Veikko Salomaa


Ontology type: schema:Person     


Person Info

NAME

Veikko

SURNAME

Salomaa

Publications in SciGraph latest 50 shown

  • 2018-12 Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients in BMC MEDICAL GENETICS
  • 2018-10 Increased Mortality Despite Successful Multifactorial Cardiovascular Risk Reduction in Healthy Men: 40-Year Follow-Up of the Helsinki Businessmen Study Intervention Trial in THE JOURNAL OF NUTRITION, HEALTH & AGING
  • 2018-06 Ceramide stearic to palmitic acid ratio predicts incident diabetes in DIABETOLOGIA
  • 2018-04 Genetic predisposition to obesity, restrained eating and changes in body weight: a population-based prospective study in INTERNATIONAL JOURNAL OF OBESITY
  • 2018-03 Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology in THE PHARMACOGENOMICS JOURNAL
  • 2018-02 Correction to: Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes in DIABETOLOGIA
  • 2018-01 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks in NATURE GENETICS
  • 2017-12-19 Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-12 Investigating the causal effect of smoking on hay fever and asthma: a Mendelian randomization meta-analysis in the CARTA consortium in SCIENTIFIC REPORTS
  • 2017-12 Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes in DIABETOLOGIA
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-12 A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors in SCIENTIFIC REPORTS
  • 2017-10 Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease in NATURE GENETICS
  • 2017-08-22 Neuregulin signaling pathway in smoking behavior in TRANSLATIONAL PSYCHIATRY
  • 2017-06 Midregional proadrenomedullin and growth differentiation factor-15 are not influenced by obesity in heart failure patients in CLINICAL RESEARCH IN CARDIOLOGY
  • 2017-04 Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-03-21 Genetic correlation between amyotrophic lateral sclerosis and schizophrenia in NATURE COMMUNICATIONS
  • 2017-03 High-sensitivity cardiac troponin I and NT-proBNP as predictors of incident dementia and Alzheimer’s disease: the FINRISK Study in JOURNAL OF NEUROLOGY
  • 2017-01 Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects in NATURE GENETICS
  • 2016-12 Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence in BMC MEDICINE
  • 2016-12 No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis in SCIENTIFIC REPORTS
  • 2016-12 Genome-wide analysis identifies 12 loci influencing human reproductive behavior in NATURE GENETICS
  • 2016-12 Apolipoproteins and HDL cholesterol do not associate with the risk of future dementia and Alzheimer’s disease: the National Finnish population study (FINRISK) in GEROSCIENCE
  • 2016-11 Genetic support for the causal role of insulin in coronary heart disease in DIABETOLOGIA
  • 2016-10 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals in NATURE GENETICS
  • 2016-10 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension in NATURE GENETICS
  • 2016-08 Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine in NATURE GENETICS
  • 2016-07 Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses in SCIENTIFIC REPORTS
  • 2016-05 Insomnia does not mediate or modify the association between MTNR1B risk variant rs10830963 and glucose levels in DIABETOLOGIA
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 Genetic causal beliefs about morbidity: associations with health behaviors and health outcome beliefs about behavior changes between 1982–2002 in the Finnish population in BMC PUBLIC HEALTH
  • 2015-10 Clinical and laboratory characteristics of active and healthy aging (AHA) in octogenarian men in AGING CLINICAL AND EXPERIMENTAL RESEARCH
  • 2015-10-01 Appetitive traits as behavioural pathways in genetic susceptibility to obesity: a population-based cross-sectional study in SCIENTIFIC REPORTS
  • 2015-10 A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease in NATURE GENETICS
  • 2015-10 Biomarkers of rapid chronic kidney disease progression in type 2 diabetes in KIDNEY INTERNATIONAL
  • 2015-06 Protein biomarkers for the prediction of cardiovascular disease in type 2 diabetes in DIABETOLOGIA
  • 2015-06 The impact of low-frequency and rare variants on lipid levels in NATURE GENETICS
  • 2015-04 Endotoxemia, nutrition, and cardiometabolic disorders in ACTA DIABETOLOGICA
  • 2015-02 Systemic exposure to a common periodontal pathogen and missing teeth are associated with metabolic syndrome in ACTA DIABETOLOGICA
  • 2014-12 A metabolic view on menopause and ageing in NATURE COMMUNICATIONS
  • 2014-12 Amerindian-specific regions under positive selection harbour new lipid variants in Latinos in NATURE COMMUNICATIONS
  • 2014-12 The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies in BMC ENDOCRINE DISORDERS
  • 2014-10 BiomarCaRE: rationale and design of the European BiomarCaRE project including 300,000 participants from 13 European countries in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2014-07 Biological insights from 108 schizophrenia-associated genetic loci in NATURE
  • 2014-04 Loss-of-function mutations in SLC30A8 protect against type 2 diabetes in NATURE GENETICS
  • 2014-03 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility in NATURE GENETICS
  • 2014-02 Drug–gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval in THE PHARMACOGENOMICS JOURNAL
  • 2013-11 Common variants associated with plasma triglycerides and risk for coronary artery disease in NATURE GENETICS
  • 2013-11 Discovery and refinement of loci associated with lipid levels in NATURE GENETICS
  • 2013-10 Systematic identification of trans eQTLs as putative drivers of known disease associations in NATURE GENETICS
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