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News

Explore the latest from SFARI

  1. SFARI’s 2018 Funding Priorities

  2. New SFARI Gene Website Launched

  3. A Conversation With Sharmila Banerjee-Basu About SFARI Gene

  4. Whole-genome sequencing of the Simons Simplex Collection: New data release

  5. Simons Variation in Individuals Project (Simons VIP): New data release

  6. SFARI July 2017 announcements: Bridge to Independence Award RFA, Recruiting SPARK participants into new research studies and more

  7. A Conversation with SFARI Bridge to Independence Investigator Sung Han

  8. SPARK: Research matching program launched

  9. A SFARI channel on bioRxiv

  10. SFARI May 2017 announcements: SPARK update, new SSC data, IMFAR and more

  11. Simons Simplex Collection: Updated medical and educational data now available

  12. IMFAR 2017: Presentations by SFARI Investigators

  13. SFARI Gene: New data release

  14. Epigenetic mechanisms beyond imprinting are widespread in the mammalian brain

  15. A Conversation with SFARI Investigator Liqun Luo

  16. Simons Foundation statement on executive order on visas and immigration

  17. SCN2A variants result in opposite effects on sodium channel function in autism and infantile seizures

  18. Identification of an amygdala circuit involved in social learning

  19. Gene-gene interactions contribute to autism

  20. SFARI announces Bridge to Independence Award finalists

  21. SFARI Gene: New data release

  22. Simons Variation in Individuals Project (Simons VIP): New data release

  23. SFARI announces 2016 Bridge to Independence Award finalists

  24. SFARI 2016 Explorer awardees announced

  25. A potentially treatable form of autism caused by impaired brain transport of amino acids

  26. SFARI announces 2016 Pilot and Research awardees

  27. SFARI 2016 Pilot and Research awardees announced

  28. Genetic mechanisms underlying physical trait differences between males and females contribute to sex bias in autism

  29. Sequencing Study in a Chinese Cohort Confirms the Importance of De Novo Mutations in Autism

  30. Predicting autism treatment outcome with imaging biomarkers

  31. CASPR2 antibodies from human maternal serum mediate autism-like phenotypes in mice

  32. DIXDC1 contributes to neurodevelopmental and psychiatric phenotypes via altered Wnt signaling

  33. Pathogenic mutations in mitochondrial DNA enriched in autism

  34. SPARK update; SFARI Social at Neuroscience 2016

  35. Neuroscience 2016: Presentations by SFARI Investigators

  36. Microglia-like cells derived from human pluripotent stem cells

  37. Dissecting the neurobehavioral phenotypes caused by loss of RAI1 from specific cell types

  38. Increased risk for autism is associated with mutations in genomic loci that have undergone accelerated evolution in humans

  39. SFARI’s 2017 funding priorities

  40. 2017 Pilot and Research Award applications: The review process

  41. 2017 Pilot and Research Awards – Request for applications

  42. Simons Variation in Individuals Project (Simons VIP): New data now available

  43. Update on Simons Simplex Collection whole-genome sequencing; Rat and iPSC models for autism research

  44. A computational approach to predicting autism risk genes

  45. Deep brain stimulation rescues neural circuit dysfunction in Rett syndrome mouse model

  46. Update on Simons Simplex Collection whole-genome sequencing data availability

  47. Human-specific BOLA2 duplication at chromosomal region 16p11.2 and the susceptibility of this locus to recurrent rearrangements

  48. Microglia excessively engulf synapses weakened by loss of MeCP2