered
by allaccessdna
Want to know more about your DNA? Curious about how your genes impact your health? All Access DNA honestly answers the questions you have about genetics, healthcare, and popular issues in genomic medicine. Host Kate Wilson utilizes her genetic expertise and experience to interview leaders and specialists in genomic health and research. Join us as we bring you understandable, scientific information about genetics!
Latest Episodes
The most recent episodes — sign up to get AI-powered summaries of each one.
- 3 days ago39 min
MTHFR Gene: What’s real, what’s not and what does it actually mean?
In today's conversation, Kate Wilson welcomes Emalyn Cork to explore the complexities of the MTHFR gene, a topic that has sparked curiosity and confusion alike in both clinical settings and the general public. Emalyn explains the complexities of the MTHFR gene, debunks common misconceptions, and discusses when genetic testing is truly necessary. Key words: MTHFR, genetics, homocysteine, genetic testing, medical misinformation, folic acid, genetic variants, health risks, clinical utility, genetic counseling Key Topics: What the MTHFR gene does in the body Common misconceptions about MTHFR variants When genetic testing for MTHFR is clinically relevant Risks of unnecessary genetic testing and treatments How to interpret genetic test results responsibly Guest bio: Emalyn is the Assistant Director of Genetic Counseling at Emory Healthcare. She works with pediatric and adult clinical genetics patients in the inpatient and outpatient settings. She graduated from Mount Sinai's genetic counseling training program in 2018 and worked as a genetic counselor in their clinic for inborn errors of metabolism before moving to Atlanta to join Emory's team in 2021. She has a special interest in metabolic and mitochondrial diseases and is passionate about the education and mentorship of genetics trainees. Resources related to today’s topic: Findageneticcounselor.org to search for a genetic counselor near you Information on MTHFR from Cleveland Clinic Give your feedback and help shape All Access DNA! Take our listener survey here: https://forms.gle/x82MKLRftpKH987s7 Sign up for our newsletter here: https://www.allaccessdna.com/newsletter Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Any inquiries on the podcast can be sent to AllAccessDNA@gmail.com Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health. The All Access DNA team includes: host, producer and editor Kate Wilson. The logo is designed by Designs by NKJ. Our Social Media Lead is Aryanah Estinvil.
- 2 weeks ago35 min
#64- Should we select embryos based on chance?
Dr. Betty Cohn discusses the complexities, ethical considerations, and current state of polygenic embryo screening and risk scores, highlighting the scientific, ethical, and societal challenges involved. Key words: polygenic embryo screening, genetic testing, reproductive ethics, risk scores, embryo selection, genetic diversity, clinical validity, reproductive autonomy, bioethics Key Topics: What polygenic embryo screening is and how it differs from single-gene testing The probabilistic nature of polygenic risk scores and their limitations Ethical implications of embryo selection based on risk scores Disparities and biases in polygenic risk scoring across ancestry groups The influence of commercial companies and lack of regulation in direct-to-consumer genetic testing The impact of societal values in embryo selection Guest bio: Betty Cohn is a postdoctoral fellow working with Dr. Anna Wexler at the University of Pennsylvania. She holds a PhD in Public Health Genetics from the University of Washington, a Master of Bioethics from the Johns Hopkins Berman Institute of Bioethics, and a B.A. from Binghamton University. Her research examines the ethical, legal, and social implications of emerging biotechnologies, including direct-to-consumer genetic testing, brain organoids, and polygenic risk scores. Her doctoral dissertation used qualitative methods to explore how individuals who discover a misattributed parentage experience through genetic testing navigate these findings, with a focus on online communities as sources of social support. LinkedIn: https://www.linkedin.com/in/bettycohn/ Twitter/X: @bettyccohn Resources related to today’s topic: “Ethical and social implications of implementing polygenic embryo screening into clinical care: A scoping review” by Betty Cohn, Dorit Barlevy, Gabriel Lazaro-Munoz “Polygenic risk scores in the clinic: Health-system leaders and primary care providers weigh in” by Susan Brown Trinidad, Stephanie M Fullerton, Betty Cohn, David R Crosslin, Gail P Jarvik “Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations” by Martin et al. Give your feedback and help shape All Access DNA! Take our listener survey here: https://forms.gle/x82MKLRftpKH987s7 Sign up for our newsletter here: https://www.allaccessdna.com/newsletter Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Any inquiries on the podcast can be sent to AllAccessDNA@gmail.com Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health. The All Access DNA team includes: host, producer and editor Kate Wilson. The logo is designed by Designs by NKJ. Our Social Media Lead is Aryanah Estinvil.
- Sep 8, 202652 min
#63-How can you cure ALS & FTD in a race against time?
In this episode, Yentli Soto Albrecht, PhD, shares her personal journey with ALS and FTD, her scientific research, and her efforts to accelerate the search for a cure. Discover how her story fuels her advocacy and innovative projects to fight these neurodegenerative diseases. Key words: ALS, FTD, genetic research, neurodegeneration, Cure C9, gene therapy, prevention trials, scientific collaboration, patient advocacy Key Topics: Genetic causes of ALS and FTD and the C9 repeat expansion Current challenges in clinical trials and drug development The role of patient advocacy and community engagement Innovative research projects and collaborations The importance of accessible biomarkers and diagnostics Guest bio: Yentli Soto Albrecht, PhD, is a 9th-year MD-PhD student at the University of Pennsylvania and will complete her medical degree in 2027. She earned her PhD in 2024 in the Douglas Wallace lab at the Children’s Hospital of Philadelphia, showing that mitochondrial oxidative phosphorylation restricts SARS-CoV-2 replication and that natural mitochondrial DNA variation modulates viral pathogenesis, work recognized with the Richard K. Root Prize for Infectious Disease Research in 2025. She was president of the American Physician Scientists Association from 2022 to 2023, managing a budget of more than $300,000 and reaching over 5,000 dual-degree applicants across her five-year tenure. She was preparing for a career as an infectious disease physician-scientist when her father was diagnosed with genetic ALS in June 2023 and she learned she carried the same C9orf72 repeat expansion that was taking his life, the most common genetic cause of both ALS and frontotemporal dementia (FTD). Her father, Frank Albrecht, died in August 2024, and six months later she pivoted to C9orf72 neurodegeneration. She has since built eleven collaborative projects across eight countries, including synchrotron imaging comparing aggregates in C9 ALS and C9 FTD, nanosensor-based biomarker discovery, drug repositioning, and the first commercial C9orf72 iPSC biorepository, which begins with her father’s cells and her own. She has secured more than $280,000 in grant funding for her collaborators and raised over $66,000 through Push Ups for ALS, a carrier-led fundraiser in her father’s memory. She co-founded CureC9, a program within EverythingALS governed by an eight-member scientific advisory board, which has raised $216,711 toward a $12 million flagship effort and meets for the third time in September to plan the first prevention trial for genetic ALS and FTD. She was the inaugural End the Legacy Community Science Liaison fellow, brings the science back to genetic carriers in lay terms through her video series Search for a Self Cure, and has accepted an offer to join Eli Lilly’s Talent Development Academy in Boston as a postdoctoral scientist in ALS disease biology and drug discovery after medical school. Next year, she will apply to neurology residency programs for a 2028 start. Dr. Soto Albrecht draws on her position as patient, scientist, and physician-in-training to accelerate therapies for familial ALS and FTD within her lifetime. Resources related to today’s topic: CureC9 website The Association for Frontotemporal Degeneration The ALS Association Compassionate Care ALS North Star ALS End the Legacy Everything ALS Breakthrough Prize Video Give your feedback and help shape All Access DNA! Take our listener survey here: https://forms.gle/x82MKLRftpKH987s7 Sign up for our newsletter here: https://www.allaccessdna.com/newsletter Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Any inquiries on the podcast can be sent to <a
- Aug 25, 202632 min
#62- Is the healthcare experience keeping genomic medicine out of reach?
In this episode, Megan Johnson discusses the disparities in genomic healthcare, focusing on how healthcare experiences influence participation and trust, especially among underrepresented groups. She explores the genomic healthcare disparity cycle, the importance of diversity in genetic research, and strategies to improve patient engagement and understanding. Key words: genomic healthcare disparities, underrepresented groups, healthcare experience, genetic research, trust in medicine, diversity in genomics, patient engagement, healthcare access, genetic counseling, health equity Key Topics: The genomic healthcare disparity cycle and its impact Importance of diversity and inclusion in genetic research Role of healthcare providers in improving patient trust and understanding The influence of social determinants on access to genomic healthcare The potential of community-based research and primary care integration Steps to address systemic barriers and improve health equity Guest bio: Megan is a clinical genetic counselor who helps patients and their families understand and make decisions around complex genetic information. Her research into how healthcare experiences shape genomic healthcare disparities grew out of a long-standing commitment to equity, one that took root growing up in a rural community with limited access to specialized care. She's dedicated to making genetic counseling accessible and meaningful for patients of all ages. Resources related to today’s topic: Johnson, M.D., Hite, A., Richmond, J. et al. Healthcare experiences and the cycle of genomic healthcare disparities: A cross-sectional study utilizing the ‘All of Us’ research program. J Community Genet 17, 88 (2026). https://doi.org/10.1007/s12687-026-00921-8 All of Us Research Program from the National Institutes of Health Give your feedback and help shape All Access DNA! Take our listener survey here: https://forms.gle/x82MKLRftpKH987s7 Sign up for our newsletter here: https://www.allaccessdna.com/newsletter Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Any inquiries on the podcast can be sent to AllAccessDNA@gmail.com Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health. The All Access DNA team includes: host, producer and editor Kate Wilson. The logo is designed by Designs by NKJ. Our Social Media Lead is Aryanah Estinvil
- Aug 11, 202640 min
How does Jack's Basket celebrate people with Down syndrome?
Carissa shares her inspiring journey of parenting her son Jack, diagnosed with Down syndrome, and how it led to the creation of Jack's Basket—an organization dedicated to supporting families and changing perceptions about Down syndrome. Keywords: Down syndrome, Jack's Basket, parenting, advocacy, community support, diagnosis communication, celebration, inclusion, healthcare training Key Topics: The impact of diagnosis communication on families The role of community and support networks for families with children with Down syndrome The mission and activities of Jack’s Basket in providing hope and resources The importance of celebrating individuals with Down syndrome and promoting inclusion Strategies for healthcare providers to deliver unexpected news empathetically Guest Bio: Carissa Carroll, M.Ed., is the founder and CEO of Jack’s Basket, an organization born from her heart after her son Jack was diagnosed with Down syndrome. Driven by a deep commitment and clear mission, Carissa is passionate about celebrating the lives of individuals with Down syndrome. She has a deep love for learning, constantly seeking to grow and understand more. Building meaningful relationships is a priority for her. Carissa leads all growth efforts, inspiring communities to embrace and celebrate individuals facing an unexpected diagnosis with dignity and hope. With an undergraduate degree from Bethel University and a Master of Education from the University of Minnesota, Carissa brings her background in education to equip medical providers with compassionate communication tools to deliver the Down syndrome diagnosis without bias. Her mission is to transform how families experience this moment, ensuring they feel supported, connected, and fully know that their child is worthy of celebration. As a connector, innovator, and dedicated advocate, Carissa writes, speaks, and leads strategic initiatives to expand Jack’s Basket’s reach and impact. She collaborates closely with the organization’s board, volunteers, and donors, fostering a community that values individuals, connection, and celebration. When she’s not advocating for families and shaping the future of Jack’s Basket, Carissa enjoys early morning runs with friends, quality time with her husband, and cherishing moments with her three children. She remains deeply inspired by individuals with Down syndrome and energized by the positive change that Jack’s story and the organization continue to create. Here are more resources related to today’s topic: Jack’s Basket Website “Communicating Unexpected News” Curriculum You Make Me Better Annual Gala Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Any inquiries on the podcast can be sent to AllAccessDNA@gmail.com Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health. The All Access DNA team includes: host, producer and editor Kate Wilson. The logo is designed by Designs by NKJ. Our Social Media Lead is Aryanah Estinvil.
- Jul 28, 202644 min
#60: How do I know if I have a hereditary bleeding disorder?
In this episode, we explore bleeding disorders, their symptoms, diagnosis, and management, with expert Kaylee Dollerschell. Learn how these conditions affect individuals, especially women, and discover resources for support and treatment. Key words: bleeding disorders, hemophilia, von Willebrand, heavy menstrual bleeding, diagnosis, treatment, genetic counseling, patient resources Key Topics: What is a bleeding disorder and how it affects the body Signs and symptoms of bleeding disorders Diagnosis and testing for bleeding disorders Treatment options including gene therapy Impact of bleeding disorders on pregnancy and daily life Guest bio: Kaylee is a hematology genetic counselor at the University of Colorado and Children's Hospital Colorado. She works with patients and families with hereditary bleeding & clotting conditions along with other hereditary blood & cancer disorders. She graduated from Colorado State University and worked at two start-up genetic testing companies before returning to school for her master's in genetic counseling. She graduated with her master's in genetic counseling from Augustana-Sanford Genetic Counseling Program in 2019. She's been with University of Colorado/Children's Hospital Colorado since then. She loves her work within the hereditary bleeding disorders community. During her free time, she enjoys the outdoors of Colorado, volleyball, camping, hunting, and spending time with friends & family. Resources related to today’s topic: Findageneticcounselor.org to search for a genetic counselor near you National Bleeding Disorder Foundation Foundation for Women and Girls with Blood Disorders World Federation of Hemophilia Dismissed Film- Bleeding Disorders Bombardier Blood- documentary Give your feedback and help shape All Access DNA! Take our listener survey here: https://forms.gle/x82MKLRftpKH987s7 Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Any inquiries on the podcast can be sent to AllAccessDNA@gmail.com Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health. The All Access DNA team includes: host, producer and editor Kate Wilson. The logo is designed by Designs by NKJ. Our Social Media Lead is Aryanah Estinvil.
- Jul 14, 202632 min
Are athletics in my DNA? Genetic testing & performance coaching
Dr. Jeremy Koenig shares how he came to performance genomics through his own athletic background, and the conversation explores how genetic information can inform training, injury risk, and coaching- without being treated as a prediction of destiny. Key words: Precision Health, Athletic Genomics, Genetics in Sports, Genetic Counseling, Injury Risk, Training Optimization, Personalized Coaching, DNA Testing Key Insights The most impactful knowledge is context-driven Genetic information is a navigational tool, not fate Genes don’t guarantee Olympic success Athletic genetic profiles can include info on metabolism & injury protection Guest bio: Jeremy Koenig is a PhD Biochemist, former professional athlete and the Founder of Iris Infinity. Jeremy built The DNA of Things podcast as a room where the brightest minds in genomics, longevity, and human performance can share their work directly with the people it matters to most. The guests are the story — he just makes sure they're heard. As the founder of Iris Infinity — one of the world's leading DNA analysis platforms — he's spent two decades at the intersection of biology, technology, and athletics. That experience shapes the questions, but the answers belong to the experts. Give your feedback and help shape All Access DNA! Take our listener survey here: https://forms.gle/x82MKLRftpKH987s7 Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Any inquiries on the podcast can be sent to AllAccessDNA@gmail.com Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health. The All Access DNA team includes: host, producer and editor Kate Wilson. The logo is designed by Designs by NKJ. Our Social Media Lead is Aryanah Estinvil.
- Jun 30, 202639 min
#58-Could epilepsy & seizures be genetic?
In this interview, we learn what epilepsy is, its causes, and the role of genetics in diagnosis and treatment. Beth Sheidley, a genetic counselor, explains the fundamentals of epilepsy, its genetic components, and the latest advancements in genetic testing. Take our listener survey here: https://forms.gle/x82MKLRftpKH987s7 Keywords: epilepsy, genetic testing, genetic counseling, seizures, pediatric neurology, genetic causes, epilepsy treatment, genetic diagnosis, brain disorders, clinical trials Key Topics: Clinical presentation of epilepsy and various known causes Differences between unprovoked and provoked seizures Genetic factors in epilepsy Role of genetic counseling in both diagnosis and management Guest Bio: Ms. Sheidley is a licensed genetic counselor with over 30 years of experience in clinical genetic counseling, research, and teaching. Her areas of expertise include autism, epilepsy, psychiatric illness and both prenatal and pediatric genetic counseling. She received her BS degree from Cornell University in 1990 and her MS in genetic counseling from Brandeis University in 1994, where she served as Professor of the Practice/Co-Director of Research and Professional Development from 2005 to June 2014. Ms. Sheidley is the Director of Genetic Counseling for the Department of Neurology at Boston Children’s Hospital where she co-founded the first Epilepsy Genetics Program in the United States. Ms. Sheidley also co-founded and chairs EpiGC, an international network of genetic counselors who specialize in epilepsy genetics. Ms. Sheidley was the lead author of a systematic review of the epilepsy genetics literature on behalf of the National Society of Genetic Counselors (NSGC) and co-authored the resulting practice guideline adopted by NSGC and endorsed by the AES. She is a Co-Investigator for the Gene-STEPS study at Boston Children’s, which enrolls infants with recent seizure onset for rapid whole genome sequencing. https://www.linkedin.com/in/beth-rosen-sheidley-4994654/ Resources: Findageneticcounselor.org to search for a genetic counselor near you Rare Epilepsy Network (REN) Epilepsy Foundation Please subscribe to this podcast on Apple Podcasts, Spotify, YouTube or wherever you get your podcasts to stay updated on new episodes of All Access DNA. Listen to past episodes on your favorite podcast play by searching “All Access DNA” or by streaming from our website at allaccessdna.podbean.com Any inquiries on the podcast can be sent to AllAccessDNA@gmail.com Note that this podcast is for entertainment and education and is not intended to be a substitute for professional medical advice. Please consult your physician with any questions you may have regarding your health. The All Access DNA team includes: host, producer and editor Kate Wilson. The logo is designed by Designs by NKJ. Our Social Media Lead is Casey Lepley.
Get All Access DNA summaries in your inbox
Free AI-powered daily recaps. Key takeaways, quotes, and mentions — in a 5-minute read.
Get Free Summaries →Free forever for up to 3 podcasts. No credit card required.
You Might Also Like
Listeners also like.
Genetics Unzipped
Explores stories from the world of genetics, from Mendel's experiments to modern genome research.
The Peter Attia Drive
Conversations with experts on health, longevity, performance, and critical thinking led by physician Peter Attia.
The Gift
Individuals discover life-altering family secrets and identity revelations through DNA testing.
Red Pill Your Healthcast
Two healthcare providers discuss overlooked health issues and empower listeners to make informed decisions for their families.
Extend Podcast with Darshan Shah, MD
Explores science-backed strategies and expert insights to extend healthspan and optimize longevity through actionable health protocols.
The Biohacking Standards
A deep dive into biohacking fundamentals—nutrition, movement, sleep, and mindfulness—grounded in science and holistic wellness principles.
The Genius Life
A health and science journalist explores cutting-edge research and practical strategies for optimizing brain function and overall wellness.
Health Optimization Medicine Podcast
Experts discuss science-based strategies for health optimization, performance, and human potential through targeted interventions.
Health vs Hype with the American Medical Association
A medical expert debunks viral health trends and misinformation with science-backed insights from physicians.
FoundMyFitness
A podcast exploring health, science, nutrition, aging, and fitness.
Fully Alive: Unlocking the secrets to your healthier, happier, longer life
Explores science and lifestyle strategies to enhance health, purpose, and longevity.
Decoded | Unlock The Secrets of Human Behavior, Emotion and Motivation
Analyzes subconscious patterns in human behavior and provides methods to change them.
About All Access DNA
Want to know more about your DNA? Curious about how your genes impact your health? All Access DNA honestly answers the questions you have about genetics, healthcare, and popular issues in genomic medicine. Host Kate Wilson utilizes her genetic expertise and experience to interview leaders and specialists in genomic health and research. Join us as we bring you understandable, scientific information about genetics!
Customized Recaps
AI-powered recaps with compact key takeaways, quotes, and insights.
Straight to Your Inbox
Get key takeaways from All Access DNA in a 5-minute read.
Save Hours Every Week
Stay current on your favorite podcasts without falling behind.
Frequently Asked Questions
What is Podzilla's All Access DNA daily summary?
It's a free AI-powered email that summarizes new episodes of All Access DNA as soon as they're published. You get the key takeaways, notable quotes, and links & mentions — all in a quick read.
How does the All Access DNA podcast summary work?
When a new episode drops, our AI transcribes and analyzes it, then generates a personalized summary tailored to your interests and profession. It's delivered to your inbox every morning.
Is this an official All Access DNA product?
No. Podzilla is an independent service that summarizes publicly available podcast content. We're not affiliated with or endorsed by allaccessdna.
Can I get summaries of other podcasts too?
Absolutely! The free plan covers up to 3 podcasts. Upgrade to Pro for 15, or Premium for 50. Browse our full catalog at /podcasts.
How often does All Access DNA release new episodes?
All Access DNA publishes biweekly. Our AI generates a summary within hours of each new episode.
What topics does All Access DNA cover?
All Access DNA covers topics including Science, Medicine, Fitness, Health & Fitness, Life Sciences. Our AI identifies the specific themes in each episode and highlights what matters most to you.
Start getting All Access DNA summaries tomorrow morning.
Free forever for up to 3 podcasts. No credit card required.
Free forever for up to 3 podcasts. No credit card required.