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Tommaso Mazza

Head

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Italy

Research Interests

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Professors in Italy Professors in Cell Biology Cell Biology professors in Italy

About

Tommaso Mazza is the Head at Fondazione Policlinico Universitario Agostino Gemelli in Italy. His research areas encompass epigenetics, microbiome studies, and genetic insights into various health conditions, as reflected in his recent publications. He has contributed to understanding the implications of DNA methylation in dental stem cells, microbial profiling in pancreatic ductal adenocarcinoma, and genetic factors in autism spectrum disorders.

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Collaborators (10)

Michela BUGLIONE DI MONALE E BASTIA

Prof

University of Brescia

ITALY

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lorenza putignani

Associate Professor

Ospedale Pediatrico Bambino Gesù

ITALY

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Fabio Francesco di Mola

Ricercatore senior

University of Chieti-Pescara

ITALY

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Jan Červený

Head of Domain

Global Change Research Institute CAS

CZECH REPUBLIC

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mario caccese

Istituto Oncologico Veneto

ITALY

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Gael Nicolas

PUPH

University of Rouen

FRANCE

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Gloria ANDERSON

Agostino Gemelli University Polyclinic

ITALY

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Alba Fiorentino

Associated Professor

LUM Jean Monnet University

ITALY

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Roberto Pola

Assistant Professor

Tufts University School of Medicine

UNITED STATES

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Roberta Angelini

Researcher

Consiglio Nazionale delle Ricerche

ITALY

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Tommaso Mazza

Research Interests

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About

Articles (26)

Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome.

GDF-11, GDF-15, Jag-1, and leptin in neuronal-derived extracellular vesicles as aging-related biomarkers to identify individuals at risk of Alzheimer's dementia: A pilot study

A review of reviews of the prevalence of molecular biomarkers in vulvar cancer and their implications for prognosis refinement and treatment strategies

Global prevalence of hereditary hemorrhagic telangiectasia-associated variants estimated by analysis of large-scale genomic databases

Inflammatory bowel disease (IBD) is associated with increased intestinal extrachromosomal circular DNA: an emerging biomarker for IBD type and activity

AMPK Pathway Activation Markers in GBM: Expression Patterns and Clinical Associations in a Real-World Study

Rare <i>AFG3L2</i> and <i>POLG</i> Variants Suggest a Role for Mitochondrial Dysfunction in Enteric Neuronal Vulnerability in Idiopathic Achalasia

Fibrosis and Perinatal Features Correlated with Telomere Shortening in Pediatric Metabolic Dysfunction-Associated Steatotic Liver Disease

Transcriptional Control of Hepatocellular Carcinoma Cells Aggressiveness by AAV2/8-Mediated Delivery of Human Centenarian-Associated SIRT6 N308K/A313S

Unsupervised synchronization of molecular dynamics trajectories via graph embedding and time warping

Epigenetic Signatures of Dental Stem Cells: Insights into DNA Methylation and Noncoding RNAs

Could the Microbial Profiling of Normal Pancreatic Tissue from Healthy Organ Donors Contribute to Understanding the Intratumoral Microbiota Signature in Pancreatic Ductal Adenocarcinoma?

Gut microbiome composition changes in obstructive sleep apnoea syndrome also in relation to excessive daytime sleepiness.

Downregulation of Aging-Associated Gene SUCLG1 Marks the Aggressiveness of Liver Disease

Functional and <i>In Silico</i> Characterization of ALPL Gene Variants Reveals Genotype–Phenotype Correlations in Italian Hypophosphatasia Patients

A miRNA expression profiling of breast cancer to develop a metastases predictor model and identify new molecular players of metastatic outgrowth

Circulating histones as potential biomarkers of MASLD-MASH-HCC progression

Comprehensive Molecular Screening by Next Generation Sequencing of Gastrointestinal Stromal Tumors (GISTs): In Silico Analysis and Classification of Rare KIT Exon 11 Mutations

Development of a microRNA-based prognostic model for accurate prediction of distant metastasis in breast cancer patients

E-ABIN: an explainable module for anomaly detection in biological networks

Two Novel Biallelic Variants in the <i>FARSA</i> Gene: The First Italian Case and a Literature Review

Unveiling genetic insights: Array-CGH and WES discoveries in a cohort of 122 children with essential autism spectrum disorder.

Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome's clinical and molecular spectrum through NALCN &lt;i&gt;in-silico&lt;/i&gt; structural analysis.

DNA methylation patterns of circadian and ultradian genes are altered in the peripheral blood of patients with hidradenitis suppurativa.

Extracellular Histones Profiles of Pediatric H3K27-Altered Diffuse Midline Glioma.

A Missense Variant Affecting the N-Terminal Domain of the Laminin-332 β3 Chain Results in a Distinct Form of Junctional Epidermolysis Bullosa With Altered Granulation Tissue Response and No New Blistering: A Second Family Report.

Collaborators (10)

Michela BUGLIONE DI MONALE E BASTIA

lorenza putignani

Fabio Francesco di Mola

Jan Červený

mario caccese

Gael Nicolas

Gloria ANDERSON

Alba Fiorentino

Roberto Pola

Roberta Angelini

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Widening the infantile hypotonia with psychomotor retardation and characteristic Facies-1 Syndrome's clinical and molecular spectrum through NALCN <i>in-silico</i> structural analysis.