Daniel speaks about the films to be screened at the festival and the film he produced about his son's rare disease, Menkes Disease.
All in Interview
#66 Dr. Susan Capasso on Genetic Counseling
Her personal journey to become a genetic counselor and advice for students.
#64 Dan Faszczyk on Kolgene
Co-Founder/CEO of Kolgene explains the platform connecting clinicians with genetic labs around the world. His company streamlines the process of looking for labs, communicating with them and ordering the tests.
#63 Rare Disease Day 2017
NORD's event in Hartford is recapped including interviews with a patient advocate, Michelle Cotton, and a Connecticut representative, Dave W. Yaccarino.
#62 Cytogenetics Basics
A Clinical Cytogeneticist talks about the field of cytogenetics which studies chromosomes.
#61 Wes Wilson on Tumor Progression Epigenetics
Discussion on the epigenetics of tumor progression in pediatric cancer, how it differs between types of cancer, and using it to diagnosis and alter treatments.
#60 Dan Donovan on Onevoice
Co-Founder/CEO of Onevoice shares how his new community building software solution supports the rare disease community.
#59 Scott Weissman on Genetic Counseling Private Practice
Discuss the subfields of genetic counseling cardiogenetics, hereditary cancer genetics, direct-to-consumer tests and carrier screening.
#58 Joanne Kamens on Gender Equality in Science
Dr. Joanne Kamens discusses gender equality in work environments, specifically in scientific fields and finding different careers in science through networking.
#56 Brianne Kirkpatrick on Ancestry Genetic Testing
Entrepreneur/genetic counselor discusses the importance of family health history awareness month, ancestry DNA testing and other direct-to-consumer genetic tests.
#55 Sharon Begley on CRISPR, a BRCA Event
A science communicator of 40 years, Sharon Begley, shares her insight on CRISPR’s impact on advances in research. Event about the environmental factor of breast cancer is reviewed.
#53 Ginger Nichols on MotherToBaby
Genetic counselor, Ginger Nichols, shares about what the MotherToBaby service offers and other information for pregnant and nursing women.
#52 Charcot Marie Tooth Interview
Patient advocates Bernadette Scarduzio and Allison Moore share about CMT, their documentary and the Hereditary Neuropathy Foundation.
#51 Nevena Hristozova on Stress Proteins in Plants
Nevena Hristozova joins me on the show all the way from Brussels! We discuss her research with chaperones - stress related proteins, in plants under unfavorable environmental conditions.
#50 Dr. Melina Fan about Addgene
Dr. Melina Fan joins me on the show to discuss plasmids. Dr. Fan is the Chief Scientific Officer and a co-founder of Addgene. Addgene is a nonprofit organization that operates a plasmid repository for the research community. Dr. Fan explains what plasmids are, highlights cool genes that are inserted into plasmids and how Addgene's plasmid repository works.
#49 Brittany Gancarz on Prenatal Genetic Counseling
Prenatal genetic counselor Brittany Gancarz talks about the field of genetic counseling, busts a few genetic counseling myths and announces a new genetic counseling program in Connecticut!
#48 Dr. Ellen Elliott on lncRNAs and CRISPR
Dr. Ellen Elliott discusses her research of lncRNAs in TH2 cells and asthma. and how she uses CRISPR to do it.
#47 Sharon Turcotte on lncRNAs
What a lncRNA is, its function in gene expression, the diseases associated, how the CRISPR-Cas can modify it.
#45 Hole In The Wall Gang Camp
Former camper and current camp counselor, Ester Wasserman shares the magic of camp, how it was founded, what it offers to seriously ill children campers and her own experience through the years.
#41 Rare Disease Day 2016
February 29th is the rarest day of the year and that means it's Rare Disease Day! Throughout the world NORD (The National Organization of Rare Diseases) has hosted Rare Disease Day events. I attended the Connecticut Rare Disease Day at the State House in Hartford and interviewed a few of the presenters including Jackie and Eloise Stager, founders of JaxLegacy, John Hopper, the director of the Fibrolamellar Cancer Foundation and Maddie Shaw, leader of Maddie's Herd.