Congratulations to Nadia Wallace, an undergraduate working in Dr. Lawrence T. Reiter’s lab, on being the second...
Latest News
Dup15q Clinical Trial Locations Open
NEW US Dup15q Clinical Trial Location Open: Children's Hospital Los Angeles. Interested in enrolling at CHLA?...
LADDER Family-Friendly Reports
LADDER has some new family-friendly resources that you can view on the LADDER website! In May, LADDER launched a...
6th Annual Big Give Event
Each May our community comes together, as we go LIVE for our annual BIG GIVE event. The BIG GIVE event brings a...
Rare Epilepsy Partnership Award
Dup15q Alliance is proud to be selected for the Cure Epilepsy Rare Epilepsy Partnership Award. This award is co-funded...
Dup15q Alliance Named an Official Charity Partner of the 2023 TCS New York City Marathon
Dup15q Alliance has been Named an Official Charity Partner of the 2023 TCS New York City Marathon Dup15q Alliance has...
The New Year Brings New Changes
Thank you, David Gifford, for your past 4 years of Service to the Dup15q Alliance as Board Chair. "Being the Board...
First New Co-Chairs of the Dup15q Alliance Board
Greetings to our Dup15q families and friends! Lisa Feehery and I are both honored and excited to be taking on the...
Get involved in Rare Disease Day!
February 28, 2023 is the designated “Rare Disease Awareness Day” across the world. Dup15q Syndrome is 1 of 7,000 Rare...
Single gene insufficient to account for dup15q, Angelman traits
BY ANGIE VOYLES ASKHAM / 18 NOVEMBER 2022 Spectrum News: https://doi.org/10.53053/SRCT6791 Multiple genes shape the...
LADDER Database Family-friendly Reports
LADDER Database Family-friendly Reports LADDER shares de-identified information (which means it cannot be traced back...
CNV Road Map
Neurodevelopmental copy-number variants: A roadmap to improving outcomes by uniting patient advocates, researchers,...