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Hepcidin is potential regulator for renin activity

PloS one, 2022-04, Vol.17 (4), p.e0267343-e0267343

2022

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Comparison of three troponins as predictors of future cardiovascular events--prospective results from the FINRISK and BiomaCaRE studies

PloS one, 2014-03, Vol.9 (3), p.e90063-e90063

2014

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Hematocrit value at early middle age predicts hypertension at late middle age; the Tampere adult population cardiovascular risk study, a 30-year follow-up

Preventive medicine reports, 2023-06, Vol.33, p.102192-102192, Article 102192

2023

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Functional Inducible Nitric Oxide Synthase Gene Variants Associate With Hypertension: A Case-Control Study in a Finnish Population-The TAMRISK Study

Medicine (Baltimore), 2015-11, Vol.94 (46), p.e1958-e1958

2015

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Genetic variant coding for iron regulatory protein HFE contributes to hypertension, the TAMRISK study

Medicine (Baltimore), 2015-01, Vol.94 (4), p.e464-e464

2015

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Genetic variation in bone morphogenetic proteins family members (BMPs 2 and 4) and hypertension risk in middle-aged men: The TAMRISK study

Medicine (Baltimore), 2017-12, Vol.96 (51), p.e9362-e9362

2017

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Minor variant of rs 16827043 in the iron regulator hemojuvelin gene (HJV) contributes to hypertension: The TAMRISK study

Medicine (Baltimore), 2017-02, Vol.96 (5), p.e6052-e6052

2017

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Contribution of fatty acid transporter (CD36) genetic variant rs1761667 to body mass index, the TAMRISK study

Scandinavian journal of clinical and laboratory investigation, 2015-05, Vol.75 (3), p.254-258

2015

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ESR1 genetic variants, haplotypes and the risk of coronary heart disease and ischemic stroke in the Finnish population: A prospective follow-up study

Atherosclerosis, 2010-07, Vol.211 (1), p.200-202

2010

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A functional variant in the serine-threonine kinase coding gene is associated with hypertension: a case-control study in a Finnish population, the Tampere adult population cardiovascular risk study

Journal of hypertension, 2013-03, Vol.31 (3), p.516-520

2013

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Periodic cohort health examinations in the TAMRISK study show untoward increases in body mass index and blood pressure during 15 years of follow-up

BMC public health, 2012-08, Vol.12 (1), p.654-654, Article 654

2012

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Family history of hypertension enhances age-dependent rise in blood pressure, a 15-year follow-up, the Tampere adult population cardiovascular risk study

Medicine (Baltimore), 2023-09, Vol.102 (39), p.e35366-e35366

2023

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Contribution of SLC7A1 genetic variant to hypertension, the TAMRISK study

BMC medical genetics, 2013-07, Vol.14 (1), p.69-69, Article 69

2013

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Late-life coronary heart disease mortality of Finnish war veterans in the TAMRISK study, a 28-year follow-up

BMC public health, 2011-02, Vol.11 (1), p.71-71, Article 71

2011

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The gene variant for desmin rs1058261 may protect against combined cancer and cardiovascular death, the Tampere adult population cardiovascular risk study

Medicine (Baltimore), 2022-10, Vol.101 (40), p.e31005-e31005

2022

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Apolipoprotein E genotype is related to plasma levels of C-reactive protein and lipids and to longevity in nonagenarians

Clinical endocrinology (Oxford), 2006-03, Vol.64 (3), p.265-270

2006

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Coronary artery wall atherosclerosis in relation to the estrogen receptor 1 gene polymorphism: an autopsy study

Journal of molecular medicine (Berlin, Germany), 2002-03, Vol.80 (3), p.176-180

2002

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COX-2 Gene Promoter Polymorphism and Coronary Artery Disease in Middle-Aged Men: The Helsinki Sudden Death Study

Mediators of Inflammation, 2008-01, Vol.2008 (2008), p.126-130

2008

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Variant rs6749447 (T > G) in the serine threonine kinase gene is associated with cardiovascular complications, the Tampere adult population cardiovascular risk study

Medicine (Baltimore), 2021-10, Vol.100 (42), p.e27566-e27566

2021

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Association of apolipoprotein E polymorphism with outcome after aneurysmal subarachnoid hemorrhage : A preliminary study

Stroke (1970), 2001-05, Vol.32 (5), p.1181-1184

2001

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Positive Association of the JAG1 rs1327235 Genotype with Coronary Artery Disease in Men, the Tampere Adult Population Cardiovascular Risk Study

Genetic testing and molecular biomarkers, 2020-10, Vol.24 (10), p.681-684

2020

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Association of a Chromosome Locus 9p21.3 CDKN2B-AS1 Variant rs4977574 with Hypertension: The TAMRISK Study

Genetic testing and molecular biomarkers, 2018-05, Vol.22 (5), p.327-330

2018

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Association of the Collagen Type IV Alpha 1 Chain Gene rs3783107 GG Genotype with Hypertension, Asthma, and Eczema: The Tampere Adult Population Cardiovascular Risk Study

Genetic testing and molecular biomarkers, 2020-01, Vol.24 (1), p.6-9

2020

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Myeloperoxidase Gene Variation as a Determinant of Atherosclerosis Progression in the Abdominal and Thoracic Aorta: An Autopsy Study

Laboratory investigation, 2003-07, Vol.83 (7), p.919-925

2003

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No Association of nineteenCOX-2 gene variants to preclinical markers of atherosclerosis The Cardiovascular Risk in Young Finns Study

BMC medical genetics, 2012-07, Vol.13 (1), p.32-32

2012

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Hepcidin is potential regulator for renin activity

Comparison of three troponins as predictors of future cardiovascular events--prospective results from the FINRISK and BiomaCaRE studies

Hematocrit value at early middle age predicts hypertension at late middle age; the Tampere adult population cardiovascular risk study, a 30-year follow-up

Functional Inducible Nitric Oxide Synthase Gene Variants Associate With Hypertension: A Case-Control Study in a Finnish Population-The TAMRISK Study

Genetic variant coding for iron regulatory protein HFE contributes to hypertension, the TAMRISK study

Genetic variation in bone morphogenetic proteins family members (BMPs 2 and 4) and hypertension risk in middle-aged men: The TAMRISK study

Minor variant of rs 16827043 in the iron regulator hemojuvelin gene (HJV) contributes to hypertension: The TAMRISK study

Contribution of fatty acid transporter (CD36) genetic variant rs1761667 to body mass index, the TAMRISK study

ESR1 genetic variants, haplotypes and the risk of coronary heart disease and ischemic stroke in the Finnish population: A prospective follow-up study

A functional variant in the serine-threonine kinase coding gene is associated with hypertension: a case-control study in a Finnish population, the Tampere adult population cardiovascular risk study

Periodic cohort health examinations in the TAMRISK study show untoward increases in body mass index and blood pressure during 15 years of follow-up

Family history of hypertension enhances age-dependent rise in blood pressure, a 15-year follow-up, the Tampere adult population cardiovascular risk study

Contribution of SLC7A1 genetic variant to hypertension, the TAMRISK study

Late-life coronary heart disease mortality of Finnish war veterans in the TAMRISK study, a 28-year follow-up

The gene variant for desmin rs1058261 may protect against combined cancer and cardiovascular death, the Tampere adult population cardiovascular risk study

Apolipoprotein E genotype is related to plasma levels of C-reactive protein and lipids and to longevity in nonagenarians

Coronary artery wall atherosclerosis in relation to the estrogen receptor 1 gene polymorphism: an autopsy study

COX-2 Gene Promoter Polymorphism and Coronary Artery Disease in Middle-Aged Men: The Helsinki Sudden Death Study

Variant rs6749447 (T > G) in the serine threonine kinase gene is associated with cardiovascular complications, the Tampere adult population cardiovascular risk study

Association of apolipoprotein E polymorphism with outcome after aneurysmal subarachnoid hemorrhage : A preliminary study

Positive Association of the JAG1 rs1327235 Genotype with Coronary Artery Disease in Men, the Tampere Adult Population Cardiovascular Risk Study

Association of a Chromosome Locus 9p21.3 CDKN2B-AS1 Variant rs4977574 with Hypertension: The TAMRISK Study

Association of the Collagen Type IV Alpha 1 Chain Gene rs3783107 GG Genotype with Hypertension, Asthma, and Eczema: The Tampere Adult Population Cardiovascular Risk Study

Myeloperoxidase Gene Variation as a Determinant of Atherosclerosis Progression in the Abdominal and Thoracic Aorta: An Autopsy Study

No Association of nineteenCOX-2 gene variants to preclinical markers of atherosclerosis The Cardiovascular Risk in Young Finns Study

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