Øyvind Helgeland's picture

Øyvind Helgeland

PhD Candidate
  • E-mailoyvind.helgeland@uib.no
  • Visitor Address
    Haukelandsveien 28
    Armauer Hansens hus
    5009 Bergen
  • Postal Address
    Postboks 7804
    5020 Bergen
Academic article
  • Show author(s) (2023). Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Nature Genetics. 1807-1819.
  • Show author(s) (2023). Genetic effects on the timing of parturition and links to fetal birth weight. Nature Genetics. 559-567.
  • Show author(s) (2022). Whole-genome sequencing reveals host factors underlying critical COVID-19. Nature. 97-103.
  • Show author(s) (2022). Placental weight centiles adjusted for age, parity and fetal sex. Placenta. 87-94.
  • Show author(s) (2022). Characterization of the genetic architecture of infant and early childhood body mass index. Nature Metabolism. 344-358.
  • Show author(s) (2022). Body mass index and childhood symptoms of depression, anxiety, and attention-deficit hyperactivity disorder: A within-family Mendelian randomization study. eLIFE. 41 pages.
  • Show author(s) (2021). SeeCiTe: a method to assess CNV calls from SNP arrays using trio data. Bioinformatics. 1876-1883.
  • Show author(s) (2021). Genetic association study of childhood aggression across raters, instruments, and age. Translational Psychiatry. 1-9.
  • Show author(s) (2021). Genetic Liability for Schizophrenia and Childhood Psychopathology in the General Population. Schizophrenia Bulletin. 1179-1189.
  • Show author(s) (2021). GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility. Nature Communications. 1-14.
  • Show author(s) (2021). A fast wavelet-based functional association analysis replicates several susceptibility loci for birth weight in a Norwegian population. BMC Genomics. 9 pages.
  • Show author(s) (2020). The genetic architecture of sporadic and multiple consecutive miscarriage. Nature Communications. 1-12.
  • Show author(s) (2020). Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents. European Journal of Human Genetics. 205-215.
  • Show author(s) (2020). Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits. PLoS Genetics. 1-26.
  • Show author(s) (2020). Autozygosity mapping and time-to-spontaneous delivery in Norwegian parent-offspring trios. Human Molecular Genetics. 3845-3858.
  • Show author(s) (2019). Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. Nature Communications. 1-13.
  • Show author(s) (2019). Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nature Genetics. 804-814.
  • Show author(s) (2019). Introducing M-GCTA a software package to estimate maternal (or paternal) genetic effects on offspring phenotypes. Behavior Genetics. 51-66.
  • Show author(s) (2019). Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. Nature Communications. 1-10.
  • Show author(s) (2019). A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity. Human Molecular Genetics. 3327-3338.
  • Show author(s) (2018). Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. Human Molecular Genetics. 742-756.
  • Show author(s) (2017). Rare and low-frequency coding variants alter human adult height. Nature. 186-190.
  • Show author(s) (2016). Methylenetetrahydrofolate dehydrogenase 1 polymorphisms modify the associations of plasma glycine and serine with risk of acute myocardial infarction in patients with stable angina pectoris in WENBIT (Western Norway B Vitamin Intervention Trial). Circulation: Cardiovascular Genetics. 541-547.
  • Show author(s) (2016). B vitamin treatments modify the risk of myocardial infarction associated with a MTHFD1 polymorphism in patients with stable angina pectoris. NMCD. Nutrition Metabolism and Cardiovascular Diseases. 495-501.
  • Show author(s) (2015). Assessing the Causal Relationship of Maternal Height on Birth Size and Gestational Age at Birth: A Mendelian Randomization Analysis. PLoS Medicine. 23 pages.
Academic lecture
  • Show author(s) (2020). Which Metabo-Psychiatric Factors Affect the Risk of Anorexia Nervosa? A Mendelian Randomization Study.
Letter to the editor
  • Show author(s) (2022). A first update on mapping the human genetic architecture of COVID-19. Nature. E1-E10.
  • Show author(s) (2021). The causal effect of BMI on neurodevelopment: a within family Mendelian randomization study using MoBa. International Journal of Epidemiology. 1 pages.
  • Show author(s) (2024). Correction to: Characterization of the genetic architecture of infant and early childhood body mass index (Nature Metabolism, (2022), 4, 3, (344-358), 10.1038/s42255-022-00549-1). Nature Metabolism. 378-378.
  • Show author(s) (2023). Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight (Nature Genetics, (2023), 55, 4, (559-567), 10.1038/s41588-023-01343-9). Nature Genetics.
  • Show author(s) (2018). Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. 766-767.
Academic literature review
  • Show author(s) (2015). The chromosome 9p21 CVD- and T2D-associated regions in a Norwegian population (the HUNT2 survey). International Journal of Endocrinology. 9 pages.

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