Genetic regulatory variation in populations informs transcriptome analysis in rare disease
Pejman Mohammadi(New York Genome Center), Tuuli Lappalainen(University of Geneva), Christina Sousa(Scripps Research Institute), Beryl B. Cummings(Rapt Therapeutics (United States)), Zhuoxun Jiang(University of Chicago), Sandra Donkervoort(Government of the United States of America), Stephane E. Castel(Varian Medical Systems (United States)), Hae Kyung Im(University of Chicago), Heather E. Wheeler(Loyola University Chicago), Carsten G. Bönnemann(National Institute of Neurological Disorders and Stroke), Payam Mohassel(Johns Hopkins University), Paul Hoffman(New York Genome Center), Jonah Einson(New York Genome Center), A. Reghan Foley(National Institutes of Health), Daniel G. MacArthur(Garvan Institute of Medical Research)
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