Rosanna Asselta

Rozzano, Italy

Last Updated: 09/26/2026

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Found 152 publications

Identification of genetic variants in the FGB gene associated with congenital hypofibrinogenemia with divergent clinical phenotype.

Identification of genetic variants in the FGB gene associated with congenital hypofibrinogenemia with divergent clinical phenotype.

Journal: Annals of hematology
Published: April 16, 2026

Protein Profile of Multiple Myeloma-Derived Extracellular Vesicles for the Discovery of Novel Myeloma-Related Biomarkers.

Protein Profile of Multiple Myeloma-Derived Extracellular Vesicles for the Discovery of Novel Myeloma-Related Biomarkers.

Journal: Cancer science
Published: March 20, 2026

Integrating Host Genetics and Clinical Setting in Machine Learning Models: Predicting COVID-19 Prognosis for Healthcare Decision-Making (The FeMiNa Study).

Integrating Host Genetics and Clinical Setting in Machine Learning Models: Predicting COVID-19 Prognosis for Healthcare Decision-Making (The FeMiNa Study).

Journal: Diagnostics (Basel, Switzerland)
Published: December 09, 2025

Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity.

Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity.

Journal: EBioMedicine
Published: September 15, 2025

Genetic predisposition to elevated lipoprotein(a) in early-onset myocardial infarction.

Genetic predisposition to elevated lipoprotein(a) in early-onset myocardial infarction.

Journal: European journal of preventive cardiology
Published: August 12, 2025

Splicing-based biomarkers define a robust multigene classifier for relapsing-remitting multiple sclerosis.

Splicing-based biomarkers define a robust multigene classifier for relapsing-remitting multiple sclerosis.

Journal: Journal of translational autoimmunity
Published: July 21, 2025

Germline homologous recombination repair (gHRR) variants in bladder cancer: Preliminary evidence and clinical implications.

Germline homologous recombination repair (gHRR) variants in bladder cancer: Preliminary evidence and clinical implications.

Journal: BJUI compass
Published: July 08, 2025

Correcting CFTR mRNA splicing defects with the plant cytokine kinetin and its analogues.

Correcting CFTR mRNA splicing defects with the plant cytokine kinetin and its analogues.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: April 17, 2025

Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database.

Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database.

Journal: Research and practice in thrombosis and haemostasis
Published: March 18, 2025

Genetics Influences Telomere Length in Parkinson's Disease: A Study in Monozygotic Discordant Twins.

Genetics Influences Telomere Length in Parkinson's Disease: A Study in Monozygotic Discordant Twins.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 14, 2025

Factor XI Deficiency in apoE/FXI Double-Knockout Mice Decreases Atherosclerosis by Lowering MSR1 mRNA Expression Within the Plaque.

Factor XI Deficiency in apoE/FXI Double-Knockout Mice Decreases Atherosclerosis by Lowering MSR1 mRNA Expression Within the Plaque.

Journal: Journal of lipid and atherosclerosis
Published: February 12, 2025

A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia.

A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: January 17, 2025
Showing 1-12 of 152

Last Updated: 09/26/2026