Research by Topic: dup15q

AGENDA’s First Initiative is a Unified Registry of Family Data

Published October 17, 2018

Today, ASF announced that it will be leading the newly-launched Alliance for Genetic Etiologies of Neurodevelopmental Disorders and Autism (AGENDA). This alliance is a partnership of research and advocacy organizations focused on improving outcomes of individuals with all forms of autism by fostering a genetics-first approach to autism science. AGENDA will also work to strengthen […]

Filed under: ASD, asf, Autism, collaboration, database, dup15q, Dup15q Alliance, featured, fragile X syndrome, FRAXA, FRAXA Research Foundation, genetic, Phelan-McDermid Syndrome, Phelan-Mcdermid Syndrome Foundation, PMSF, registry, research, Rett Syndrome, Rett Syndrome Research Trust, RSRT, science, SFARI, Simons Foundation, Simons VIP, subtypes, TSA, Tuberous Sclerosis, Tuberous Sclerosis Alliance

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Dup15q Alliance Fellowship Opportunity

Published May 23, 2017

The Dup15q Alliance is offering pre- and postdoctoral fellowships to individuals studying basic science or clinical research on mutations of chromosome 15. People with mutations in a specific region of chromosome 15 also show a high prevalence of #autism and applications to investigate autism associated with Dup15 are welcomed. Applications are due by June 1st. […]

Filed under: application, Autism, dup15q, featured, fellowship, grant

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