Publications
Export 2 results:
Filters: Keyword is Polymorphism, Single Nucleotide and Author is Johnsen, Jill M [Clear All Filters]
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. Hum Mol Genet. 2022 ;31(18):3120-3132.
. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 2021 ;590(7845):290-299.
.