Funded Publications

Below is a list of publications and preprints generated with SFARI support. The list includes papers from SFARI-funded investigators as well as from researchers who used genetic/phenotypic data or biospecimens from the Simons Simplex Collection (SSC), Simons Searchlight, Simons Foundation Powering Autism Research for Knowledge (SPARK), the Autism Inpatient Collection or Autism BrainNet.

2110 Articles

Effects of eight neuropsychiatric copy number variants on human brain structure.

Modenato C., Kumar K., Moreau C., Martin-Brevet S., Huguet G., Schramm C., Jean-Louis M., Martin C.-O., Younis N., Tamer P., Douard E., Thébault-Dagher F., Côté V., Charlebois A.-R., Deguire F., Maillard A.M., Rodriguez-Herreros B., Pain A., Richetin S., 16p11.2 European Consortium, Simons Searchlight Consortium, Melie-Garcia L., Kushan L., Silva A.I., van den Bree M.B., Linden D.E.J., Owen M.J., Hall J., Lippé S., Chakravarty M., Bzdok D., Bearden C., Draganski B., Jacquemont S.

Polygenic profiles define aspects of clinical heterogeneity in ADHD.

LaBianca S., Brikell I., Helenius D., Loughnan R., Mefford J., Palmer C.E., Walker R., Gådin J.R., Krebs M., Appadurai V., Vaez M., Agerbo E., Pedersen M.G., Børglum A.D., Hougaard D.M., Mors O., Nordentoft M., Mortensen P.B., Kendler K.S., Jernigan T.L., Geschwind D., Ingason A., Dahl A.W., Zaitlen N., Dalsgaard S., Werge T.M., Schork A.J.

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.

Padhi E.M., Hayeck T.J., Cheng Z., Chatterjee S., Mannion B.J., Byrska-Bishop M., Willems M., Pinson L., Redon S., Benech C., Uguen K., Audebert-Bellanger S., Le Marechal C., Férec C., Efthymiou S., Rahman F., Maqbool S., Maroofian R., Houlden H., Musunuri R., Narzisi G., Abhyankar A., Hunter R.D., Akiyama J., Fries L.E., Ng J.K., Mehinovic E., Stong N., Allen A.S., Dickel D.E., Bernier R., Gorkin D.U., Pennacchio L., Zody M.C., Turner T.

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Research Highlights
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