Marsh A, Novarino G, Lockhart P, Leventer R. CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63. European Journal of Human Genetics. 2019;27:161-166. doi: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, et al. 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. 2019;16(3):1282-1293. doi: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 MK, Nusser Z. Improved spike inference accuracy by estimating the peak amplitude of unitary [C+] transients in weakly GCaMf-expressing hippocampal pyramidal cells. Journal of Physiology. 2019;597(11):2925–2947. doi:10.1113/JP277681
LibreCat: https://research-explorer.ista.ac.at/record/6470
DOI: 10.1113/JP277681
WoS: 000470780400013
PMID: 31006863

Oliveira B, Yahya AÇ, Novarino G. Modeling cell-cell interactions in the brain using cerebral organoids. Brain Research. 2019;1724. doi: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 LA, Novarino G. S.16.05 Illuminating the role of the e3 ubiquitin ligase cullin3 in brain development and autism. European Neuropsychopharmacology. 2019;29(Supplement 6):-. doi: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. S.16.03 A homozygous missense mutation in SL leads to autism spectrum disorder and microcephaly. European Neuropsychopharmacology. 2019;29(Supplement 6):. doi: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

Novarino G. Zika-associated microcephaly: Reduce the stress and race for the treatment. Science Translational Medicine. 2018;10(423). doi:10.1126/scitranslmed.aar7514
LibreCat: https://research-explorer.ista.ac.at/record/456
DOI: 10.1126/scitranslmed.aar7514

Tarlungeanu D-C, Novarino G. Genomics in neurodevelopmental disorders: an avenue to personalized medicine. Experimental &; Molecular Medicine. 2018;50(8). doi: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. Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology. 2018;48(2):131-138. doi: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, et al. A homozygous founder mutation in TRAPPB associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics. 2018;55(1):48-54. doi: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. The branched chain amino acids in autism spectrum disorders . 2018. doi: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, et al. Haploinsufficiency of the intellectual disability gene SET disturbs developmental gene expression and cognition. Nature Neuroscience. 2018;21(12):1717-1727. doi: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, et al. Characterization of host proteins interacting with the lymphocytic choriomeningitis virus L protein. PLoS Pathogens. 2017;13(12). doi: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. Extracerebral dysfunction in animal models of autism spectrum disorder. In: Schmeisser M, Boekers T, eds. Translational Anatomy and Cell Biology of Autism Spectrum Disorder. Vol 224. Advances in Anatomy Embryology and Cell Biology. Springer; 2017:159-187. doi: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. Genetic and pharmacological reversibility of phenotypes in mouse models of autism spectrum disorder. In: Schmeisser M, Boekers T, eds. Translational Anatomy and Cell Biology of Autism Spectrum Disorder. Vol 224. Advances in Anatomy Embryology and Cell Biology. Springer; 2017:189-211. doi: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. Modeling Alzheimer’s disease in mice with human neurons. Science Translational Medicine. 2017;9(381). doi:10.1126/scitranslmed.aam9867
LibreCat: https://research-explorer.ista.ac.at/record/656
DOI: 10.1126/scitranslmed.aam9867

Novarino G. The antisocial side of antibiotics. Science Translational Medicine. 2017;9(387). doi:10.1126/scitranslmed.aan2786
LibreCat: https://research-explorer.ista.ac.at/record/667
DOI: 10.1126/scitranslmed.aan2786

Novarino G. Rett syndrome modeling goes simian. Science Translational Medicine. 2017;9(393). doi:10.1126/scitranslmed.aan8196
LibreCat: https://research-explorer.ista.ac.at/record/689
DOI: 10.1126/scitranslmed.aan8196

Novarino G. The riddle of CH haploinsufficiency in autism spectrum disorder. Science Translational Medicine. 2017;9(399):eaao0972. doi:10.1126/scitranslmed.aao0972
LibreCat: https://research-explorer.ista.ac.at/record/702
DOI: 10.1126/scitranslmed.aao0972

Andergassen D, Dotter C, Wenzel D, et al. Mapping the mouse Allelome reveals tissue specific regulation of allelic expression. eLife. 2017;6. doi:10.7554/eLife.25125
LibreCat: https://research-explorer.ista.ac.at/record/713
DOI: 10.7554/eLife.25125

Brailoiu G, Deliu E, Barr J, et al. HIV Tat excites10.1016/j.drugalcdep.2017.04.015__receptor-like expressing neurons from rat nucleus accumbens. Drug and Alcohol Dependence. 2017;178:7-14. doi: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. More excitation for Rett syndrome. Science Translational Medicine. 2017;9(405). doi:10.1126/scitranslmed.aao4218
LibreCat: https://research-explorer.ista.ac.at/record/715
DOI: 10.1126/scitranslmed.aao4218

Novarino G. The science of love in ASD and ADHD. Science Translational Medicine. 2017;9(411). doi:10.1126/scitranslmed.aap8168
LibreCat: https://research-explorer.ista.ac.at/record/731
DOI: 10.1126/scitranslmed.aap8168

Sauerzopf U, Sacco R, Novarino G, et al. Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence. European Journal of Neuroscience. 2017;45(1):45-57. doi: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, et al. Modulation of cardiac vagal tone by bradykinin acting on nucleus ambiguus. Neuroscience. 2017;365:23-32. doi: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, et al. Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans. Genome Biology. 2016;17(1). doi: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, et al. Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder. Cell. 2016;167(6):1481-1494. doi: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, et al. Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data. Nucleic Acids Research. 2015;43(21). doi:10.1093/nar/gkv727
LibreCat: https://research-explorer.ista.ac.at/record/1497
DOI: 10.1093/nar/gkv727

Kuechler A, Zink A, Wieland T, et al. Loss-of-function variants of SET cause intellectual disability and the core phenotype of microdeletion 3.3 syndrome. European Journal of Human Genetics. 2015;23(6):753-760. doi: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, et al. Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science. 2014;343(6170):506-511. doi:10.1126/science.1247363
LibreCat: https://research-explorer.ista.ac.at/record/1916
DOI: 10.1126/science.1247363
PMID: 24482476