Terkko Navigator / Lokki, M(arja)-L(iisa)*

Osteoid Metaplasia in Femoral Artery Plaques Is Associated With the Clinical Severity of Lower Extremity Artery Disease in Men

<em>ACE</em> gene variants and sarcoidosis in a Finnish population

Exome Sequencing Identifies Susceptibility Loci for Sarcoidosis Prognosis

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

The complexity and diversity of major histocompatibility complex challenge disease association studies

Genome Analyses of &gt;200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

Salivary biomarkers in association with periodontal parameters and the periodontitis risk haplotype

Susceptibility of low-density lipoprotein particles to aggregate depends on particle lipidome, is modifiable, and associates with future cardiovascular deaths

Clinical features of patients with homozygous complement C4A or C4B deficiency

Multi-ethnic genome-wide association study for atrial fibrillation

Fatal Puumala Hantavirus Disease: Involvement of Complement Activation and Vascular Leakage in the Pathobiology

Disease marker combination enhances patient characterization in the Finnish sarcoidosis patients

Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis

Soluble HLA-DR serum levels are associated with smoking but not with acute coronary syndrome

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

C4B gene influences intestinal microbiota through complement activation in patients with paediatric-onset inflammatory bowel disease

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Genetic support for the causal role of insulin in coronary heart disease

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

HLA-B*44 May Be a Marker for Orofacial Granulomatosis

Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Plasma ceramides predict cardiovascular death in patients with stable coronary artery disease and acute coronary syndromes beyond LDL-cholesterol

Genetic Risk Scores Predict Recurrence of Acute Coronary Syndrome

Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome

Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Novel Associations Between Major Histocompatibility Complex and Pediatric-onset Inflammatory Bowel Disease

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

Directional dominance on stature and cognition in diverse human populations

Genetically determined height and coronary artery disease

Genetic studies of body mass index yield new insights for obesity biology

New genetic loci link adipose and insulin biology to body fat distribution

Resolution of HLA-B*44:02:01G, -DRB1*14:01:01G and -DQB1*03:01:01G reveals a high allelic variability among 12 European populations

Pathophysiology of a severe case of Puumala hantavirus infection successfully treated with bradykinin receptor antagonist icatibant

Low-expression variant of fatty acid-binding protein 4 favors reduced manifestations of atherosclerotic disease and increased plaque stability

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

Complement activation and regulation in preeclamptic placenta

Quality control and conduct of genome-wide association meta-analyses

Multi-ethnic fine-mapping of 14 central adiposity loci

The HLA-net GENE[RATE] pipeline for effective HLA data analysis and its application to 145 population samples from Europe and neighbouring areas

Evaluation of HLA-DRB1 imputation using a Finnish dataset

Complement C4 deficiency--a plausible risk factor for non-tuberculous mycobacteria (NTM) infection in apparently immunocompetent patients

Genetic variation on the BAT1-NFKBIL1-LTA region of major histocompatibility complex class III associates with periodontitis

Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation

Diversity of extended HLA-DRB1 haplotypes in the Finnish population

Mining the human phenome using allelic scores that index biological intermediates