London, United Kingdom

Philip L Beales


Average Co-Inventor Count = 7.0

ph-index = 1


Company Filing History:

goldMedal1 out of 832,812 
Other
 patents

Years Active: 2012

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1 patent (USPTO):Explore Patents

Title: The Innovator Behind the Gene BBS10: Philip L Beales

Introduction

Philip L Beales is a distinguished inventor based in London, GB, known for his significant contributions to the field of genetics. With a focus on medical innovations, his research and inventions aim to address complex genetic disorders, particularly Bardet-Biedl Syndrome (BBS).

Latest Patents

Beales holds a notable patent for BBS10, which pertains to diagnostic methods associated with Bardet-Biedl Syndrome. This innovative patent involves the identification of a gene, designated BBS1O, crucial to understanding this genetic disease characterized by a variety of symptoms, including obesity, diabetes, hypertension, mental retardation, renal cancer, retinopathy, and hypogonadism. The patent also describes methods for using this gene in both diagnosis and therapy of BBS, marking a significant step forward in the treatment of this condition.

Career Highlights

Beales has made a profound impact on genetic research and diagnostics. His work in understanding the complexities of Bardet-Biedl Syndrome is pivotal in the medical community, providing essential insights into the symptoms and potential treatment pathways for those affected by the syndrome.

Collaborations

Throughout his career, Beales has collaborated with prominent professionals in the field, including Nicholas Katsanis and Helene Dollfus. These collaborations have enhanced his research efforts, enabling the development of innovative solutions for genetic disorders.

Conclusion

Philip L Beales exemplifies the spirit of innovation in the realm of genetic research. His dedication to advancing diagnostic methods for Bardet-Biedl Syndrome through his patent on the BBS10 gene underscores the vital role of inventors in improving healthcare outcomes. As ongoing research continues to unfold, his contributions may lead to transformative changes in the understanding and treatment of genetic diseases.

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