Center-Authored Papers

Filters: Author is Kim, Daniel Seung  [Clear All Filters]
Journal Article
Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS et al..  2015.  Actionable exomic incidental findings in 6503 participants: challenges of variant classification.. Genome research. 25(3):305-15. Abstract
Rosenthal EA, Makaryan V, Burt AA, Crosslin DR, Kim DS, Smith JD, Nickerson DA, Reiner AP, Rich SS, Jackson RD et al..  2016.  Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.. Genetic epidemiology. Abstract
Kim DS, Kim JH, Burt AA, Crosslin DR, Burnham N, Kim CE, McDonald-McGinn DM, Zackai EH, Nicolson SC, Spray TL et al..  2016.  Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.. The Journal of thoracic and cardiovascular surgery. 151(4):1147-1151.e4. Abstract
Holzinger ER, Verma SS, Moore CB, Hall M, De R, Gilbert-Diamond D, Lanktree MB, Pankratz N, Amuzu A, Burt A et al..  2017.  Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.. BioData mining. 10:25. Abstract
Kim DS, Crosslin DR, Auer PL, Suzuki SM, Marsillach J, Burt AA, Gordon AS, Meschia JF, Nalls MA, Worrall BB et al..  2014.  Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.. Journal of lipid research. 55(6):1173-8. Abstract