Postal addressDepartment of Neuroscience Norwegian University of Science and Technology Postboks 8905 7491 Trondheim Norway
Background and activities
Scientific, academic and artistic work
A selection of recent journal publications, artistic productions, books, including book and report excerpts. See all publications in the database
- (2014) Changes in matrix metalloprotease activity and progranulin levels may contribute to the pathophysiological function of mutant leucine-rich repeat kinase 2. Glia. volum 62 (7).
- (2014) The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants. Neurobiology of Aging. volum 35 (1).
- (2014) Olfactory dysfunction in sporadic Parkinson's Disease and LRRK2 carriers. Acta Neurologica Scandinavica. volum 129 (5).
- (2014) Cheek cell-derived alpha-synuclein and DJ-1 do not differentiate Parkinson's disease from control. Neurobiology of Aging. volum 35 (2).
- (2013) Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease. Movement Disorders. volum 28 (6).
- (2013) Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium. Movement Disorders. volum 28 (12).
- (2013) Three family members with elevated plasma cobalamin, transcobalamin and soluble transcobalamin receptor (sCD320). Clinical Chemistry and Laboratory Medicine. volum 51 (3).
- (2013) IgM to S-nitrosylated protein is found intrathecally in relapsing-remitting multiple sclerosis. Journal of Neuroimmunology. volum 256 (1-2).
- (2013) Progressive multifocal leukoencephalopathy in an immunocompetent patient?. Case Reports in Neurology. volum 5.
- (2013) Found in transcription: Accurate Parkinson’s disease classification in peripheral blood. Journal of Parkinson's Disease. volum 3 (1).
- (2013) LRRTM3 Interacts with APP and BACE1 and Has Variants Associating with Late-Onset Alzheimer's Disease (LOAD). PLoS ONE. volum 8 (6).
- (2013) Ursocholanic acid rescues mitochondrial function in common forms of familial Parkinson's disease. Brain. volum 136.
- (2013) Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations. Parkinsonism & Related Disorders. volum 19 (10).
- (2013) STX6 rs1411478 is not associated with increased risk of Parkinson's disease. Parkinsonism & Related Disorders. volum 19 (5).
- (2012) Cerebrospinal fluid amyloid beta and tau in LRRK2 mutation carriers. Neurology. volum 78 (1).
- (2012) Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications. Molecular Neurodegeneration. volum 7.
- (2012) Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids. Nature Genetics. volum 44 (2).
- (2012) Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology. volum 79 (7).
- (2012) A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics. volum 49 (11).
- (2012) DJ-1 and alpha SYN in LRRK2 CSF do not correlate with striatal dopaminergic function. Neurobiology of Aging. volum 33 (4).