System Maintenance Notice

Please note that maintenance work is scheduled between 4 AM and 5 AM - CET. During this time, you may experience reduced performance. Thanks for your patience.

Corrado Romano is an expert in Genetics at University of Catania (Italy). Corrado Romano has authored 160 publications, the most recent in 2026. SLR score: 326 (community average: 125). How the SLR is computed.

LeadR Profile

Corrado Romano University of Catania Italy
326 ScienceLeadR Reputation 326

Unlock

Register Login
Network Map

Genetics

Subspecialties: Biochemistry - Neurology - Psychiatry

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: 2013 - 2026
Source: PubMed

University of Catania

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 160

Citations

Citations: 11 053 1st author: 3 Last author: 22 Unique author: 1

Main journals

Am J Med Genet A 12
Eur J Hum Genet 10
Am J Hum Genet 7
Nat Genet 7
Genes (Basel) 5

Best Journals

Cell 2
N Engl J Med 1

Breakdown by type

Click a legend label to hide or show it in the chart.

Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).
PMID 42417140 — neurodevelopmental disorders, neurodevelopment		Genet Med20261
GIT1 loss of function causes a recognizable syndromic neurodevelopmental disorder.
PMID 42360756 — cells, tissue adhesions, actins, growth, brain, phenotype, neurodevelopmental disorders, actin cytoskeleton, neurology, focal adhesions, microcephaly, neurodevelopment		Brain20260
Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases.
PMID 42016445 — undiagnosed diseases, diagnosis, therapeutics, genetic diseases, inborn		Genet Med Open20260
De novo mutation in the ARHGAP32 gene endorses the implication of GTPase-activating proteins (RhoGAP family) in idiopathic autism spectrum disorder.
PMID 41726838 — genes, autism spectrum disorder, autistic disorder, diagnosis, gtp phosphohydrolases, mutation, gtpase-activating proteins, jacobsen distal 11q deletion syndrome		Front Psychiatry20260
Dysregulation of miRNAs in Sicilian Patients with Autism Spectrum Disorder.
PMID 41595751 — cells, autism spectrum disorder, micrornas, biomarkers, autistic disorder, cardiomyopathies, autoimmunity		Biomedicines20261

LeadR Networks

Main global connection map

Sources: PubMed, OpenAlex, ClinicalTrials, EU CTIS