vered raz

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Associate Professor

Leiden University Medical Center

Netherlands

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Dr. Vered Raz is an Associate Professor at Leiden University Medical Centre in the Netherlands. Her research focuses on muscular dystrophies, emphasizing molecular and cellular mechanisms, histopathology, and the development of novel therapeutic approaches. Recent publications include studies on the structural dynamics of muscle cell aggregates, biomarkers in rare diseases, and muscle physiology in mouse models. Dr. Raz's work contributes significantly to understanding muscle-related disorders and improving treatment strategies.

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Fullbright Israel-USA

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Articles (16)

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2025

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Collaborators (9)

Tooba Abbassi-Daloii

University of Maastricht

NETHERLANDS

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Maaike van Putten

Assistant Professor

Leiden University Medical Center

NETHERLANDS

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Andreas Damianou

University of Oxford

UNITED KINGDOM

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Jessica de Greef

Assistant Professor

Leiden University Medical Center

NETHERLANDS

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Benedikt Kessler

Professor of Biochemistry and Life Science Mass Spectrometry

University of Oxford

UNITED KINGDOM

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Jan J.G.M. Verschuuren

NETHERLANDS

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Thomas H. Sharp

Leiden University Medical Center

NETHERLANDS

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Adán Pinto-Fernández

University of Oxford

UNITED KINGDOM

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H. Eka D. Suchiman

Leiden University Medical Center

NETHERLANDS

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vered raz

Research Interests

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About

Recent Grants

Articles (16)

Polyalanine Expansion in PABPN1 Alters the Structure and Dynamics of Its Nuclear Aggregates in Differentiated Muscle Cells

Histopathologic Marks of Tongue in a Mouse Model of Oculopharyngeal Muscular Dystrophy Suggest Biomechanical Defects

Calcium-Enhanced Medium-Based Delivery of Splice Modulating Antisense Oligonucleotides in 2D and 3D hiPSC-Derived Neuronal Models

A Natural History Study of Hindlimb Physiology and Histopathology in a Heterozygous OPMD Mouse Model

PABPN1 loss-of-function causes APA-shift in oculopharyngeal muscular dystrophy

High-throughput Analysis of Capillary Density in Skeletal Muscle Cross Sections.

Novel Metabolomic Approach for Identifying Pathology-Specific Biomarkers in Rare Diseases: A Case Study in Oculopharyngeal Muscular Dystrophy (OPMD)

USP18 is an essential regulator of muscle cell differentiation and maturation

Diffusion‐tensor magnetic resonance imaging captures increased skeletal muscle fibre diameters in Becker muscular dystrophy

A transcriptome atlas of leg muscles from healthy human volunteers reveals molecular and cellular signatures associated with muscle location.

The metabolic landscape in chronic rotator cuff tear reveals tissue‐region‐specific signatures

Discovering fiber type architecture over the entire muscle using data‐driven analysis

Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability.

Age-Associated Salivary MicroRNA Biomarkers for Oculopharyngeal Muscular Dystrophy

A data-driven methodology reveals novel myofiber clusters in older human muscles.

Mouse models for muscular dystrophies: an overview

Collaborators (9)

Tooba Abbassi-Daloii

Maaike van Putten

Andreas Damianou

Jessica de Greef

Benedikt Kessler

Jan J.G.M. Verschuuren

Thomas H. Sharp

Adán Pinto-Fernández

H. Eka D. Suchiman

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