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Weinert, S., Gimber, N., Deuschel, D., Stuhlmann, T., Puchkov, D., Farsi, Z.,https://doi.org/10.15252/embj.2019103358__Jentsch, T. J. (2020). Uncoupling endosomal CLC chloride/proton exchange causes severe neurodegeneration. EMBO Journal. EMBO Press.https://doi.org/10.15252/embj.2019103358 

Parenti, I., Diab, F., Gil, S. R., Mulugeta, E., Casa, V., Berutti, R.,https://doi.org/10.1016/j.celrep.2020.107647__Wendt, K. S. (2020). MA and NIPBL variants impair the heterodimerization of the cohesin loader subunits and cause Cornelia de Lange syndrome. Cell Reports. Elsevier.https://doi.org/10.1016/j.celrep.2020.107647 

Parenti, I., Garcia Rabaneda, L. E., Schön, H., &; Novarino, G. (2020). Neurodevelopmental disorders: From genetics to functional pathways. Trends in Neurosciences. Elsevier.https://doi.org/10.1016/j.tins.2020.05.004 

Morandell, J. (2020). Illuminating the role of Cul3 in autism spectrum disorder pathogenesis. Institute of Science and Technology Austria.https://doi.org/10.15479/AT:ISTA:8620 

Morandell, J., Schwarz, L. A., Basilico, B., Tasciyan, S., Nicolas, A., Sommer, C. M.,https://doi.org/10.1101/2020.01.10.902064 __Novarino, G. (n.d.). Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development. bioRxiv. Cold Spring Harbor Laboratory.https://doi.org/10.1101/2020.01.10.902064  

Basilico, B., Morandell, J., &; Novarino, G. (2020). Molecular mechanisms for targeted ASD treatments. Current Opinion in Genetics and Development. Elsevier.https://doi.org/10.1016/j.gde.2020.06.004 

Marsh, A., Novarino, G., Lockhart, P., &; Leventer, R. (2019). CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63. European Journal of Human Genetics. Springer Nature.https://doi.org/10.1038/s41431-018-0231-2 

Traxl, A., Mairinger, S., Filip, T., Sauberer, M., Stanek, J., Poschner, S.,https://doi.org/10.1021/acs.molpharmaceut.8b01217__Langer, O. (2019). Inhibition of ABC and ABC at the mouse blood-brain barrier with marketed drugs to improve brain delivery of the model ABC/ABC substrate [11C]erlotinib. Molecular Pharmaceutics. American Chemical Society.https://doi.org/10.1021/acs.molpharmaceut.8b01217 

Éltes, T., Szoboszlay, M., Szigeti, M. K., &; Nusser, Z. (2019). Improved spike inference accuracy by estimating the peak amplitude of unitary [C+] transients in weakly GCaMf-expressing hippocampal pyramidal cells. Journal of Physiology. Wiley.https://doi.org/10.1113/JP277681 

Oliveira, B., Yahya, A. Ç., &; Novarino, G. (2019). Modeling cell-cell interactions in the brain using cerebral organoids. Brain Research. Elsevier.https://doi.org/10.1016/j.brainres.2019.146458 

Morandell, J., Nicolas, A., Schwarz, L. A., &; Novarino, G. (2019). S.16.05 Illuminating the role of the e3 ubiquitin ligase cullin3 in brain development and autism. European Neuropsychopharmacology. Elsevier.https://doi.org/10.1016/j.euroneuro.2019.09.040 

Knaus, L., Tarlungeanu, D.-C., &; Novarino, G. (2019). S.16.03 A homozygous missense mutation in SL leads to autism spectrum disorder and microcephaly. European Neuropsychopharmacology. Elsevier.https://doi.org/10.1016/j.euroneuro.2019.09.039 

Dotter, C., &; Novarino, G. (2019). Supplementary data for the research paper “Haploinsufficiency of the intellectual disability gene SET disturbs developmental gene expression and cognition.”https://doi.org/10.15479/AT:ISTA:6074__Institute of Science and Technology Austria.https://doi.org/10.15479/AT:ISTA:6074 

Novarino, G. (2018). Zika-associated microcephaly: Reduce the stress and race for the treatment. Science Translational Medicine. American Association for the Advancement of Science.https://doi.org/10.1126/scitranslmed.aar7514 

Tarlungeanu, D.-C., &; Novarino, G. (2018). Genomics in neurodevelopmental disorders: an avenue to personalized medicine. Experimental &; Molecular Medicine. Springer Nature.https://doi.org/10.1038/s12276-018-0129-7 

Sacco, R., Cacci, E., &; Novarino, G. (2018). Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology. Elsevier.https://doi.org/10.1016/j.conb.2017.12.005 

Marin Valencia, I., Novarino, G., Johansen, A., Rosti, B., Issa, M., Musaev, D.,https://doi.org/10.1136/jmedgenet-2017-104627__Gleeson, J. (2018). A homozygous founder mutation in TRAPPB associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics. BMJ Publishing Group.https://doi.org/10.1136/jmedgenet-2017-104627 

Tarlungeanu, D.-C. (2018). The branched chain amino acids in autism spectrum disorders . Institute of Science and Technology Austria.https://doi.org/10.15479/AT:ISTA:th_992 

Deliu, E., Arecco, N., Morandell, J., Dotter, C., Contreras, X., Girardot, C.,https://doi.org/10.1038/s41593-018-0266-2__Novarino, G. (2018). Haploinsufficiency of the intellectual disability gene SET disturbs developmental gene expression and cognition. Nature Neuroscience. Nature Publishing Group.https://doi.org/10.1038/s41593-018-0266-2