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SFARI Gene
 
SFARI Gene: A Gene Reference Resource for Autism Research

Recent advances in research on Autism Spectrum Disorders (ASD) is uncovering putative candidate genes and loci at an accelerated pace. To address the genetic complexity of ASD, we have developed SFARI Gene, a publicly available web-portal for on-going collection, manual annotation, and visualization of genes linked to the disorder from the published literature.

We present a disease-driven database model in SFARI Gene where all genes connected to ASD are assembled from various genetic categories: candidates identified from genetic association studies, rare single gene mutations, and genes linked to syndromic autism. Genes are richly annotated for their relevance to ASD, along with in-depth annotation providing current knowledge of gene functions. The main focus of this resource is to provide an up-to-date, annotated list of ASD candidate genes in the form of reference datasets. Our goal is to capture a comprehensive view of the rapidly evolving field of autism genetics.

A recent paper describes the methodology behind SFARI Gene.

 

What Is SFARI Gene?
sfari gene microarray

Launched in 2008, SFARI Gene is the world's first genetic database for autism. Continuously updated by a team of curators, the database allows researchers to search for genes that have been linked to autism in the peer-reviewed scientific literature.

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