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40 Publications

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: 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: 689
Novarino, Gaia. “Rett Syndrome Modeling Goes Simian.” Science Translational Medicine 9, no. 393 (2017). https://doi.org/10.1126/scitranslmed.aan8196.
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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: 1228 | OA
Sauerzopf, Ulrich, Roberto Sacco, Gaia Novarino, Marco Niello, Ana Weidenauer, Nicole Praschak Rieder, Harald Sitte, and Matthaeus Willeit. “Are Reprogrammed Cells a Useful Tool for Studying Dopamine Dysfunction in Psychotic Disorders? A Review of the Current Evidence.” European Journal of Neuroscience 45, no. 1 (2017): 45–57. https://doi.org/10.1111/ejn.13418.
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2016 | Journal Article | IST-REx-ID: 1183 | OA
Tarlungeanu, Dora-Clara, Elena Deliu, Christoph Dotter, Majdi Kara, Philipp Janiesch, Mariafrancesca Scalise, Michele Galluccio, et al. “Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder.” Cell 167, no. 6 (2016): 1481–94. https://doi.org/10.1016/j.cell.2016.11.013.
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2016 | Journal Article | IST-REx-ID: 1240 | OA
Kornienko, Aleksandra, Christoph Dotter, Philipp Guenzl, Heinz Gisslinger, Bettina Gisslinger, Ciara Cleary, Robert Kralovics, Florian Pauler, and Denise Barlow. “Long Non-Coding RNAs Display Higher Natural Expression Variation than Protein-Coding Genes in Healthy Humans.” Genome Biology 17, no. 1 (2016). https://doi.org/10.1186/s13059-016-0873-8.
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2015 | Journal Article | IST-REx-ID: 1789 | OA
Kuechler, Alma, Alexander Zink, Thomas Wieland, Hermann Lüdecke, Kirsten Cremer, Leonardo Salviati, Pamela Magini, 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 23, no. 6 (2015): 753–60. https://doi.org/10.1038/ejhg.2014.165.
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2015 | Journal Article | IST-REx-ID: 1497 | OA
Andergassen, Daniel, Christoph Dotter, Tomasz Kulinski, Philipp Guenzl, Philipp Bammer, Denise Barlow, Florian Pauler, and Quanah Hudson. “Allelome.PRO, a Pipeline to Define Allele-Specific Genomic Features from High-Throughput Sequencing Data.” Nucleic Acids Research 43, no. 21 (2015). https://doi.org/10.1093/nar/gkv727.
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2014 | Journal Article | IST-REx-ID: 1916 | OA
Novarino, Gaia, Ali Fenstermaker, Maha Zaki, Matan Hofree, Jennifer Silhavy, Andrew Heiberg, Mostafa Abdellateef, et al. “Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders.” Science 343, no. 6170 (2014): 506–11. https://doi.org/10.1126/science.1247363.
View | DOI | Download Submitted Version (ext.) | PubMed | Europe PMC
 

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