Salt Lake City, UT, United States of America

Donna M Shattuck-Eidens



Average Co-Inventor Count = 5.5

ph-index = 6

Forward Citations = 136(Granted Patents)


Company Filing History:


Years Active: 1994-2000

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8 patents (USPTO):Explore Patents

Title: Innovations by Donna M. Shattuck-Eidens in Breast and Ovarian Cancer Research

Introduction

Donna M. Shattuck-Eidens is an accomplished inventor based in Salt Lake City, UT, known for her significant contributions to the field of human genetics. With a total of eight patents to her name, her work has greatly impacted the understanding and diagnosis of breast and ovarian cancer.

Latest Patents

Her latest patents focus on the isolation and detection of the BRCA1 gene, which is known to predispose individuals to breast and ovarian cancer. These patents encompass methods for identifying germline and somatic mutations within the BRCA1 gene. The inventions not only aid in diagnosing predisposition to these cancers but also address somatic mutations in other forms of human cancers. Moreover, her patents delve into potential therapeutic avenues, including gene therapy and drug screening, focused on treatments for cancers associated with BRCA1 mutations.

Career Highlights

Donna M. Shattuck-Eidens has had a notable career, working with leading organizations such as Myriad Genetics, Inc. and the University of Utah Research Foundation. Her research and innovative inventions have played a crucial role in advancing cancer genetics, establishing her as a key figure in the battle against breast and ovarian cancer.

Collaborations

Throughout her career, Donna has collaborated with prominent professionals in the field, including Mark H. Skolnick and David E. Goldgar. These collaborations have enriched her research and broadened the reach and impact of her innovations.

Conclusion

Donna M. Shattuck-Eidens exemplifies the spirit of innovation within the field of genetics, particularly concerning breast and ovarian cancer susceptibility. Her patents reflect a deep commitment to enhancing medical understanding and improving patient outcomes through cutting-edge research in human genetics.

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