Kathrin Meyer

Assistant Professor

Ohio State University

United States

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Kathrin Meyer is an Assistant Professor at The Ohio State University, specializing in gene therapy for neuromuscular and neurodegenerative disorders. Her recent research includes studies on the MeCP2 gene therapy for Pitt Hopkins syndrome, AAV9 interventions for FOXG1 syndrome, and the therapeutic potential of viral vectors in treating conditions like spinal muscular atrophy. Dr. Meyer is dedicated to advancing personalized medicine approaches and improving therapeutic delivery systems in her field.

Articles (15)

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2022

Collaborators (14)

Carlo Baggio

University of California, Riverside

UNITED STATES

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Olivier Scheidegger

SWITZERLAND

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Stephen J Kolb

The Ohio State University Wexner Medical Center

UNITED STATES

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Julieth Sierra-Delgado

Assistant Research Professor

University of Missouri

UNITED STATES

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Nitin Chakravarti

Assistant Professor

Thomas Jefferson University

UNITED STATES

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priyanka tripathi

University of Maastricht

NETHERLANDS

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Iryna Ethell

UNITED STATES

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Bhuvaneish Thangaraj Selvaraj

University of Edinburgh

UNITED KINGDOM

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Dora Brites

Senior Researcher and Invited Full Professor

Universidade de Lisboa Faculdade de Farmácia

PORTUGAL

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Nicolas Wein

Assistant Professor

Nationwide Children's Hospital

UNITED STATES

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Meisam Naeimi Kararoudi

Research Assistant Professor

Ohio State University

UNITED STATES

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Soo-Kyung Lee

Professor

University at Buffalo - North Campus

UNITED STATES

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Maria Clara Franco

Associate Professor (tenured)

Florida International University

UNITED STATES

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Ana Rita Vaz

Professor Auxiliar

Universidade de Lisboa Faculdade de Farmácia

PORTUGAL

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Kathrin Meyer

Research Interests

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Articles (15)

MeCP2 gene therapy ameliorates disease phenotype in mouse model for Pitt Hopkins syndrome

The postnatal injection of AAV9-FOXG1 rescues corpus callosum agenesis and other brain deficits in the mouse model of FOXG1 syndrome

In-depth comparison of Anc80L65 and AAV9 retinal targeting and characterization of cross-reactivity to multiple AAV serotypes in humans

In Vitro Modeling as a Tool for Testing Therapeutics for Spinal Muscular Atrophy and IGHMBP2-Related Disorders.

Opportunities for mitochondrial disease gene therapy.

Early postnatal administration of an AAV9 gene therapy is safe and efficacious in CLN3 disease.

Prevalence of Neutralizing Antibodies against Adeno-Associated Virus Serotypes 1, 2, and 9 in Non-Injected Latin American Patients with Heart Failure-ANVIAS Study.

AAV-based gene therapy ameliorated CNS-specific GPI defect in mouse models.

Editorial: Personalized medicine for neuromuscular disorders.

CuATSM effectively ameliorates ALS patient astrocyte-mediated motor neuron toxicity in human in vitro models of amyotrophic lateral sclerosis.

PolyGA targets the ER stress-adaptive response by impairing GRP75 function at the MAM in C9ORF72-ALS/FTD.

EphA4 targeting agents protect motor neurons from cell death induced by amyotrophic lateral sclerosis -astrocytes.

Optimization and validation of CAR transduction into human primary NK cells using CRISPR and AAV.

Neurotoxic Astrocytes Directly Converted from Sporadic and Familial ALS Patient Fibroblasts Reveal Signature Diversities and miR-146a Theragnostic Potential in Specific Subtypes.

Emerging Perspectives on Gene Therapy Delivery for Neurodegenerative and Neuromuscular Disorders

Collaborators (14)

Carlo Baggio

Olivier Scheidegger

Stephen J Kolb

Julieth Sierra-Delgado

Nitin Chakravarti

priyanka tripathi

Iryna Ethell

Bhuvaneish Thangaraj Selvaraj

Dora Brites

Nicolas Wein

Meisam Naeimi Kararoudi

Soo-Kyung Lee

Maria Clara Franco

Ana Rita Vaz

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