Center-Authored Papers

Filters: Author is Worrall, Bradford B  [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 
C
van der Laan SW, Fall T, Soumaré A, Teumer A, Sedaghat S, Baumert J, Zabaneh D, van Setten J, Isgum I, Galesloot TE et al..  2016.  Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study.. Journal of the American College of Cardiology. 68(9):934-45. Abstract
G
Traylor M, Farrall M, Holliday EG, Sudlow C, Hopewell JC, Cheng Y-C, Fornage M, Ikram AM, Malik R, Bevan S et al..  2012.  Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies.. Lancet neurology. 11(11):951-962. Abstract
Huang J, Huffman JE, Yamkauchi M, Trompet S, Asselbergs FW, Sabater-Lleal M, Trégouët D-A, Chen W-M, Smith NL, Kleber ME et al..  2014.  Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2.. Arteriosclerosis, thrombosis, and vascular biology. Abstract
I
Bookman EB, Din-Lovinescu C, Worrall BB, Manolio TA, Bennett SN, Laurie C, Mirel DB, Doheny KF, Anderson GL, Wehr K et al..  2013.  Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).. Genome medicine. 5(1):7. Abstract
L
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM et al..  2017.  Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.. Nature genetics. 49(6):946-952. Abstract
Malik R, Traylor M, Pulit SL, Bevan S, Hopewell JC, Holliday EG, Zhao W, Abrantes P, Amouyel P, Attia JR et al..  2016.  Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.. Neurology. 86(13):1217-26. Abstract
M
Carty CL, Keene KL, Cheng Y-C, Meschia JF, Chen W-M, Nalls M, Bis JC, Kittner SJ, Rich SS, Tajuddin S et al..  2015.  Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.. Stroke; a journal of cerebral circulation. 46(8):2063-8. Abstract
R
Auer PL, Nalls M, Meschia JF, Worrall BB, Longstreth WT, Seshadri S, Kooperberg C, Burger KM, Carlson CS, Carty CL et al..  2015.  Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.. JAMA neurology. 72(7):781-8. 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
S
Malik R, Freilinger T, Winsvold BS, Anttila V, Vander Heiden J, Traylor M, de Vries B, Holliday EG, Terwindt GM, Sturm J et al..  2015.  Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.. Neurology. Abstract