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Author

Valerio Caputo

Observed name: V. Caputo
ORCID: 0000-0002-3503-3318
Observed ORCID: 0000-0002-3503-3318
OpenAlex ID: A5062548065
Application of Precision Medicine in Neurodegenerative Diseases
2018 · Claudia Strafella, Valerio Caputo, et al. · Frontiers in Neurology · 110
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Towards the application of precision medicine in Age-Related Macular Degeneration
2017 · Raffaella Cascella, Claudia Strafella, et al. · Progress in Retinal and Eye Research · 76
Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications
2020 · Claudia Strafella, Valerio Caputo, et al. · Genes · 70
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Overview of the molecular determinants contributing to the expression of Psoriasis and Psoriatic Arthritis phenotypes
2020 · Valerio Caputo, Claudia Strafella, et al. · Journal of Cellular and Molecular Medicine · 62
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Pharmacogenomics: An Update on Biologics and Small-Molecule Drugs in the Treatment of Psoriasis
2021 · Valerio Caputo, Claudia Strafella, et al. · Genes · 48
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P63 in health and cancer
2015 · Stefania Gonfloni, Valerio Caputo, et al. · The International Journal of Developmental Biology · 48
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Multi-Layer Picture of Neurodegenerative Diseases: Lessons from the Use of Big Data through Artificial Intelligence
2021 · Andrea Termine, Carlo Fabrizio, et al. · Journal of Personalized Medicine · 44
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Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants
2017 · Raffaella Cascella, Claudia Strafella, et al. · Oncotarget · 38
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Investigation of Genetic Variations of IL6 and IL6R as Potential Prognostic and Pharmacogenetics Biomarkers: Implications for COVID-19 and Neuroinflammatory Disorders
2020 · Claudia Strafella, Valerio Caputo, et al. · Life · 37
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Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era
2019 · Stefania Zampatti, Luca Colantoni, et al. · Neurogenetics · 34
Deregulation of ncRNA in Neurodegenerative Disease: Focus on circRNA, lncRNA and miRNA in Amyotrophic Lateral Sclerosis
2021 · Paola Ruffo, Claudia Strafella, et al. · Frontiers in Genetics · 33
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Characterization of a natural variant of human NDP52 and its functional consequences on mitophagy
2021 · Anthea Di Rita, Daniela F. Angelini, et al. · Cell Death and Differentiation · 32
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Interpreting Mixture Profiles: Comparison Between Precision ID GlobalFiler™ NGS STR Panel v2 and Traditional Methods
2020 · Michele Ragazzo, Stefania Carboni, et al. · Genes · 23
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The Role of Epigenetic Control of Mitochondrial (Dys)Function in MASLD Onset and Progression
2023 · Valerio Caputo, Giovanni Tarantino, et al. · Nutrients · 21
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Update on the Molecular Aspects and Methods Underlying the Complex Architecture of FSHD
2022 · Valerio Caputo, Domenica Megalizzi, et al. · Cells · 21
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Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis
2019 · M.L. Musumeci, F. Fiorentini, et al. · Journal of the European Academy of Dermatology and Venereology · 21
Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD
2023 · Claudia Strafella, Valerio Caputo, et al. · Frontiers in Genetics · 20
RNAseq-Based Prioritization Revealed COL6A5, COL8A1, COL10A1 and MIR146A as Common and Differential Susceptibility Biomarkers for Psoriasis and Psoriatic Arthritis: Confirmation from Genotyping Analysis of 1417 Italian Subjects
2020 · Valerio Caputo, Claudia Strafella, et al. · International Journal of Molecular Sciences · 20
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The variability of SMCHD1 gene in FSHD patients: evidence of new mutations
2019 · Claudia Strafella, Valerio Caputo, et al. · Human Molecular Genetics · 19
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D4Z4 Methylation Levels Combined with a Machine Learning Pipeline Highlight Single CpG Sites as Discriminating Biomarkers for FSHD Patients
2022 · Valerio Caputo, Domenica Megalizzi, et al. · Cells · 18
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Evaluation of OpenArray™ as a Genotyping Method for Forensic DNA Phenotyping and Human Identification
2021 · Michele Ragazzo, Giulio Puleri, et al. · Genes · 18
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A
2019 · Claudia Strafella, Valeria Errichiello, et al. · International Journal of Molecular Sciences · 18
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Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from ADH1B, CYP1A2 and MTHFR
2022 · Shila Barati, Carlo Fabrizio, et al. · Genes · 15
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Immune System and Neuroinflammation in Idiopathic Parkinson’s Disease: Association Analysis of Genetic Variants and miRNAs Interactions
2021 · Claudia Strafella, Valerio Caputo, et al. · Frontiers in Genetics · 15
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Genetic Determinants Highlight the Existence of Shared Etiopathogenetic Mechanisms Characterizing Age-Related Macular Degeneration and Neurodegenerative Disorders
2021 · Claudia Strafella, Valerio Caputo, et al. · Frontiers in Neurology · 15
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Works count: 61
Citation count: 1,103
H-index: 19
I10-index: 37
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