Kaya Kvarme Jacobsen
Stilling
Førsteamanuensis, 1. amanuensis/koordinator medisinstudiet i Førde
Tilhørighet
Forskergrupper
Kort info
Forskning på genetiske risikofaktorer for barneortopediske tilstander som hofteleddsdysplasi, patellofemoral dysplasi og klumpfot.
Publikasjoner
2025
- Jacobsen, Kaya Kvarme; Kristiansen, Hege; Gundersen, Trude et al. (2025). The epidemiology of hip dysplasia in the nationwide Norwegian Mother, Father, and Child Cohort Study. (ekstern lenke)
- Laborie, Lene Bjerke; Sera, Francesco; Jacobsen, Kaya Kvarme et al. (2025). Childhood growth associated with hip shapes at skeletal maturity: the Bergen Hip Cohort Study. (ekstern lenke)
2024
- Rosendahl, Karen; Laborie, Lene Bjerke; Rasmussen, Hanne et al. (2024). Neonatal Ultrasound and Radiographic Markers of Hip Dysplasia in Young Adults.. (ekstern lenke)
- Jacobsen, Kaya Kvarme; Laborie, Lene Bjerke; Kristiansen, Hege et al. (2024). Genetics of hip dysplasia - a systematic literature review. (ekstern lenke)
- Laborie, Lene Bjerke; Rasmussen, Hanne; Jacobsen, Kaya Kvarme et al. (2024). Neonatal Ultrasound and Radiographic Markers of Hip Dysplasia in Young Adults. (ekstern lenke)
2016
- Hegvik, Tor-Arne; Jacobsen, Kaya Kvarme; Fredriksen, Mats et al. (2016). A candidate gene investigation of methylphenidate response in adult attention-deficit/hyperactivity disorder patients: results from a naturalistic study. (ekstern lenke)
- Jacobsen, Kaya Kvarme; Haavik, Jan (2016). Genetic susceptibility across neuropsychiatric disorders – genome-wide, candidate gene and interaction analyses. (ekstern lenke)
- Klein, Marieke; Berger, Stefanie; Hoogman, Martine et al. (2016). Meta-analysis of the DRD5 VNTR in persistent ADHD. (ekstern lenke)
- Zayats, Tetyana; Jacobsen, Kaya Kvarme; Kleppe, Rune et al. (2016). Exome chip analyses in adult attention deficit hyperactivity disorder. (ekstern lenke)
2015
- Myrum, Craig; Giddaluru, Sudheer; Jacobsen, Kaya Kvarme et al. (2015). Common variants in the ARC gene are not associated with cognitive abilities. (ekstern lenke)
- Sánchez-Mora, Cristina; Ramos-Quiroga, Josep Antonio; Bosch, Rosa et al. (2015). Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder. (ekstern lenke)
- Jacobsen, Kaya Kvarme; Kleppe, Rune; Johansson, Stefan et al. (2015). Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE. (ekstern lenke)
- Jacobsen, Kaya Kvarme; Nievergelt, Caroline M.; Zayats, Tetyana et al. (2015). Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder. (ekstern lenke)
2011
- Sánchez-Mora, Cristina; Ribases, Marta; Casas, Miquel et al. (2011). Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four european populations. (ekstern lenke)
- Reif, Andreas; Nguyen, T. Trang; Weissflog, Lena et al. (2011). DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders. (ekstern lenke)
2010
- Johansson, Stefan; Halmøy, Anne; Mavroconstanti, Thegna et al. (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. (ekstern lenke)
- Landaas, Elisabeth Thoverud; Johansson, Stefan; Jacobsen, Kaya Kvarme et al. (2010). An international multicenter association study of the serotonin transporter gene in persistent ADHD. (ekstern lenke)
- Ødegaard, Ketil Joachim; Greenwood, Tifany A.; Johansson, Stefan et al. (2010). A genome-wide association study of bipolar disorder and comorbid migraine. (ekstern lenke)