Speaker Profile
Biography
Timothy Yu, MD, PhD, is recognized as a leader in the field of gene therapy, particularly in the development of personalized gene therapies for individuals with rare genetic disorders. A graduate of Harvard College, he completed MD-PhD training at UCSF, neurology residency at Massachusetts General Hospital and Brigham and Women’s Hospital, and a fellowship in neurogenetics at Boston Children’s Hospital. He joined the faculty of Boston Children’s Hospital in the Division of Genetics and Genomics in 2013. He is also an Associate Member at the Broad Institute Dr. Yu’s research group works at the intersection of genomics, informatics, and neurobiology with a focus on understanding and treating disorders of brain development. He was an early pioneer in methodology for genome sequencing and interpretation, which he applied to discover genes responsible for brain development and autism. He is also recognized for having developed the world’s first individualized genomic medicine: milasen, an antisense oligonucleotide targeting a unique genetic mutation causing a child’s fatal neurodegenerative condition – in under one year. Milasen was the first in a pilot series of individualized therapeutics for severe neurogenetic conditions that his team has since created. It also inspired efforts to advance individualized therapeutics for dozens of neglected genetic conditions worldwide, including the N-of-1 Collaborative, an international coalition founded by Dr. Yu to advance scientific, regulatory, and ethical best practices for this budding field. Dr. Yu has authored more than 80 scientific publications and has been recognized with numerous awards and honors, including the NORD Rare Impact Award, the Global Genes Rare Champion award, and the ANA Denny-Brown Young Neurologic Scholar award. He is dedicated to advancing precision medicine and improving patient outcomes through his research and clinical practice.
Session Abstract – PMWC 2027 Silicon Valley
Track Chair:
Catriona Jamieson, UC San Diego
PMWC Award Ceremony
• Emmanuelle Charpentier, Max Planck (J. Craig Venter Visionary Award · Nobel Laureate)
• Jay Bradner, Amgen (Pioneer)
• Adrian Krainer, Cold Spring Harbor Laboratory (Luminary)
• Randy Schekman, UC Berkeley (Nobel Laureate, Pioneer)
Featured Speakers
• Emmanuelle Charpentier, Max Planck
• Randy Schekman, UC Berkeley
• Jay Bradner, Amgen
• Adrian Krainer, Cold Spring Harbor Laboratory
• Alexis C. Komor, UC San Diego
• Nicole Gaudelli, GV
• Rachel Haurwitz, Caribou Bio
• Gene Yeo, UC San Diego
• Timothy Yu, Boston Children's / Harvard
• Shicheng Guo, Arrowhead Pharmaceuticals
• Mark A. Kay, Stanford
• Niren Murthy, UC Berkeley
• Ben Deverman, Broad Institute
• Stanley Crooke, n-Lorem / Ionis
Programming Protein Fate
Molecular glues, degraders, and induced proximity crossing into medicines.
Genome Editing Beyond the First Wave
Base, prime, and CRISPR-enabled editing moving from correction to clinic.
RNA Editing, Splice Modulation & Programmable RNA
RNA editing, ASOs, and splice modulation with chemistry already reaching patients.
In Vivo Delivery & Vector Engineering
AAV, LNP, and next-generation vectors that decide what is treatable.
From N-of-1 to Platform
Evidence, CMC, regulation, and access for individualized genetic medicines.
PMWC Hall of Impact
Previous Speakers Include
Nobel laureates, technology founders, regulators, CEOs and scientific pioneers who have taken the PMWC stage.