|
| 37946686 | Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD. | Am J Med Genet B Neuropsychiatr Genet | 2024 |
| 38052102 | Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity. | Hum Reprod | 2024 |
| 37244984 | DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals. | BMC Genom Data | 2023 |
| 37937776 | Actionable Genotypes and Their Association with Life Span in Iceland. | N Engl J Med | 2023 |
| 37794188 | Large-scale plasma proteomics comparisons through genetics and disease associations. | Nature | 2023 |
| 37486023 | Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor. | Ann Neurol | 2023 |
| 37464041 | Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. | Nat Med | 2023 |
| 37414856 | Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study. | Commun Med (Lond) | 2023 |
| 37400429 | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. | Nat Commun | 2023 |
| 37301908 | Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. | Nat Commun | 2023 |
| 37294764 | Sequence variants affecting voice pitch in humans. | Sci Adv | 2023 |
| 36151456 | Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample. | Mol Psychiatry | 2022 |
| 33615640 | Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs. | Hum Brain Mapp | 2022 |
| 35859178 | The sequences of 150,119 genomes in the UK Biobank. | Nature | 2022 |
| 35726068 | Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. | Nat Genet | 2022 |
| 35659384 | Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes. | Biol Psychiatry | 2022 |
| 35470158 | Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset. | Ann Rheum Dis | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 35298028 | A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam. | Epilepsia | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 36415660 | Thirty novel sequence variants impacting human intracranial volume. | Brain Commun | 2022 |
| 33846298 | HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry. | Transl Psychiatry | 2021 |
| 36070241 | Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases. | BMJ Open | 2021 |
| 33602968 | A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy. | Sci Rep | 2021 |
| 33453761 | Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study. | Lancet Child Adolesc Health | 2021 |
| 33315477 | Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in <i>LDLR</i>. | Circ Genom Precis Med | 2021 |
| 33169150 | Data Resource Profile: The Copenhagen Hospital Biobank (CHB). | Int J Epidemiol | 2021 |
| 32989287 | Genome-wide association study identifies 48 common genetic variants associated with handedness. | Nat Hum Behav | 2021 |
| 34857953 | Large-scale integration of the plasma proteome with genetics and disease. | Nat Genet | 2021 |
| 34773122 | Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. | Nat Genet | 2021 |
| 34620984 | A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo. | Commun Biol | 2021 |
| 34145379 | Predicting the probability of death using proteomics. | Commun Biol | 2021 |
| 34140119 | Cognition in Schizophrenia. | Biol Psychiatry | 2021 |
| 31712720 | Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. | Mol 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 |
| 33931204 | Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition. | Biol Psychiatry | 2021 |
| 31665216 | Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. | JAMA Psychiatry | 2020 |
| 33239738 | Large genome-wide association study identifies three novel risk variants for restless legs syndrome. | Commun Biol | 2020 |
| 30705424 | Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. | Mol Psychiatry | 2020 |
| 33035477 | Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming. | Curr Biol | 2020 |
| 32702746 | Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease. | Eur Heart J | 2020 |
| 32061372 | Identification of Genetic Loci Shared Between Attention-Deficit/Hyperactivity Disorder, Intelligence, and Educational Attainment. | Biol Psychiatry | 2020 |
| 32029921 | Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. | Nat Genet | 2020 |
| 31619746 | Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study. | Sci Rep | 2019 |
| 31209380 | Genome-wide association study implicates CHRNA2 in cannabis use disorder. | Nat Neurosci | 2019 |
| 31160808 | Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. | Nat Genet | 2019 |
| 31104508 | Comparing migraine with and without aura to healthy controls using RNA sequencing. | Cephalalgia | 2019 |
| 31065058 | GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study. | Sci Rep | 2019 |
| 30992453 | A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy. | Nat Commun | 2019 |
| 30988515 | Roadmap for a precision-medicine initiative in the Nordic region. | Nat Genet | 2019 |