Please note that LibreCat no longer supports Internet Explorer versions 8 or 9 (or earlier).
We recommend upgrading to the latest Internet Explorer, Google Chrome, or Firefox.
37 Publications
2019 | Journal Article | IST-REx-ID: 6896
B. Oliveira, A. Ç. Yahya, and G. Novarino, “Modeling cell-cell interactions in the brain using cerebral organoids,” Brain Research, vol. 1724, 2019.
View
| DOI
| PubMed | Europe PMC
2018 | Thesis | IST-REx-ID: 395 | 
D.-C. Tarlungeanu, The branched chain amino acids in autism spectrum disorders . IST Austria, 2018.
View
| Files available
| DOI
2018 | Journal Article | IST-REx-ID: 5888 |
D.-C. Tarlungeanu and G. Novarino, “Genomics in neurodevelopmental disorders: an avenue to personalized medicine,” Experimental & Molecular Medicine, vol. 50, no. 8, 2018.
View
| Files available
| DOI
| PubMed | Europe PMC
2018 | Journal Article | IST-REx-ID: 3 |
E. Deliu et al., “Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition,” Nature Neuroscience, vol. 21, no. 12, pp. 1717–1727, 2018.
View
| Files available
| DOI
2018 | Journal Article | IST-REx-ID: 691 |
I. Marin Valencia et al., “A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features,” Journal of Medical Genetics, vol. 55, no. 1, pp. 48–54, 2018.
View
| DOI
| Download (ext.)
| PubMed | Europe PMC
2017 | Journal Article | IST-REx-ID: 1228 |
U. Sauerzopf 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, vol. 45, no. 1, pp. 45–57, 2017.
View
| Files available
| DOI
2017 | Journal Article | IST-REx-ID: 540 |
K. Khamina et al., “Characterization of host proteins interacting with the lymphocytic choriomeningitis virus L protein,” PLoS Pathogens, vol. 13, no. 12, 2017.
View
| Files available
| DOI
2017 | Journal Article | IST-REx-ID: 714 |
G. Brailoiu et al., “HIV Tat excites D1 receptor-like expressing neurons from rat nucleus accumbens,” Drug and Alcohol Dependence, vol. 178, pp. 7–14, 2017.
View
| DOI
| Download (ext.)
| PubMed | Europe PMC
2017 | Journal Article | IST-REx-ID: 713 |
D. Andergassen et al., “Mapping the mouse Allelome reveals tissue specific regulation of allelic expression,” eLife, vol. 6, 2017.
View
| Files available
| DOI
2017 | Book Chapter | IST-REx-ID: 623
E. Hill Yardin, S. Mckeown, G. Novarino, and A. Grabrucker, “Extracerebral dysfunction in animal models of autism spectrum disorder,” in Translational Anatomy and Cell Biology of Autism Spectrum Disorder, vol. 224, M. Schmeisser and T. Boekers, Eds. Springer, 2017, pp. 159–187.
View
| DOI
2017 | Book Chapter | IST-REx-ID: 634
J. Schroeder, E. Deliu, G. Novarino, and M. Schmeisser, “Genetic and pharmacological reversibility of phenotypes in mouse models of autism spectrum disorder,” in Translational Anatomy and Cell Biology of Autism Spectrum Disorder, vol. 224, M. Schmeisser and T. Boekers, Eds. Springer, 2017, pp. 189–211.
View
| DOI
2017 | Journal Article | IST-REx-ID: 747 |
E. Brǎiloiu et al., “Modulation of cardiac vagal tone by bradykinin acting on nucleus ambiguus,” Neuroscience, vol. 365, pp. 23–32, 2017.
View
| DOI
| Download (ext.)
| PubMed | Europe PMC
2016 | Journal Article | IST-REx-ID: 1240 |
A. Kornienko et al., “Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans,” Genome Biology, vol. 17, no. 1, 2016.
View
| Files available
| DOI
2016 | Journal Article | IST-REx-ID: 1183 |
D.-C. Tarlungeanu et al., “Impaired amino acid transport at the blood brain barrier is a cause of autism spectrum disorder,” Cell, vol. 167, no. 6, pp. 1481–1494, 2016.
View
| Files available
| DOI
2015 | Journal Article | IST-REx-ID: 1497 |
D. Andergassen et al., “Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data,” Nucleic Acids Research, vol. 43, no. 21, 2015.
View
| Files available
| DOI
2015 | Journal Article | IST-REx-ID: 1789 |
A. Kuechler et al., “Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome,” European Journal of Human Genetics, vol. 23, no. 6, pp. 753–760, 2015.
View
| DOI
| Download (ext.)
| PubMed | Europe PMC
2014 | Journal Article | IST-REx-ID: 1916 |
G. Novarino et al., “Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders,” Science, vol. 343, no. 6170, pp. 506–511, 2014.
View
| DOI
| Download (ext.)
| PubMed | Europe PMC