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.

2015 Articles

Dissociable cellular and genetic mechanisms of cortical thinning at different life stages.

Modabbernia A., Vidal-Pineiro D., Agartz I., Andreassen O.A., Ayesa-Arriola R., Bertolino A., Boomsma D.I., Bourque J., Breier A., Brodaty H., Brouwer R.M., Buitelaar J.K., Canales-Rodríguez E.J., Caseras X., Conrod P.J., Crespo-Facorro B., Crivello F., Crone E.A., de Zubicaray G.I., Dickie E.W., Dima D., Frenzel S., Fisher S., Franke B., Glahn D.C., Grabe H.-J., Grotegerd D., Gruber O., Guerrero-Pedraza A., Gur R.E., Gur R.C., Hartman C.A., Hoekstra P.J., Hulshoff Pol H.E., Jahanshad N., Jernigan T.L., Jiang J., Kalnin A.J., Kochan N.A., Mazoyer B., McDonald B.C., McMahon K.L., Nyberg L., Oosterlaan J., Pomarol-Clotet E., Radua J., Sachdev P.S., Satterthwaite T.D., Salvador R., Sarro S., Saykin A.J., Schumann G., Smoller J.W., Sommer I.E., Espeseth T., Thomopoulos S.I., Trollor J.N., van ‘t Ent D., Voineskos A., Wang Y., Weber B., Westlye L.T., Whalley H.C., Williams S.C., Wittfeld K., Wright M.J., Thompson P.M., Paus T., Frangou S.

The link between autism and sex-specific neuroanatomy, and associated cognition and gene expression.

Floris D.L., Peng H., Warrier V., Lombardo M., Pretzsch C.M., Moreau C., Tsompanidis A., Gong W., Mennes M., Llera A., van Rooij D., Oldehinkel M., Forde N., Charman T., Tillmann J., Banaschewski T., Moessnang C., Durston S., Holt R.J., Ecker C., Dell’Acqua F., Loth E., Bourgeron T., Murphy D., Marquand A.F., Lai M.-C., Buitelaar J.K., Baron-Cohen S., Beckmann C.F., EU-AIMS LEAP Group.

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.

Marcogliese P.C., Deal S.L., Andrews J., Harnish J.M., Bhavana V.H., Graves H.K., Jangam S., Luo X., Liu N., Bei D., Chao Y.-H., Hull B., Lee P.-T., Pan H., Bhadane P., Huang M.-C., Longley C.M., Chao H.-T., Chung H.-l., Haelterman N.A., Kanca O., Manivannan S.N., Rossetti L.Z., German R.J., Gerard A., Schwaibold E.M.C., Fehr S., Guerrini R., Vetro A., England E., Murali C.N., Barakat T.S., van Dooren M.F., Wilke M., van Slegtenhorst M., Lesca G., Sabatier I., Chatron N., Brownstein C.A., Madden J.A., Agrawal P.B., Keren B., Courtin T., Perrin L., Brugger M., Roser T., Leiz S., Mau-Them F.T., Delanne J., Sukarova-Angelovska E., Trajkova S., Rosenhahn E., Strehlow V., Platzer K., Keller R., Pavinato L., Brusco A., Rosenfeld J.A., Marom R., Wangler M., Yamamoto S.

SETBP1 variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental disorder.

Wong M.M., Kampen R.A., Braden R.O., Alagöz G., Hildebrand M.S., Barnett C., Barnett M., Brusco A., Carli D., de Vries B.B.A., Dingemans A.J., Elmslie F., Ferrero G.B., Jansen N.A., van de Laar I.M.B.H., Moroni A., Mowat D., Murray L., Novara F., Peron A., Scheffer I.E., Sirchia F., Turner S.J., Vignoli A., Vino A., Weber S., Chung W., Gerard M., López-González V., Palmer E., Morgan A.T., van Bon B.W., Fisher S.

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