Philadelphia, PA, United States of America

Scott J Dooley

USPTO Granted Patents = 4 

Average Co-Inventor Count = 6.0

ph-index = 1

Forward Citations = 5(Granted Patents)


Company Filing History:


Years Active: 2021-2025

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4 patents (USPTO):Explore Patents

Title: Innovations by Scott J. Dooley: Pioneering Advances in Ocular Gene Therapy

Introduction

Scott J. Dooley, an inventive mind based in Philadelphia, PA, has focused his research on groundbreaking advancements in ocular gene therapy. With a notable record of two patents, Dooley has made significant contributions to the medical field, particularly in the treatment of hereditary ocular diseases.

Latest Patents

Dooley's latest inventions are at the forefront of genetic research. His first patent revolves around trans-splicing molecules designed to correct mutations in the ABCA4 and CEP290 genes. These innovations hold potential for treating disorders associated with these mutations, such as Stargardt Disease and Leber congenital amaurosis 10. The second patent elaborates on the use of nucleic acid trans-splicing molecules to replace defected exons in targeted ocular genes, enhancing therapeutic strategies for conditions like Stargardt's Disease.

Career Highlights

Throughout his career, Scott J. Dooley has worked with prestigious institutions, notably the University of Pennsylvania and Ascidian Therapeutics, Inc. His expertise and innovative approach have helped pave the way for new treatments that can positively impact countless patients suffering from genetic ocular diseases.

Collaborations

Collaboration has been key to Dooley's successful research endeavors. He has worked alongside notable figures such as Jean Bennett and Jeannette Bennicelli, leveraging their collective knowledge to further the field of gene therapy and ocular disease treatment.

Conclusion

Scott J. Dooley's contributions to ocular gene therapy exemplify the innovative spirit that drives medical advancements today. With two patents under his belt and ongoing collaborations, Dooley continues to be a vital part of the evolution of therapies aimed at curing hereditary ocular conditions. His work serves as an inspiration and a beacon of hope for many patients worldwide.

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