Publications by authors named "Alice Traversa"

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Variable Intrafamilial Cardiac Phenotype Segregating With a TBX20 Missense Variant in the Putative Transcriptional Activation Domain.
Gioia Mastromoro, Alice Traversa, Daniele Guadagnolo, Carolina Putotto, Viviana Caputo

Am J Med Genet A· December 2025

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Electromagnetic Transduction Therapy (EMTT) Enhances Tenocyte Regenerative Potential: Evidence for Senolytic-like Effects and Matrix Remodeling.
Matteo Mancini, Mario Vetrano, Alice Traversa, Carlo Cauli, Simona Ceccarelli

Int J Mol Sci· July 2025

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Deciphering the Transcriptional Metabolic Profile of Adipose-Derived Stem Cells During Osteogenic Differentiation and Epigenetic Drug Treatment.
Giulia Gerini, Alice Traversa, Fabrizio Cece, Matteo Cassandri, Paola Pontecorvi

Cells· January 2025

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Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impaction.
Agnese Giovannetti, Rosanna Guarnieri, Francesco Petrizzelli, Sara Lazzari, Gabriella Padalino, Alice Traversa

J Dent Sci· October 2024

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SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline.
Katherine A Wood, R Spencer Tong, Marialetizia Motta, Viviana Cordeddu, Eleanor R Scimone, Alice Traversa

Am J Hum Genet· September 2024

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Polyethylene Micro/Nanoplastics Exposure Induces Epithelial-Mesenchymal Transition in Human Bronchial and Alveolar Epithelial Cells.
Alice Traversa, Emanuela Mari, Paola Pontecorvi, Giulia Gerini, Enrico Romano

Int J Mol Sci· September 2024

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Exploring non-coding genetic variability in ACE2: Functional annotation and in vitro validation of regulatory variants.
Agnese Giovannetti, Sara Lazzari, Manuel Mangoni, Alice Traversa, Tommaso Mazza

Gene· July 2024

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Additional lesions identified by genomic microarrays are associated with an inferior outcome in low-risk chronic lymphocytic leukaemia patients.
Gian Matteo Rigolin, Alice Traversa, Viviana Caputo, Ilaria Del Giudice, Antonella Bardi

Br J Haematol· September 2023

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Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities.
Edoardo Pisa, Alice Traversa, Viviana Caputo, Angela Maria Ottomana, Jonas Hauser

Front Cell Neurosci· January 2023

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MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variants.
Agnese Giovannetti, Salvatore Daniele Bianco, Alice Traversa, Noemi Panzironi, Alessandro Bruselles

Hum Mutat· September 2022

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Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis.
Giulia Napoli, Noemi Panzironi, Alice Traversa, Caterina Catalanotto, Valentina Pace

Mol Neurobiol· August 2022

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Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges-Systematic Review of the Literature and Meta-Analysis.
Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, Enrica Marchionni, Alice Traversa

Diagnostics (Basel)· February 2022

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Exposure to 3'Sialyllactose-Poor Milk during Lactation Impairs Cognitive Capabilities in Adulthood.
Edoardo Pisa, Alberto Martire, Valentina Chiodi, Alice Traversa, Viviana Caputo

Nutrients· November 2021

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Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode.
Jonas Hauser, Edoardo Pisa, Alejandro Arias Vásquez, Flavio Tomasi, Alice Traversa

Mol Psychiatry· July 2021

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GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations.
Maria Luce Genovesi, Daniele Guadagnolo, Enrica Marchionni, Agnese Giovannetti, Alice Traversa

Bone· March 2021

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Unusual Segregation of APP Mutations in Monogenic Alzheimer Disease.
Gioia Mastromoro, Stefano Gambardella, Enrica Marchionni, Rosa Campopiano, Alice Traversa

Neurodegener Dis· August 2020

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Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance.
Alice Traversa, Enrica Marchionni, Agnese Giovannetti, Maria L Genovesi, Noemi Panzironi

Mol Genet Genomic Med· August 2020

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Genomic and physiological resilience in extreme environments are associated with a secure attachment style.
Viviana Caputo, Maria Giuseppina Pacilli, Ivan Arisi, Tommaso Mazza, Rossella Brandi, Alice Traversa

Transl Psychiatry· June 2020

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Small 7p22.3 microdeletion: Case report of Snx8 haploinsufficiency and neurological findings.
Gioia Mastromoro, Anna Capalbo, Cristiana Alessia Guido, Barbara Torres, Maria Fabbretti, Alice Traversa

Eur J Med Genet· April 2020

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Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism.
Simone Martinelli, Viviana Cordeddu, Serena Galosi, Ambra Lanzo, Eleonora Palma, Alice Traversa

Parkinsonism Relat Disord· March 2020

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Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy-Walker malformation.
Alice Traversa, Silvia Bernardo, Alessandro Paiardini, Agnese Giovannetti, Enrica Marchionni

Mol Genet Genomic Med· January 2020

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Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies.
Ersilia Barbato, Alice Traversa, Rosanna Guarnieri, Agnese Giovannetti, Maria Luce Genovesi

Arch Oral Biol· July 2018

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Biallelic mutations in early-onset, variably progressive neurodegeneration.
Valentina Muto, Elisabetta Flex, Zachary Kupchinsky, Guido Primiano, Hamid Galehdari, Alice Traversa

Neurology· July 2018

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Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies.
Marcello Niceta, Emilia Stellacci, Karen W Gripp, Giuseppe Zampino, Maria Kousi, Alice Traversa

Am J Hum Genet· May 2015

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Novel SMAD4 mutation causing Myhre syndrome.
Viviana Caputo, Gianfranco Bocchinfuso, Marco Castori, Alice Traversa, Antonio Pizzuti

Am J Med Genet A· July 2014

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