Luana Licata

University of Rome Tor Vergata

Italy

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Articles (16)

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2025

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2024

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2024

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2024

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2022

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2022

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2022

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2021

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2021

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2021

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2021

Collaborators (19)

Pier Luigi Martelli

Full professor

University of Bologna

ITALY

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Sandra Orchard

European Bioinformatics Institute

UNITED KINGDOM

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Colin Logie

NETHERLANDS

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ANGEL ALONSO

Associate Lecturer in Personalised Medicine

Universidad de Navarra

SPAIN

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Livia Perfetto

Assistant Professor (RTDB)

ITALY

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Rita Casadio

University of Bologna

ITALY

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Giuseppe Testa

Head

ITALY

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Sylvie RICARD-BLUM

Professor

Université Claude Bernard Lyon 1

FRANCE

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Lucia Monaco

ITALY

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Alessandro Vitriolo

Adjunct Professor

Università degli Studi di Torino

ITALY

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Andreas Zanzoni

Associate Professor (MCU)

Aix-Marseille University

FRANCE

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Jesualdo Tomás Fernández Breis

Professor

Universidad de Murcia

SPAIN

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Pascale Gaudet

SIB Swiss Institute of Bioinformatics

SWITZERLAND

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Wout Bittremieux

University of Antwerp

BELGIUM

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Gianni Cesareni

University of Rome Tor Vergata

ITALY

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Luisa Castagnoli

Full Professor

University of Rome Tor Vergata

ITALY

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simona panni

Assistan Professor Molecular Biology

University of Calabria

ITALY

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Matthias Futschik

UK Health Security Agency

UNITED KINGDOM

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Andrew Jones

Professor

University of Liverpool

UNITED KINGDOM

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Luana Licata

Research Interests

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Articles (16)

A tissue-specific atlas of protein–protein associations enables prioritization of candidate disease genes

Correction: Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders

Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders

The landscape of cancer-rewired GPCR signaling axes.

Proteomics Standards Initiative at Twenty Years: Current Activities and Future Work.

SIGNOR 3.0, the SIGnaling network open resource 3.0: 2022 update

The landscape of microRNA interaction annotation: analysis of three rare disorders as a case study

Resources and tools for rare disease variant interpretation

The Intricacy of the Viral-Human Protein Interaction Networks: Resources, Data, and Analyses.

A Resource to Infer Molecular Paths Linking Cancer Mutations to Perturbation of Cell Metabolism.

The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

IMEx Databases: Displaying Molecular Interactions into a Single, Standards-Compliant Dataset.

The gene regulation knowledge commons: the action area of GREEKC.

A Resource for the Network Representation of Cell Perturbations Caused by SARS-CoV-2 Infection

Phosphomatics: interactive interrogation of substrate-kinase networks in global phosphoproteomics datasets.

Integrating Patient-Specific Information into Logic Models of Complex Diseases: Application to Acute Myeloid Leukemia.

Collaborators (19)

Pier Luigi Martelli

Sandra Orchard

Colin Logie

ANGEL ALONSO

Livia Perfetto

Rita Casadio

Giuseppe Testa

Sylvie RICARD-BLUM

Lucia Monaco

Alessandro Vitriolo

Andreas Zanzoni

Jesualdo Tomás Fernández Breis

Pascale Gaudet

Wout Bittremieux

Gianni Cesareni

Luisa Castagnoli

simona panni

Matthias Futschik

Andrew Jones

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