Research Updates
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 Stats
LADDER Saturday Stats from the LADDER Database Today’s Saturday Stat: Nearly 45% of dup15q participants in LADDER are...
Progress on the 15q Newborn Screening
Progress on the 15q Newborn Screening Just 11 short months ago, Dup15q Alliance, Foundation for Prader Willi Syndrome...
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,...
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...
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