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Valentina Fodale

Observed names: Fodale, V., Fodale, Valentina, V. Fodale
Institution: IRBM
ORCID: 0000-0002-9870-2101
Observed ORCID: 0000-0002-9870-2101
OpenAlex ID: A5083010556
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome
2006 · Marco Tartaglia, Len A Pennacchio, et al. · Nature Genetics · 590
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Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
2009 · Viviana Cordeddu, Elia Di Schiavi, et al. · Nature Genetics · 430
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Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia
2008 · Elisabetta Flex, Valentina Petrangeli, et al. · The Journal of Experimental Medicine · 346
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Mechanism of Cell Adaptation
2011 · Valentina Fodale, Mariaelena Pierobon, et al. · The Cancer Journal · 178
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin
2008 · Hans Christian Hennies, Uwe Kornak, et al. · Nature Genetics · 162
Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis
2014 · E. Flex, M. Jaiswal, et al. · Human Molecular Genetics · 152
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Validation of Ultrasensitive Mutant Huntingtin Detection in Human Cerebrospinal Fluid by Single Molecule Counting Immunoassay
2017 · Valentina Fodale, Roberto Boggio, et al. · Journal of Huntington s Disease · 56
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Widespread and sustained target engagement in Huntington’s disease minipigs upon intrastriatal microRNA-based gene therapy
2021 · Astrid Vallès, Melvin M. Evers, et al. · Science Translational Medicine · 51
Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome
2013 · Elisabetta Flex, Andrea Ciolfi, et al. · Journal of Medical Genetics · 49
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Phosphoproteomic Analysis of Signaling Pathways in Head and Neck Squamous Cell Carcinoma Patient Samples
2011 · Mitchell J. Frederick, Amy J. VanMeter, et al. · American Journal Of Pathology · 49
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Quantifying autophagy using novel LC3B and p62 TR-FRET assays
2018 · Alberto Bresciani, Maria Carolina Spiezia, et al. · PLoS ONE · 48
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Polyglutamine expansion affects huntingtin conformation in multiple Huntington’s disease models
2017 · Manuel Daldin, Valentina Fodale, et al. · Scientific Reports · 41
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Polyglutamine- and Temperature-Dependent Conformational Rigidity in Mutant Huntingtin Revealed by Immunoassays and Circular Dichroism Spectroscopy
2014 · Valentina Fodale, Natalie C. Kegulian, et al. · PLoS ONE · 41
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AAV5-miHTT-mediated huntingtin lowering improves brain health in a Huntington’s disease mouse model
2022 · Sarah B Thomson, Anouk Stam, et al. · Brain · 32
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Analysis of mutant and total huntingtin expression in Huntington’s disease murine models
2020 · Valentina Fodale, Roberta Pintauro, et al. · Scientific Reports · 31
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Discovery of a Novel Series of Imidazopyrazine Derivatives as Potent SHP2 Allosteric Inhibitors
2023 · Esther Torrente, Valentina Fodale, et al. · ACS Medicinal Chemistry Letters · 27
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SHOC2 subcellular shuttling requires the KEKE motif-rich region andN-terminal leucine-rich repeat domain and impacts on ERK signalling
2016 · Marialetizia Motta, Giovanni Chillemi, et al. · Human Molecular Genetics · 22
Induction of Both CD8+ and CD4+ T-Cell–Mediated Responses in Colorectal Cancer Patients by Colon Antigen-1
2008 · Cristina Maccalli, Veronica Di Cristanziano, et al. · Clinical Cancer Research · 15
Quantifying Huntingtin Protein in Human Cerebrospinal Fluid Using a Novel Polyglutamine Length-Independent Assay
2022 · Valentina Fodale, Roberta Pintauro, et al. · Journal of Huntington s Disease · 10
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Identification and Optimization of RNA-Splicing Modulators as Huntingtin Protein-Lowering Agents for the Treatment of Huntington’s Disease
2023 · Longbin Liu, Karine Malagu, et al. · Journal of Medicinal Chemistry · 9
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I05 Sustained mutant huntingtin lowering in the brain and cerebrospinal fluid of huntington disease minipigs mediated by AAV5-MIHTT gene therapy
2018 · Astrid Valls, Cynthia Brouwers, et al. · Journal of Neurology Neurosurgery & Psychiatry · 3
Erratum: Corrigendum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome
2007 · Marco Tartaglia, Len A Pennacchio, et al. · Nature Genetics · 3
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Conformational modulation mediated by polyglutamine expansion in CAG repeat expansion disease-associated proteins
2016 · Margherita Verani, Maria Bustamante, et al. · Biochemical and Biophysical Research Communications · 2
Development and validation of highly selective monoclonal antibodies for the detection of huntingtin neoepitopes
2026 · Antonino Missineo, Licia Tomei, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 1
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Cyclic Peptide Inhibitors of the MLH1-MSH3 Interaction as a Potential Therapeutic Strategy for Huntington's Disease
2026 · Tasir S Haque, Federica Orvieto, et al. · ChemRxiv · 1
Works count: 39
Citation count: 2,349
H-index: 17
I10-index: 19
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