Kristin McKay, Executive Director of Project Alive, is dedicated to accelerating treatments, expanding care, and supporting families affected by Hunter Syndrome, a disease that impacted her brother and now her son.
All in Interview
Kristin McKay, Executive Director of Project Alive, is dedicated to accelerating treatments, expanding care, and supporting families affected by Hunter Syndrome, a disease that impacted her brother and now her son.
Geana Dyer, BS, RN, the Founder of the Cockayne Syndrome Foundation shares her experience parenting 5-year-old Ronin, filmed at the New England Regional Genetics Group (NERGG) conference.
In the pilot episode of Gene Pool Media’s newest podcast the host Amber Sher, CGC is interviewed about the intersection of genetics, medicine, and faith.
Greenwood Genetics Center’s Dr. Nikhil Sahajpal reveals how OGM is changing clinical diagnostics from missed structural variants to new gene disease association.
A leading expert in pediatric genetics and skeletal disorders, Dr. Janet Laegare, provides her expertise.
Drs. Christine Eng, Eric Green, and Marina Sirota share highlights of their presentations at this week’s AGBT Precision Health 2025 Meeting in California.
Beyond The Thesis with Papa PhD episode where Kira Dineen is interviewed by Dr. David Mendes about science communications, networking, and GC grad school apps.
Explore how MGI’s genomic innovation is transforming rare diseases (and even dual diagnoses) care in Turkey and around the globe from Dr. Serdar Ceylaner and Alice Peng.
Quest Diagnostics' Kristy Bouvier and Kathleen O’Brien explore how pharmacogenetics testing can optimize medications, prevent side effects, and improve treatment.
Live from NYC’s Cocktails & Chromosomes, patient advocate Jena Robertson and researcher Dr. Will Mannherz share personal stories and new breakthroughs bringing telomere biology disorders to a clinical trial this fall.
Former NIH communicators Jenny Montooth, Sarah Alex Bates, and Britny Kish (Founders of The Science Underground) weigh in on science communication strategies including their memes that took them from 15M to 80M impressions.
Bioethicist Dr. Madison Kilbride sheds light on controversial ethical issues surrounding genetic testing through this interview led by Sarah Lawrence student Shaun Miller.
Former NIH communicators Jenny Montooth, Sarah Alex Bates, and Britny Kish (Founders of The Science Underground) weigh in on science communication strategies including their memes that took them from 15M to 80M impressions.
When William was diagnosed with DMD, his family set out to raise $2.2 million to design a cure with CRISPR.
Behind the scenes of Beast Games, and the bigger battle the Allens are fighting.
Episode drop from Demystifying Genetics, a show in our brand new science podcast network, Gene Pool Media!
Episode drop from All Access DNA, a show in our brand new science podcast network, Gene Pool Media!