Bruno Marino is an expert in Cardiology at Sapienza University of Rome (Italy). As of July 2026, ScienceLeadR ranks Bruno Marino in the top 1% of experts worldwide for Cardiovascular Abnormalities, Congenital Abnormalities and Heart Defects, Congenital. Bruno Marino has authored 662 publications, the most recent in 2026. SLR score: 1,526 (community average: 125). How the SLR is computed.

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Cardiology

Subspecialties: Genetics - Pediatrics - Anesthesiology

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Expert Rankings

Top experts on the MeSH terms this expert works on

Organizations

Career arc: 1987 - 2026

Source: PubMed

Sapienza University of Rome

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 662

Citations

Citations: 18 241 1st author: 66 Last author: 164 Unique author: 13


Best Journals

Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Morphological and functional echocardiographic findings in pediatric patients diagnosed with hypermobile Ehlers-Danlos syndrome.
PMID 42099513 — ehlers-danlos syndrome, echocardiography
Front Pediatr20260
Genome-wide tandem repeat expansions modify schizophrenia risk in the presence of a 22q11.2 deletion.
PMID 41986744 — genes, mental disorders, genome, schizophrenia, neurosciences, tandem repeat sequences
Mol Psychiatry20260
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.
PMID 41891037 — heart defects, congenital, genetic variation, genes, heart diseases, heart, phenotype, wounds and injuries, genetic background, demography
medRxiv20260
Comment on Othman et al. Ventricular Topology in Congenital Heart Defects Associated with Heterotaxy: Can We Find Patterns Reflecting the Syndrome-Specific Tendency for Visceral Symmetry? J. Cardiovasc. Dev. Dis. 2025, 12, 430.
PMID 41745315 — heart defects, congenital, heart
J Cardiovasc Dev Dis20260
Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 Deletions.
PMID 41360439 — heart defects, congenital, genes, heart diseases, heart, chromosome deletion, prevalence, chromosome aberrations, chromosomes
Clin Genet20250

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