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.
All in Interview
#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.
#222 Wilson’s Disease with Naseem Amin
Naseem Amin, CEO of Orphalan, explores Wilson’s disease and current FDA-approved treatments.
#221 Genetic Counseling in South Africa with Samantha Bayley and Tina-Marié Wessels
University of Cape Town student, Samantha Bayley, and professor, Tina-Marié Wessels, discuss the genetic counseling field in South Africa.
#220 Microfluidics with Franz Pruefer
Scientist and biotech engineer, Franz Pruefer, discusses the many applications of microfluidics.
#219 It Happened To Me Podcast: Genetic Counselors for Rare Diseases
Episode drop of “It Happened To Me” with Kira Dineen sharing how genetic counselors can help people with rare diseases.