Center-Authored Papers

Filters: Author is Gordon, Adam S  [Clear All Filters]
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
G
Gordon AS, Tabor HK, Johnson AD, Snively BM, Assimes TL, Auer PL, Ioannidis JPA, Peters U, Robinson JG, Sucheston LE et al..  2013.  Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.. Human molecular genetics. Abstract
K
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
T
Tabor HK, Auer PL, Jamal SM, Chong JX, Yu J-H, Gordon AS, Graubert TA, O'Donnell CJ, Rich SS, Nickerson DA et al..  2014.  Pathogenic variants for mendelian and complex traits in exomes of 6,517 European and african americans: implications for the return of incidental results.. American journal of human genetics. 95(2):183-93. Abstract