Publications

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Author Title [ Year(Desc)]
Filters: Author is Strober, Benjamin J  [Clear All Filters]
2017
Li, X. et al. The impact of rare variation on gene expression across tissues. Nature 550, 239-243 (2017).
2019
Frésard, L. et al. Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts. Nat Med 25, 911-919 (2019).
2020
Ferraro, N. M. et al. Transcriptomic signatures across human tissues identify functional rare genetic variation. Science 369, (2020).
2021
de Goede, O. M. et al. Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease. Cell 184, 2633-2648.e19 (2021).