Discover New Advances in the world of genetics, from technology like CRISPR to rare diseases to new research. For over a decade, multi-award winning podcast "DNA Today" has brought you the voices of…

Victoria Gray is the FIRST person to be cured with a genetic condition using CRISPR, in this podcast interview she shares about her sickle cell pain crises and medical racism experiences prior to…

Dr. Heather Cheng, prostate cancer expert, discusses the PROMISE Study for prostate cancer patients.

Precipio COO, Zaki Sabet, discusses issues in the diagnostic process of hematologic cancers in this interview by Kira Dineen.

Dana-Farber/Boston Children’s Dr. Lisa Diller provides insight on newborn screening for childhood cancer conditions like retinoblastoma and Li-Fraumeni syndrome.

Patient advocates Bernadette Scarduzio and Allison Moore share about CMT, their documentary and the Hereditary Neuropathy Foundation.

Four current graduate students discuss how to prepare and what to expect during the first year.

Investigational therapies for primary mitochondrial myopathy are discussed with Dr. Alejandro Dorenbaum in honor of rare disease month.

Amber Olsen and Faith McGown of the United MSD Foundation discuss Multiple Sulfatase Deficiency.

Rosalind Franklin's contribution to the discovery of the structure of DNA is explored, her role may be bigger than you think.

Gregor Mendel has been called the father of genetics due to his ground breaking discoveries from his pea plant experiments. Be sure to check out dnapodcast.com to learn more or contact at…

Three Genetic Counselors who recently took the American boards exam share their experience and offer advice.

DNA Today ’s Communication Lead, Corinne Merlino, shares about her rare congenital birth defect that affects craniofacial development and how it influenced her to become a genetic counselor.

Best DNA Podcasts to Listen to ⋅ 1. Once Upon A Gene ⋅ 2. Base by Base ⋅ 3. Science Facts & Fallacies ⋅ 4. Finding Family DNA ⋅ 5. Beyond the Sequence ⋅ 6. DNA Surprises ⋅ 7. DNA: ID

Fellow podcaster (Being Rare) and the CEO/President of the E.WE Foundation shares her experience parenting a child with Trisomy 18 and the resources she created for fellow parents.

“You are (not) the father!” NBC’s Maury Povich joins us for a discussion on paternity testing.

Read the 2026 report to understand the burden of Alzheimer's and dementia on individuals, caregivers, government and the nation's health care system.

Pro genealogist Nicka Smith discusses direct to consumer DNA testing and its role in retracing African American Ancestry.

Victoria Gray is the FIRST person to be cured with a genetic condition using CRISPR, in this podcast interview she shares about her sickle cell pain crises and medical racism experiences prior to…

Podcast episode exploring protecting transgender and non-binary patients during times of unprecedented legislation, creating psychologically safe and inclusive medical environments, supporting access…

Victoria Gray is the FIRST person to be cured with a genetic condition using CRISPR, in this podcast interview she shares about her sickle cell pain crises and medical racism experiences prior to…

Episode drop of “It Happened To Me” sharing the story of a heartbreaking Tay Sachs diagnosis inspiring a career in carrier screening.

Author and law professor, Jorge Contreras, give an overview of his latest novel, The Genome Defense.

Hear about epigenetics in this 30 minute podcast interview. Discussion includes epigenetic disorders (Prader–Willi, Angelman, Beckwith-Wiedemann syndrome), testing for epigenetic (EpiSign), and…

Resources to observe National Asian & Pacific Islander HIV/AIDS Awareness Day on May 19 and highlight the impact of HIV in Asian and Pacific Islander (API)…

Betsy Humphreys, Karen Volle and Karina Mancini share their experience with the New Hampshire-Maine Leadership Education Neurodevelopmental Disabilities (LEND) program.

Explore reflections written by Kevin Alexander on PKU, newborn screening, rare disease, and mental health advocacy at PKU Journal.

Patient Advocate and Motivational Speaker shares his journey with Huntington Disease.

Rare disease patient leader Gunnar Esiason shares about his journey with cystic fibrosis and how he utilizes his experience to advocate for the community. He is director of patient outreach at the…

Atticus Shaffer of The Middle on ABC discusses life with osteogenesis imperfecta and his acting career.

Learn how to extract DNA from fruit to celebrate DNA Day.

Dr. Patrick Short, Sano Genetics CEO, shares about our understanding of autism genetics and current research studies in this podcast episode.

Representatives from the Parkinson’s Foundation and the Hispanic Parkinson’s Advisory Council explore Parkinson’s disease including diversity in genetic research.

Genetic Counselor, Laura Hercher, discusses the US Supreme Court’s decision to overturn Roe v. Wade and the consequences of this decision for the genetic counseling community and people who may need…

Tune into this podcast episode to learn how to: improve clinic experiences for transgender and gender non-conforming patients, go beyond standards for gender affirming family history collection,…

Author Laura Kieger and her son, Dr. Alexander Kieger, share their family’s courageous, century-long struggle with a rare genetic cancer syndrome.

Naseem Amin, CEO of Orphalan, explores Wilson’s disease and current FDA-approved treatments.

New podcast launch! Check out the first episode of the official Journal of Genetic Counseling Podcast, “DNA Dialogues”.

Patient advocate talks about her hereditary cancer syndrome and offers her expertise and experience.

In this podcast episode, Lauren Potter shares her experience playing Becky Jackson on all six seasons of Fox's hit TV show, Glee. Lauren also speaks to her advocacy work including being appointed to…

Podcast episode exploring protecting transgender and non-binary patients during times of unprecedented legislation, creating psychologically safe and inclusive medical environments, supporting access…

First episode of the N-Lorem Foundations’ “Patient Empowerment Program” features an actor turned patient advocate and a pediatric geneticist.

Fellow podcaster (Being Rare) and the CEO/President of the E.WE Foundation shares her experience parenting a child with Trisomy 18 and the resources she created for fellow parents.

A glaucoma surgeon and Wilmer Johns Hopkins researcher shares about risk factors, development, and screening for glaucoma.