Frederick, MD, United States of America

Randall Johnson


Average Co-Inventor Count = 5.0

ph-index = 1

Forward Citations = 6(Granted Patents)


Company Filing History:


Years Active: 2015

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1 patent (USPTO):Explore Patents

Title: The Innovations of Randall Johnson

Introduction

Randall Johnson is an accomplished inventor based in Frederick, MD (US). He has made significant contributions to the field of genetics, particularly in understanding renal diseases. His work focuses on identifying genetic predispositions that can lead to serious health conditions.

Latest Patents

Randall Johnson holds a patent for "Single nucleotide polymorphisms associated with renal disease." This patent outlines methods for determining the genetic predisposition of individuals to develop renal diseases, such as focal segmental glomerulosclerosis (FSGS) or end-stage kidney disease. The methods involve detecting one or more haplotype blocks comprising at least two tag single nucleotide polymorphisms (SNPs) in a non-coding region of the MYH9 gene. Additionally, the patent describes an array for detecting genetic predisposition to renal disease using probes complementary to the tag SNPs in the non-coding region of the MYH9 gene.

Career Highlights

Randall Johnson is associated with the United States of America, as represented by the Secretary, Department of Health and Human Services. His work has been pivotal in advancing the understanding of genetic factors that contribute to renal diseases. He has been recognized for his innovative approaches and methodologies in this critical area of health research.

Collaborations

Some of his notable coworkers include Cheryl Winkler and George E Nelson. Their collaborative efforts have contributed to the success of various research initiatives aimed at improving health outcomes related to renal diseases.

Conclusion

Randall Johnson's contributions to the field of genetics and renal disease research highlight the importance of innovation in medical science. His patent and collaborative work continue to pave the way for advancements in understanding genetic predispositions to health conditions.

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