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News

Explore the latest from SFARI

  1. High-Resolution Rodent Movement Tracking Provides the Opportunity To Link Autism Risk Genes With Behavioral Presentations

  2. A Machine-Learning Framework for Prioritizing Disease-Associated Enhancers

  3. SFARI Gene To Introduce EAGLE, a New ASD-Relevance Gene Scoring System

  4. Altered Hormone Signaling in the Brainstem Causes Motor Delays in 16p11.2 Mice

  5. RhoA Overactivation May Underlie Smaller Brain Volumes in Cul3 Mutant Mice

  6. Tandem Repeat Mutations in Autism

  7. Perceptual Impairments and Altered Excitatory–Inhibitory Activity in Cntnap2 Knockout Mice

  8. Fetal Responses to Maternal Infection May Help Explain Prevalence of Autism in Males

  9. Study Using SPARK Data Uncovers New Inherited Genetic Risks for Autism

  10. Probing the Neural Circuits of Social Interactions in Monkeys

  11. Excessive Dendritic Spine Clusters in MECP2 Duplication Syndrome Mouse Model

  12. Large Cohorts Aid in Genotype-Phenotype Analyses

  13. Sensory Habituation Is Reduced in Autism

  14. Rare Inherited Variants in Previously Unsuspected Genes May Confer Significant Risk for Autism

  15. Impaired Long–Range Communication and Reduced Anxiety–Related Behavior in Pogz Deficient Mice

  16. Pupil Responses Predict Reward Sensitivity and Autism Status

  17. Cellular System To Screen ASD Risk Gene Function

  18. 2021 Autism BrainNet Appreciation Award: Recipients Announced

  19. Mitochondrial Deficiency and Fragile X Syndrome

  20. Neural Circuitry of Sociability in Mice

  21. Sex Differential Effects of Excitation-Inhibition Imbalance in Autism

  22. ASD Risk Genes and Homeostatic Plasticity

  23. Parental Influence on Language Development in Infants at High and Low Risk for Autism

  24. Mutations in ACTL6B Are Linked to a Form of Recessive Autism

  25. MeCP2 and VIP-Interneurons

  26. Role of WNT Signaling in Tbr1-Mutant Phenotypes

  27. Functional Impact of PTEN Missense Mutations

  28. Molecular Mechanisms of Fragile X Syndrome

  29. Microexon Splicing and Translation in ASD

  30. First 1,000 Participants in RI-CART Study

  31. Foxp1 and the Striatum

  32. Paraventricular Oxytocin Neurons Support Social Behavior

  33. USP9X Mutation Defines a Neurodevelopmental Syndrome

  34. Exome Sequencing Identifies New ASD Risk Genes

  35. Shank3 Is Necessary for Homeostatic Plasticity

  36. Shank3 Mutation R1117X Affects Interneuron Function

  37. C. elegans Screen for ASD Risk Gene–Associated Phenotypes

  38. Cell-Type-Specific Effects of Loss of Autophagy in the Striatum

  39. Genetic Mutations Linked to Kleefstra Syndrome Converge on Similar Neuronal Hyperactivity Phenotypes

  40. Autism Spectrum Disorder Risk Assessment Through Quantification of Sperm Mosaicism

  41. Neural Encoding of Social Signals in Mice

  42. Neuroimmune Mechanisms in Autism Mouse Models

  43. Noise Hypersensitivity in PTCHD1-Associated ASD

  44. Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder Have a Similar Profile of Rare Mutations

  45. T-Lymphocytes Target Astrocytes in the Postmortem Autism Brain

  46. Binocular Rivalry: A Noninvasive Biomarker of Inhibitory Signaling in the Brain?

  47. Modulating the Expression and Activity of the Potassium-Chloride Cotransporter KCC2

  48. Allelic Imbalance in ASD-Associated Gene Expression