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  • Showing 1-11 of 11 Results
2016
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.Chami, N., Chen MH, Slater AJ, Eicher JD, Evangelou E., Tajuddin SM, Love-Gregory L., Kacprowski T., Schick UM, Nomura A., Giri A., Lessard S., Brody JA, Schurmann C., Pankratz N., Yanek LR, Manichaikul A., Pazoki R., Mihailov E., Hill WD, et al. American journal of human genetics, 2016/06/21, (2016) Read More / View Supplemental Materials
Abstract
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.Eicher, JD, Chami N., Kacprowski T., Nomura A., Chen MH, Yanek LR, Tajuddin SM, Schick UM, Slater AJ, Pankratz N., Polfus L., Schurmann C., Giri A., Brody JA, Lange LA, Manichaikul A., Hill WD, Pazoki R., Elliot P., Evangelou E., et al. American journal of human genetics, 2016/06/21, (2016) Read More / View Supplemental Materials
Abstract
Orosomucoid, Carotid Plaque, and Incidence of Stroke.Berntsson, J., Östling G., Persson M., Smith JG, Hedblad B., and Engström G. Stroke; a journal of cerebral circulation, 2016/06/14, (2016) Read More / View Supplemental Materials
Abstract
Total and Differential Leukocyte Counts in Relation to Incidence of Diabetes Mellitus: A Prospective Population-Based Cohort Study.Borné, Y., Smith JG, Nilsson PM, Melander O., Hedblad B., and Engström G. PloS one, 2016/01/01, Volume 11, Issue 2, p.e0148963, (2016) Read More / View Supplemental Materials
Abstract
2015
Dimethylglycine Deficiency and the Development of Diabetes mellitus.Magnusson, M., Wang TJ, Clish C., Engström G., Nilsson P., Gerszten RE, and Melander O. Diabetes, 2015/03/20, (2015) Read More / View Supplemental Materials
Abstract
Risk profiles for aortic dissection and ruptured or surgically treated aneurysms: a prospective cohort study.Landenhed, M., Engström G., Gottsäter A., Caulfield MP, Hedblad B., Newton-Cheh C., Melander O., and Smith JG Journal of the American Heart Association, 2015/01/21, Volume 4, Issue 1, (2015) Read More / View Supplemental Materials
Abstract
2014
Twelve-Single Nucleotide Polymorphism Genetic Risk Score Identifies Individuals at Increased Risk for Future Atrial Fibrillation and Stroke.Tada, H., Shiffman D., Smith JG, Sjögren M., Lubitz SA, Ellinor PT, Louie JZ, Catanese JJ, Engström G., Devlin JJ, Kathiresan S., and Melander O. Stroke; a journal of cerebral circulation, 2014/08/14, (2014) Read More / View Supplemental Materials
Abstract
Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.Hamrefors, V., Hedblad B., Hindy G., Smith JG, Almgren P., Engström G., Sjögren M., Gränsbo K., Orho-Melander M., and Melander O. PloS one, 2014/01/22, Volume 9, Issue 1, p.e85893, (2014) Read More / View Supplemental Materials
Abstract
2012
Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.Gustav Smith, J., Almgren P., Engström G., Hedblad B., Platonov PG, Newton-Cheh C., and Melander O. Journal of internal medicine, 2012/06/12, (2012) Read More / View Supplemental Materials
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2011
Low Plasma Level of Atrial Natriuretic Peptide Predicts Development of Diabetes: The Prospective Malmo Diet and Cancer Study.Magnusson, M., Jujic A., Hedblad B., Engström G., Persson M., Struck J., Morgenthaler NG, Nilsson P., Newton-Cheh C., Wang TJ, and Melander O. The Journal of clinical endocrinology and metabolism, 2011/11/23, (2011) Read More / View Supplemental Materials
Abstract
2009
Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study.Smith, JG, Melander O., Lövkvist H., Hedblad B., Engström G., Nilsson P., Carlson J., Berglund G., Norrving B., and Lindgren A. Circulation. Cardiovascular genetics, 2009/04/01, Volume 2, Issue 2, p.159-64, (2009) Read More / View Supplemental Materials
Abstract
  • Showing 1-11 of 11 Results