GATC Event Schedule
November 11, 2025
8:00 am - 8:30 am
Registration, Breakfast and CoffeeFoyerGrand A + B8:30 am - 8:40am
Welcome and Opening RemarksEric KelsicGrand A + B8:40 - 9:00am
How and Why to Cure Prion DiseaseSonia VallabhGrand A + B9:00 - 9:45am
Genetic Agency ConversationsMisha GloubermanGrand A + B9:45 - 10:05am
Break10:05 - 10:25am
Rare Disease Access to Gene Therapy: Update on ASGCT RoleTerence FlotteGrand A + B10:25 - 10:40 am
Dyno Therapeutics: Empowering Patients with Genetic AgencyEric KelsicGrand A + B10:40 - 10:50 am
Break10:50 - 12:50 pm
Platform Sessions with DiscussionsBroadening Patient ImpactGrand CIntroduction to SessionTyson BertmaringGene Therapy as a Disruptive TechnologyJim WilsonRethinking how we fund, build and sustain the next generation of therapiesLaura Lande-DinerGenetic Surgery for Genetic Agency: building a procedural model for delivering ultra rare disease therapiesWinston YanFocal Administration of AAV Therapies for Severe Neurological DiseasesJosh LeemanSilencing the Critics: Scaling Gene Therapy for Human and Animal HealthDan OliverSolving Gene DeliveryGrand DDyno-bn8, safe and therapeutic gene delivery for muscle gene therapiesAdrian VeresCircular single-stranded DNA: Building the next generation of genetic cargoFloris EngelhardtShuttling precision genetic medicines into the CNS using human TfR1-binding AAV capsidsBen DevermanTRACER Capsid Platform for Systemic Gene Delivery to the CNSMathieu NonnenmacherAmplifying the promise of RNA medicines to empower genetic agencyCory SagoAI-powered drug delivery: Unlocking programmable scienceYogev DebbiRedefining Gene Delivery Through Plant-Based ManufacturingDaniel GibbsManufacturing agency via scalable methodsGaurav VenkataramanGenetic Information & InterventionGrand EIntroduction to SessionEric KelsicAI-Programmable Gene Insertion: A Path to Genetic Agency for AllJohn FinnGenetic medicine platforms at the AAV-RNA InterfaceAravind AsokanAgency begins with knowing what to doMartin Borch JensenMassively Multiplexed In Vivo Screening of AI-Designed Proteins Enables Programmable Tissue TargetingPierce OgdenThe future of genetic medicine: smarter platforms, broader access, deeper impactFederico MingozziFunction-First Biologics Engineering in the Era of Genetic AgencyEmma WestGenetic agency through programmable biology toolsJonathan Gootenberg & Omar AbudayyehFireside ChatEric Kelsic, George Church & Kevin DaviesAI meets Genetic AgencyCommonwealth A+BIntroduction to AI for genetic agencySam SinaiAccelerating the pace of scientific discoveryDaniel BurkhardtTreating cancer like the polygenic disease that it isNima AlidoustModeling missense variants to gain insight into causal human biologyHilary FinucaneAdvancing Genetic Agency via Programmable BiologicsPranam ChatterjeeBoltzGen: Toward Universal Binder DesignHannes StärkDemocratizing gene editing with AIHilary EatonScaling generative models for functional protein designAva AminiCode to Cure: Build Models, Agents, AI-XR Co-scientists to Drive Biomedical InnovationLe CongInnovation and Genetic Agency in the Age of AIAndrew GiesselPanel Discussion: The role of AI agents in the future of discovery, development and technologies that enable genetic agencyFay Lin, Le Cong, Andrew Giessel, Elahe Vedadi & David Levy-Booth12:50 - 1:50pm
Buffet LunchFoyerGrand A + B1:50 - 2:10pm
AI & Genetic AgencyGeorge ChurchGrand A + B2:10 - 2:30pm
Three Eras of Genetic Medicine: Creating the PathSylke PoehlingGrand A + B2:30 - 3:40pm
Roundtable ConversationsFor the detailed list of roundtable topics click hereGrand A + B3:40 - 4:00pm
Break4:00 - 4:30pm
Fireside ChatVictoria Gray & Eric KelsicGrand A+B4:30 - 4:50pm
The Parents’ Journey Through Drug Development: The Angelman Syndrome story of making the impossible possibleAllyson BerentGrand A+B4:50 - 5:20pm
Reflections and ClosingEric Kelsic & Misha GloubermanGrand A+B5:20 - 7:00pm
Reception and Happy HourFoyer