Rosalba Carrozzo

Research Assistant, Head of the Cell Biology Section/Biologist

Ospedale Pediatrico Bambino Gesù

Italy

Research Interests

Explore related searches

Professors in Italy Professors in Medical Science Medical Science professors in Italy

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Rosalba Carrozzo is a Research Assistant and Head of the Cell Biology Section at Ospedale Pediatrico Bambino Gesù in Italy. Her research areas encompass molecular genetics, cellular biology, and the impact of genetic mutations on neurological and developmental disorders. Recent articles authored by her include studies on the epigenetic signature of MORC2, imaging-based molecular interactions in laminopathic cells, and clinical insights into various genetic mutations associated with complex health conditions.

Articles (12)

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Collaborators (6)

Nikolina Sekulić

Associate professor

University of Oslo

NORWAY

View details

sandra moreno

Università degli Studi di Roma La Sapienza

ITALY

View details

Barbara Peruzzi

Università Cattolica del Sacro Cuore

ITALY

View details

Stefano Leone

Sapienza University of Rome

ITALY

View details

Vincenzo Leuzzi

associated professor of Child Neurology and Psychiatry

Università degli Studi di Roma La Sapienza

ITALY

View details

Annalisa Grimaldi

Associate Professor

University of Insubria

ITALY

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Rosalba Carrozzo

Research Interests

Explore related searches

Contact this professor

About

Articles (12)

Pleiotropic effects of MORC2 derive from its epigenetic signature

Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy.

De Novo <i>DNM1L</i> Mutation in a Patient with Encephalopathy, Cardiomyopathy and Fatal Non-Epileptic Paroxysmal Refractory Vomiting

Biallelic variants in GTPBP3: New patients, phenotypic spectrum, and outcome

Case report: A safeguard in the sea of variants of uncertain significance: a case study on child with high risk neuroblastoma and acute myeloid leukemia

Imaging-Based Molecular Interaction Between Src and Lamin A/C Mechanosensitive Proteins in the Nucleus of Laminopathic Cells

TERT Extra-Telomeric Roles: Antioxidant Activity and Mitochondrial Protection

GLUT-1 changes in paediatric Huntington disease brain cortex and fibroblasts: an observational case-control study

Inflammatory profile in mitochondrial diseases: A cohort study

AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian Patients

Biallelic CLPB mutation associated with isolated neutropenia and 3‐MGA‐uria

Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausal

Collaborators (6)

Nikolina Sekulić

sandra moreno

Barbara Peruzzi

Stefano Leone

Vincenzo Leuzzi

Annalisa Grimaldi

Make your next move.