Tournier, N., et al. “Complete Inhibition of ABC and ABC at the Blood-Brain Barrier by Co-Infusion of Erlotinib and Tariquidar to Improve Brain Delivery of the Model ABC/ABC Substrate [11C]Erlotinib.”10.1177/0271678X20965500__Journal of Cerebral Blood Flow and Metabolism, vol. 41, no. 7, SAGE Publications, 2021, pp. 1634–46, doi:10.1177/0271678X20965500.

Cordella, Federica, et al. “Antibiotics Treatment Modulates Microglia–Synapses Interaction.”10.3390/cells10102648__Cells, vol. 10, no. 10, 2648, MDPI, 2021, doi:10.3390/cells10102648.

Morandell, Jasmin, et al. “Cul3 Regulates Cytoskeleton Protein Homeostasis and Cell Migration during a Critical Window of Brain Development.”10.1038/s41467-021-23123-x__Nature Communications, vol. 12, no. 1, 3058, Springer Nature, 2021, doi:10.1038/s41467-021-23123-x.

Avagliano, Laura, et al. “Chromatinopathies: A Focus on Cornelia de Lange Syndrome.”10.1111/cge.13674__Clinical Genetics, vol. 97, no. 1, Wiley, 2020, pp. 3–11, doi:10.1111/cge.13674.

Latorre-Pellicer, Ana, et al. “Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes.”10.3390/ijms21031042__International Journal of Molecular Sciences, vol. 21, no. 3, 1042, MDPI, 2020, doi:10.3390/ijms21031042.

Weinert, Stefanie, et al. “Uncoupling Endosomal CLC Chloride/Proton Exchange Causes Severe Neurodegeneration.”10.15252/embj.2019103358__EMBO Journal, vol. 39, e103358, EMBO Press, 2020, doi:10.15252/embj.2019103358.

Parenti, Ilaria, et al. “MA and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange Syndrome.”10.1016/j.celrep.2020.107647__Cell Reports, vol. 31, no. 7, 107647, Elsevier, 2020, doi:10.1016/j.celrep.2020.107647.

Parenti, Ilaria, et al. “Neurodevelopmental Disorders: From Genetics to Functional Pathways.”10.1016/j.tins.2020.05.004__Trends in Neurosciences, vol. 43, no. 8, Elsevier, 2020, pp. 608–21, doi:10.1016/j.tins.2020.05.004.

Morandell, Jasmin. Illuminating the Role of Cul3 in Autism Spectrum Disorder Pathogenesis. Institute of Science and Technology Austria, 2020, doi:10.15479/AT:ISTA:8620.

Morandell, Jasmin, et al. “Cul3 Regulates Cytoskeleton Protein Homeostasis and Cell Migration during a Critical Window of Brain Development.”10.1101/2020.01.10.902064 __BioRxiv, Cold Spring Harbor Laboratory, doi:10.1101/2020.01.10.902064 .

Basilico, Bernadette, et al. “Molecular Mechanisms for Targeted ASD Treatments.”10.1016/j.gde.2020.06.004__Current Opinion in Genetics and Development, vol. 65, no. 12, Elsevier, 2020, pp. 126–37, doi:10.1016/j.gde.2020.06.004.

Marsh, Ashley, et al. “CUGC for Pontocerebellar Hypoplasia Type 9 and Spastic Paraplegia-63.”10.1038/s41431-018-0231-2__European Journal of Human Genetics, vol. 27, Springer Nature, 2019, pp. 161–66, doi:10.1038/s41431-018-0231-2.

Traxl, Alexander, 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.”10.1021/acs.molpharmaceut.8b01217__Molecular Pharmaceutics, vol. 16, no. 3, American Chemical Society, 2019, pp. 1282–93, doi:10.1021/acs.molpharmaceut.8b01217.

Éltes, Tímea, et al. “Improved Spike Inference Accuracy by Estimating the Peak Amplitude of Unitary [C+] Transients in Weakly GCaMf-Expressing Hippocampal Pyramidal Cells.”10.1113/JP277681__Journal of Physiology, vol. 597, no. 11, Wiley, 2019, pp. 2925–2947, doi:10.1113/JP277681.

Oliveira, Bárbara, et al. “Modeling Cell-Cell Interactions in the Brain Using Cerebral Organoids.”10.1016/j.brainres.2019.146458__Brain Research, vol. 1724, 146458, Elsevier, 2019, doi:10.1016/j.brainres.2019.146458.

Morandell, Jasmin, et al. “S.16.05 Illuminating the Role of the10.1016/j.euroneuro.2019.09.040__Ubiquitin Ligase Cullin3 in Brain Development and Autism.”10.1016/j.euroneuro.2019.09.040__European Neuropsychopharmacology, vol. 29, no. Supplement 6, Elsevier, 2019, pp. –12, doi:10.1016/j.euroneuro.2019.09.040.

Knaus, Lisa, et al. “S.16.03 A Homozygous Missense Mutation in SL Leads to Autism Spectrum Disorder and Microcephaly.”10.1016/j.euroneuro.2019.09.039__European Neuropsychopharmacology, vol. 29, no. Supplement 6, Elsevier, 2019, p. , doi:10.1016/j.euroneuro.2019.09.039.

Novarino, Gaia. “Zika-Associated Microcephaly: Reduce the Stress and Race for the Treatment.”10.1126/scitranslmed.aar7514__Science Translational Medicine, vol. 10, no. 423, eaar7514, American Association for the Advancement of Science, 2018, doi:10.1126/scitranslmed.aar7514.

Tarlungeanu, Dora-Clara, and Gaia Novarino. “Genomics in Neurodevelopmental Disorders: An Avenue to Personalized Medicine.”10.1038/s12276-018-0129-7__Experimental &; Molecular Medicine, vol. 50, no. 8, 100, Springer Nature, 2018, doi:10.1038/s12276-018-0129-7.

Sacco, Roberto, et al. “Neural Stem Cells in Neuropsychiatric Disorders.”10.1016/j.conb.2017.12.005__Current Opinion in Neurobiology, vol. 48, no. 2, Elsevier, 2018, pp. 131–38, doi:10.1016/j.conb.2017.12.005.