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

The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

Tailoring Multi-Dimensional Outcomes to Level of Functional Recovery after Traumatic Brain Injury

Elucidating the relationship between migraine risk and brain structure using genetic data

Health care utilization and outcomes in older adults after Traumatic Brain Injury: A CENTER-TBI study

Whole-genome sequencing reveals host factors underlying critical COVID-19

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease

Genome-wide risk prediction of common diseases across ancestries in one million people

Serum metabolome associated with severity of acute traumatic brain injury

Discrepancy between disability and reported well-being after traumatic brain injury

Surgery versus conservative treatment for traumatic acute subdural haematoma: a prospective, multicentre, observational, comparative effectiveness study

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Rare coding variants in ten genes confer substantial risk for schizophrenia

Vibrational Spectroscopy for the Triage of Traumatic Brain Injury Computed Tomography Priority and Hospital Admissions

New insights into the genetic etiology of Alzheimer's disease and related dementias

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

A genome-wide association study of outcome from traumatic brain injury

Genetic associations of protein-coding variants in human disease

Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes

Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

<em>NCOR2</em> is a novel candidate gene for migraine-epilepsy phenotype

How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development

Effect of frailty on 6-month outcome after traumatic brain injury: a multicentre cohort study with external validation

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma

The relation of severe malocclusion to patients' mental and behavioral disorders, growth, and speech problems

Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers

Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

Genomic prediction of alcohol-related morbidity and mortality

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

Identification of pathogenic variant enriched regions across genes and gene families

Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power

Multivariate Genome-wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

Polygenic burden in focal and generalized epilepsies

Distinct gene-set burden patterns underlie common generalized and focal epilepsies

Extended Coagulation Profiling in Isolated Traumatic Brain Injury: A CENTER-TBI Analysis

Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer

Dissecting the contribution of single nucleotide polymorphisms in <em>CCR9</em> and <em>CCL25</em> genomic regions to the celiac disease phenotype

Can We Cluster ICU Treatment Strategies for Traumatic Brain Injury by Hospital Treatment Preferences?

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

Explaining Outcome Differences between Men and Women following Mild Traumatic Brain Injury

Mapping the human genetic architecture of COVID-19

Reaction Time and Visual Memory in Connection to Hazardous Drinking Polygenic Scores in Schizophrenia, Schizoaffective Disorder and Bipolar Disorder

Questionnaires vs Interviews for the Assessment of Global Functional Outcomes After Traumatic Brain Injury

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