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High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms.
Kurki MI, Gaál EI, Kettunen J, Lappalainen T, Menelaou A, Anttila V, van 't Hof FN, von Und Zu Fraunberg M, Helisalmi S, Hiltunen M, Lehto H, Laakso A, Kivisaari R, Koivisto T, Ronkainen A, Rinne J, Kiemeney LA, Vermeulen SH, Kaunisto MA, Eriksson JG, Aromaa A, Perola M, Lehtimäki T, Raitakari OT, Salomaa V, Gunel M, Dermitzakis ET, Ruigrok YM, Rinkel GJ, Niemelä M, Hernesniemi J, Ripatti S, de Bakker PI, Palotie A, Jääskeläinen JE. Kurki MI, et al. Among authors: salomaa v. PLoS Genet. 2014 Jan 30;10(1):e1004134. doi: 10.1371/journal.pgen.1004134. eCollection 2014 Jan. PLoS Genet. 2014. PMID: 24497844 Free PMC article.
Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.
Komulainen K, Alanne M, Auro K, Kilpikari R, Pajukanta P, Saarela J, Ellonen P, Salminen K, Kulathinal S, Kuulasmaa K, Silander K, Salomaa V, Perola M, Peltonen L. Komulainen K, et al. Among authors: salomaa v. PLoS Genet. 2006 May;2(5):e69. doi: 10.1371/journal.pgen.0020069. Epub 2006 May 12. PLoS Genet. 2006. PMID: 16699592 Free PMC article.
Gender differences in genetic risk profiles for cardiovascular disease.
Silander K, Alanne M, Kristiansson K, Saarela O, Ripatti S, Auro K, Karvanen J, Kulathinal S, Niemelä M, Ellonen P, Vartiainen E, Jousilahti P, Saarela J, Kuulasmaa K, Evans A, Perola M, Salomaa V, Peltonen L. Silander K, et al. Among authors: salomaa v. PLoS One. 2008;3(10):e3615. doi: 10.1371/journal.pone.0003615. Epub 2008 Oct 31. PLoS One. 2008. PMID: 18974842 Free PMC article.
The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.
Karvanen J, Silander K, Kee F, Tiret L, Salomaa V, Kuulasmaa K, Wiklund PG, Virtamo J, Saarela O, Perret C, Perola M, Peltonen L, Cambien F, Erdmann J, Samani NJ, Schunkert H, Evans A; MORGAM Project. Karvanen J, et al. Among authors: salomaa v. Genet Epidemiol. 2009 Apr;33(3):237-46. doi: 10.1002/gepi.20374. Genet Epidemiol. 2009. PMID: 18979498 Free PMC article.
Common variants at 30 loci contribute to polygenic dyslipidemia.
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, Kaplan L, Bennett D, Li Y, Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, Guiducci C, Burtt NP, Parish S, Clarke R, Zelenika D, Kubalanza KA, Morken MA, Scott LJ, Stringham HM, Galan P, Swift AJ, Kuusisto J, Bergman RN, Sundvall J, Laakso M, Ferrucci L, Scheet P, Sanna S, Uda M, Yang Q, Lunetta KL, Dupuis J, de Bakker PI, O'Donnell CJ, Chambers JC, Kooner JS, Hercberg S, Meneton P, Lakatta EG, Scuteri A, Schlessinger D, Tuomilehto J, Collins FS, Groop L, Altshuler D, Collins R, Lathrop GM, Melander O, Salomaa V, Peltonen L, Orho-Melander M, Ordovas JM, Boehnke M, Abecasis GR, Mohlke KL, Cupples LA. Kathiresan S, et al. Among authors: salomaa v. Nat Genet. 2009 Jan;41(1):56-65. doi: 10.1038/ng.291. Epub 2008 Dec 7. Nat Genet. 2009. PMID: 19060906 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: salomaa v. Ann Med. 2009;41(3):234-40. doi: 10.1080/07853890802668530. Ann Med. 2009. PMID: 19160088 Free PMC article.
986 results