Dr. Brian Shirts discusses ConnectMyVariant and the importance of connecting individuals with the same cancer variants.
All in Interview
#174 Pharmacogenomics with Fulgent Genetics
Gregory Kellogg, Director of Genetic Counseling at Fulgent Genetics explores pharmacogenomics.
#173 GRIN1 with Keith McArthur
Keith McArthur shares about his son Bryson’s GRIN1 rare disease diagnosis and his family's experience connecting with others in the community.
#172 PhenoTips: Advances in Rare Disease Diagnosis
Drs. Stephen Kingsmore, Marshall Summar, and Ellen Thomas join Dr. Pawel Buczkowicz to discuss the diagnostic odyssey in this installment of the PhenoTips Speaker Series.
#171 Farber Disease with Aceragen
In honor of Rare Disease Month we explore Farber Disease with Dr. Alex Solyom and Katie Crosby of Aceragen.
#170 Mitochondrial Disorders with Alejandro Dorenbaum
Investigational therapies for primary mitochondrial myopathy are discussed with Dr. Alejandro Dorenbaum in honor of rare disease month.
#169 Cytogenomics with Phase Genomics
Next generation cytogenomic applications in the reproductive genetics and oncology spaces are explored with Dr. Ivan Liachko and Dr. Stephen Eacker.
#168 Polygenic Risk Scores with Giordano Bottà
Allelica CEO and Co-Founder explains the power of PRS to assess people’s risk of common diseases.
#167 PhenoTips: Future of Cancer Genetics
Dr. Banu Arun and Dr. Mark Robson discuss how to prepare practitioners for the future of cancer genetics in this installment of the PhenoTips Speaker Series.
#166 Beta Thalassemia with Radhika Sawh
A genetic counselor discusses the genetics of beta thalassemia and shares her personal experience with the genetic condition.
#165 Sequencing for Cancer Risk with Sandra Balladares
Scientist and breast cancer survivor explores how to utilize Illumina’s sequencing technology to assess inherited cancer risk.
#164 Parkinson’s Disease with the Parkinson’s Foundation
Representatives from the Parkinson’s Foundation and the Hispanic Parkinson’s Advisory Council explore Parkinson’s disease including diversity in genetic research.
#163 Rachel Pastiloff & Krystle Davis On Prader-Willi Syndrome
A mother/advocate and a researcher share their unique insights on Prader-Willi Syndrome.
#162 PhenoTips: Future of Genetic Counseling
Genetic Counselors explore the future of the field in this installment of the PhenoTips Speaker Series.
#161 Phenotips: Digital Tools in Genetic Counseling
Genetic Counselors explore the Adoption and Impact of Digital Tools in Genetic Counseling in this installment of the PhenoTips Speaker Series.
#159 Black Cancer Genes on Breast Cancer
Attorney /Patient Advocate Erika Stallings and Genetic Counselor Dena Goldberg discuss breast cancer in the Black patients.
#158 Mark Kiel on ALS Genetics
The Chief Science Officer and Co-Founder of Genomenon shares his insight on the genetics of ALS.
#157 NSGC 2021 Recap
Laura Hercher covers the Texas SB 8 abortion law and its impact on genetic counseling . Sally Rodríguez shares insight on the racial disparities in carrier screening.
#156 Rich Horgan on Duchenne Muscular Dystrophy (DMD)
The Founder and President of Cure Rare Disease discusses treatments for Duchenne Muscular Dystrophy.
#154 Kenneth Kovan & David Berd on Haptenized Vaccines
BioVaxys’ Kenneth Kovan and Dr. David Berd discuss vaccine platforms for viral infections and cancers.