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.
#218 LEND Program with Betsy Humphreys, Karen Volle & Karina Mancini
Betsy Humphreys, Karen Volle and Karina Mancini share their experience with the New Hampshire-Maine Leadership Education Neurodevelopmental Disabilities (LEND) program.
#217 SynGAP1 with Mike Graglia and Elli Brimble
Patient advocate Mike Graglia and genetic counselor Elli Brimble discuss SynGAP1-related disorders.
#216 African American Ancestry with Nicka Smith
Pro genealogist Nicka Smith discusses direct to consumer DNA testing and its role in retracing African American Ancestry.
#215 Preventative Health via Whole Exome Sequencing
The Founder and CEO of Panacea discusses utilizing whole exome sequencing for preventive health.