Salomaa V - Search Results

1

Exome-wide association study of plasma lipids in >300,000 individuals.

Liu DJ, Peloso GM, Yu H, Butterworth AS, Wang X, Mahajan A, Saleheen D, Emdin C, Alam D, Alves AC, Amouyel P, Di Angelantonio E, Arveiler D, Assimes TL, Auer PL, Baber U, Ballantyne CM, Bang LE, Benn M, Bis JC, Boehnke M, Boerwinkle E, Bork-Jensen J, Bottinger EP, Brandslund I, Brown M, Busonero F, Caulfield MJ, Chambers JC, Chasman DI, Chen YE, Chen YI, Chowdhury R, Christensen C, Chu AY, Connell JM, Cucca F, Cupples LA, Damrauer SM, Davies G, Deary IJ, Dedoussis G, Denny JC, Dominiczak A, Dubé MP, Ebeling T, Eiriksdottir G, Esko T, Farmaki AE, Feitosa MF, Ferrario M, Ferrieres J, Ford I, Fornage M, Franks PW, Frayling TM, Frikke-Schmidt R, Fritsche LG, Frossard P, Fuster V, Ganesh SK, Gao W, Garcia ME, Gieger C, Giulianini F, Goodarzi MO, Grallert H, Grarup N, Groop L, Grove ML, Gudnason V, Hansen T, Harris TB, Hayward C, Hirschhorn JN, Holmen OL, Huffman J, Huo Y, Hveem K, Jabeen S, Jackson AU, Jakobsdottir J, Jarvelin MR, Jensen GB, Jørgensen ME, Jukema JW, Justesen JM, Kamstrup PR, Kanoni S, Karpe F, Kee F, Khera AV, Klarin D, Koistinen HA, Kooner JS, Kooperberg C, Kuulasmaa K, Kuusisto J, Laakso M, Lakka T, Langenberg C, Langsted A, Launer LJ, Lauritzen T, Liewald DCM, Lin L… See abstract for full author list ➔ Liu DJ, et al. Among authors: salomaa v. Nat Genet. 2017 Dec;49(12):1758-1766. doi: 10.1038/ng.3977. Epub 2017 Oct 30. Nat Genet. 2017. PMID: 29083408 Free PMC article.

2

Sequence polymorphism at the human apolipoprotein AII gene ( APOA2): unexpected deficit of variation in an African-American sample.

Fullerton SM, Clark AG, Weiss KM, Taylor SL, Stengård JH, Salomaa V, Boerwinkle E, Nickerson DA. Fullerton SM, et al. Among authors: salomaa v. Hum Genet. 2002 Jul;111(1):75-87. doi: 10.1007/s00439-002-0763-x. Epub 2002 Jun 14. Hum Genet. 2002. PMID: 12136239

3

Contributions of 18 additional DNA sequence variations in the gene encoding apolipoprotein E to explaining variation in quantitative measures of lipid metabolism.

Stengård JH, Clark AG, Weiss KM, Kardia S, Nickerson DA, Salomaa V, Ehnholm C, Boerwinkle E, Sing CF. Stengård JH, et al. Among authors: salomaa v. Am J Hum Genet. 2002 Sep;71(3):501-17. doi: 10.1086/342217. Epub 2002 Aug 5. Am J Hum Genet. 2002. PMID: 12165926 Free PMC article.

4

MORGAM (an international pooling of cardiovascular cohorts).

Evans A, Salomaa V, Kulathinal S, Asplund K, Cambien F, Ferrario M, Perola M, Peltonen L, Shields D, Tunstall-Pedoe H, Kuulasmaa K; MORGAM Project. Evans A, et al. Among authors: salomaa v. Int J Epidemiol. 2005 Feb;34(1):21-7. doi: 10.1093/ije/dyh327. Epub 2004 Nov 23. Int J Epidemiol. 2005. PMID: 15561751 Review. No abstract available.

5

Total and cause specific mortality among participants and non-participants of population based health surveys: a comprehensive follow up of 54 372 Finnish men and women.

Jousilahti P, Salomaa V, Kuulasmaa K, Niemelä M, Vartiainen E. Jousilahti P, et al. Among authors: salomaa v. J Epidemiol Community Health. 2005 Apr;59(4):310-5. doi: 10.1136/jech.2004.024349. J Epidemiol Community Health. 2005. PMID: 15767385 Free PMC article.

6

Evaluating whole genome amplification via multiply-primed rolling circle amplification for SNP genotyping of samples with low DNA yield.

Silander K, Komulainen K, Ellonen P, Jussila M, Alanne M, Levander M, Tainola P, Kuulasmaa K, Salomaa V, Perola M, Peltonen L, Saarela J. Silander K, et al. Among authors: salomaa v. Twin Res Hum Genet. 2005 Aug;8(4):368-75. doi: 10.1375/1832427054936664. Twin Res Hum Genet. 2005. PMID: 16176722

7

Contribution of regulatory and structural variations in APOE to predicting dyslipidemia.

Stengård JH, Kardia SL, Hamon SC, Frikke-Schmidt R, Tybjaerg-Hansen A, Salomaa V, Boerwinkle E, Sing CF. Stengård JH, et al. Among authors: salomaa v. J Lipid Res. 2006 Feb;47(2):318-28. doi: 10.1194/jlr.M500491-JLR200. Epub 2005 Nov 29. J Lipid Res. 2006. PMID: 16317171 Free PMC article.

8

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.

9

Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts.

Alanne M, Kristiansson K, Auro K, Silander K, Kuulasmaa K, Peltonen L, Salomaa V, Perola M. Alanne M, et al. Among authors: salomaa v. Hum Genet. 2007 Nov;122(3-4):355-65. doi: 10.1007/s00439-007-0402-7. Epub 2007 Jul 20. Hum Genet. 2007. PMID: 17641917

10

Combined effects of thrombosis pathway gene variants predict cardiovascular events.

Auro K, Alanne M, Kristiansson K, Silander K, Kuulasmaa K, Salomaa V, Peltonen L, Perola M. Auro K, et al. Among authors: salomaa v. PLoS Genet. 2007 Jul;3(7):e120. doi: 10.1371/journal.pgen.0030120. Epub 2007 Jun 7. PLoS Genet. 2007. PMID: 17677000 Free PMC article.

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