Viviana Caputo

Sapienza University of Rome — Italy

Biochemistry, Genetics and Molecular Biology · Life Sciences

30h-index7.0kcitations91works2.62yr avg
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Research Topics

RNA modifications and cancer(8), Genomics and Rare Diseases(8), Genetics and Neurodevelopmental Disorders(8), Parkinson's Disease Mechanisms and Treatments(7), MicroRNA in disease regulation(6)

Publications91 total

Unsupervised synchronization of molecular dynamics trajectories via graph embedding and time warping
Bioinformatics·2026Open Access
nAPOGEE: A machine-learning platform for clinically actionable pathogenicity assessment of all mitochondrial noncoding variants
2025Open Access
NetMD: Unsupervised Synchronization of Molecular Dynamics Trajectories via Graph Embedding and Time Warping
2025Open Access
Epigenetic Signatures of Dental Stem Cells: Insights into DNA Methylation and Noncoding RNAs
Applied Sciences·2025Open Access
Variable Intrafamilial Cardiac Phenotype Segregating With a <scp> <i>TBX20</i> </scp> Missense Variant in the Putative Transcriptional Activation Domain
American Journal of Medical Genetics Part A·2025
Craniofacial and Dental Anomalies of a Patient Carrying Two <scp>MicroRNA</scp> Variants: A Proof‐Of‐Concept Case Report
Clinical Case Reports·2025Open Access
Phenotypic traits and family history in patients with 22q11.2 deletion syndrome and generalized epilepsy: A multicenter case–control study
Epilepsia·2024
Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome’s clinical and molecular spectrum through NALCN in-silico structural analysis
Frontiers in Genetics·2024· 2 citedOpen Access
Craniofacial and dental anomalies of a patient characterized by microRNA polymorphisms: a case report.
2024Open Access
Unconventional p65/p52 NF-κB module regulates key tumor microenvironment-related genes in breast tumor-associated macrophages (TAMs)
Life Sciences·2024· 4 citedOpen Access
Dominantly acting variants in ATP6V1C1 and ATP6V1B2 cause a multisystem phenotypic spectrum by altering lysosomal and/or autophagosome function
Human Genetics and Genomics Advances·2024· 8 citedOpen Access
SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline
The American Journal of Human Genetics·2024· 15 citedOpen Access
Biallelic Variants of <scp><i>MRPS36</i></scp> Cause a New Form of Leigh Syndrome
Movement Disorders·2024· 3 citedOpen Access
Exploring non-coding genetic variability in ACE2: Functional annotation and in vitro validation of regulatory variants
Gene·2024Open Access
Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impaction
Journal of Dental Sciences·2024· 7 citedOpen Access
APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants
Nature Communications·2023· 32 citedOpen Access
Additional lesions identified by genomic microarrays are associated with an inferior outcome in low‐risk chronic lymphocytic leukaemia patients
British Journal of Haematology·2023· 2 citedOpen Access
Investigating Mitochondrial Gene Expression Patterns in Drosophila melanogaster Using Network Analysis to Understand Aging Mechanisms
Applied Sciences·2023· 8 citedOpen Access
APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants
2023Open Access
P-173 Extended molecular profiling in patients with biliary tract cancers: Impact of the BRCAness phenotype in patients management
Annals of Oncology·2023Open Access
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Frequent Co-authors

Marco Tartaglia(19), Bruno Dallapiccola(18), Antonio Pizzuti(14), Andrea Ciolfi(13), Alice Traversa(12), Enza Maria Valente(11), Lorenzo Stella(9), Anna Rita Bentivoglio(7), Giuseppe Zampino(6), Gianfranco Bocchinfuso(6), Francesco Brancati(6), Tommaso Mazza(6), Alberto Albanese(5), Giovanni Battista Ferrero(5), Simone Macrı̀(5), Francesco Petrizzelli(5), Massimo Carella(5), Pietro Cortelli(4), Nicholas Wood(4), Elisabetta Flex(4)