P.M. Knappskog
Haukeland University Hospital(NO)University of Bergen(NO)
Publications by Year
Research Areas
Attention Deficit Hyperactivity Disorder, Metabolism and Genetic Disorders, Bipolar Disorder and Treatment, Neurotransmitter Receptor Influence on Behavior, Mitochondrial Function and Pathology
Most-Cited Works
- → A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication(2010)291 cited
- → Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene(1995)200 cited
- → A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes(2008)191 cited
- → Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzyme(1995)182 cited
- → Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder(2007)125 cited
- → Genetic analyses of dopamine related genes in adult ADHD patients suggest an association with the DRD5‐microsatellite repeat, but not with DRD4 or SLC6A3 VNTRs(2007)94 cited
- → Meta‐analysis of brain‐derived neurotrophic factor p.Val66Met in adult ADHD in four European populations(2009)66 cited
- → A forensic DNA profiling system for Northern European brown bears (Ursus arctos)(2012)57 cited
- → Attention-Deficit/Hyperactivity Disorder Symptoms in Offspring of Mothers With Impaired Serotonin Production(2010)55 cited
- → An international multicenter association study of the serotonin transporter gene in persistent ADHD(2010)55 cited