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Nicholas Katsanis is a Greek human geneticist known for research on the molecular basis of rare inherited disorders, especially ciliopathies. He is recognized for discoveries in Bardet–Biedl syndrome, contributions to the concepts of modifier alleles and genetic burden, and for developing multi-model functional genomics platforms. Katsanis has held faculty positions at the Johns Hopkins University Institute of Genetic Medicine and at Duke University, where he founded the Center for Human Disease Modeling.
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