Publications
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Filters: Keyword is Whole Genome Sequencing and Author is Gao, Yan [Clear All Filters]
Rare coding variants in RCN3 are associated with blood pressure. BMC Genomics. 2022 ;23(1):148.
. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. Nat Commun. 2022 ;13(1):7592.
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