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29 Publications

2019 | Journal Article | IST-REx-ID: 105
Marsh, A., Novarino, G., Lockhart, P., & Leventer, R. (2019). CUGC for pontocerebellar hypoplasia type 9 and spastic paraplegia-63. European Journal of Human Genetics, 27, 161–166. https://doi.org/10.1038/s41431-018-0231-2
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2019 | Journal Article | IST-REx-ID: 6896
Oliveira, B., Yahya, A. Ç., & Novarino, G. (2019). Modeling cell-cell interactions in the brain using cerebral organoids. Brain Research, 1724, 146458. https://doi.org/10.1016/j.brainres.2019.146458
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2019 | Research Data | IST-REx-ID: 6074
Dotter, C., & Novarino, G. (2019). Supplementary data for the research paper “Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.” IST Austria. https://doi.org/10.15479/AT:ISTA:6074
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2019 | Journal Article | IST-REx-ID: 6088
Traxl, A., Mairinger, S., Filip, T., Sauberer, M., Stanek, J., Poschner, S., … Langer, O. (2019). Inhibition of ABCB1 and ABCG2 at the mouse blood-brain barrier with marketed drugs to improve brain delivery of the model ABCB1/ABCG2 substrate [11C]erlotinib. Molecular Pharmaceutics, 16(3), 1282–1293. https://doi.org/10.1021/acs.molpharmaceut.8b01217
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2019 | Journal Article | IST-REx-ID: 6470
Éltes, T., Szoboszlay, M., Szigeti, M. K., & Nusser, Z. (2019). Improved spike inference accuracy by estimating the peak amplitude of unitary [Ca2+] transients in weakly GCaMP6f-expressing hippocampal pyramidal cells. Journal of Physiology. https://doi.org/10.1113/JP277681
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2018 | Thesis | IST-REx-ID: 395   OA
Tarlungeanu, D.-C. (2018). The branched chain amino acids in autism spectrum disorders . IST Austria. https://doi.org/10.15479/AT:ISTA:th_992
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2018 | Journal Article | IST-REx-ID: 456
Novarino, G. (2018). Zika-associated microcephaly: Reduce the stress and race for the treatment. Science Translational Medicine, 10(423). https://doi.org/10.1126/scitranslmed.aar7514
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2018 | Journal Article | IST-REx-ID: 691   OA
Marin Valencia, I., Novarino, G., Johansen, A., Rosti, B., Issa, M., Musaev, D., … Gleeson, J. (2018). A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics, 55(1), 48–54. https://doi.org/10.1136/jmedgenet-2017-104627
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2018 | Journal Article | IST-REx-ID: 546
Sacco, R., Cacci, E., & Novarino, G. (2018). Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology, 48(2), 131–138. https://doi.org/10.1016/j.conb.2017.12.005
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2018 | Journal Article | IST-REx-ID: 5888   OA
Tarlungeanu, D.-C., & Novarino, G. (2018). Genomics in neurodevelopmental disorders: an avenue to personalized medicine. Experimental & Molecular Medicine, 50(8). https://doi.org/10.1038/s12276-018-0129-7
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