Co-Founder Nargol Faravashi and Genetic Counselor Christin Coffeen share considerations before and after testing.
All in Interview
#115 Dr. Daria Julkowska on The European Joint Program on Rare Diseases
Celebrate Rare Disease Month with the Coordinator of the EJPRD discussing rare disease research.
#114 Matt Burgess on Australasia Genetic Counseling
Private Practice Australian Genetic Counselor Transitions to Clinical Science Liaison Role in the US.
#113 Lauren Winter on Dental Genetics
Genetic counseling graduate student shares current understanding of dental genetics including her thesis project.
#112 Sam Toy on Pediatric Genetic Counseling
A genetic counselor shares about the pediatric genetic counseling speciality.
#109 Shenela Lakhani on Genetic Counseling in Qatar
First genetic counselor in Qatar shares her experience.
#108 Dr. Becky Winslow on Pharmacogenomics
Dr. Becky Winslow, a Doctor of Clinical Pharmacy, shares her insight about pharmacogenomics.
#107 Eleanor Griffith on Grey Genetics
Founder of Grey Genetics, Eleanor Griffith, shares about her telehealth genetic counseling company.
#106 Sano Genetics on Autism Genetics
Dr. Patrick Short, Sano Genetics CEO, shares about our understanding of autism genetics and current research studies in this podcast episode.
#105 Secret Sequence on Genetic Privacy
Jason Corbiere and Austin Maier, founders of Secret Sequence, discuss data security of genetic tests results.
#104 Genetics of Opioid Addiction
Scientists from the Camden Opioid Research Initiative share their research focusing on the role genetics plays in this drug addiction.
#103 Brianne Kirkpatrick on Adoptee Genetic Testing
Genetic counselor and Founder of WatershedDNA offers advice for adoptees and donor conceived people on genetic testing.
#102 Seth Rotberg on Huntington Disease
Patient Advocate and Motivational Speaker shares his journey with Huntington Disease.
#100 Carl Zimmer on Human Heredity
Award-winning New York Times columnist and the author of 13 science books discusses his latest book about hereditary.
#99 Coriell Institute on Biobanking
Nahid Turan (Chief Laboratory Officer) and Alissa Resch (Chief Scientific Officer) share about biobanking’s role in research and development.
#98 Lydia Seiders on Aplastic Anemia
Maryland State Ambassador for NORD brings her passion for patient advocacy for the rare disease community including her daughter known as #EmmaStrong.
#96 Jim Cavan on Backpack Health
A mobile and cloud-based app that helps people with chronic, serious and rare health concerns better manage their health journeys.
#95 Kieger Family on Familial Adenomatous Polyposis
Author Laura Kieger and her son, Dr. Alexander Kieger, share their family’s courageous, century-long struggle with a rare genetic cancer syndrome.
#94 Legend of Sumeria: A Genetics Graphic Novel
Dr. Biju Parekkadan, Co-Creator and Scientific Director of Legend of Sumeria, discusses the science, bioethics, and art behind this hard science graphic novel.
#93 Team Telomere
A community for telomere biology disorders discusses dyskeratosis congenita.