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453 results

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Page 1
Common genetic variants associated with sudden cardiac death: the FinSCDgen study.
Lahtinen AM, Noseworthy PA, Havulinna AS, Jula A, Karhunen PJ, Kettunen J, Perola M, Kontula K, Newton-Cheh C, Salomaa V. Lahtinen AM, et al. Among authors: jula a. PLoS One. 2012;7(7):e41675. doi: 10.1371/journal.pone.0041675. Epub 2012 Jul 23. PLoS One. 2012. PMID: 22844511 Free PMC article.
Gender differences in the treatment and secondary prevention of CHD at population level.
Kattainen A, Salomaa V, Jula A, Antero Kesäniemi Y, Kukkonen-Harjula K, Kähönen M, Majahalme S, Moilanen L, Nieminen MS, Aromaa A, Reunanen A. Kattainen A, et al. Among authors: jula a. Scand Cardiovasc J. 2005 Dec;39(6):327-33. doi: 10.1080/14017430500233417. Scand Cardiovasc J. 2005. PMID: 16352484 Free article.
Metabolic syndrome and arterial stiffness: the Health 2000 Survey.
Sipilä K, Koivistoinen T, Moilanen L, Nieminen T, Reunanen A, Jula A, Salomaa V, Kaaja R, Kööbi T, Kukkonen-Harjula K, Majahalme S, Kähönen M. Sipilä K, et al. Among authors: jula a. Metabolism. 2007 Mar;56(3):320-6. doi: 10.1016/j.metabol.2006.10.008. Metabolism. 2007. PMID: 17292719
Metabolic syndrome and carotid intima media thickness in the Health 2000 Survey.
Sipilä K, Moilanen L, Nieminen T, Reunanen A, Jula A, Salomaa V, Kaaja R, Kukkonen-Harjula K, Lehtimäki T, Kesäniemi YA, Koivistoinen T, Nieminen MS, Tuomilehto J, Kähönen M. Sipilä K, et al. Among authors: jula a. Atherosclerosis. 2009 May;204(1):276-81. doi: 10.1016/j.atherosclerosis.2008.08.029. Epub 2008 Sep 4. Atherosclerosis. 2009. PMID: 18848324
Common candidate gene variants are associated with QT interval duration in the general population.
Marjamaa A, Newton-Cheh C, Porthan K, Reunanen A, Lahermo P, Väänänen H, Jula A, Karanko H, Swan H, Toivonen L, Nieminen MS, Viitasalo M, Peltonen L, Oikarinen L, Palotie A, Kontula K, Salomaa V. Marjamaa A, et al. Among authors: jula a. J Intern Med. 2009 Apr;265(4):448-58. doi: 10.1111/j.1365-2796.2008.02026.x. Epub 2009 Oct 25. J Intern Med. 2009. PMID: 19019189 Free PMC article.
High prevalence of four long QT syndrome founder mutations in the Finnish population.
Marjamaa A, Salomaa V, Newton-Cheh C, Porthan K, Reunanen A, Karanko H, Jula A, Lahermo P, Väänänen H, Toivonen L, Swan H, Viitasalo M, Nieminen MS, Peltonen L, Oikarinen L, Palotie A, Kontula K. Marjamaa A, et al. Among authors: jula a. Ann Med. 2009;41(3):234-40. doi: 10.1080/07853890802668530. Ann Med. 2009. PMID: 19160088 Free PMC article.
Prevalence, awareness and treatment of hypertension in Finland during 1982-2007.
Kastarinen M, Antikainen R, Peltonen M, Laatikainen T, Barengo NC, Jula A, Salomaa V, Jousilahti P, Nissinen A, Vartiainen E, Tuomilehto J. Kastarinen M, et al. Among authors: jula a. J Hypertens. 2009 Aug;27(8):1552-9. doi: 10.1097/HJH.0b013e32832c41cd. J Hypertens. 2009. PMID: 19412128
OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism.
Perttilä J, Merikanto K, Naukkarinen J, Surakka I, Martin NW, Tanhuanpää K, Grimard V, Taskinen MR, Thiele C, Salomaa V, Jula A, Perola M, Virtanen I, Peltonen L, Olkkonen VM. Perttilä J, et al. Among authors: jula a. J Mol Med (Berl). 2009 Aug;87(8):825-35. doi: 10.1007/s00109-009-0490-z. Epub 2009 Jun 25. J Mol Med (Berl). 2009. PMID: 19554302 Free PMC article.
453 results