SFARI | SFARI Funded Publications

Robust and replicable measurement for prepulse inhibition of the acoustic startle response.

Miller E.A., Kastner D., Grzybowski M.N., Dwinell M.R., Geurts A.M., Frank L.

FOXP1 negatively regulates intrinsic excitability in D2 striatal projection neurons by promoting inwardly rectifying and leak potassium currents.

Khandelwal N., Cavalier S., Rybalchenko V., Kulkarni A., Anderson A.G., Konopka G., Gibson J.

Resting and functional pupil response metrics indicate features of reward sensitivity and ASD in children.

DiCriscio A.S., Troiani V.

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.

Harris H.K., Nakayama T., Lai J., Zhao B., Argyrou N., Gubbels C.S., Soucy A., Genetti C.A., Suslovitch V., Rodan L.H., Tiller G.E., Lesca G., Gripp K.W., Asadollahi R., Hamosh A., Applegate C.D., Turnpenny P.D., Simon M.E.H., Volker-Touw C.M.L., van Gassen K.L.I., van Binsbergen E., Pfundt R., Gardeitchik T., de Vries B.B.A., Immken L.L., Buchanan C., Willing M., Toler T.L., Fassi E., Baker L., Vansenne F., Wang X., Ambrus J.L., Jr., Fannemel M., Posey J.E., Agolini E., Novelli A., Rauch A., Boonsawat P., Fagerberg C.R., Larsen M.J., Kibaek M., Labalme A., Poisson A., Payne K.K., Walsh L.E., Aldinger K.A., Balciuniene J., Skraban C., Gray C., Murrell J., Bupp C.P., Pascolini G., Grammatico P., Broly M., Küry S., Nizon M., Rasool I.G., Zahoor M.Y., Kraus C., Reis A., Iqbal M., Uguen K., Audebert-Bellanger S., Ferec C., Redon S., Baker J., Wu Y., Zampino G., Syrbe S., Brosse I., Abou Jamra R., Dobyns W.B., Cohen L.L., Blomhoff A., Mignot C., Keren B., Courtin T., Agrawal P.B., Beggs A., Yu T.

Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.

Huguet G., Schramm C., Douard E., Tamer P., Main A., Monin P., England J., Jizi K., Renne T., Poirier M., Nowak S., Martin C.-O., Younis N., Knoth I.S., Jean-Louis M., Saci Z., Auger M., Tihy F., Mathonnet G., Maftei C., Léveillé F., Porteous D., Davies G., Redmond P., Harris S.E., Hill W.D., Lemyre E., Schumann G., Bourgeron T., Pausova Z., Paus T., Karama S., Lippé S., Deary I.J., Almasy L., Labbe A., Glahn D., Greenwood C.M.T., Jacquemont S.

Brain gene co-expression networks link complement signaling with convergent synaptic pathology in schizophrenia.

Kim M., Haney J.R., Zhang P., Hernandez L.M., Wang L.-K., Perez-Cano L., Olde Loohuis L.M., de la Torre-Ubieta L., Gandal M.

Adaptive behavior profiles of intellectually gifted children with autism spectrum disorder.

Dempsey J., Ahmed K., Simon A.R., Hayutin L.G., Monteiro S., Dempsey A.G.

A large-scale investigation into the role of classical HLA loci in multiple types of severe infections, with a focus on overlaps with autoimmune and mental disorders.

Nudel R., Allesøe R.L., Thompson W.K., Werge T., Rasmussen S., Benros M.E.

Differences in social brain function in autism spectrum disorder are linked to the serotonin transporter.

Wong N.M.L., Dipasquale O., Turkheimer F., Findon J.L., Wichers R.H., Dimitrov M., Murphy C.M., Stoencheva V., Robertson D.M., Murphy D., Daly E., McAlonan G.

Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions.

Moreau C.A., Kumar K., Harvey A., Huguet G., Urchs S., Douard E.A., Schultz L.M., Sharmarke H., Jizi K., Martin C.-O., Younis N., Tamer P., Rolland T., Martineau J.-L., Orban P., Shin D., Silva A.I., Hall J., van den Bree M.B., Owen M.J., Linden D.E.J., Labbe A., Maillard A.M., Nowakowski T., Lippé S., Bearden C., Almasy L., Glahn D.C., Thompson P.M., Bourgeron T., Bellec P., Jacquemont S.