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Author

Valentina Melzi

Observed name: V. Melzi
ORCID: 0000-0003-4984-6800
Observed ORCID: 0000-0003-4984-6800
OpenAlex ID: A5037428787
MicroRNA expression analysis identifies a subset of downregulated miRNAs in ALS motor neuron progenitors
2018 · Mafalda Rizzuti, Giuseppe Filosa, et al. · Scientific Reports · 62
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Synaptotagmin 13 is neuroprotective across motor neuron diseases
2020 · M. Nizzardo, M. Taiana, et al. · Acta Neuropathologica · 50
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Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons
2018 · Federica Rizzo, Monica Nizzardo, et al. · Brain · 43
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Shaping the Neurovascular Unit Exploiting Human Brain Organoids
2024 · Mafalda Rizzuti, Valentina Melzi, et al. · Molecular Neurobiology · 38
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Stathmins and Motor Neuron Diseases: Pathophysiology and Therapeutic Targets
2022 · Delia Gagliardi, Elisa Pagliari, et al. · Biomedicines · 33
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Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes
2022 · Mafalda Rizzuti, Valentina Melzi, et al. · Cellular and Molecular Life Sciences · 33
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Mutational analysis of COQ2 in patients with MSA in Italy
2016 · Dario Ronchi, Ernesto Di Biase, et al. · Neurobiology of Aging · 32
Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown–Vialetto disease that is partially rescued by riboflavin
2017 · Federica Rizzo, Agnese Ramirez, et al. · Scientific Reports · 29
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A novel homozygous PLA2G6 mutation causes dystonia-parkinsonism
2015 · M.C. Malaguti, V. Melzi, et al. · Parkinsonism & Related Disorders · 27
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot–Marie–Tooth type 2A
2023 · Federica Rizzo, Silvia Bono, et al. · Cellular and Molecular Life Sciences · 21
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A de novo C19orf12 heterozygous mutation in a patient with MPAN
2017 · Edoardo Monfrini, Valentina Melzi, et al. · Parkinsonism & Related Disorders · 21
Genomic and transcriptomic advances in amyotrophic lateral sclerosis
2023 · Mafalda Rizzuti, Luca Sali, et al. · Ageing Research Reviews · 20
Juvenile dystonia-parkinsonism syndrome caused by a novel p.S941Tfs1X ATP13A2 (PARK9) mutation
2015 · D. Martino, V. Melzi, et al. · Parkinsonism & Related Disorders · 15
Mutations in TMEM230 are rare in autosomal dominant Parkinson's disease
2017 · Gabriele Buongarzone, Edoardo Monfrini, et al. · Parkinsonism & Related Disorders · 12
Targeting STMN2 for neuroprotection and neuromuscular recovery in Spinal Muscular Atrophy: evidence from in vitro and in vivo SMA models
2024 · Elisa Pagliari, Michela Taiana, et al. · Cellular and Molecular Life Sciences · 10
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SCARB1 downregulation in adrenal insufficiency with Allgrove syndrome
2023 · Giacomo Bitetto, Gianluca Lopez, et al. · Orphanet Journal of Rare Diseases · 9
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Unveiling amyotrophic lateral sclerosis complexity: insights from proteomics, metabolomics, and microbiomics
2025 · Simone Scarcella, Lorenzo Brambilla, et al. · Brain Communications · 6
Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired
2022 · Michela Taiana, Alessandra Govoni, et al. · Journal of Neurology Neurosurgery & Psychiatry · 6
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iPSC ‐derived human cortical organoids display profound alterations of cellular homeostasis following SARS ‐ CoV ‐2 infection and Spike protein exposure
2025 · Gioia Cappelletti, Lorenzo Brambilla, et al. · The FASEB Journal · 5
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Generation of two hiPSC lines (UMILi027-A and UMILi028-A) from early and late-onset Congenital Central hypoventilation Syndrome (CCHS) patients carrying a polyalanine expansion mutation in the PHOX2B gene
2022 · Ana Lucia Cuadros Gamboa, Roberta Benfante, et al. · Stem Cell Research · 5
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A point-of-care test for miR-129–5p detection at sub-atto molar concentrations exploiting plasmonic pollen probes combined with complementary DNA
2025 · Laura Pasquardini, Rosalba Pitruzzella, et al. · Sensors and Actuators Reports · 1
RNAi/gene therapy combined approach as therapeutic strategy for Charcot-Marie-Tooth 2A (S58.005)
2019 · Federica Rizzo, Silvia Bono, et al. · Neurology · 1
A Subset of Axonal and Synaptic Genes with Altered Expression/Splicing in SMA-MNs Harbours a Common Motif that Interacts with SMN/SYNCRIP Complex (S29.005)
2018 · Federica Rizzo, Monica Nizzardo, et al. · Neurology · 1
SARS-CoV-2 infection and Spike protein exposure alter iPSC-derived human brain organoid homeostasis.
2023 · Gioia Cappelletti, Lorenzo Brambilla, et al. · The Journal of Immunology
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Expanding the genotypic and phenotypic spectrum of Beta‐propeller protein‐associated neurodegeneration
2020 · Edoardo Monfrini, Pierluigi Tocco, et al. · European Journal of Neurology
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Works count: 29
Citation count: 478
H-index: 13
I10-index: 15
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