5 Publications

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[5]
2020 | Preprint | IST-REx-ID: 7800 | OA
Morandell, J., Schwarz, L. A., Basilico, B., Tasciyan, S., Nicolas, A., Sommer, C. M., … Novarino, G. (n.d.). Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development. BioRxiv. Cold Spring Harbor Laboratory.
View | Files available | Download Preprint (ext.)
 
[4]
2020 | Journal Article | IST-REx-ID: 8131 | OA
Basilico, B., Morandell, J., & Novarino, G. (2020). Molecular mechanisms for targeted ASD treatments. Current Opinion in Genetics and Development, 65(12), 126–137. https://doi.org/10.1016/j.gde.2020.06.004
View | Files available | DOI | PubMed | Europe PMC
 
[3]
2019 | Journal Article | IST-REx-ID: 7415
Morandell, J., Nicolas, A., Schwarz, L. A., & Novarino, G. (2019). S.16.05 Illuminating the role of the e3 ubiquitin ligase cullin3 in brain development and autism. European Neuropsychopharmacology, 29(Supplement 6), S11–S12. https://doi.org/10.1016/j.euroneuro.2019.09.040
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[2]
2018 | Journal Article | IST-REx-ID: 3 | OA
Deliu, E., Arecco, N., Morandell, J., Dotter, C., Contreras, X., Girardot, C., … Novarino, G. (2018). Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition. Nature Neuroscience, 21(12), 1717–1727. https://doi.org/10.1038/s41593-018-0266-2
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[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie, M., Breuss, M., Tian, G., Hansen, A. H., Cristofoli, F., Morandell, J., … Van Esch, H. (2015). Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics, 97(6), 790–800. https://doi.org/10.1016/j.ajhg.2015.10.014
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5 Publications

Mark all

[5]
2020 | Preprint | IST-REx-ID: 7800 | OA
Morandell, J., Schwarz, L. A., Basilico, B., Tasciyan, S., Nicolas, A., Sommer, C. M., … Novarino, G. (n.d.). Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development. BioRxiv. Cold Spring Harbor Laboratory.
View | Files available | Download Preprint (ext.)
 
[4]
2020 | Journal Article | IST-REx-ID: 8131 | OA
Basilico, B., Morandell, J., & Novarino, G. (2020). Molecular mechanisms for targeted ASD treatments. Current Opinion in Genetics and Development, 65(12), 126–137. https://doi.org/10.1016/j.gde.2020.06.004
View | Files available | DOI | PubMed | Europe PMC
 
[3]
2019 | Journal Article | IST-REx-ID: 7415
Morandell, J., Nicolas, A., Schwarz, L. A., & Novarino, G. (2019). S.16.05 Illuminating the role of the e3 ubiquitin ligase cullin3 in brain development and autism. European Neuropsychopharmacology, 29(Supplement 6), S11–S12. https://doi.org/10.1016/j.euroneuro.2019.09.040
View | DOI
 
[2]
2018 | Journal Article | IST-REx-ID: 3 | OA
Deliu, E., Arecco, N., Morandell, J., Dotter, C., Contreras, X., Girardot, C., … Novarino, G. (2018). Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition. Nature Neuroscience, 21(12), 1717–1727. https://doi.org/10.1038/s41593-018-0266-2
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie, M., Breuss, M., Tian, G., Hansen, A. H., Cristofoli, F., Morandell, J., … Van Esch, H. (2015). Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics, 97(6), 790–800. https://doi.org/10.1016/j.ajhg.2015.10.014
View | DOI
 

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