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 
LibreCat: https://research-explorer.ista.ac.at/record/8131
DOI: 10.1016/j.gde.2020.06.004
WoS: 000598918900019
PMID: 32659636

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 
LibreCat: https://research-explorer.ista.ac.at/record/105
DOI: 10.1038/s41431-018-0231-2
WoS: 000454111500019
PMID: 30089829

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 
LibreCat: https://research-explorer.ista.ac.at/record/6088
DOI: 10.1021/acs.molpharmaceut.8b01217
WoS: 000460600400031
PMID: 30694684

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 
LibreCat: https://research-explorer.ista.ac.at/record/6470
DOI: 10.1113/JP277681
WoS: 000470780400013
PMID: 31006863

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 
LibreCat: https://research-explorer.ista.ac.at/record/6896
DOI: 10.1016/j.brainres.2019.146458
WoS: 000491646600033
PMID: 31521639

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 
LibreCat: https://research-explorer.ista.ac.at/record/7415
DOI: 10.1016/j.euroneuro.2019.09.040
WoS: 000502657500021

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 
LibreCat: https://research-explorer.ista.ac.at/record/7414
DOI: 10.1016/j.euroneuro.2019.09.039
WoS: 000502657500020

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 
LibreCat: https://research-explorer.ista.ac.at/record/6074
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/456
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/5888
DOI: 10.1038/s12276-018-0129-7
WoS: 000441266700006
PMID: 30089840

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 
LibreCat: https://research-explorer.ista.ac.at/record/546
DOI: 10.1016/j.conb.2017.12.005
WoS: 000427101600018

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 
LibreCat: https://research-explorer.ista.ac.at/record/691
DOI: 10.1136/jmedgenet-2017-104627
WoS: 000418199800007
PMID: 28626029

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 
LibreCat: https://research-explorer.ista.ac.at/record/395
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/3
DOI: 10.1038/s41593-018-0266-2
WoS: 000451324700010

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 
LibreCat: https://research-explorer.ista.ac.at/record/540
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/623
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/634
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/656
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/667
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/689
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/702
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/713
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/714
DOI: 10.1016/j.drugalcdep.2017.04.015
PMID: 28623807

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 
LibreCat: https://research-explorer.ista.ac.at/record/715
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/731
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/1228
DOI: 10.1111/ejn.13418
WoS: 000392487100005
PMID: 27690184

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 
LibreCat: https://research-explorer.ista.ac.at/record/747
DOI: 10.1016/j.neuroscience.2017.09.034
WoS: 000415966200003
PMID: 28951324

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 
LibreCat: https://research-explorer.ista.ac.at/record/1240
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/1183
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/1497
DOI: 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 
LibreCat: https://research-explorer.ista.ac.at/record/1789
DOI: 10.1038/ejhg.2014.165
PMID: 25138099

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 
LibreCat: https://research-explorer.ista.ac.at/record/1916
DOI: 10.1126/science.1247363
PMID: 24482476