Export 5 results:[ Author] Title Year
Filters: Keyword is Mutation [Clear All Filters]
Estimating the selective effects of heterozygous protein-truncating variants from human exome data. Nat Genet 49, 806-810 (2017).
Identification of cancer driver genes based on nucleotide context. Nat Genet 52, 208-218 (2020).
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts. Nat Med 25, 911-919 (2019).
Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes. Nat Genet 50, 1366-1374 (2018).