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

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

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

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

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

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

A large-scale genome-wide association study meta-analysis of cannabis use disorder

Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

Genome-wide association study identifies 48 common genetic variants associated with handedness

A data-driven medication score predicts 10-year mortality among aging adults

Prediction of Global Functional Outcome and Post-Concussive Symptoms after Mild Traumatic Brain Injury: External Validation of Prognostic Models in the Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI) S

Correction to: Frequency of fatigue and its changes in the first 6 months after traumatic brain injury: results from the CENTER-TBI study

Extensions of Multiple-Group Item Response Theory Alignment: Application to Psychiatric Phenotypes in an International Genomics Consortium

Differences between Men and Women in Treatment and Outcome after Traumatic Brain Injury

GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer

Predictors of Access to Rehabilitation in the Year Following Traumatic Brain Injury: A European Prospective and Multicenter Study

Tracheal intubation in traumatic brain injury: a multicentre prospective observational study

Frequency of fatigue and its changes in the first 6 months after traumatic brain injury: results from the CENTER-TBI study

Health-related quality of life after traumatic brain injury: deriving value sets for the QOLIBRI-OS for Italy, The Netherlands and The United Kingdom

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

Complement genes contribute sex-biased vulnerability in diverse disorders

Informed consent procedures in patients with an acute inability to provide informed consent: Policy and practice in the CENTER-TBI study

The effect of LRRK2 loss-of-function variants in humans

Transcript expression-aware annotation improves rare variant interpretation

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

Evaluating drug targets through human loss-of-function genetic variation

A structural variation reference for medical and population genetics

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