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33 Publications

2020 | Journal Article | IST-REx-ID: 7488   OA
Latorre-Pellicer, Ana, Ángela Ascaso, Laura Trujillano, Marta Gil-Salvador, Maria Arnedo, Cristina Lucia-Campos, Rebeca Antoñanzas-Pérez, et al. “Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes.” International Journal of Molecular Sciences 21, no. 3 (2020): 1042. https://doi.org/10.3390/ijms21031042.
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2020 | Journal Article | IST-REx-ID: 7149
Avagliano, Laura, Ilaria Parenti, Paolo Grazioli, Elisabetta Di Fede, Chiara Parodi, Milena Mariani, Frank J. Kaiser, Angelo Selicorni, Cristina Gervasini, and Valentina Massa. “Chromatinopathies: A Focus on Cornelia de Lange Syndrome.” Clinical Genetics 97, no. 1 (2020): 3–11. https://doi.org/10.1111/cge.13674.
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2019 | Journal Article | IST-REx-ID: 105
Marsh, Ashley, Gaia Novarino, Paul Lockhart, and Richard Leventer. “CUGC for Pontocerebellar Hypoplasia Type 9 and Spastic Paraplegia-63.” European Journal of Human Genetics 27 (2019): 161–66. https://doi.org/10.1038/s41431-018-0231-2.
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2019 | Research Data | IST-REx-ID: 6074   OA
Dotter, Christoph, and Gaia Novarino. Supplementary Data for the Research Paper “Haploinsufficiency of the Intellectual Disability Gene SETD5 Disturbs Developmental Gene Expression and Cognition.” IST Austria, 2019. https://doi.org/10.15479/AT:ISTA:6074.
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2019 | Journal Article | IST-REx-ID: 6896
Oliveira, Bárbara, Aysan Çerağ Yahya, and Gaia Novarino. “Modeling Cell-Cell Interactions in the Brain Using Cerebral Organoids.” Brain Research 1724 (2019). https://doi.org/10.1016/j.brainres.2019.146458.
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2019 | Journal Article | IST-REx-ID: 7414
Knaus, Lisa, Dora-Clara Tarlungeanu, and Gaia Novarino. “S.16.03 A Homozygous Missense Mutation in SLC7A5 Leads to Autism Spectrum Disorder and Microcephaly.” European Neuropsychopharmacology 29, no. Supplement 6 (2019): S11. https://doi.org/10.1016/j.euroneuro.2019.09.039.
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2019 | Journal Article | IST-REx-ID: 7415
Morandell, Jasmin, Armel Nicolas, Lena A Schwarz, and Gaia Novarino. “S.16.05 Illuminating the Role of the E3 Ubiquitin Ligase Cullin3 in Brain Development and Autism.” European Neuropsychopharmacology 29, no. Supplement 6 (2019): S11–12. https://doi.org/10.1016/j.euroneuro.2019.09.040.
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2019 | Journal Article | IST-REx-ID: 6088
Traxl, Alexander, Severin Mairinger, Thomas Filip, Michael Sauberer, Johann Stanek, Stefan Poschner, Walter Jäger, et al. “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, no. 3 (2019): 1282–93. https://doi.org/10.1021/acs.molpharmaceut.8b01217.
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2019 | Journal Article | IST-REx-ID: 6470
Éltes, Tímea, Miklos Szoboszlay, Margit Katalin Szigeti, and Zoltan Nusser. “Improved Spike Inference Accuracy by Estimating the Peak Amplitude of Unitary [Ca2+] Transients in Weakly GCaMP6f-Expressing Hippocampal Pyramidal Cells.” Journal of Physiology 597, no. 11 (2019): 2925–2947. https://doi.org/10.1113/JP277681.
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2018 | Thesis | IST-REx-ID: 395   OA
Tarlungeanu, Dora-Clara. The Branched Chain Amino Acids in Autism Spectrum Disorders . IST Austria, 2018. https://doi.org/10.15479/AT:ISTA:th_992.
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2018 | Journal Article | IST-REx-ID: 456
Novarino, Gaia. “Zika-Associated Microcephaly: Reduce the Stress and Race for the Treatment.” Science Translational Medicine 10, no. 423 (2018). https://doi.org/10.1126/scitranslmed.aar7514.
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2018 | Journal Article | IST-REx-ID: 691   OA
Marin Valencia, Isaac, Gaia Novarino, Anide Johansen, Başak Rosti, Mahmoud Issa, Damir Musaev, Gifty Bhat, et al. “A Homozygous Founder Mutation in TRAPPC6B Associates with a Neurodevelopmental Disorder Characterised by Microcephaly Epilepsy and Autistic Features.” Journal of Medical Genetics 55, no. 1 (2018): 48–54. https://doi.org/10.1136/jmedgenet-2017-104627.
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2018 | Journal Article | IST-REx-ID: 546
Sacco, Roberto, Emanuele Cacci, and Gaia Novarino. “Neural Stem Cells in Neuropsychiatric Disorders.” Current Opinion in Neurobiology 48, no. 2 (2018): 131–38. https://doi.org/10.1016/j.conb.2017.12.005.
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2018 | Journal Article | IST-REx-ID: 5888   OA
Tarlungeanu, Dora-Clara, and Gaia Novarino. “Genomics in Neurodevelopmental Disorders: An Avenue to Personalized Medicine.” Experimental & Molecular Medicine 50, no. 8 (2018). https://doi.org/10.1038/s12276-018-0129-7.
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2018 | Journal Article | IST-REx-ID: 3
Deliu, Elena, Niccoló Arecco, Jasmin Morandell, Christoph Dotter, Ximena Contreras, Charles Girardot, Eva Käsper, et al. “Haploinsufficiency of the Intellectual Disability Gene SETD5 Disturbs Developmental Gene Expression and Cognition.” Nature Neuroscience 21, no. 12 (2018): 1717–27. https://doi.org/10.1038/s41593-018-0266-2.
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2017 | Journal Article | IST-REx-ID: 667
Novarino, Gaia. “The Antisocial Side of Antibiotics.” Science Translational Medicine 9, no. 387 (2017). https://doi.org/10.1126/scitranslmed.aan2786.
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2017 | Journal Article | IST-REx-ID: 713   OA
Andergassen, Daniel, Christoph Dotter, Dyniel Wenzel, Verena Sigl, Philipp Bammer, Markus Muckenhuber, Daniela Mayer, et al. “Mapping the Mouse Allelome Reveals Tissue Specific Regulation of Allelic Expression.” ELife 6 (2017). https://doi.org/10.7554/eLife.25125.
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2017 | Journal Article | IST-REx-ID: 656
Novarino, Gaia. “Modeling Alzheimer’s Disease in Mice with Human Neurons.” Science Translational Medicine 9, no. 381 (2017). https://doi.org/10.1126/scitranslmed.aam9867.
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2017 | Journal Article | IST-REx-ID: 702
Novarino, Gaia. “The Riddle of CHD8 Haploinsufficiency in Autism Spectrum Disorder.” Science Translational Medicine 9, no. 399 (2017): eaao0972. https://doi.org/10.1126/scitranslmed.aao0972.
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2017 | Journal Article | IST-REx-ID: 714
Brailoiu, Gabriela, Elena Deliu, Jeffrey Barr, Linda Console Bram, Alexandra Ciuciu, Mary Abood, Ellen Unterwald, and Eugen Brǎiloiu. “HIV Tat Excites D1 Receptor-like Expressing Neurons from Rat Nucleus Accumbens.” Drug and Alcohol Dependence 178 (2017): 7–14. https://doi.org/10.1016/j.drugalcdep.2017.04.015.
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