Almgren P - Search Results

1

Dipping and variability of blood pressure and heart rate at night are heritable traits.

Fava C, Burri P, Almgren P, Arcaro G, Groop L, Lennart Hulthén U, Melander O. Fava C, et al. Among authors: almgren p. Am J Hypertens. 2005 Nov;18(11):1402-7. doi: 10.1016/j.amjhyper.2005.05.011. Am J Hypertens. 2005. PMID: 16280271

2

Heritability of ambulatory and office blood pressure phenotypes in Swedish families.

Fava C, Burri P, Almgren P, Groop L, Hulthén UL, Melander O. Fava C, et al. Among authors: almgren p. J Hypertens. 2004 Sep;22(9):1717-21. doi: 10.1097/00004872-200409000-00015. J Hypertens. 2004. PMID: 15311099

3

The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes.

Fava C, Montagnana M, Almgren P, Rosberg L, Guidi GC, Berglund G, Melander O. Fava C, et al. Among authors: almgren p. J Hypertens. 2007 Jan;25(1):111-6. doi: 10.1097/HJH.0b013e3280103a5a. J Hypertens. 2007. PMID: 17143181

4

Association between adducin-1 G460W variant and blood pressure in Swedes is dependent on interaction with body mass index and gender.

Fava C, Montagnana M, Almgren P, Rosberg L, Guidi GC, Berglund G, Melander O. Fava C, et al. Among authors: almgren p. Am J Hypertens. 2007 Sep;20(9):981-9. doi: 10.1016/j.amjhyper.2007.04.007. Am J Hypertens. 2007. PMID: 17765140

5

Determinants of kidney function in Swedish families: role of heritable factors.

Fava C, Montagnana M, Burri P, Almgren P, Minuz P, Hulthén UL, Melander O. Fava C, et al. Among authors: almgren p. J Hypertens. 2008 Sep;26(9):1773-9. doi: 10.1097/HJH.0b013e3283060f1d. J Hypertens. 2008. PMID: 18698211

6

Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome.

Fava C, Montagnana M, Guerriero M, Almgren P, von Wowern F, Minuz P, Melander O. Fava C, et al. Among authors: almgren p. J Hypertens. 2009 Sep;27(9):1794-803. doi: 10.1097/HJH.0b013e32832d3f9c. J Hypertens. 2009. PMID: 19593211

7

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

8

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

9

A genome wide scan for early onset primary hypertension in Scandinavians.

von Wowern F, Bengtsson K, Lindgren CM, Orho-Melander M, Fyhrquist F, Lindblad U, Råstam L, Forsblom C, Kanninen T, Almgren P, Burri P, Katzman P, Groop L, Hulthén UL, Melander O. von Wowern F, et al. Among authors: almgren p. Hum Mol Genet. 2003 Aug 15;12(16):2077-81. doi: 10.1093/hmg/ddg206. Hum Mol Genet. 2003. PMID: 12913078

10

The V433M variant of the CYP4F2 is associated with ischemic stroke in male Swedes beyond its effect on blood pressure.

Fava C, Montagnana M, Almgren P, Rosberg L, Lippi G, Hedblad B, Engström G, Berglund G, Minuz P, Melander O. Fava C, et al. Among authors: almgren p. Hypertension. 2008 Aug;52(2):373-80. doi: 10.1161/HYPERTENSIONAHA.108.114199. Epub 2008 Jun 23. Hypertension. 2008. PMID: 18574070

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