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L. Calzari · SciRah

Researcher profile · Semantic Scholar

L. Calzari

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L. Calzari — researcher profile on SciRah

h-index: 19
Works: 68
Citations: 1,053

Most-cited papers

(Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome
A. Mussa, S. Russo, A. De Crescenzo, A. Freschi +17 more
2015European Journal of Human Genetics133 citations Open access
Semantic Scholar
Stochastic epigenetic mutations (DNA methylation) increase exponentially in human aging and correlate with X chromosome inactivation skewing in females
D. Gentilini, P. Garagnani, S. Pisoni, M. Bacalini +5 more
2015Aging88 citations Open access
Semantic Scholar
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation
H. Demond, Z. Anvar, B. Jahromi, A. Sparago +9 more
2019Genome Medicine69 citations Open access
Semantic Scholar
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes
S. Russo, L. Calzari, A. Mussa, E. Mainini +19 more
2016Clinical Epigenetics64 citations Open access
Semantic Scholar
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
M. Cubellis, Laura Pignata, A. Verma, A. Sparago +9 more
2020Clinical Epigenetics57 citations Open access
Semantic Scholar
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
T. Eggermann, Elzem Yapici, J. Bliek, A. Pereda +15 more
2022Clinical Epigenetics46 citations Open access
Semantic Scholar
Fetal growth patterns in Beckwith–Wiedemann syndrome
A. Mussa, S. Russo, A. De Crescenzo, A. Freschi +17 more
2016Clinical Genetics42 citations
Semantic Scholar
DNA Methylation in the Diagnosis of Monogenic Diseases
Flavia Cerrato, A. Sparago, F. Ariani, Fulvia Brugnoletti +19 more
2020Genes41 citations Open access
Semantic Scholar
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
M. Calvello, S. Tabano, P. Colapietro, S. Maitz +12 more
2013Epigenetics41 citations Open access
Semantic Scholar
Heterogeneity of Cellular Senescence: Cell Type-Specific and Senescence Stimulus-Dependent Epigenetic Alterations
K. Kwiatkowska, E. Mavrogonatou, Adamantia Papadopoulou, C. Sala +10 more
2023Cells32 citations Open access
Semantic Scholar
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype
A. Sparago, A. Verma, M. Patricelli, Laura Pignata +12 more
2019Clinical Epigenetics29 citations Open access
Semantic Scholar
iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability.
Valentina Alari, S. Russo, B. Terragni, P. Ajmone +11 more
2018Stem Cell Research29 citations Open access
Semantic Scholar
Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
A. Peron, Ilaria Catusi, Maria Paola Recalcati, L. Calzari +3 more
2020Frontiers in Neurology28 citations Open access
Semantic Scholar
Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes
D. Mackay, J. Bliek, M. Lombardi, S. Russo +10 more
2019Genetics Research26 citations Open access
Semantic Scholar
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates
Marta Viggiano, F. Ceroni, Paola Visconti, A. Posar +13 more
2024npj Genomic Medicine22 citations Open access
Semantic Scholar
Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID-19 infection: insights from a genome-wide DNA methylation study
L. Calzari, D. F. Dragani, L. Zanotti, Elvira Inglese +15 more
2024Clinical Epigenetics22 citations Open access
Semantic Scholar
Epigenome Wide Association and Stochastic Epigenetic Mutation Analysis on Cord Blood of Preterm Birth
E. Spada, L. Calzari, Luigi Corsaro, T. Fazia +6 more
2020International Journal of Molecular Sciences22 citations Open access
Semantic Scholar
Genome-Wide DNA Methylation Analysis of a Cohort of 41 Patients Affected by Oculo-Auriculo-Vertebral Spectrum (OAVS)
V. Guida, L. Calzari, M. Fadda, F. Piceci-Sparascio +19 more
2021International Journal of Molecular Sciences21 citations Open access
Semantic Scholar
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith–Wiedemann progeny
P. Tannorella, L. Calzari, C. Daolio, E. Mainini +7 more
2022Clinical Epigenetics20 citations Open access
Semantic Scholar
Role of epigenetics in the clinical evolution of COVID-19 disease. Epigenome-wide association study identifies markers of severe outcome
L. Calzari, Lucia Zanotti, Elvira Inglese, F. Scaglione +7 more
2023European Journal of Medical Research19 citations Open access
Semantic Scholar
Taurine Administration Recovers Motor and Learning Deficits in an Angelman Syndrome Mouse Model
S. Guzzetti, L. Calzari, L. Buccarello, V. Cesari +6 more
2018International Journal of Molecular Sciences18 citations Open access
Semantic Scholar
Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation
L. Calzari, M. Barcella, Valentina Alari, D. Braga +7 more
2020Molecular Neurobiology17 citations Open access
Semantic Scholar
Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study
Alberto Brusati, S. Peverelli, L. Calzari, C. Tiloca +10 more
2023Frontiers in Aging Neuroscience15 citations Open access
Semantic Scholar
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases
P. Tannorella, D. Minervino, S. Guzzetti, Alessandro Vimercati +11 more
2021Genes13 citations Open access
Semantic Scholar
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes
M. Crippa, M. T. Bonati, L. Calzari, Chiara Picinelli +12 more
2019Frontiers in Genetics13 citations Open access
Semantic Scholar
High-Resolution Whole-Genome DNA Methylation Revealed Unique Signatures of Painful Diabetic Neuropathy
K. Kwiatkowska, P. Garagnani, Massimiliano Bonafé, M. Bacalini +12 more
2025Diabetes12 citations Open access
Semantic Scholar
Genes for RNA-binding proteins involved in neural-specific functions and diseases are downregulated in Rubinstein-Taybi iNeurons
L. Larizza, L. Calzari, Valentina Alari, S. Russo
2021Neural Regeneration Research11 citations Open access
Semantic Scholar
Painful diabetic neuropathy is associated with accelerated epigenetic aging
K. Kwiatkowska, P. Garagnani, Massimiliano Bonafé, M. Bacalini +10 more
2025GeroScience10 citations Open access
Semantic Scholar
Association Between TTV Viremia, Chronic Inflammation, and Ischemic Heart Disease Risk: Insights From MARK-AGE and Report-Age Projects
R. Giacconi, Francesco Piacenza, F. Maggi, A. Bürkle +31 more
2024The journals of gerontology. Series A, Biological sciences and medical sciences10 citations Open access
Semantic Scholar
Extensive Placental Methylation Profiling in Normal Pregnancies
O. Rondinone, Alessio Murgia, Jole Costanza, S. Tabano +13 more
2021International Journal of Molecular Sciences10 citations Open access
Semantic Scholar
Blood oxidative stress and metallothionein expression in Rett syndrome: Probing for markers
Maria Pintaudi, E. Veneselli, A. Voci, A. Vignoli +9 more
2016World Journal of Biological Psychiatry10 citations Open access
Semantic Scholar
Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations.
Valentina Alari, S. Russo, D. Rovina, M. Garzo +11 more
2019Stem Cell Research8 citations Open access
Semantic Scholar
Comprehensive genetic and epigenetic characterization of Lynch‐like syndrome patients
F. Pirini, L. Calzari, G. Tedaldi, M. Tebaldi +15 more
2025International Journal of Cancer7 citations Open access
Semantic Scholar
Association of an inflammaging score based on IL-6, IL-10 and CXCL9, and frailty with long-term mortality in hospitalized older adults
Matilde Sbriscia, S. Fantone, M. di Rosa, F. Marchegiani +36 more
2025Immunity & Ageing6 citations
Semantic Scholar
Investigating the Epigenetic Landscape of Major Depressive Disorder: A Genome-Wide Meta-Analysis of DNA Methylation Data, Including New Insights into Stochastic Epigenetic Mutations and Epivariations
G. N. Baldrighi, Rebecca Cavagnola, L. Calzari, Davide Sacco +3 more
2024Biomedicines6 citations Open access
Semantic Scholar
Circulating Bacterial DNA as a Novel Blood-Based Biomarker in Type 2 Diabetes Mellitus (DM2): Results from the PROMOTERA Study
R. Giacconi, P. D'Aquila, Fabiola Olivieri, D. Gentilini +16 more
2025International Journal of Molecular Sciences5 citations Open access
Semantic Scholar
Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver–Russell Syndrome and Focus on the IGF1R Gene
Alessandro Vimercati, P. Tannorella, S. Guzzetti, L. Calzari +20 more
2024Journal of Clinical Endocrinology and Metabolism5 citations Open access
Semantic Scholar
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism
D. Gentilini, M. Muzza, T. De Filippis, M. Vigone +9 more
2022Journal of Endocrinological Investigation5 citations Open access
Semantic Scholar
Correction: Epigenetic patterns, accelerated biological aging, and enhanced epigenetic drift detected 6 months following COVID‑19 infection: insights from a genome‑wide DNA methylation study
L. Calzari, D. F. Dragani, L. Zanotti, Elvira Inglese +15 more
2024Clinical Epigenetics3 citations
Semantic Scholar
B Cells Isolated from Individuals Who Do Not Respond to the HBV Vaccine Are Characterized by Higher DNA Methylation-Estimated Aging Compared to Responders
K. Kwiatkowska, Simona Anticoli, Stefano Salvioli, L. Calzari +7 more
2024Vaccines3 citations Open access
Semantic Scholar
Epigenetic Drift Is Involved in the Efficacy of HBV Vaccination
Francesca Ferraresi, Simona Anticoli, Stefano Salvioli, C. Pirazzini +9 more
2024Vaccines3 citations Open access
Semantic Scholar
Epigenetic aging differences between Wichí and Criollos from Argentina
Vincenzo Iannuzzi, S. Sarno, M. Sazzini, Paolo Abondio +15 more
2023Evolution, Medicine and Public Health3 citations Open access
Semantic Scholar
Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum
Alessandro Vimercati, P. Tannorella, Eleonora Orlandini, L. Calzari +7 more
2023Frontiers in Genetics3 citations Open access
Semantic Scholar
Erratum to: A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes
S. Russo, L. Calzari, A. Mussa, E. Mainini +19 more
2016Clinical Epigenetics3 citations Open access
Semantic Scholar
Methylation patterns associated with TTV load in geriatric hospitalized patients: an exploratory functional analysis
Carlo Fortunato, P. G. Spezia, Federica Novazzi, G. V. Badillo Pazmay +20 more
2025GeroScience2 citations Open access
Semantic Scholar
Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder
E. Bacchelli, Marta Viggiano, F. Ceroni, Paola Visconti +13 more
2023Research Square2 citations Open access
Semantic Scholar
Notch, SUMOylation, and ESR-Mediated Signalling Are the Main Molecular Pathways Showing Significantly Different Epimutation Scores between Expressing or Not Oestrogen Receptor Breast Cancer in Three Public EWAS Datasets
Luigi Corsaro, Davide Gentilini, L. Calzari, V. Gambino
2023Cancers2 citations Open access
Semantic Scholar
Epimutation analysis reveals involvement of SLIT2/ROBO signaling pathway in painful diabetic neuropathy
K. Kwiatkowska, P. Garagnani, Francesca Ferraresi, Massimiliano Bonafé +13 more
2026Human Genomics1 citations Open access
Semantic Scholar
Follicular Lymphoma Microenvironment Traits Associated with Event-Free Survival
M. Tumedei, F. Piccinini, I. Azzali, F. Pirini +18 more
2023International Journal of Molecular Sciences1 citations Open access
Semantic Scholar
Interconnected Gene Networks Underpin the Clinical Overlap of HNRNPH1-Related and Rubinstein–Taybi Intellectual Disability Syndromes
L. Larizza, Valentina Alari, L. Calzari, S. Russo
2021Frontiers in Neuroscience1 citations Open access
Semantic Scholar

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S. Russo×23
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S. Russo — researcher profile on SciRah
L. Larizza×15
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L. Larizza — researcher profile on SciRah
D. Gentilini×12
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D. Gentilini — researcher profile on SciRah
D. Gentilini×9
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M. Bacalini — researcher profile on SciRah

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A. Mussa — researcher profile on SciRah