Terkko Navigator / Palotie, A(arno)* (FIMM)

Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families

A cross-population atlas of genetic associations for 220 human phenotypes

Reaction Time and Visual Memory in Connection to Alcohol Use in Persons with Bipolar Disorder

Effects of pnpla3 i148m on hepatic lipid and very low-density lipoprotein metabolism in humans

Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans

Occurrence and timing of withdrawal of life-sustaining measures in traumatic brain injury patients: a CENTER-TBI study

Primary versus early secondary referral to a specialized neurotrauma center in patients with moderate/severe traumatic brain injury: a CENTER TBI study

Lifetime risk of rheumatoid arthritis-associated interstitial lung disease in <em>MUC5B</em> mutation carriers

Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

Fluid balance and outcome in critically ill patients with traumatic brain injury (CENTER-TBI and OzENTER-TBI): a prospective, multicentre, comparative effectiveness study

Management of arterial partial pressure of carbon dioxide in the first week after traumatic brain injury: results from the CENTER-TBI study

Pathological Computed Tomography Features Associated With Adverse Outcomes After Mild Traumatic Brain Injury: A TRACK-TBI Study With External Validation in CENTER-TBI

Genetics of Cluster Headache takes a leap

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences

Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population

Reaction Time and Visual Memory in Connection with Alcohol Use in Schizophrenia and Schizoaffective Disorder

Identifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics

ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes

Association of structural variation with cardiometabolic traits in Finns

Persistent postconcussive symptoms in children and adolescents with mild traumatic brain injury receiving initial head computed tomography

Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries

Author Correction: Evaluating drug targets through human loss-of-function genetic variation

Author Correction: A structural variation reference for medical and population genetics

Author Correction: Transcript expression-aware annotation improves rare variant interpretation

Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans

Author Correction: Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals

Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants

Combined effects of genotype and childhood adversity shape variability of DNA methylation across age

The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease

Author Correction: The effect of LRRK2 loss-of-function variants in humans

Missing Data in Prediction Research: A Five-Step Approach for Multiple Imputation, Illustrated in the CENTER-TBI Study

Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes

Sleep apnoea is a risk factor for severe COVID-19

The role of polygenic risk and susceptibility genes in breast cancer over the course of life

Global Characterisation of Coagulopathy in Isolated Traumatic Brain Injury (iTBI): A CENTER-TBI Analysis

Cerebral small vessel disease genomics and its implications across the lifespan

Understanding the relationship between cognitive performance and function in daily life after traumatic brain injury

High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health

Effects of TM6SF2 E167K on hepatic lipid and very low-density lipoprotein metabolism in humans

Outcome Prediction after Moderate and Severe Traumatic Brain Injury: External Validation of Two Established Prognostic Models in 1742 European Patients

Habitual sleep disturbances and migraine: a Mendelian randomization study

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants