Dale R. Nyholt
Queensland University of Technology
250 papers found
A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts
The genetic architecture of sporadic and multiple consecutive miscarriage
Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity
A comparative study of multi-omics integration tools for cancer driver gene identification and tumour subtyping
Associations of autozygosity with a broad range of human phenotypes
Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium
Novel hypotheses emerging from GWAS in migraine?
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Identification of common genetic risk variants for autism spectrum disorder
Erratum to: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (Nature Communications, (2018), 9, 1, (4774), 10.1038/s41467-018-06649-5)
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium
Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank
Linking migraine frequency with family history of migraine
Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels
Analysis of shared heritability in common disorders of the brain.
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses
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