Kari-Matti Mäkelä

发表

Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error

Peter K. Joshi, Milly S. Tedja, Claire L. Simpson, 2016, Nature Communications.

Association of Neuroimmune Guidance Cue Netrin-1 and Its Chemorepulsive Receptor UNC5B With Atherosclerotic Plaque Expression Signatures and Stability in Human(s): Tampere Vascular Study (TVS)

T. Lehtimäki, M. Kähönen, R. Laaksonen, 2013, Circulation. Cardiovascular genetics.

Afamin predicts the prevalence and incidence of nonalcoholic fatty liver disease

F. Kronenberg, T. Lehtimäki, J. Viikari, 2021, Clinical chemistry and laboratory medicine.

Vascular cell adhesion molecule 1, soluble Fas and hepatocyte growth factor as predictors of mortality in nonagenarians: The Vitality 90+ study

T. Lehtimäki, N. Mononen, L. Lyytikäinen, 2013, Experimental Gerontology.

A Novel MMP12 Locus Is Associated with Large Artery Atherosclerotic Stroke Using a Genome-Wide Age-at-Onset Informed Approach

Niku Oksala, Peter M. Rothwell, Braxton D. Mitchell, 2014, PLoS genetics.

Reply: Intestinal cholesterol absorption and cardiovascular risk.

T. Lehtimäki, O. Raitakari, W. März, 2014, Journal of the American College of Cardiology.

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Claire L. Simpson, David M. Evans, C. Gieger, 2014, Human Genetics.

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Gabriëlle H S Buitendijk, Claire L. Simpson, David M. Evans, 2013, Nature Genetics.

Polymorphism in alpha 2A adrenergic receptor gene is associated with sialorrhea in schizophrenia patients on clozapine treatment

T. Lehtimäki, N. Mononen, O. Kampman, 2014, Human psychopharmacology.

High intestinal cholesterol absorption is associated with cardiovascular disease and risk alleles in ABCG8 and ABO: evidence from the LURIC and YFS cohorts and from a meta-analysis.

T. Lehtimäki, W. März, B. Boehm, 2013, Journal of the American College of Cardiology.

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Gabriëlle H S Buitendijk, David M. Evans, A. Hofman, 2013, Nature Genetics.

Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

Claire L. Simpson, David M. Evans, C. Gieger, 2016, Scientific Reports.

Clinical Management of Epilepsy With Glutamic Acid Decarboxylase Antibody Positivity: The Interplay Between Immunotherapy and Anti-epileptic Drugs

J. Peltola, A. Hietaharju, A. Brander, 2018, Front. Neurol..

Evidence HDAC9 Genetic Variant Associated With Ischemic Stroke Increases Risk via Promoting Carotid Atherosclerosis

T. Lehtimäki, J. Bis, H. Markus, 2013, Stroke.

Genome-Wide Association Study Identifies 3 Genomic Loci Significantly Associated With Serum Levels of Homoarginine: The AtheroRemo Consortium

T. Lehtimäki, O. Raitakari, W. März, 2013, Circulation. Cardiovascular genetics.

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

C. Sudlow, T. Lehtimäki, P. Rothwell, 2016, Scientific Reports.

Synergistic Expression of Histone Deacetylase 9 and Matrix Metalloproteinase 12 in M4 Macrophages in Advanced Carotid Plaques.

T. Lehtimäki, N. Klopp, T. Illig, 2017, European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery.

Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.

T. Lehtimäki, J. Viikari, O. Raitakari, 2014, European heart journal.

Complementary prediction of cardiovascular events by estimated apo- and lipoprotein concentrations in the working age population. The Health 2000 Study

T. Lehtimäki, A. Jula, A. Reunanen, 2013, Annals of medicine.

Genome-Wide Association Study Pinpoints a New Functional Apolipoprotein B Variant Influencing Oxidized Low-Density Lipoprotein Levels But Not Cardiovascular Events: AtheroRemo Consortium

T. Lehtimäki, T. Laitinen, J. Viikari, 2013, Circulation. Cardiovascular genetics.

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Jonathan H. Morgan, M. P. Concas, Adriana I. Iglesias, 2018, Nature Genetics.

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

C. Sudlow, T. Lehtimäki, P. Rothwell, 2016, Scientific Reports.

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

T. Lehtimäki, P. Rothwell, M. Dichgans, 2022 .

High intestinal cholesterol absorption is associated with cardiovascular disease and risk alleles in ABCG8 and ABO: evidence from the LURIC and YFS cohorts and from a meta-analysis.

T. Lehtimäki, B. Boehm, M. Kleber, 2013, Journal of the American College of Cardiology.

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Claire L. Simpson, C. Gieger, T. Lehtimäki, 2014, Human Genetics.