Bayswater, Australia

Graham McClorey

USPTO Granted Patents = 30 

Average Co-Inventor Count = 3.0

ph-index = 25

Forward Citations = 1,914(Granted Patents)


Company Filing History:


Years Active: 2010-2022

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30 patents (USPTO):Explore Patents

Title: Graham McClorey: Innovator in Antisense Oligonucleotide Technology

Introduction

Graham McClorey, a distinguished inventor based in Bayswater, Australia, has made significant contributions to the field of biotechnology. With an impressive portfolio of 30 patents, his work primarily focuses on the development of antisense oligonucleotides. These innovations are instrumental in advancing therapeutic techniques for various genetic disorders.

Latest Patents

Among his latest patents is the groundbreaking work titled "Antisense oligonucleotides for inducing exon skipping and methods of use thereof." This innovative antisense molecule is capable of binding to a selected target site to induce exon skipping in the dystrophin gene, as outlined in SEQ ID NO: 1 to 202. Another notable patent is similar in nature, also addressing the induction of exon skipping in the dystrophin gene, specified in SEQ ID NO: 1 to 214. These patents reflect his commitment to addressing critical challenges in genetic therapies.

Career Highlights

Graham McClorey is associated with The University of Western Australia, where he continues to push the boundaries of research in the field of molecular biology. His career is marked by a focus on innovative solutions that promote better health outcomes and greater understanding of genetic diseases.

Collaborations

Throughout his career, Graham has collaborated with notable colleagues, including Stephen Donald Wilton and Sue Fletcher. These collaborations have enriched his research, enabling him to harness diverse expertise and drive forward innovative projects in antisense technology.

Conclusion

Graham McClorey's pioneering work in antisense oligonucleotide technology establishes him as a significant figure in biotechnology. With numerous patents that highlight his remarkable contributions, he continues to influence the future of genetic therapies, making strides toward improved treatment options for patients with genetic disorders.

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