Alessia Cavazza

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 4

Top Topics

Acute Myeloid Leukemia

Newly Diagnosed

Ejection Fraction

Top Venues

Human gene therapy

Nature communications

University College London

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University College London Apr 11 2016

United Kingdom

Lecturer/Assistant Professor in Gene Therapy :: Great Ormond Street Institute of Child Health

Dana Farber Cancer Institute

United States

Postdoctoral Fellow :: Center for Functional Cancer Epigenetics

Publications

Rajeev Rai, Zohar Steinberg, Marianna Romito, Federica Zinghirino, Yi-Ting Hu, Nathan White, Asma Naseem, Adrian J Thrasher, Giandomenico Turchiano, Alessia Cavazza
CRISPR/Cas9-Based Disease Modeling and Functional Correction of Interleukin 7 Receptor Alpha Severe Combined Immunodeficiency in T-Lymphocytes and Hematopoietic Stem Cells. Human gene therapy 35 (7-8) (2024)
Rajeev Rai, Zohar Steinberg, Marianna Romito, Federica Zinghirino, Yi-Ting Hu, Nathan White, Asma Naseem, Adrian J Thrasher, Giandomenico Turchiano, Alessia Cavazza
CRISPR/Cas9-Based Disease Modeling and Functional Correction of Interleukin 7 Receptor Alpha Severe Combined Immunodeficiency in T-Lymphocytes and Hematopoietic Stem Cells. Human gene therapy (2024)
Rajeev Rai, Zohar Steinberg, Marianna Romito, Federica Zinghirino, Yi-Ting Hu, Nathan White, Asma Naseem, Adrian J Thrasher, Giandomenico Turchiano, Alessia Cavazza
CRISPR/Cas9-Based Disease Modeling and Functional Correction of Interleukin 7 Receptor Alpha Severe Combined Immunodeficiency in T-Lymphocytes and Hematopoietic Stem Cells. Human gene therapy 35 (7-8) (2024)
Rajeev Rai, Marianna Romito, Elizabeth Rivers, Giandomenico Turchiano, Georges Blattner, Winston Vetharoy, Dariusz Ladon, Geoffroy Andrieux, Fang Zhang, Marta Zinicola, Diego Leon-Rico, Giorgia Santilli, Adrian J Thrasher, Alessia Cavazza
Targeted gene correction of human hematopoietic stem cells for the treatment of Wiskott - Aldrich Syndrome. Nature communications 11 (1) (2020)