Viviana Caputo

7.0k total citations
52 papers, 1.8k citations indexed

About

Viviana Caputo is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Viviana Caputo has authored 52 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Genetics and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Viviana Caputo's work include RNA modifications and cancer (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Viviana Caputo is often cited by papers focused on RNA modifications and cancer (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Viviana Caputo collaborates with scholars based in Italy, United States and Switzerland. Viviana Caputo's co-authors include Bruno Dallapiccola, Enza Maria Valente, Emanuele Bellacchio, Laura Silvestri, Luigia Atorino, Giorgio Casari, Antonio Pizzuti, Anna Rita Bentivoglio, Alberto Albanese and Antonio Emanuele Elia and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and PLoS ONE.

In The Last Decade

Viviana Caputo

50 papers receiving 1.8k citations

Peers

Countries citing papers authored by Viviana Caputo

Since Specialization

Citations

This map shows the geographic impact of Viviana Caputo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Viviana Caputo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Viviana Caputo more than expected).

Fields of papers citing papers by Viviana Caputo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Viviana Caputo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Viviana Caputo. The network helps show where Viviana Caputo may publish in the future.

Co-authorship network of co-authors of Viviana Caputo

This figure shows the co-authorship network connecting the top 25 collaborators of Viviana Caputo. A scholar is included among the top collaborators of Viviana Caputo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Viviana Caputo. Viviana Caputo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Unconventional p65/p52 NF-κB module regulates key tumor microenvironment-related genes in breast tumor-associated macrophages (TAMs) 2024 ·Life Sciences ·(unknown), (unknown), Antonella Bordin, Francesca Pagano, Viviana Caputo, Chiara Parisi	1
2	Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome 2024 ·Movement Disorders ·Serena Galosi, Cecilia Mancini, (unknown), Paolo Calligari, Viviana Caputo, Francesca Nardecchia, Claudia Carducci, Lambertus P. van den Heuvel, Simone Pizzi, Alessandro Bruselles, Marcello Niceta, Simone Martinelli, Richard J. Rodenburg, Marco Tartaglia, Vincenzo Leuzzi	2
3	Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities 2023 ·Frontiers in Cellular Neuroscience ·(unknown), Alice Traversa, Viviana Caputo, (unknown), Jonas Hauser, Simone Macrı̀	7
4	Protection against Ischemic Heart Disease: A Joint Role for eNOS and the KATP Channel 2023 ·International Journal of Molecular Sciences ·Paolo Severino, Andrea D’Amato, Massimo Mancone, Alberto Palazzuoli, Marco Valerio Mariani, Silvia Prosperi, (unknown), Carlo Lavalle, Giovanni B. Forleo, Lucia Ilaria Birtolo, Viviana Caputo, Fabio Miraldi, Cristina Chimenti, Roberto Badagliacca, Viviana Maestrini, Raffaele Palmirotta, Carmine Dario Vizza, Francesco Fedele	3
5	APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants 2023 ·Nature Communications ·(unknown), Luca Parca, (unknown), Tommaso Biagini, (unknown), (unknown), (unknown), Massimo Carella, Vincent Procaccio, Marie T. Lott, (unknown), Angelo L. Vescovi, Douglas C. Wallace, Viviana Caputo, Tommaso Mazza	20
6	Investigating Mitochondrial Gene Expression Patterns in Drosophila melanogaster Using Network Analysis to Understand Aging Mechanisms 2023 ·Applied Sciences ·(unknown), (unknown), (unknown), (unknown), Tommaso Biagini, (unknown), (unknown), Pietro Hiram Guzzi, Antonio Novelli, Viviana Caputo, Tommaso Mazza	2
7	Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study 2022 ·Genes ·Carolina Putotto, Federica Pulvirenti, Flaminia Pugnaloni, (unknown), Marta Unolt, Silvia Anaclerio, Viviana Caputo, Laura Bernardini, Elisa Messina, Corrado Moretti, Luigi Tarani, Bruno Marino, Paolo Versacci	3
8	Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode 2021 ·Molecular Psychiatry ·Jonas Hauser, (unknown), Alejandro Arias Vásquez, (unknown), Alice Traversa, Valentina Chiodi, François‐Pierre Martin, Norbert Sprenger, Oksana Lukjančenko, (unknown), Sylviane Métairon, Nora Schneider, Pascal Steiner, Alberto Martire, Viviana Caputo, Simone Macrı̀	64
9	Prenatal expression of d-aspartate oxidase causes early cerebral d-aspartate depletion and influences brain morphology and cognitive functions at adulthood 2020 ·Amino Acids ·(unknown), (unknown), Anna Maio, Tommaso Nuzzo, Yasuaki Saitoh, Masumi Katane, Andrea M. Isidori, Viviana Caputo, Pina Marotta, Geppino Falco, Maria Egle De Stefano, Hiroshi Homma, Alessandro Usiello, Francesco Errico	19
10	New insights on the influence of free d-aspartate metabolism in the mammalian brain during prenatal and postnatal life 2020 ·Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics ·Francesco Errico, Mariella Cuomo, Nadia Canu, Viviana Caputo, Alessandro Usiello	28
11	Prediction and visualization data for the interpretation of sarcomeric and non-sarcomeric DNA variants found in patients with hypertrophic cardiomyopathy 2016 ·Data in Brief ·Irene Bottillo, (unknown), Viviana Caputo, Alessandro Paiardini, (unknown), Carmelilia De Bernardo, Silvia Majore, Marco Castori, Elisabetta Zachara, Federica Re, Paola Grammatico	1
12	Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes 2016 ·European Journal of Paediatric Neurology ·Elisa Giorgio, Alessandro Brussino, Elisa Biamino, Elga Fabia Belligni, Alessandro Bruselles, Andrea Ciolfi, Viviana Caputo, Simone Pizzi, Alessandro Calcia, Eleonora Di Gregorio, Simona Cavalieri, Cecilia Mancini, Elisa Pozzi, Marta Ferrero, Evelise Riberi, I Borelli, Antonio Amoroso, Giovanni Battista Ferrero, Marco Tartaglia, Alfredo Brusco	11
13	The Emerging Role of MicroRNA in Schizophrenia 2015 ·CNS & Neurological Disorders - Drug Targets ·Viviana Caputo, Andrea Ciolfi, Simone Macrı̀, Antonio Pizzuti	26
14	Ago1 and Ago2 differentially affect cell proliferation, motility and apoptosis when overexpressed in SH-SY5Y neuroblastoma cells 2011 ·FEBS Letters ·Chiara Parisi, Corinna Giorgi, (unknown), Laura Braccini, Giovanna Maresca, Igea D’Agnano, Viviana Caputo, (unknown), (unknown), Carlo Cogoni, Caterina Catalanotto	27
15	Insights into the interaction of sortilin with proneurotrophins: A computational approach 2008 ·Neuropeptides ·Alessandro Paiardini, Viviana Caputo	16
16	Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian family 2004 ·European Journal of Human Genetics ·Antonio Novelli, Enza Maria Valente, Laura Bernardini, (unknown), Lorenzo Sinibaldi, Viviana Caputo, Pietro Cavalli, Bruno Dallapiccola	10
17	Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33–q34 2002 ·Annals of Neurology ·Enza Maria Valente, Francesco Brancati, Viviana Caputo, Enrico Bertini, Clarice Patrono, (unknown), Bruno Dallapiccola	24
18	Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene 2002 ·Movement Disorders ·Giovanni Defazio, Francesco Brancati, Enza Maria Valente, Viviana Caputo, Antonio Pizzuti, Davide Martino, Giovanni Abbruzzese, Paolo Livrea, Alfredo Berardelli, Bruno Dallapiccola	34
19	Novel Italian family supports clinical and genetic heterogeneity of primary adult‐onset torsion dystonia 2002 ·Movement Disorders ·Francesco Brancati, Giovanni Defazio, Viviana Caputo, Enza Maria Valente, Antonio Pizzuti, Paolo Livrea, Alfredo Berardelli, Bruno Dallapiccola	19
20	PARK6 is a common cause of familial parkinsonism 2002 ·Neurological Sciences ·Enza Maria Valente, Francesco Brancati, Viviana Caputo, Elizabeth Graham, Mary B. Davis, Alessandro Ferraris, Monique M.B. Breteler, Thomas Gasser, Vincenzo Bonifati, Anna Rita Bentivoglio, Giovanna De Michele, Alexandra D�rr, Pietro Cortelli, Alessandro Filla, G. Meco, Ben A. Oostra, Alexis Brice, Alberto Albanese, Bruno Dallapiccola, Nicholas Wood	32

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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