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| 33949298 | Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study. | Psychological Medicine | 2023 |
| 37666001 | Genome-Wide Association study of susceptibility to respiratory syncytial virus hospitalization in young children < 5 years of age. | | 2023 |
| 37798380 | Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. | Nat Genet | 2023 |
| 37464041 | Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. | Nat Med | 2023 |
| 36810956 | Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locus. | | 2023 |
| 36697501 | Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks. | Commun Biol | 2023 |
| 36477816 | Deep Learning for Cross-Diagnostic Prediction of Mental Disorder Diagnosis and Prognosis Using Danish Nationwide Register and Genetic Data. | JAMA Psychiatry | 2023 |
| 36694575 | The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvement. | Brain Commun | 2023 |
| 36918911 | Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants. | | 2023 |
| 36786322 | DNA-methylation and immunological response in medication overuse headache. | | 2023 |
| 35139346 | Accounting for age of onset and family history improves power in genome-wide association studies. | Am J Hum Genet | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 36163277 | Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups. | Nat Genet | 2022 |
| 35381269 | Genome-wide study of early and severe childhood asthma identifies interaction between CDHR3 and GSDMB. | J Allergy Clin Immunol | 2022 |
| 36272495 | Methylation microarray-based detection of clinical copy-number aberrations in CLL benchmarked to standard FISH analysis. | Genomics | 2022 |
| 35996886 | Genetic assortative mating for schizophrenia and bipolar disorder. | Eur Psychiatry | 2022 |
| 35927488 | Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder. | Nat Genet | 2022 |
| 36778135 | The female protective effect against autism spectrum disorder. | Cell Genom | 2022 |
| 36457050 | A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions. | Behavioral and Brain Functions | 2022 |
| 34092057 | IGHV-associated methylation signatures more accurately predict clinical outcomes of chronic lymphocytic leukemia patients than IGHV mutation load. | Haematologica | 2022 |
| 35317884 | Increased transmission of SARS-CoV-2 in Denmark during UEFA European championships. | Epidemiology and Infection | 2022 |
| 34794811 | Concordance and comorbidities among monozygotic twins with tic disorders. | Journal of Psychiatric Research | 2022 |
| 35272746 | Molecular epidemiology of the SARS-CoV-2 variant Omicron BA.2 sub-lineage in Denmark, 29 November 2021 to 2 January 2022. | Eurosurveillance | 2022 |
| 34664785 | Evaluating the interrelations between the autism polygenic score and psychiatric family history in risk for autism. | Autism Research | 2022 |
| 34817560 | Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. | JAMA Psychiatry | 2022 |
| 34531895 | Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis. | Front Genet | 2021 |
| 36324662 | Genome-wide by Environment Interaction Study of Stressful Life Events and Hospital-Treated Depression in the iPSYCH2012 Sample. | Biol Psychiatry Glob Open Sci | 2021 |
| 33972578 | Bortezomib induces methylation changes in neuroblastoma cells that appear to play a significant role in resistance development to this compound. | Scientific Reports | 2021 |
| 33910498 | Co-occurring hydrocephalus in autism spectrum disorder: a Danish population-based cohort study. | Journal of Neurodevelopmental Disorders | 2021 |
| 34006849 | Pharmacogenetic genotype and phenotype frequencies in a large Danish population-based case-cohort sample. | Translational Psychiatry | 2021 |
| 34002096 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. | Nat Genet | 2021 |
| 33439215 | Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status. | JAMA Psychiatry | 2021 |
| 33293699 | Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder. | Eur J Hum Genet | 2021 |
| 33226468 | Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci. | Child's Nervous System | 2021 |
| 34680906 | EWAS of Monozygotic Twins Implicate a Role of mTOR Pathway in Pathogenesis of Tic Spectrum Disorder. | Genes | 2021 |
| 34465810 | Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study. | Scientific Reports | 2021 |
| 34915977 | Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021. | Eurosurveillance | 2021 |
| 34449527 | Implementation of SCID Screening in Denmark. | International Journal of Neonatal Screening | 2021 |
| 34599460 | Idiopathic early ovarian aging: is there a relation with premenopausal accelerated biological aging in young women with diminished response to ART? | | 2021 |
| 31049583 | Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse. | Cardiovascular Research | 2020 |
| 31803957 | Genetic liability to ADHD and substance use disorders in individuals with ADHD. | Addiction | 2020 |
| 31748690 | A major role for common genetic variation in anxiety disorders. | Mol Psychiatry | 2020 |
| 31577390 | Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk. | Autism Research | 2020 |
| 32152699 | A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness. | Hum Genet | 2020 |
| 33096046 | A large-scale genome-wide association study meta-analysis of cannabis use disorder. | Lancet Psychiatry | 2020 |
| 33239672 | The genetic architecture of sporadic and multiple consecutive miscarriage. | Nat Commun | 2020 |
| 32635940 | Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study. | BMC Neuroscience | 2020 |
| 32959868 | The Duffy-null genotype and risk of infection. | Human Molecular Genetics | 2020 |
| 32735934 | Genetic liability to major depression and risk of childhood asthma. | Brain, Behavior, and Immunity | 2020 |