Platelet glycoprotein Ibα HPA-2 Met/VNTR B haplotype as a genetic predictor of myocardial infarction and Sudden cardiac DeathMIKKELSSON, Jussi; PEROLA, Markus; PENTTILÄ, Antti et al.Circulation (New York, N.Y.). 2001, Vol 104, Num 8, pp 876-880, issn 0009-7322Article

Platelet collagen receptor GPIa (C807T/HPA-5) haplotype is not associated with an increased risk of fatal coronary events in middle-aged menMIKKELSSON, Jussi; PEROLA, Markus; PENTTILÄ, Antti et al.Atherosclerosis. 2002, Vol 165, Num 1, pp 111-118, issn 0021-9150Article

ACE gene and physical activity, blood pressure, and hypertension: a population study in FinlandFUENTES, Ricardo M; PEROLA, Markus; NISSINEN, Aulikki et al.Journal of applied physiology (1985). 2002, Vol 92, Num 6, pp 2508-2512, issn 8750-7587Article

Lessons from studying monogenic disease for common diseasePELTONEN, Leena; PEROLA, Markus; NAUKKARINEN, Jussi et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R67-R74, NSArticle

Heritability and risk factors of uterine fibroids : The Finnish Twin Cohort StudyLUOTO, Riitta; KAPRIO, Jaakko; RUTANEN, Eeva-Marja et al.Maturitas (Amsterdam). 2000, Vol 37, Num 1, pp 15-26, issn 0378-5122Conference Paper

Platelet membrane collagen receptor glycoprotein VI polymorphism is associated with coronary thrombosis and fatal myocardial infarction in middle-aged menOLLIKAINEN, Elina; MIKKELSSON, Jussi; PEROLA, Markus et al.Atherosclerosis. 2004, Vol 176, Num 1, pp 95-99, issn 0021-9150, 5 p.Article

Association Analysis of Allelic Variants of USF1 in Coronary AtherosclerosisKRISTIANSSON, Kati; ILVESKOSKI, Erkki; LEHTIMÄKI, Terho et al.Arteriosclerosis, thrombosis, and vascular biology. 2008, Vol 28, Num 5, pp 983-989, issn 1079-5642, 7 p.Article

Polymorphisms in the nephrin gene and diabetic nephropathy in type 1 diabetic patientsPETTERSSON-FERNHOLM, Kim; FORSBLOM, Carol; PEROLA, Markus et al.Kidney international. 2003, Vol 63, Num 4, pp 1205-1210, issn 0085-2538, 6 p.Article

Glycoprotein IIIa P1^A1/A2 polymorphism and sudden cardiac deathMIKKELSSON, Jussi; PEROLA, Markus; LAIPPALA, Pekka et al.Journal of the American College of Cardiology. 2000, Vol 36, Num 4, pp 1317-1323, issn 0735-1097Article

C-reactive protein-associated genetic variants and cancer risk: Findings from FINRISK 1992, FINRISK 1997 and Health 2000 studiesHEIKKILÄ, Katriina; SILANDER, Kaisa; SALOMAA, Veikko et al.European journal of cancer (1990). 2011, Vol 47, Num 3, pp 404-412, issn 0959-8049, 9 p.Article

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyVOIGHT, Benjamin F; PELOSO, Gina M; SCHUNKERT, Heribert et al.Lancet (British edition). 2012, Vol 380, Num 9841, pp 572-580, issn 0140-6736, 9 p.Article

Age-dependent association between hepatic lipase gene C-480T polymorphism and the risk of pre-hospital sudden cardiac death : The Helsinki Sudden Death StudyFAN, Yue-Mei; LEHTIMFIKI, Terho; RONTU, Riikka et al.Atherosclerosis. 2007, Vol 192, Num 2, pp 421-427, issn 0021-9150, 7 p.Article

Sweet taste preferences are partly genetically determined : identification of a trait locus on chromosome 16KESKITALO, Kaisu; KNAAPILA, Antti; KALLELA, Mikko et al.The American journal of clinical nutrition. 2007, Vol 86, Num 1, pp 55-63, issn 0002-9165, 9 p.Article

Association of the endothelial nitric oxide synthase gene polymorphism with risk of coronary artery disease and myocardial infarction in middle-aged menKUNNAS, Tarja A; ILVESKOSKI, Erkki; KARHUNEN, Pekka J et al.Journal of molecular medicine (Berlin. Print). 2002, Vol 80, Num 9, pp 605-609, issn 0946-2716Article

Coronary artery complicated lesion area is related to functional polymorphism of matrix metalloproteinase 9 gene an autopsy studyPÖLLÄNEN, Perttu J; KARHUNEN, Pekka J; MIKKELSSON, Jussi et al.Arteriosclerosis, thrombosis, and vascular biology. 2001, Vol 21, Num 9, pp 1446-1450, issn 1079-5642Article

Genetic variation of the interleukin-1 family and nongenetic factors determining the interleukin-1 receptor antagonist phenotypesLUOTOLA, Kari; PIETILÄ, Arto; SALOMAA, Veikko et al.Metabolism, clinical and experimental. 2010, Vol 59, Num 10, pp 1520-1527, issn 0026-0495, 8 p.Article

Evaluation of HapMap data in six populations of European descentLUNDMARK, Per E; LILJEDAHL, Ulrika; BOOMSMA, Dorret I et al.European journal of human genetics. 2008, Vol 16, Num 9, pp 1142-1150, issn 1018-4813, 9 p.Article

Food neophobia shows heritable variation in humansKNAAPILA, Antti; TUORILA, Hely; SILVENTOINEN, Karri et al.Physiology & behavior. 2007, Vol 91, Num 5, pp 573-578, issn 0031-9384, 6 p.Article

MORGAM (an international pooling of cardiovascular cohorts)EVANS, Alun; SALOMAA, Veikko; KUULASMAA, Kari et al.International journal of epidemiology. 2005, Vol 34, Num 1, pp 21-27, issn 0300-5771, 7 p.Article

Association of paraoxonase-1 M55L genotype and alcohol consumption with coronary atherosclerosis: the Helsinki Sudden Death StudyRONTU, Riikka; LEHTIMÄKI, Terho; ILVESKOSKI, Erkki et al.Pharmacogenetics (London). 2004, Vol 14, Num 8, pp 479-485, issn 0960-314X, 7 p.Article

Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3KOIVUKOSKI, Liisa; FISHER, Sheila A; RAO, Dabeeru C et al.Human molecular genetics (Print). 2004, Vol 13, Num 19, pp 2325-2332, issn 0964-6906, 8 p.Article

Smoking-dependent association between paraoxonase 1 M/L55 genotype and coronary atherosclerosis in males: an autopsy studyRONTU, Riikka; KARHUNEN, Pekka J; ILVESKOSKI, Erkki et al.Atherosclerosis. 2003, Vol 171, Num 1, pp 31-37, issn 0021-9150, 7 p.Article

Coronary artery calcification is related to functional polymorphism of matrix metalloproteinase 3: the Helsinki Sudden Death StudyPÖLLÄNEN, Perttu J; LEHTIMÄKI, Terho; SYRJÄKOSKI, Kirsi et al.Atherosclerosis. 2002, Vol 164, Num 2, pp 329-335, issn 0021-9150Article

Promoter polymorphism of the CD14 endotoxin receptor gene as a risk factor for alcoholic liver diseaseJÄRVEIÄINEN, Harri A; ORPANA, Arto; PEROLA, Markus et al.Hepatology (Baltimore, Md.). 2001, Vol 33, Num 5, pp 1148-1153, issn 0270-9139Article

Apolipoprotein E variation at the sequence haplotype level : Implications for the origin and maintenance of a major human polymorphismFULLERTON, Stephanie M; CLARK, Andrew G; SING, Charles F et al.American journal of human genetics. 2000, Vol 67, Num 4, pp 881-900, issn 0002-9297Article