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) (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.