Kaya Kvarme Jacobsen
Stilling
førsteamanuensis, 1. amanuensis/koordinator medisinstudiet i Førde
Tilhørighet
- E-post
- kaya.jacobsen@uib.no
- Besøksadresse
-
Førd Sentralsjukehus Nasjonalt Register for Leddproteser, Møllendalsbakken 7
5009 Bergen - Postadresse
-
Postboks 7804
5020 Bergen
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
2015
- Kaya Kvarme Jacobsen; Rune Kleppe; Stefan Johansson 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)
- Craig Myrum; Sudheer Giddaluru; Kaya Kvarme Jacobsen et al. (2015). Common variants in the ARC gene are not associated with cognitive abilities. (ekstern lenke)
- Kaya Kvarme Jacobsen; Caroline M. Nievergelt; Tetyana Zayats et al. (2015). Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder. (ekstern lenke)
- Cristina Sánchez-Mora; Josep Antonio Ramos-Quiroga; Rosa Bosch 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)
2025
- Lene Bjerke Laborie; Francesco Sera; Kaya Kvarme Jacobsen et al. (2025). Childhood growth associated with hip shapes at skeletal maturity: the Bergen Hip Cohort Study. (ekstern lenke)
- Kaya Kvarme Jacobsen; Hege Kristiansen; Trude Gundersen et al. (2025). The epidemiology of hip dysplasia in the nationwide Norwegian Mother, Father, and Child Cohort Study. (ekstern lenke)
2016
- Tetyana Zayats; Kaya Kvarme Jacobsen; Rune Kleppe et al. (2016). Exome chip analyses in adult attention deficit hyperactivity disorder. (ekstern lenke)
- Kaya Kvarme Jacobsen; Jan Haavik (2016). Genetic susceptibility across neuropsychiatric disorders – genome-wide, candidate gene and interaction analyses. (ekstern lenke)
- Marieke Klein; Stefanie Berger; Martine Hoogman et al. (2016). Meta-analysis of the DRD5 VNTR in persistent ADHD. (ekstern lenke)
- Tor-Arne Hegvik; Kaya Kvarme Jacobsen; Mats Fredriksen et al. (2016). A candidate gene investigation of methylphenidate response in adult attention-deficit/hyperactivity disorder patients: results from a naturalistic study. (ekstern lenke)
2010
- Stefan Johansson; Anne Halmøy; Thegna Mavroconstanti 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)
- Ketil Joachim Ødegaard; Tifany A. Greenwood; Stefan Johansson et al. (2010). A genome-wide association study of bipolar disorder and comorbid migraine. (ekstern lenke)
- Elisabeth Thoverud Landaas; Stefan Johansson; Kaya Kvarme Jacobsen et al. (2010). An international multicenter association study of the serotonin transporter gene in persistent ADHD. (ekstern lenke)
2024
- Karen Rosendahl; Lene Bjerke Laborie; Hanne Rasmussen et al. (2024). Neonatal Ultrasound and Radiographic Markers of Hip Dysplasia in Young Adults.. (ekstern lenke)
- Kaya Kvarme Jacobsen; Lene Bjerke Laborie; Hege Kristiansen et al. (2024). Genetics of hip dysplasia - a systematic literature review. (ekstern lenke)
- Lene Bjerke Laborie; Hanne Rasmussen; Kaya Kvarme Jacobsen et al. (2024). Neonatal Ultrasound and Radiographic Markers of Hip Dysplasia in Young Adults. (ekstern lenke)
2011
- Cristina Sánchez-Mora; Marta Ribases; Miquel Casas 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)
- Andreas Reif; T. Trang Nguyen; Lena Weissflog et al. (2011). DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders. (ekstern lenke)
- Kaya Kvarme Jacobsen; Jan Haavik (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. (ekstern lenke)