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Christopher D. Brown, Ph.D. is a faculty member at the Perelman School of Medicine at the University of Pennsylvania. His research expertise centers on understanding how genotypes contribute to phenotypes, particularly by identifying and characterizing functional human non-coding sequence variation. Dr. Brown aims to comprehend the mechanisms by which non-coding variants function, with a particular emphasis on complex human diseases. His research leverages both high-throughput experimental and computational approaches to massively parallelize assays that interrogate non-coding DNA function, as well as employing methods to fine-map causal variants associated with human disease. He completed his Bachelor of Science in Biochemistry at the University of Nebraska-Lincoln in 2001 and earned his Ph.D. in Genetics from Stanford University in 2007.
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