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Research by Topic: dup15q
AGENDA’s First Initiative is a Unified Registry of Family Data
Published October 17, 2018Today, 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
Dup15q Alliance Fellowship Opportunity
Published May 23, 2017The 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