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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

    Resource for Applying

    • Open Funding Opportunities
    • Policies & Procedures
    • Instructional Videos
    • Past Funded Work
  • Supported Work

    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) Autism Rat Models Consortium

Autism Rat Models Consortium: Publications

From ARC

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Results

  1. A framework for the interpretation of de novo mutation in human disease.

    Nat. Genet., August 31, 2014

    K. Samocha, E. Robinson, S. Sanders, Stevens C., Sabo A., McGrath L.M., et al.

  2. The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism.

    Am. J. Med. Genet. C Semin. Med. Genet., August 31, 2014

    Vandeweyer G., Helsmoortel C., Van Dijck A., Vulto-van Silfhout A.T., Coe B.P., R. Bernier, et al.

  3. Opposing brain differences in 16p11.2 deletion and duplication carriers.

    J. Neurosci., August 19, 2014

    Qureshi A.Y., Mueller S., Snyder A.Z., P. Mukherjee, Berman J.I., T. Roberts, et al.

  4. Dysfunctional dopaminergic neurotransmission in asocial BTBR mice.

    Transl. Psychiatry, August 18, 2014

    Squillace M., Dodero L., Federici M., Migliarini S., Errico F., Napolitano F., et al.

  5. Plasma oxytocin concentrations and OXTR polymorphisms predict social impairments in children with and without autism spectrum disorder.

    Proc. Natl. Acad. Sci. USA, August 18, 2014

    K. Parker, Garner J.P., Libove R.A., Hyde S.A., Hornbeak K.B., Carson D.S., et al.

  6. Microglia function during brain development: New insights from animal models.

    Brain Res., August 14, 2014

    Bilimoria P.M. and B. Stevens

  7. Facial emotion recognition in agenesis of the corpus callosum.

    J. Neurodev. Disord., August 13, 2014

    Bridgman M.W., Brown W.S., Spezio M.L., Leonard M.K., and Paul L.K.

  8. Testing the accuracy of an observation-based classifier for rapid detection of autism risk.

    Transl. Psychiatry, August 11, 2014

    Duda M., Kosmicki J.A., and D. Wall

  9. CC2D1A regulates human intellectual and social function as well as NF-kappaB signaling homeostasis.

    Cell Rep., August 6, 2014

    Manzini M.C., Xiong L., Shaheen R., Tambunan D.E., Di Costanzo S., Mitisalis V., et al.

  10. Violations of personal space by individuals with autism spectrum disorder.

    PLoS One, August 5, 2014

    Kennedy D.P.

  11. Longitudinal patterns of repetitive behavior in toddlers with autism.

    J. Child Psychol. Psychiatry, July 31, 2014

    Wolff J.J., K. Botteron, S. Dager, J. Elison, Estes A.M., Gu H., et al.

  12. No increase in autism associated genetic events in children conceived by assisted reproductive technology.

    Fertil. Steril., July 31, 2014

    Ackerman S., Wenegrat J., Rettew D., Althoff R., and R. Bernier

  13. Neurons in the human amygdala selective for perceived emotion.

    Proc. Natl. Acad. Sci. USA, July 28, 2014

    Wang S., Tudusciuc O., Mamelak A.N., Ross I.B., and Rutishauser U.

  14. Optogenetic insights on the relationship between anxiety-related behaviors and social deficits.

    Front. Behav. Neurosci., July 15, 2014

    Allsop S.A., Vander Weele C.M., Wichmann R., and Tye K.M.

  15. Disruptive CHD8 mutations define a subtype of autism early in development.

    Cell, July 13, 2014

    R. Bernier, Golzio C., Xiong B., H. Stessman, Coe B.P., Penn O., et al.

  16. CNTNAP4 differentially contributes to GABAergic and dopaminergic synaptic transmission.

    Nature, July 9, 2014

    Karayannis T., Au E., Patel J.C., Kruglikov I., Markx S., Delorme R., et al.

  17. Beta2-adrenergic receptor agonist ameliorates phenotypes and corrects microRNA-mediated IGF1 deficits in a mouse model of Rett syndrome.

    Proc. Natl. Acad. Sci. USA, July 7, 2014

    Mellios N., Woodson J., Garcia R.I., Crawford B., Sharma J., Sheridan S.D., et al.

  18. Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome.

    Proc. Natl. Acad. Sci. USA, July 7, 2014

    Castro J., Garcia R.I., Kwok S., Banerjee A., Petravicz J., Woodson J., et al.

  19. Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors.

    Cell, July 2, 2014

    Rothwell P.E., Fuccillo M.V., Maxeiner S., Hayton S.J., Gokce O., Lim B.K., et al.

  20. Developmental regression among children with autism spectrum disorders: Onset, duration, and effects on functional outcomes.

    Res. Autism Spectr. Disord., July 1, 2014

    R. Goin-Kochel, Esler A.N., S. Kanne, and Hus V.

  21. Emotion dysregulation and the core features of autism spectrum disorder.

    J. Autism Dev. Disord., June 30, 2014

    Samson A.C., Phillips J.M., K. Parker, Shah S., Gross J.J., and A. Hardan

  22. Largely typical patterns of resting-state functional connectivity in high-functioning adults with autism

    Cereb. Cortex, June 30, 2014

    Tyszka J.M., Kennedy D.P., and Paul L.K.

  23. Natural neural projection dynamics underlying social behavior.

    Cell, June 18, 2014

    Gunaydin L.A., Grosenick L., Finkelstein J.C., Kauvar I.V., Fenno L.E., Adhikari A., et al.

  24. Unlocking epigenetic codes in neurogenesis.

    Genes Dev., June 14, 2014

    Yao B. and P. Jin

  25. A role for dendritic mGluR5-mediated local translation of ARC/ARG3.1 in MEF2-dependent synapse elimination.

    Cell Rep., June 11, 2014

    Wilkerson J.R., N. Tsai, Maksimova M.A., Wu H., Cabalo N.P., Loerwald K.W., et al.

  26. Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.

    Am. J. Hum. Genet., June 4, 2014

    Blumenthal I, Ragavendran A., Erdin S., Klei L., Sugathan A., Guide J.R., et al.

  27. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

    Autism Res., May 31, 2014

    P. Chaste, S. Sanders, Mohan K.N., Klei L., Song Y., Murtha M.T., et al.

  28. Brief report: Arrested development of audiovisual speech perception in autism spectrum disorders.

    J. Autism Dev. Disord., May 31, 2014

    Stevenson R.A., Siemann J.K., Woynaroski T.G., Schneider B.C., Eberly H.E., Camarata S.M., et al.

  29. The autism brain imaging data exchange: Towards a large-scale evaluation of the intrinsic brain architecture in autism.

    Mol. Psychiatry, May 31, 2014

    A. Di Martino, Yan C.G., Li Q., Denio E., F. Castellanos, Alaerts K., et al.

  30. Internet-based, randomized, controlled trial of omega-3 fatty acids for hyperactivity in autism.

    J. Am. Acad. Child Adolesc. Psychiatry, May 31, 2014

    S. Bent, R. Hendren, Zandi T., K. Law, Choi J.E., Widjaja F., et al.

  31. Snx14 regulates neuronal excitability, promotes synaptic transmission, and is imprinted in the brain of mice.

    PLoS One, May 22, 2014

    Huang H.S., Yoon B.J., Brooks S., Bakal R., Berrios J., Larsen R.S., et al.

  32. Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.

    Cell Rep., May 21, 2014

    Portmann T., Yang M., Mao R., Panagiotakos G., Ellegood J., Dolen G., et al.

  33. The impact of multisensory integration deficits on speech perception in children with autism spectrum disorders.

    Front. Psychol., May 20, 2014

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

  34. Dopaminergic dynamics contributing to social behavior.

    Cold Spring Harb. Symp. Quant. Biol., May 14, 2014

    Gunaydin L.A. and K. Deisseroth

  35. Neurosteroids promote phosphorylation and membrane insertion of extrasynaptic GABAA receptors.

    Proc. Natl. Acad. Sci. USA, May 12, 2014

    Abramian A.M., Comenencia-Ortiz E., Modgil A., Vien T.N., Nakamura Y., Moore Y.E., et al.

  36. Fragile X mental retardation protein regulates synaptic and behavioral plasticity to repeated cocaine administration.

    Neuron, May 6, 2014

    Smith L.N., Jedynak J.P., Fontenot M.R., Hale C.F., Dietz K.C., Taniguchi M., et al.

  37. De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.

    Am. J. Hum. Genet., April 30, 2014

    Xia F., Bainbridge M.N., Tan T.Y., M. Wangler, Scheuerle A.E., Zackai E.H., et al.

  38. The Rhode Island Consortium for Autism Research and Treatment (RI-CART): A new statewide autism collaborative.

    R. I. Med. J. (2013), April 30, 2014

    Gerber A., E. Morrow, S. Sheinkopf, and Anders T.

  39. Aberrant white matter microstructure in children with 16p11.2 deletions.

    J. Neurosci., April 29, 2014

    Owen J.P., Chang Y.S., Pojman N.J., Bukshpun P., Wakahiro M.L., Marco E.J., et al.

  40. Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.

    Mol. Autism, April 28, 2014

    A. Gupta, Pirruccello M., Cheng F., Kang H.J., T. Fernandez, Baskin J.M., et al.

  41. CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration.

    Cell, April 23, 2014

    Schaffer A.E., Eggens V.R., Caglayan A.O., Reuter M.S., Scott E., N. Coufal, et al.

  42. The potential of accelerating early detection of autism through content analysis of YouTube videos.

    PLoS One, April 15, 2014

    Fusaro V.A., Daniels J., Duda M., DeLuca T.F., D’Angelo O., Tamburello J., et al.

  43. Circuit-selective striatal synaptic dysfunction in the SAPAP3 knockout mouse model of obsessive-compulsive disorder.

    Biol. Psychiatry, April 14, 2014

    Wan Y., Ade K.K., Caffall Z., Ilcim Ozlu M., C. Eroglu, G. Feng, et al.

  44. Loss of Tet enzymes compromises proper differentiation of embryonic stem cells.

    Dev. Cell, April 13, 2014

    Dawlaty M.M., Breiling A., Le T., Barrasa M.I., Raddatz G., Gao Q., et al.

  45. Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

    Nat. Commun., April 10, 2014

    Corominas R., Yang X., Lin G.N., Kang S., Shen Y., Ghamsari L., et al.

  46. Chromatin regulators, phenotypic robustness, and autism risk.

    Front. Genet., April 9, 2014

    Suliman R., Ben-David E., and S. Shifman

  47. Equivalent neural responses in children and adolescents with and without autism during judgments of affect.

    Dev. Cogn. Neurosci., April 7, 2014

    Vander Wyk B.C., Hoffman F., and K. Pelphrey

  48. Investigation of maternal genotype effects in autism by genome-wide association.

    Autism Res., March 31, 2014

    Yuan H. and J. Dougherty

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