User profiles for "author:Veikko Salomaa"

Veikko Salomaa

Finnish Institute for Health and Welfare
Verified email at thl.fi
Cited by 201355

Analysis of shared heritability in common disorders of the brain

Brainstorm Consortium, V Anttila, B Bulik-Sullivan… - Science, 2018 - science.org
INTRODUCTION Brain disorders may exhibit shared symptoms and substantial
epidemiological comorbidity, inciting debate about their etiologic overlap. However, detailed …

Atrial fibrillation and stroke: mortality and causes of death after the first acute ischemic stroke

MM Kaarisalo, P Immonen-Räihä, RJ Marttila… - Stroke, 1997 - Am Heart Assoc
Background and Purpose Atrial fibrillation (AF) is a risk factor for stroke. This study was
undertaken to determine the influence of AF on the mortality of stroke patients and on the …

[HTML][HTML] Risk thresholds for alcohol consumption: combined analysis of individual-participant data for 599 912 current drinkers in 83 prospective studies

AM Wood, S Kaptoge, AS Butterworth, P Willeit… - The Lancet, 2018 - thelancet.com
Background Low-risk limits recommended for alcohol consumption vary substantially across
different national guidelines. To define thresholds associated with lowest risk for all-cause …

Biological insights from 108 schizophrenia-associated genetic loci

C Pantelis, GN Papadimitriou, S Papiol… - Nature, 2014 - nature.com
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of
alleles, including common alleles of small effect that might be detected by genome-wide …

Biological, clinical and population relevance of 95 loci for blood lipids

TM Teslovich, K Musunuru, AV Smith, AC Edmondson… - Nature, 2010 - nature.com
Plasma concentrations of total cholesterol, low-density lipoprotein cholesterol, high-density
lipoprotein cholesterol and triglycerides are among the most important risk factors for …

[HTML][HTML] FinnGen provides genetic insights from a well-phenotyped isolated population

MI Kurki, J Karjalainen, P Palta, TP Sipilä… - Nature, 2023 - nature.com
Population isolates such as those in Finland benefit genetic research because deleterious
alleles are often concentrated on a small number of low-frequency variants (0.1%≤ minor …

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

Heart Attack Risk in Puget Sound. Schwartz Stephen … - Nature …, 2009 - nature.com
We conducted a genome-wide association study testing single nucleotide polymorphisms
(SNPs) and copy number variants (CNVs) for association with early-onset myocardial …

[HTML][HTML] Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

BF Voight, GM Peloso, M Orho-Melander… - The Lancet, 2012 - thelancet.com
Background High plasma HDL cholesterol is associated with reduced risk of myocardial
infarction, but whether this association is causal is unclear. Exploiting the fact that genotypes …

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

H Schunkert, IR König, S Kathiresan, MP Reilly… - Nature …, 2011 - nature.com
We performed a meta-analysis of 14 genome-wide association studies of coronary artery
disease (CAD) comprising 22,233 individuals with CAD (cases) and 64,762 controls of …

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Meta-Analyses of Glucose and Insulin-related traits … - Nature …, 2012 - nature.com
To extend understanding of the genetic architecture and molecular basis of type 2 diabetes
(T2D), we conducted a meta-analysis of genetic variants on the Metabochip, including …