Chiara Tocco, Michele Bertacchi, Michèle Studer. Front Mol Neurosci 2021
Times Cited: 2
Times Cited: 2
Times Cited
Times Co-cited
Similarity
COUP-TFI regulates the balance of cortical patterning between frontal/motor and sensory areas.
Maria Armentano, Shen-Ju Chou, Giulio Srubek Tomassy, Axel Leingärtner, Dennis D M O'Leary, Michèle Studer. Nat Neurosci 2007
Maria Armentano, Shen-Ju Chou, Giulio Srubek Tomassy, Axel Leingärtner, Dennis D M O'Leary, Michèle Studer. Nat Neurosci 2007
100
The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations.
Chun-An Chen, Daniëlle G M Bosch, Megan T Cho, Jill A Rosenfeld, Marwan Shinawi, Richard Alan Lewis, John Mann, Parul Jayakar, Katelyn Payne, Laurence Walsh,[...]. Genet Med 2016
Chun-An Chen, Daniëlle G M Bosch, Megan T Cho, Jill A Rosenfeld, Marwan Shinawi, Richard Alan Lewis, John Mann, Parul Jayakar, Katelyn Payne, Laurence Walsh,[...]. Genet Med 2016
50
Nonsense-mediated decay approaches the clinic.
Jill A Holbrook, Gabriele Neu-Yilik, Matthias W Hentze, Andreas E Kulozik. Nat Genet 2004
Jill A Holbrook, Gabriele Neu-Yilik, Matthias W Hentze, Andreas E Kulozik. Nat Genet 2004
50
More evidence for seizure-induced neuron loss: is hippocampal sclerosis both cause and effect of epilepsy?
T P Sutula, A Pitkänen. Neurology 2001
T P Sutula, A Pitkänen. Neurology 2001
50
Growth in children with chronic kidney disease: role of nutrition, growth hormone, dialysis, and steroids.
Elizabeth G Ingulli, Robert H Mak. Curr Opin Pediatr 2014
Elizabeth G Ingulli, Robert H Mak. Curr Opin Pediatr 2014
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Neurobiological bases of autism-epilepsy comorbidity: a focus on excitation/inhibition imbalance.
Yuri Bozzi, Giovanni Provenzano, Simona Casarosa. Eur J Neurosci 2018
Yuri Bozzi, Giovanni Provenzano, Simona Casarosa. Eur J Neurosci 2018
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A neurodegenerative perspective on mitochondrial optic neuropathies.
Patrick Yu-Wai-Man, Marcela Votruba, Florence Burté, Chiara La Morgia, Piero Barboni, Valerio Carelli. Acta Neuropathol 2016
Patrick Yu-Wai-Man, Marcela Votruba, Florence Burté, Chiara La Morgia, Piero Barboni, Valerio Carelli. Acta Neuropathol 2016
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Human iPSC-Derived Cerebral Organoids Model Cellular Features of Lissencephaly and Reveal Prolonged Mitosis of Outer Radial Glia.
Marina Bershteyn, Tomasz J Nowakowski, Alex A Pollen, Elizabeth Di Lullo, Aishwarya Nene, Anthony Wynshaw-Boris, Arnold R Kriegstein. Cell Stem Cell 2017
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The human hippocampus: cognitive maps or relational memory?
Dharshan Kumaran, Eleanor A Maguire. J Neurosci 2005
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NR2F1 mediated down-regulation of osteoblast differentiation was rescued by bone morphogenetic protein-2 (BMP-2) in human MSC.
Muthurangan Manikandan, Sarah Abuelreich, Mona Elsafadi, Hussain Alsalman, Hassan Almalak, Abdulaziz Siyal, Jamil Amjad Hashmi, Abdullah Aldahmash, Moustapha Kassem, Musaad Alfayez,[...]. Differentiation 2018
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The Optic Nerve Hypoplasia Spectrum: Review of the Literature and Clinical Guidelines.
Anna Ryabets-Lienhard, Carly Stewart, Mark Borchert, Mitchell E Geffner. Adv Pediatr 2016
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Neurodevelopmental Disorders: From Genetics to Functional Pathways.
Ilaria Parenti, Luis G Rabaneda, Hanna Schoen, Gaia Novarino. Trends Neurosci 2020
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Molecular logic of neocortical projection neuron specification, development and diversity.
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Characteristics of Brains in Autism Spectrum Disorder: Structure, Function and Connectivity across the Lifespan.
Sungji Ha, In-Jung Sohn, Namwook Kim, Hyeon Jeong Sim, Keun-Ah Cheon. Exp Neurobiol 2015
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Optic nerve hypoplasia syndrome: a review of the epidemiology and clinical associations.
Pamela Garcia-Filion, Mark Borchert. Curr Treat Options Neurol 2013
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Medial temporal lobe contributions to cued retrieval of items and contexts.
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Netrin-1 and DCC mediate axon guidance locally at the optic disc: loss of function leads to optic nerve hypoplasia.
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Epileptic seizures.
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Chronic cortical visual impairment in children: aetiology, prognosis, and associated neurological deficits.
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Autism spectrum and obsessive-compulsive disorders: OC behaviors, phenotypes and genetics.
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Whole genome sequencing unveils genetic heterogeneity in optic nerve hypoplasia.
Sara Dahl, Maria Pettersson, Jesper Eisfeldt, Anna Katharina Schröder, Ronny Wickström, Kristina Teär Fahnehjelm, Britt-Marie Anderlid, Anna Lindstrand. PLoS One 2020
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Sustained Pax6 Expression Generates Primate-like Basal Radial Glia in Developing Mouse Neocortex.
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Astrocytes as Guardians of Neuronal Excitability: Mechanisms Underlying Epileptogenesis.
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50
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome Presenting as New-Onset Psychosis in a 32-Year-Old Man: A Case Report and Literature Review.
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50
Effect of Seizures on the Developing Brain and Cognition.
Gregory L Holmes. Semin Pediatr Neurol 2016
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50
Recent advances in cortical visual impairment.
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Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction.
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50
Missense NR2F1 variant in monozygotic twins affected with the Bosch-Boonstra-Schaaf optic atrophy syndrome.
Catia Mio, Federico Fogolari, Laura Pezzoli, Angela V D'Elia, Maria Iascone, Giuseppe Damante. Mol Genet Genomic Med 2020
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50
Manneristic behaviors of visually impaired children.
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50
Dynamic expression of NR2F1 and SOX2 in developing and adult human cortex: comparison with cortical malformations.
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50
COUP-TF Genes, Human Diseases, and the Development of the Central Nervous System in Murine Models.
Xiong Yang, Su Feng, Ke Tang. Curr Top Dev Biol 2017
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Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.
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50
Synaptic, transcriptional and chromatin genes disrupted in autism.
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Drug-based modulation of endogenous stem cells promotes functional remyelination in vivo.
Fadi J Najm, Mayur Madhavan, Anita Zaremba, Elizabeth Shick, Robert T Karl, Daniel C Factor, Tyler E Miller, Zachary S Nevin, Christopher Kantor, Alex Sargent,[...]. Nature 2015
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Nonsense-mediated decay in genetic disease: friend or foe?
Jake N Miller, David A Pearce. Mutat Res Rev Mutat Res 2014
Jake N Miller, David A Pearce. Mutat Res Rev Mutat Res 2014
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Motor development and delay: advances in assessment of motor skills in autism spectrum disorders.
Rujuta B Wilson, Peter G Enticott, Nicole J Rinehart. Curr Opin Neurol 2018
Rujuta B Wilson, Peter G Enticott, Nicole J Rinehart. Curr Opin Neurol 2018
50
COUP-TFI: an intrinsic factor for early regionalization of the neocortex.
C Zhou, S Y Tsai, M J Tsai. Genes Dev 2001
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50
FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders.
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Renal-coloboma syndrome: report of a novel PAX2 gene mutation.
G W Chung, A O Edwards, L A Schimmenti, G S Manligas, Y H Zhang, R Ritter. Am J Ophthalmol 2001
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COUP-TFI mitotically regulates production and migration of dentate granule cells and modulates hippocampal Cxcr4 expression.
Joséphine Parisot, Gemma Flore, Michele Bertacchi, Michèle Studer. Development 2017
Joséphine Parisot, Gemma Flore, Michele Bertacchi, Michèle Studer. Development 2017
50
The topography of corticopontine projections is controlled by postmitotic expression of the area-mapping gene Nr2f1.
Chiara Tocco, Martin Øvsthus, Jan G Bjaalie, Trygve B Leergaard, Michèle Studer. Development 2022
Chiara Tocco, Martin Øvsthus, Jan G Bjaalie, Trygve B Leergaard, Michèle Studer. Development 2022
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Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS) initially diagnosed as ALG6-CDG: Functional evidence for benignity of the ALG6 c.391T>C (p.Tyr131His) variant and further expanding the BBSOAS phenotype.
Rodrigo Tzovenos Starosta, Jessica Tarnowski, Filippo Pinto E Vairo, Kimiyo Raymond, Graeme Preston, Eva Morava. Eur J Med Genet 2020
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A staged screening of registered drugs highlights remyelinating drug candidates for clinical trials.
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The intolerance to functional genetic variation of protein domains predicts the localization of pathogenic mutations within genes.
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Clinical whole-exome sequencing results impact medical management.
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Early-Life Exposure to Environmental Air Pollution and Autism Spectrum Disorder: A Review of Available Evidence.
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Agyria (lissencephaly) with anomalous pyramidal crossing. Case report and review of literature.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.