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Frontiers in Molecular Neuroscience|January 3, 2022
Structural and Functional Aspects of the Neurodevelopmental Gene NR2F1: From Animal Models to Human PathologyChiara Tocco, Michele Bertacchi, Michèle Studer
Cells|April 23, 2022
Pathophysiological Heterogeneity of the BBSOA Neurodevelopmental SyndromeMichele Bertacchi, Chiara Tocco, Christian P Schaaf, et al.
Development (Cambridge, England)|March 9, 2022
The topography of corticopontine projections is controlled by postmitotic expression of the area-mapping gene Nr2f1Chiara Tocco, Martin Øvsthus, Jan G Bjaalie, et al.
Plos Biology|August 8, 2023
Lmo4 synergizes with Fezf2 to promote direct in vivo reprogramming of upper layer cortical neurons and cortical glia towards deep-layer neuron identitiesTorsten Felske, Chiara Tocco, Sophie Péron, et al.
Scientific Data|November 12, 2024
Spatially integrated cortico-subcortical tracing data for analyses of rodent brain topographical organizationMartin Øvsthus, Maaike M H van Swieten, Maja A Puchades, et al.
Neurobiology of Disease|February 26, 2024
Structural interhemispheric connectivity defects in mouse models of BBSOAS: Insights from high spatial resolution 3D white matter tractographyJean Christophe Deloulme, Maxime Leclercq, Olivier Deschaux, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 24, 2020
COUP-TFI/Nr2f1 Orchestrates Intrinsic Neuronal Activity during Development of the Somatosensory CortexIsabel Del Pino, Chiara Tocco, Elia Magrinelli, et al.
NPJ Parkinson'S Disease|October 9, 2025
Investigating the ageing-Parkinson's disease nexus: standardisation of in vitro models and techniques by the PD-AGE networkAlexander G Bury, Alicja Olejnik, Chiara Tocco, et al.
Nature Medicine|March 13, 2019
Altered neuronal migratory trajectories in human cerebral organoids derived from individuals with neuronal heterotopiaJohannes Klaus, Sabina Kanton, Christina Kyrousi, et al.
Cell Death & Disease|October 28, 2016
ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephalyVincent El Ghouzzi, Federico T Bianchi, Ivan Molineris, et al.
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