Valeria Cinquina

8PUBLICATIONS
11CO-AUTHORS
BiomechanicsEpigenetics (incl. genome methylation and epigenomics)Respiratory diseasesMolecular evolutionNeonatology
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Publications (8)

|Mar 07, 2026
Proximity extension assay-based serum proteomic profiling identifies shared protein signatures in hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders.

Valeria Cinquina, Giulia Carini, Nicola Chiarelli

|Jan 08, 2025
Integrative Multi-Omics Approach in Vascular Ehlers-Danlos Syndrome: Further Insights into the Disease Mechanisms by Proteomic Analysis of Patient Dermal Fibroblasts.

Nicola Chiarelli, Valeria Cinquina, Nicoletta Zoppi

|Sep 03, 2024
Bridging the Diagnostic Gap for Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders: Evidence of a Common Extracellular Matrix Fragmentation Pattern in Patient Plasma as a Potential Biomarker.

Marco Ritelli, Nicola Chiarelli, Valeria Cinquina

|Sep 29, 2023
Looking back and beyond the 2017 diagnostic criteria for hypermobile Ehlers-Danlos syndrome: A retrospective cross-sectional study from an Italian reference center.

Marco Ritelli, Nicola Chiarelli, Valeria Cinquina

|Jan 04, 2023
Truncating variants in the penultimate exon of TGFBR1 escaping nonsense-mediated mRNA decay cause Loeys-Dietz syndrome.

Paola Fortugno, Rosanna Monetta, Valeria Cinquina

|Dec 23, 2022
RNA-Seq of Dermal Fibroblasts from Patients with Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders Supports Their Categorization as a Single Entity with Involvement of Extracellular Matrix Degrading and Proinflammatory Pathomechanisms.

Marco Ritelli, Nicola Chiarelli, Valeria Cinquina

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Frequent Collaborators

7 joint publications

Marco Ritelli

7 joint publications

Marina Colombi

4 joint publications

Nicola Chiarelli

3 joint publications

Nicoletta Zoppi