Sara Castagnola

Centre National de la Recherche Scientifique — France

Biochemistry, Genetics and Molecular Biology · Life Sciences

8h-index387citations13works0.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(12), Autism Spectrum Disorder Research(4), Ubiquitin and proteasome pathways(3), Congenital heart defects research(3), RNA and protein synthesis mechanisms(2)

Publications13 total

Missense mutation of Fmr1 results in impaired AMPAR-mediated plasticity and socio-cognitive deficits in mice
Nature Communications·2021· 38 citedOpen Access
Agonist-induced functional analysis and cell sorting associated with single-cell transcriptomics characterizes cell subtypes in normal and pathological brain
Genome Research·2020· 9 citedOpen Access
Agonist-induced Functional Analysis and Cell Sorting, a novel tool to select and analyze neurons: Fragile X as a proof of concept
2020Open Access
Abnormal AMPAR-mediated synaptic plasticity, cognitive and autistic-like behaviors in a missense <i>Fmr1</i> mutant mouse model of Fragile X syndrome
2020Open Access
Reduction of Fmr1 mRNA Levels Rescues Pathological Features in Cortical Neurons in a Model of FXTAS
Molecular Therapy — Nucleic Acids·2019· 16 citedOpen Access
Dissecting the role of calcium signaling in Fragile X syndrome
HAL (Le Centre pour la Communication Scientifique Directe)·2019Open Access
Le rôle de la signalisation calcique dans le Syndrome de l'X fragile
ZooKeys·2019Open Access
New Insights Into the Role of Cav2 Protein Family in Calcium Flux Deregulation in Fmr1-KO Neurons
Frontiers in Molecular Neuroscience·2018· 22 citedOpen Access
Involvement of Phosphodiesterase 2A Activity in the Pathophysiology of Fragile X Syndrome
Cerebral Cortex·2018· 43 cited
HITS-CLIP in various brain areas reveals new targets and new modalities of RNA binding by fragile X mental retardation protein
Nucleic Acids Research·2018· 153 citedOpen Access
Sumoylation regulates FMRP-mediated dendritic spine elimination and maturation
Nature Communications·2018· 69 citedOpen Access
The Search for an Effective Therapy to Treat Fragile X Syndrome: Dream or Reality?
Frontiers in Synaptic Neuroscience·2017· 34 citedOpen Access
Screening for the major cystic fibrosis mutation in non-Caucasian populations.
PubMed·1991· 3 cited

Frequent Co-authors

Barbara Bardoni(10), Thomas Maurin(8), Frédéric Brau(7), Marielle Jarjat(6), Stéphane Martin(5), Sébastien Delhaye(5), Anouar Khayachi(4), Gwénola Poupon(4), Alessandra Folci(4), Kévin Lebrigand(3), Pietro Picerno(3), Carole Gwizdek(3), Magda Chafaï(3), Marta Curto Prieto(3), Marie Pronot(3), Emmanuel Deval(3), Sara Schiavi(3), Viviana Trezza(3), Agnès Paquet(2), Małgorzata Drozd(2)