Home
Kaya Kvarme Jacobsen's picture

Kaya Kvarme Jacobsen

Guest Researcher
  • E-mailkaya.jacobsen@uib.no
  • Visitor Address
    Haukeland Universitetssykehus Laboratoriebygget, 7. etg. Heis øst
    5009 Bergen
  • Postal Address
    Postboks 7804
    5020 Bergen
Academic article
  • Show author(s) (2024). Neonatal Ultrasound and Radiographic Markers of Hip Dysplasia in Young Adults. Pediatrics.
  • Show author(s) (2023). COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study. Osteoarthritis and Cartilage Open. 1-7.
  • Show author(s) (2018). Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC. Brain and Behavior. 1-12.
  • Show author(s) (2016). Meta-analysis of the DRD5 VNTR in persistent ADHD. European Neuropsychopharmacology. 1527-1532.
  • Show author(s) (2016). Exome chip analyses in adult attention deficit hyperactivity disorder. Translational Psychiatry. 7 pages.
  • Show author(s) (2016). A candidate gene investigation of methylphenidate response in adult attention-deficit/hyperactivity disorder patients: results from a naturalistic study. Journal of Neural Transmission. 859-865.
  • Show author(s) (2015). Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder . Journal of Affective Disorders. 453-461.
  • Show author(s) (2015). Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 423-432.
  • Show author(s) (2015). Common variants in the ARC gene are not associated with cognitive abilities. Brain and Behavior. 8 pages.
  • Show author(s) (2015). Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder. Neuropsychopharmacology. 915-926.
  • Show author(s) (2013). DISC1 in adult ADHD patients: An association study in two European samples. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 227-234.
  • Show author(s) (2011). Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four european populations. American Journal of Medical Genetics. 600-612.
  • Show author(s) (2011). DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders. Neuropsychopharmacology. 2318-2327.
  • Show author(s) (2010). Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations. American Journal of Medical Genetics. 1008-1015.
  • Show author(s) (2010). An international multicenter association study of the serotonin transporter gene in persistent ADHD. Genes, Brain and Behavior. 449-458.
  • Show author(s) (2010). A genome-wide association study of bipolar disorder and comorbid migraine. Genes, Brain and Behavior. 673-680.
Doctoral dissertation
  • Show author(s) (2016). Genetic susceptibility across neuropsychiatric disorders – genome-wide, candidate gene and interaction analyses.
Medical Student Research Thesis
  • Show author(s) (2011). Disrupted in schizophrenia 1 (DISC1) as a novel candidate gene in attention-deficit/hyperactivity disorder (ADHD) – association with rs1538979 in a Norwegian sample of adult ADHD patients.

More information in national current research information system (CRIStin)