Dup15q Alliance is proud to be selected for the Cure Epilepsy Rare Epilepsy Partnership Award. This award is co-funded...
Research Updates
Consistent, convergent pathways link two forms of autism
Consistent, convergent pathways link two forms of autism BYÂ ANGIE VOYLES ASKHAMÂ / Spectrum News /Â 15 NOVEMBER...
Single gene insufficient to account for dup15q, Angelman traits
Single gene insufficient to account for dup15q, Angelman traits BYÂ ANGIE VOYLES ASKHAMÂ Â /Â Spectrum News / 18...
Ciitizen Research Opportunity
Ciitizen Research Opportunity Dup15q Alliance has been presented with a new opportunity provided by Invitae, a leading...
CANDID Conference Presentations Are Available Online
Consortium for Autism, Neurodevelopmental Disorders & Digestive Diseases (CANDID) is a  collaboration between...
CURE Epilepsy Partnership Grant for Dup15q!
Calling Dup15q Researchers, we are excited to be part of the CURE Epilepsy Partnership Grant. CURE Epilepsy...
Sign up for Text Alerts
Big things are coming and we don't want you to miss them! Sign up for our NEW Research and Clinical Trial Text Alerts!...
First complete sequence of the human genome
We are so excited about the recent announcement of the first complete sequence of the human genome. The complete...
LADDER Learning Network
Dup15q Alliance and Angelman Syndrome Foundation partner to launch the LADDER Learning Network, showing continued...
ASF/Dup15q Science Symposium
The Dup15q Alliance Research Symposium is the largest dup15q specific research meeting in the world. The Symposium...
Copy number variants’ impact on autism
Source: Spectrum News Population study downgrades some copy number variants’ impact on autism BY CHARLES Q....
Dup15q in the News! New test to screen newborns…..
New test to screen newborns for rare genetic disorders paves the way for earlier diagnosis and treatment....