Novarino, Gaia. “More Excitation for Rett Syndrome.”10.1126/scitranslmed.aao4218__Science Translational Medicine, vol. 9, no. 405, aao4218, American Association for the Advancement of Science, 2017, doi:10.1126/scitranslmed.aao4218.
LibreCat: https://research-explorer.ista.ac.at/record/715
DOI: 10.1126/scitranslmed.aao4218

Novarino, Gaia. “The Science of Love in ASD and ADHD.”10.1126/scitranslmed.aap8168__Science Translational Medicine, vol. 9, no. 411, ea, American Association for the Advancement of Science, 2017, doi:10.1126/scitranslmed.aap8168.
LibreCat: https://research-explorer.ista.ac.at/record/731
DOI: 10.1126/scitranslmed.aap8168

Sauerzopf, Ulrich, et al. “Are Reprogrammed Cells a Useful Tool for Studying Dopamine Dysfunction in Psychotic Disorders? A Review of the Current Evidence.”10.1111/ejn.13418__European Journal of Neuroscience, vol. 45, no. 1, Wiley-Blackwell, 2017, pp. 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, Eugen, et al. “Modulation of Cardiac Vagal Tone by Bradykinin Acting on Nucleus Ambiguus.”10.1016/j.neuroscience.2017.09.034__Neuroscience, vol. 365, Elsevier, 2017, pp. 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, Aleksandra, et al. “Long Non-Coding RNAs Display Higher Natural Expression Variation than Protein-Coding Genes in Healthy Humans.”10.1186/s13059-016-0873-8__Genome Biology, vol. 17, no. 1, 14, BioMed Central, 2016, doi:10.1186/s13059-016-0873-8.
LibreCat: https://research-explorer.ista.ac.at/record/1240
DOI: 10.1186/s13059-016-0873-8

Tarlungeanu, Dora-Clara, et al. “Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder.”10.1016/j.cell.2016.11.013__Cell, vol. 167, no. 6, Cell Press, 2016, pp. 1481–94, 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, Daniel, et al. “Allelome.PRO, a Pipeline to Define Allele-Specific Genomic Features from High-Throughput Sequencing Data.”10.1093/nar/gkv727__Nucleic Acids Research, vol. 43, no. 21, e146, Oxford University Press, 2015, doi:10.1093/nar/gkv727.
LibreCat: https://research-explorer.ista.ac.at/record/1497
DOI: 10.1093/nar/gkv727

Kuechler, Alma, et al. “Loss-of-Function Variants of SET Cause Intellectual Disability and the Core Phenotype of Microdeletion 3.3 Syndrome.”10.1038/ejhg.2014.165__European Journal of Human Genetics, vol. 23, no. 6, Nature Publishing Group, 2015, pp. 753–60, doi:10.1038/ejhg.2014.165.
LibreCat: https://research-explorer.ista.ac.at/record/1789
DOI: 10.1038/ejhg.2014.165
PMID: 25138099

Novarino, Gaia, et al. “Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders.”10.1126/science.1247363__Science, vol. 343, no. 6170, American Association for the Advancement of Science, 2014, pp. 506–11, doi:10.1126/science.1247363.
LibreCat: https://research-explorer.ista.ac.at/record/1916
DOI: 10.1126/science.1247363
PMID: 24482476