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 

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 

Khamina, K., Lercher, A., Caldera, M., Schliehe, C., Vilagos, B., Sahin, M.,https://doi.org/10.1371/journal.ppat.1006758__Bergthaler, A. (2017). Characterization of host proteins interacting with the lymphocytic choriomeningitis virus L protein. PLoS Pathogens. Public Library of Science.https://doi.org/10.1371/journal.ppat.1006758 

Hill Yardin, E., Mckeown, S., Novarino, G., &; Grabrucker, A. (2017). Extracerebral dysfunction in animal models of autism spectrum disorder. In M. Schmeisser &; T. Boekers (Eds.), Translational Anatomy and Cell Biology of Autism Spectrum Disorder (Vol. 224, pp. 159–187). Springer.https://doi.org/10.1007/978-3-319-52498-6_9 

Schroeder, J., Deliu, E., Novarino, G., &; Schmeisser, M. (2017). Genetic and pharmacological reversibility of phenotypes in mouse models of autism spectrum disorder. In M. Schmeisser &; T. Boekers (Eds.), Translational Anatomy and Cell Biology of Autism Spectrum Disorder (Vol. 224, pp. 189–211). Springer.https://doi.org/10.1007/978-3-319-52498-6_10 

Novarino, G. (2017). Modeling Alzheimer’s disease in mice with human neurons. Science Translational Medicine. American Association for the Advancement of Science.https://doi.org/10.1126/scitranslmed.aam9867 

Novarino, G. (2017). The antisocial side of antibiotics. Science Translational Medicine. American Association for the Advancement of Science.https://doi.org/10.1126/scitranslmed.aan2786 

Novarino, G. (2017). Rett syndrome modeling goes simian. Science Translational Medicine. American Association for the Advancement of Science.https://doi.org/10.1126/scitranslmed.aan8196 

Novarino, G. (2017). The riddle of CH haploinsufficiency in autism spectrum disorder. Science Translational Medicine. American Association for the Advancement of Science.https://doi.org/10.1126/scitranslmed.aao0972 

Andergassen, D., Dotter, C., Wenzel, D., Sigl, V., Bammer, P., Muckenhuber, M.,https://doi.org/10.7554/eLife.25125__Hudson, Q. (2017). Mapping the mouse Allelome reveals tissue specific regulation of allelic expression. ELife. eLife Sciences Publications.https://doi.org/10.7554/eLife.25125 

Brailoiu, G., Deliu, E., Barr, J., Console Bram, L., Ciuciu, A., Abood, M.,https://doi.org/10.1016/j.drugalcdep.2017.04.015__Breiloiu, E. (2017). HIV Tat exciteshttps://doi.org/10.1016/j.drugalcdep.2017.04.015__receptor-like expressing neurons from rat nucleus accumbens. Drug and Alcohol Dependence. Elsevier.https://doi.org/10.1016/j.drugalcdep.2017.04.015 

Novarino, G. (2017). More excitation for Rett syndrome. Science Translational Medicine. American Association for the Advancement of Science.https://doi.org/10.1126/scitranslmed.aao4218 

Novarino, G. (2017). The science of love in ASD and ADHD. Science Translational Medicine. American Association for the Advancement of Science.https://doi.org/10.1126/scitranslmed.aap8168 

Sauerzopf, U., Sacco, R., Novarino, G., Niello, M., Weidenauer, A., Praschak Rieder, N.,https://doi.org/10.1111/ejn.13418__Willeit, M. (2017). Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence. European Journal of Neuroscience. Wiley-Blackwell.https://doi.org/10.1111/ejn.13418 

Breiloiu, E., Mcguire, M., Shuler, S., Deliu, E., Barr, J., Abood, M., &; Brailoiu, G. (2017). Modulation of cardiac vagal tone by bradykinin acting on nucleus ambiguus. Neuroscience. Elsevier.https://doi.org/10.1016/j.neuroscience.2017.09.034 

Kornienko, A., Dotter, C., Guenzl, P., Gisslinger, H., Gisslinger, B., Cleary, C.,https://doi.org/10.1186/s13059-016-0873-8__Barlow, D. (2016). Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans. Genome Biology. BioMed Central.https://doi.org/10.1186/s13059-016-0873-8 

Tarlungeanu, D.-C., Deliu, E., Dotter, C., Kara, M., Janiesch, P., Scalise, M.,https://doi.org/10.1016/j.cell.2016.11.013__Novarino, G. (2016). Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder. Cell. Cell Press.https://doi.org/10.1016/j.cell.2016.11.013 

Andergassen, D., Dotter, C., Kulinski, T., Guenzl, P., Bammer, P., Barlow, D.,https://doi.org/10.1093/nar/gkv727__Hudson, Q. (2015). Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data. Nucleic Acids Research. Oxford University Press.https://doi.org/10.1093/nar/gkv727 

Kuechler, A., Zink, A., Wieland, T., Lüdecke, H., Cremer, K., Salviati, L.,https://doi.org/10.1038/ejhg.2014.165__Engels, H. (2015). Loss-of-function variants of SET cause intellectual disability and the core phenotype of microdeletion 3.3 syndrome. European Journal of Human Genetics. Nature Publishing Group.https://doi.org/10.1038/ejhg.2014.165 

Novarino, G., Fenstermaker, A., Zaki, M., Hofree, M., Silhavy, J., Heiberg, A.,https://doi.org/10.1126/science.1247363__Gleeson, J. (2014). Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science. American Association for the Advancement of Science.https://doi.org/10.1126/science.1247363