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Arianna Vino

Showing results (1-10 of 15) with videos related to

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European Journal of Human Genetics : EJHG|April 9, 2015
A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairmentReymundo Lozano, Arianna Vino, Cristina Lozano, et al.
Human Mutation|April 14, 2025
Genome Sequencing of Idiopathic Speech DelayElse Eising, Arianna Vino, Heather L Mabie, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 7, 2018
Rare variants in axonogenesis genes connect three families with sound-color synesthesiaAmanda K Tilot, Katerina S Kucera, Arianna Vino, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 2, 2019
Toward Robust Functional Neuroimaging Genetics of CognitionJulia Uddén, Annika Hultén, Katarina Bendtz, et al.
Molecular Psychiatry|August 20, 2025
De novo protein-coding gene variants in developmental stutteringElse Eising, Ivana Dzinovic, Arianna Vino, et al.
The Oncologist|November 11, 2011
Prevalence of Borrelia burgdorferi infection in a series of 98 primary cutaneous lymphomasMaurilio Ponzoni, Andrés J M Ferreri, Silvia Mappa, et al.
Human Molecular Genetics|January 25, 2018
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disordersSara B Estruch, Sarah A Graham, Martí Quevedo, et al.
Human Molecular Genetics|December 29, 2022
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactionsElliot Sollis, Joery den Hoed, Marti Quevedo, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
Plos One|June 29, 2016
A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal GyrusYoung Jae Woo, Tao Wang, Tulio Guadalupe, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
European Journal of Human Genetics : EJHG|April 9, 2015
A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairmentReymundo Lozano, Arianna Vino, Cristina Lozano, et al.
Human Mutation|April 14, 2025
Genome Sequencing of Idiopathic Speech DelayElse Eising, Arianna Vino, Heather L Mabie, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 7, 2018
Rare variants in axonogenesis genes connect three families with sound-color synesthesiaAmanda K Tilot, Katerina S Kucera, Arianna Vino, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 2, 2019
Toward Robust Functional Neuroimaging Genetics of CognitionJulia Uddén, Annika Hultén, Katarina Bendtz, et al.
Molecular Psychiatry|August 20, 2025
De novo protein-coding gene variants in developmental stutteringElse Eising, Ivana Dzinovic, Arianna Vino, et al.
The Oncologist|November 11, 2011
Prevalence of Borrelia burgdorferi infection in a series of 98 primary cutaneous lymphomasMaurilio Ponzoni, Andrés J M Ferreri, Silvia Mappa, et al.
Human Molecular Genetics|January 25, 2018
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disordersSara B Estruch, Sarah A Graham, Martí Quevedo, et al.
Human Molecular Genetics|December 29, 2022
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactionsElliot Sollis, Joery den Hoed, Marti Quevedo, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
Plos One|June 29, 2016
A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal GyrusYoung Jae Woo, Tao Wang, Tulio Guadalupe, et al.
Pageof 2