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Simons Foundation
Simons Foundation

Autism Research Initiative (SFARI)

  • Funding

    Explore open funding opportunities for autism research.

    Funding Opportunities

    Early Career Awards

    • Fellows to Faculty Award
    • Shenoy Undergraduate Research Fellowship in Neuroscience (SURFiN)

    Investigator Awards

    • New Ideas

    Symposia & Travel Awards

    • Conferences & Courses Award

    Shared Programs

    • Pivot Fellowship
    • Simons Society of Fellows

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    • Open Funding Opportunities
    • Policies & Procedures
    • Instructional Videos
    • Past Funded Work
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    SFARI has supported over 750 investigators studying autism-related research.

    Research Highlights

    Research

    • SFARI Investigators
    • Funded Projects
    • Publications

    Data Access & Tools

    • SFARI Base
    • SFARI Gene

    Centers & Initiatives

    • Simons Center for the Social Brain
    • Simons Initiative for the Developing Brain

    Collaborations & Consortia

    • SFARI Sex Differences
    • Autism Rat Models Consortium
  • Resources

    Access data, biospecimens and participant cohorts through SFARI Base.

    SFARI Base

    Cohorts & Tissue Banks

    • SPARK
    • Simons Searchlight
    • Simons Simplex Collection
    • Autism BrainNet
    • Autism Inpatient Collection

    Other Resources

    • Animal Models
    • Biospecimens
    • Research Match

    Data Access & Tools

    • SFARI Base
    • SFARI Gene
    • SFARI Genomes Browser
    • Genotypes & Phenotypes in Families
  • News

    See the latest news and updates from SFARI.

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    SFARI’s mission is to advance the basic science of autism and related neurodevelopmental disorders.

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Autism Research Initiative (SFARI) Research

Research: Funded Publications

Explore publications and preprints from SFARI-funded investigators and researchers using SFARI-supported data and resources.

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  1. Keeping time in the brain: Autism spectrum disorder and audiovisual temporal processing.

    Autism Res., June 30, 2016

    Stevenson R.A., Segers M., Ferber S., Barense M.D., Camarata S., and M. Wallace

  2. SHANK3 controls maturation of social reward circuits in the VTA.

    Nat. Neurosci., June 30, 2016

    Bariselli S., Tzanoulinou S., Glangetas C., Prévost-Solié C., Pucci L., Viguié J., et al.

  3. Deletion and duplication of 16p11.2 are associated with opposing effects on visual evoked potential amplitude.

    Mol. Autism, June 26, 2016

    LeBlanc J.J. and C. Nelson

  4. Persistent neuronal UBE3A expression in the suprachiasmatic nucleus of Angelman syndrome model mice.

    Sci. Rep., June 15, 2016

    Jones K.A., Han J.E., DeBruyne J.P., and B. Philpot

  5. Central amygdala somatostatin neurons gate passive and active defensive behaviors.

    J. Neurosci., June 14, 2016

    Yu K., Garcia da Silva P., Albeanu D.F., and B. Li

  6. SMASH, a fragmentation and sequencing method for genomic copy number analysis.

    Genome Res., May 31, 2016

    Wang Z., Andrews P., Kendall J., Ma B., Hakker I., Rodgers L., et al.

  7. Relationship between M100 auditory evoked response and auditory radiation microstructure in 16p11.2 deletion and duplication carriers.

    AJNR Am. J. Neuroradiol., May 31, 2016

    Berman J.I., Chudnovskaya D., Blaskey L., Kuschner E., P. Mukherjee, S. Nagarajan, et al.

  8. High frequency stimulation at the subthalamic nucleus suppresses excessive self-grooming in autism-like mouse models.

    Neuropsychopharmacology, May 31, 2016

    Chang A.D., Berges V.A., Chung S.J., Fridman G.Y., Baraban J.M., and I. Reti

  9. Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.

    Mol. Psychiatry, May 30, 2016

    Loviglio M.N., Leleu M., Männik K., Passeggeri M., Giannuzzi G., van der Werf I., et al.

  10. Neural circuits underlying mother's voice perception predict social communication abilities in children.

    Proc. Natl. Acad. Sci. USA, May 30, 2016

    Abrams D.A., Chen T., Odriozola P., Cheng K.M., Baker A.E., Padmanabhan A., et al.

  11. Transcriptome analysis of cortical tissue reveals shared sets of downregulated genes in autism and schizophrenia.

    Transl. Psychiatry, May 23, 2016

    Ellis S.E., Panitch R., West A.B., and D. Arking

  12. 22q11.2 duplication syndrome: Elevated rate of autism spectrum disorder and need for medical screening.

    Mol. Autism, May 5, 2016

    Wenger T.L., Miller J.S., DePolo L.M., de Marchena A.B., Clements C.C., Emanuel B.S., et al.

  13. Transgenic labeling of parvalbumin-expressing neurons with tdTomato.

    Neuroscience., May 2, 2016

    Kaiser T., Ting J.T., Monteiro P., and G. Feng

  14. Cellular correlates of selfish spermatogonial selection.

    Andrology, April 30, 2016

    Maher G.J., Rajpert-De Meyts E., A. Goriely, and Wilkie A.O.

  15. 16p11.2 locus modulates response to satiety before the onset of obesity.

    Int. J. Obes. (Lond.), April 30, 2016

    Maillard A.M., Hippolyte L., Rodriguez-Herreros B., Chawner S.J., Dremmel D., Agüera Z., et al.

  16. Auditory evoked M100 response latency is delayed in children with 16p11.2 deletion but not 16p11.2 duplication.

    Cereb. Cortex, April 30, 2016

    Jenkins J. 3rd, Chow V., Blaskey L., Kuschner E., Qasmieh S., Gaetz L., et al.

  17. Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.

    Nat. Genet., April 30, 2016

    E. Robinson, B. St Pourcain, Anttila V., Kosmicki J.A., Bulik-Sullivan B., Grove J., et al.

  18. Brief report: Further examination of self-injurious behaviors in children and adolescents with autism spectrum disorders.

    J. Autism Dev. Disord., April 30, 2016

    Dempsey J., Dempsey A.G., Guffey D., Minard C.G., and R. Goin-Kochel

  19. Neocortical neurogenesis and the etiology of autism spectrum disorder.

    Neurosci. Biobehav. Rev., April 30, 2016

    A. Packer

  20. Maternal loss of UBE3A impairs experience-driven dendritic spine maintenance in the developing visual cortex.

    J. Neurosci., April 26, 2016

    Kim H., Kunz P.A., Mooney R., B. Philpot, and Smith S.L.

  21. Neurobiology of social behavior abnormalities in autism and Williams syndrome.

    Nat. Neurosci., April 25, 2016

    Barak B. and G. Feng

  22. CNView: a visualization and annotation tool for copy number variation from whole-genome sequencing.

    bioRxiv, April 20, 2016

    Collins R.L., Stone M.R., Brand H., Glessner J.T., and M. Talkowski

  23. Putative microcircuit-level substrates for attention are disrupted in mouse models of autism.

    Biol. Psychiatry, April 14, 2016

    Luongo F.J., Horn M.E., and V. Sohal

  24. The genetics-driven revival in neuropsychiatric drug development.

    Biol. Psychiatry, April 14, 2016

    M. Gandal and D. Geschwind

  25. Sex differences in cerebellar synaptic transmission and sex-specific responses to autism-linked GABRB3 mutations in mice.

    Elife, April 13, 2016

    Mercer A.A., Palarz K.J., Tabatadze N., Woolley C.S., and I. Raman

  26. Robust classification of protein variation using structural modelling and large-scale data integration.

    Nucleic Acids Res., April 6, 2016

    Baugh E.H., Simmons-Edler R., Müller C.L., Alford R.F., N. Volfovsky, and Bonneau R.

  27. Thalamic reticular impairment underlies attention deficit in PTCHD1Y/- mice.

    Nature, April 6, 2016

    Wells M.F., Wimmer R.D., Schmitt L.I., G. Feng, and M. Halassa

  28. Frequency and complexity of de novo structural mutation in autism.

    Am. J. Hum. Genet., April 6, 2016

    Brandler W.M., Antaki D., Gujral M., Noor A., Rosanio G., Chapman T.R., et al.

  29. GABAergic neuron-specific loss of UBE3A causes Angelman syndrome-like EEG abnormalities and enhances seizure susceptibility.

    Neuron, April 5, 2016

    Judson M.C., M. Wallace, Sidorov M.S., Burette A.C., Gu B., van Woerden G.M., et al.

  30. Clinical phenotype of the recurrent 1q21.1 copy-number variant.

    Genet. Med., March 31, 2016

    R. Bernier, Steinman K.J., Reilly B., Wallace A.S., E. Sherr, Pojman N., et al.

  31. Is there concordance in attitudes and beliefs between parents and scientists about autism spectrum disorder?

    Autism, March 31, 2016

    Fischbach R.L., Harris M.J., Ballan M.S., G. Fischbach, and Link B.G.

  32. An expanded sequence context model broadly explains variability in polymorphism levels across the human genome.

    Nat. Genet., March 31, 2016

    Aggarwala V. and Voight B.F.

  33. No difference in cross-modal attention or sensory discrimination thresholds in autism and matched controls.

    Vision Res., March 31, 2016

    Haigh S.M., Heller L.M., A. Gupta, I. Dinstein, Minshew N.J., and M. Behrmann

  34. Anatomical abnormalities in autism?

    Cereb. Cortex, March 31, 2016

    Haar S., Berman S., M. Behrmann, and I. Dinstein

  35. Feedback modulation of neural network synchrony and seizure susceptibility by Mdm2-p53-Nedd4-2 signaling.

    Mol. Brain, March 21, 2016

    Jewett K.A., Christian C.A., Bacos J.T., K. Lee, Zhu J., and N. Tsai

  36. Unifying views of autism spectrum disorders: A consideration of autoregulatory feedback loops.

    Neuron, March 15, 2016

    Mullins C., G. Fishell, and R. Tsien

  37. Prenatal neurogenesis in autism spectrum disorders.

    Front. Chem., March 14, 2016

    Kaushik G. and K. Zarbalis

  38. Disruption of POGZ is associated with intellectual disability and autism spectrum disorders.

    Am. J. Hum. Genet., March 2, 2016

    H. Stessman, Willemsen M.H., Fenckova M., Penn O., Hoischen A., Xiong B., et al.

  39. Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.

    BMC Genomics, March 1, 2016

    Tao Y., Gao H., Ackerman B., Guo W., Saffen D., and Shugart Y.Y.

  40. Altered functional connectivity networks in acallosal and socially impaired BTBR mice.

    Brain Struct. Funct., March 1, 2016

    Sforazzini F., Bertero A., Dodero L., David G., Galbusera A., Scattoni M.L., et al.

  41. Language differences at 12 months in infants who develop autism spectrum disorder.

    J. Autism Dev. Disord., February 29, 2016

    Lazenby D.C., Sideridis G.D., Huntington N., Prante M., Dale P.S., Curtin S., et al.

  42. Understanding the experience of stigma for parents of children with autism spectrum disorder and the role stigma plays in families' lives.

    J. Autism Dev. Disord., February 29, 2016

    Kinnear S.H., Link B.G., Ballan M.S., and Fischbach R.L.

  43. Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.

    Nat. Neurosci., February 29, 2016

    Tai D.J., Ragavendran A., Manavalan P., Stortchevoi A., Seabra C.M., Erdin S., et al.

  44. Visualization of cortical, subcortical and deep brain neural circuit dynamics during naturalistic mammalian behavior with head-mounted microscopes and chronically implanted lenses.

    Nat. Protoc., February 29, 2016

    Resendez S.L., Jennings J.H., Ung R.L., Namboodiri V.M., Zhou Z.C., Otis J.M., et al.

  45. Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes.

    Proc. Natl. Acad. Sci. USA, February 29, 2016

    Maher G.J., McGowan S.J., Giannoulatou E., Verrill C., A. Goriely, and Wilkie A.O.

  46. Enhanced social attention in female infant siblings at risk for autism.

    J. Am. Acad. Child Adolesc. Psychiatry, February 29, 2016

    Chawarska K., Macari S., Powell K., DiNicola L., and F. Shic

  47. The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring.

    Science, February 25, 2016

    G. Choi, Y. Yim, Wong H., Kim S., Kim H., Kim S.V., et al.

  48. Molecular subtyping and improved treatment of neurodevelopmental disease.

    Genome Med., February 24, 2016

    H. Stessman, T. Turner, and E. Eichler

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