Almgren P - Search Results

1

Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.

Smith JG, Almgren P, Engström G, Hedblad B, Platonov PG, Newton-Cheh C, Melander O. Smith JG, et al. Among authors: almgren p. J Intern Med. 2012 Dec;272(6):573-82. doi: 10.1111/j.1365-2796.2012.02563.x. Epub 2012 Jul 27. J Intern Med. 2012. PMID: 22690879 Free PMC article.

2

Assessment of conventional cardiovascular risk factors and multiple biomarkers for the prediction of incident heart failure and atrial fibrillation.

Smith JG, Newton-Cheh C, Almgren P, Struck J, Morgenthaler NG, Bergmann A, Platonov PG, Hedblad B, Engström G, Wang TJ, Melander O. Smith JG, et al. Among authors: almgren p. J Am Coll Cardiol. 2010 Nov 16;56(21):1712-9. doi: 10.1016/j.jacc.2010.05.049. J Am Coll Cardiol. 2010. PMID: 21070922 Free PMC article.

3

Genetic polymorphisms for estimating risk of atrial fibrillation in the general population: a prospective study.

Smith JG, Newton-Cheh C, Almgren P, Melander O, Platonov PG. Smith JG, et al. Among authors: almgren p. Arch Intern Med. 2012 May 14;172(9):742-4. doi: 10.1001/archinternmed.2012.786. Arch Intern Med. 2012. PMID: 22782207 Free PMC article. No abstract available.

4

Prediction of blood pressure changes over time and incidence of hypertension by a genetic risk score in Swedes.

Fava C, Sjögren M, Montagnana M, Danese E, Almgren P, Engström G, Nilsson P, Hedblad B, Guidi GC, Minuz P, Melander O. Fava C, et al. Among authors: almgren p. Hypertension. 2013 Feb;61(2):319-26. doi: 10.1161/HYPERTENSIONAHA.112.202655. Epub 2012 Dec 10. Hypertension. 2013. PMID: 23232644

5

A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis.

Hamrefors V, Hedblad B, Engström G, Almgren P, Sjögren M, Melander O. Hamrefors V, et al. Among authors: almgren p. J Intern Med. 2012 Mar;271(3):271-81. doi: 10.1111/j.1365-2796.2011.02472.x. Epub 2011 Nov 21. J Intern Med. 2012. PMID: 22017383 Free article.

6

Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction.

Gränsbo K, Almgren P, Sjögren M, Smith JG, Engström G, Hedblad B, Melander O. Gränsbo K, et al. Among authors: almgren p. J Intern Med. 2013 Sep;274(3):233-40. doi: 10.1111/joim.12063. Epub 2013 Mar 25. J Intern Med. 2013. PMID: 23480785 Free article.

7

Novel and conventional biomarkers for prediction of incident cardiovascular events in the community.

Melander O, Newton-Cheh C, Almgren P, Hedblad B, Berglund G, Engström G, Persson M, Smith JG, Magnusson M, Christensson A, Struck J, Morgenthaler NG, Bergmann A, Pencina MJ, Wang TJ. Melander O, et al. Among authors: almgren p. JAMA. 2009 Jul 1;302(1):49-57. doi: 10.1001/jama.2009.943. JAMA. 2009. PMID: 19567439 Free PMC article.

8

The common functional polymorphism -50G>T of the CYP2J2 gene is not associated with ischemic coronary and cerebrovascular events in an urban-based sample of Swedes.

Fava C, Montagnana M, Almgren P, Hedblad B, Engström G, Berglund G, Minuz P, Melander O. Fava C, et al. Among authors: almgren p. J Hypertens. 2010 Feb;28(2):294-9. doi: 10.1097/HJH.0b013e328333097e. J Hypertens. 2010. PMID: 19851119

9

Homozygosity for the EPHX2 K55R polymorphism increases the long-term risk of ischemic stroke in men: a study in Swedes.

Fava C, Montagnana M, Danese E, Almgren P, Hedblad B, Engström G, Berglund G, Minuz P, Melander O. Fava C, et al. Among authors: almgren p. Pharmacogenet Genomics. 2010 Feb;20(2):94-103. doi: 10.1097/FPC.0b013e3283349ec9. Pharmacogenet Genomics. 2010. PMID: 20065888

10

Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes.

Fava C, Danese E, Montagnana M, Sjögren M, Almgren P, Engström G, Nilsson P, Hedblad B, Guidi GC, Minuz P, Melander O. Fava C, et al. Among authors: almgren p. J Hypertens. 2011 Mar;29(3):484-91. doi: 10.1097/HJH.0b013e328342b2c1. J Hypertens. 2011. PMID: 21178783

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