SFARI

Chandelier cartridge density is reduced in the prefrontal cortex in autism.

Amina S., Falcone C., Wolf-Ochoa M.W., Vakilzadeh G., Allen E., Perez-Castro R., Kargar M., Noctor S., Martínez-Cerdeño V.

Broad frequency sensitivity and complex neural coding in the larval zebrafish auditory system.

Poulsen R.E., Scholz L.A., Constantin L., Favre-Bulle I., Vanwalleghem G.C., Scott E.

A unified resource and configurable model of the synapse proteome and its role in disease.

Sorokina O., Mclean C., Croning M.D.R., Heil K.F., Wysocka E., He X., Sterratt D., Grant S.G.N., Simpson T.I., Armstrong J.D.

Genoppi is an open-source software for robust and standardized integration of proteomic and genetic data.

Pintacuda G., Lassen F.H., Hsu Y.-H.H., Kim A., Martín J.M., Malolepsza E., Lim J.K., Fornelos N., Eggan K. C., Lage K.

Optimising a simple fully convolutional network for accurate brain age prediction in the PAC 2019 challenge.

Gong W., Beckmann C.F., Vedaldi A., Smith S.M., Peng H.

Integrating barcoded neuroanatomy with spatial transcriptional profiling enables identification of gene correlates of projections.

Sun Y.-C., Chen X., Fischer S., Lu S., Zhan H., Gillis J., Zador A.M.

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.

Zhu N., Swietlik E.M., Welch C.L., Pauciulo M.W., Hagen J.J., Zhou X., Guo Y., Karten J., Pandya D., Tilly T., Lutz K.A., Martin J.M., Treacy C.M., Rosenzweig E.B., Krishnan U., Coleman A.W., Gonzaga-Juaregui C., Lawrie A., Trembath R.C., Wilkins M.R., Regeneron Genetics Center, PAH Biobank Enrolling Centers’ Investigators, NIHR BioResource for Translational Research - Rare Diseases, National Cohort Study of Idiopathic and Heritable PAH, Morrell N.W., Shen Y., Gräf S., Nichols W.C., Chung W.

Funded Publications