Dr. Richard Wenzel shares about his experience learning that his father was not his genetic father and commentary on how healthcare providers should disclose results to patients.
#241 NBC's Maury Povich on Paternity Testing
“You are (not) the father!” NBC’s Maury Povich joins us for a discussion on paternity testing.
#240 Young Adult Patient Advocacy with Sneha Dave
Sneha Dave, Founder and Executive Director of Generation Patient, discusses her experience as a young adult patient advocate for ulcerative colitis.
#239 Duty To Warn with Janice Berliner
Genetic Counselor Janice Berliner shares about her second genetics novel, “In Good Conscience”.
#238 Secondary Findings with Caralynn Wilczewski and Andrea Alvarez
Genetic testing secondary findings and a study exploring what they mean for the patients who receive them. Learn more in this 30 minute podcast episode with a patient advocate and an expert from the NIH.
#237 Digital Tools for Cancer Outreach with Michelle Bowman
Australian cancer genetic counselor, Michelle Bowman discusses utilizing digital tools to reach patients who can benefit from cancer genetic counseling.
#236 Assessing for Alzheimer’s Disease with Quest Diagnostics
Genetic Counselor Susan Hanh shares new risk assessment advances like Quests tests and Patient Advocate Rebecca Chopp shares about her diagnosis and experience.
#235 Genetic Counseling History: ABGC Formation
Genetic Counselors, Ed Kloza and Ann Platt Walker, discuss the formation of the American Board of Genetic Counseling (ABGC) in this 30 minute podcast episode.
#234 Genetic Counseling History: 1st NSGC Conference
Seasoned genetic counselors, Michelle Fox and Debra Collins, take us back in time to the first NSGC conference!
#233 At-Home Non-Invasive Prenatal Screening with Juno Diagnostics
Dr. Allison Rodgers and Katie Sagaser of Juno Diagnostics give an overview of new advances in non-invasive prenatal screening (NIPS) utilizing only a few drops of blood.
#232 Entrepreneurship in Genetics with Matt Tschirgi
Genetic counselor and entrepreneur, Matt Tschirgi, shares insights he has learned from running his own company and a survey from others.
#231 ChatGPT and AI In Genetics with Daniel Uribe
Genobank.io’s founder explores how AI will transform healthcare and genomics with chatbots and data privacy.
#230 Cancer Pharmacogenetics with Dr. Jamie Fettig
Dr. Jamie Fettig, Founder/CEO of TrueGene Diagnostics, shares how his team is eliminating variants of unknown significance and pharmacogenetics in oncology.
#229 Pharmacogenomics with Avni Santani
Dr. Avni Santani, CMO of Veritas (LetsGetChecked), provides an overview of pharmacogenomics.
#228 Trisomy 13 and Trisomy 18 with Divya Ramachandra
Genetic counselor, Divya Ramachandra, provides a fresh perspective on the life expectancy and symptoms of trisomy 13 and trisomy 18.
#227 Limb-Girdle Muscular Dystrophies with Louise Rodino-Klapac and Livija Medne
Dr. Louise Rodino-Klapac of Sarepta Therapeutics and Livija Medne of the Children’s Hospital of Philadelphia discuss limb-girdle muscular dystrophy (LGMD).
#226 NICU Whole Genome Sequencing with Hong Li and Madhuri Hegde
Geneticists Hong Li and Madhuri Hegde explore the utilization of rapid whole genome sequencing in the NICU setting.
#225 Fetal Antigen Noninvasive Prenatal Testing (NIPT) with BillionToOne
Jen Hoskovec, BillionToOne’s Senior Director of Medical Affairs, discusses noninvasive prenatal testing (NIPT) for fetal antigen.
#224 Single-Gene Noninvasive Prenatal Testing (NIPT) with BillionToOne
Oguzhan Atay and Jen Hoskovec of BillionToOne discuss UNITY Screen non-invasive prenatal testing (NIPT) for recessive conditions.
#223 PhenoTips: Rare Disease Diagnosis Workflow
Learn how to build integrated workflows for rare disease diagnosis from PhenoTips’ Dr. Orion Buske and Charles Keenan.