Gaia Novarino

IST Austria, Klosterneuburg, Niederösterreich, Austria 
"Gaia Novarino"
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Villa CE, Cheroni C, Dotter CP, et al. (2022) CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories. Cell Reports. 39: 110615
Vasic V, Jones MSO, Haslinger D, et al. (2021) Translating the Role of mTOR- and RAS-Associated Signalopathies in Autism Spectrum Disorder: Models, Mechanisms and Treatment. Genes. 12
Basilico B, Morandell J, Novarino G. (2020) Molecular mechanisms for targeted ASD treatments. Current Opinion in Genetics & Development. 65: 126-137
Parenti I, Rabaneda LG, Schoen H, et al. (2020) Neurodevelopmental Disorders: From Genetics to Functional Pathways. Trends in Neurosciences
Knaus L, Tarlungeanu D, Novarino G. (2019) S.16.03 A homozygous missense mutation in SLC7A5 leads to autism spectrum disorder and microcephaly European Neuropsychopharmacology. 29: S11
Deliu E, Arecco N, Morandell J, et al. (2018) Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition. Nature Neuroscience
Tărlungeanu DC, Novarino G. (2018) Genomics in neurodevelopmental disorders: an avenue to personalized medicine. Experimental & Molecular Medicine. 50: 100
Sacco R, Cacci E, Novarino G. (2017) Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology. 48: 131-138
Marin-Valencia I, Novarino G, Johansen A, et al. (2017) A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features. Journal of Medical Genetics
Novarino G. (2017) Rett syndrome modeling goes simian. Science Translational Medicine. 9
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