SFARI 2020 Research awardees announced

Neural signals. Multielectrode arrays (MEA) are able to identify mutation-specific phenotypes in neuronal networks, such as those generated from human induced pluripotent stem cells (hiPSCs). Correction of aberrant phenotypes on MEA is one of several platforms that awardees Michael Boland and Wayne Frankel will use to test therapeutic efficacy in mice and hiPSC models of STXBP1 haploinsufficiency. Image credit: Andrew Ressler/Boland lab

The Simons Foundation Autism Research Initiative (SFARI) is pleased to announce that it intends to fund eight grants in response to the 2020 Research Award request for applications (RFA).

The grants awarded in response to this RFA will support research that investigates genetic and epigenetic mechanisms, neural circuits changes and the development of genetic therapies in autism spectrum disorder (ASD).

SFARI intends to provide approximately $9 million in funding over the next four years to 11 investigators as part of this award program.

“Congratulations to all of the investigators who’ve received funding in this cycle,” says SFARI director Louis Reichardt. “These research projects promise to move the field forward by answering important open questions, and we look forward to hearing about the findings in the coming years.”

Awardee Michael Boland, an assistant professor at Columbia University Medical Center, says: “Now that many ASD risk variants have been identified, an important next step is to test the efficacy of different therapeutic approaches based on these findings. My lab, together with Wayne Frankel’s at Columbia University Irving Medical Center, will use our SFARI funding to develop and test multiple genetic therapy approaches for the ability to correct phenotypes in cellular and mouse models of STXBP1 haploinsufficiency. We expect that this research will help identify a path forward to improve outcomes for individuals with these genetic changes and their families.”

The projects that SFARI intends to fund in this cycle include:

Michael Boland, Ph.D. and Wayne Frankel, Ph.D. (Columbia University Medical Center)
Development of genetic therapies for STXBP1 haploinsufficiency

Dan Feldman, Ph.D. (University of California, Berkeley)
Population coding in sensory cortex in multiple mouse models of autism

Andreas Frick, Ph.D. (INSERM, University of Bordeaux) and Stefan H. Heinemann, Ph.D. (Friedrich-Schiller-Universität Jena)
Targeting neocortical alterations to improve atypical sensory experience in mouse and human ASD models

Michael Greenberg, Ph.D. (Harvard Medical School)
Neuronal activity-dependent chromatin remodeling in autism neurobiology

Jingjing Li, Ph.D. and Arnold Kriegstein, M.D., Ph.D. (University of California, San Francisco)
Identifying the altered gene regulatory networks at single-cell resolution along the trajectory of brain development in autism spectrum disorders

Gaia Novarino, Ph.D. (Institute of Science and Technology Austria)
Critical windows and reversibility of ASD associated with mutations in chromatin remodelers

Benjamin Philpot, Ph.D. (University of North Carolina at Chapel Hill)
Neuron type-specific roles of UBE3A: E-I imbalance and seizures

Elise Robinson, Sc.D. (Broad Institute, Harvard T.H. Chan School of Public Health)
Characterizing the convergent molecular mechanisms of common and rare ASD-associated genetic variation

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