From Possibility to Progress: A New Era in SMS Research

For years, families living with Smith Magenis Syndrome have waited for more than symptom management—for a path toward treatments that address the biology of SMS itself. Today, that path is beginning to emerge. Our new Spring Appeal shares why this moment in SMS research is different, how advances centered around the RAI1 gene are creating new possibilities, and why the next several years could be transformational for the SMS community. This is a moment where science, urgency, and opportunity are converging—and what we do now matters. Read our full letter here and learn how you can help accelerate the future of SMS research. Read More


2025 Year In Review – SAP Chair Message

At the SMSRF, our research strategy is built around one goal: turning strong science into meaningful impact for individuals living with SMS and their families. Because SMS biology is complex, and because families deserve progress that is both real and durable, we focus on supporting work that is scientifically rigorous, strategically chosen, and aligned with a clear long-term path toward therapies. Read More


2025 Year In Review – President’s Message

Fifteen years ago, the Smith-Magenis Syndrome Research Foundation was founded on the belief that families, clinicians, and researchers working together could move the science forward and improve the lives of individuals living with Smith-Magenis syndrome. For many of us, this mission is deeply personal, shaped by the daily realities of loving and supporting someone with SMS. Read More


Stanford University Project

Two World-Class Institutions, One Goal: A Breakthrough for Smith-Magenis SyndromeDr. Wei-Hsiang Huang (McGill University) and Dr. Xiaojing Gao (Stanford University)... Read More


Announcing Our New Executive Director

After an extensive search process, led by members of the Board of Directors, we are pleased to announce that Angela Weaver has been selected as Executive Director, beginning January 2023.