New data were added to SFARI Gene in April 2018. This data release included updated gene scores for candidate autism risk genes, as well as the addition of new genes, animal models, and copy number variant loci associated with autism.
News
Subscribe to our newsletter and receive SFARI funding announcements and news
New Simons VIP Phase 2 data were recently added to SFARI Base. This data release included data from individuals with 16p11.2 copy number variants (CNVs), 1q21.1 CNVs and mutations in the following single genes: ADNP, ASXL3, DYRK1A, FOXP1, GRIN2B, HIVEP2, MED13L, PACS1, PPP2R5D, SCN2A, SETBP1, STXBP1 and SYNGAP1.
SFARI announces the launch of HumanBase, a Simons Foundation interactive web server for predictions and information about human genes, pathways and disorders.
SFARI announces that a new article summarizing the first year’s activities of SPARK — a SFARI-funded study that aims to recruit, engage and retain 50,000 individuals with autism spectrum disorder (ASD) and their family members — was published in the journal Neuron.
SFARI is happy to announce a new addition to the gene-scoring module of SFARI Gene: scores and rankings from an additional six published approaches to evaluating the strength of the evidence implicating each gene in autism risk.
SFARI is pleased to announce that it has awarded 13 grants in response to the Explorer Awards request for applications this year.
SFARI is pleased to announce that it has selected seven finalists in response to the 2017 Bridge to Independence Award request for applications.
New data were added to SFARI Gene in October 2017. This data release included updated gene scores for candidate autism risk genes, new rodent models and new genes and copy number variant loci associated with autism.
- Previous Page
- Viewing
- Next Page