- Works count
- 310
- Citation count
- 21,722
- H-index
- 68
- i10-index
- 211
Research interests
Publications
Clinical Correlations With Lewy Body Pathology inLRRK2-Related Parkinson Disease
JAMA Neurology · 2014 · https://doi.org/10.1001/jamaneurol.2014.2704
DNAJC13 mutations in Parkinson disease
Human Molecular Genetics · 2013 · https://doi.org/10.1093/hmg/ddt570
Alpha‐synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease
Movement Disorders · 2013 · 10.1002/mds.25421
Large-scale replication and heterogeneity in Parkinson disease genetic loci
Neurology · 2012 · https://doi.org/10.1212/wnl.0b013e318264e353
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
The American Journal of Human Genetics · 2011 · https://doi.org/10.1016/j.ajhg.2011.08.009
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
Nature Genetics · 2011 · https://doi.org/10.1038/ng.1027
VPS35 Mutations in Parkinson Disease
The American Journal of Human Genetics · 2011 · https://doi.org/10.1016/j.ajhg.2011.06.001
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
Nature Genetics · 2011 · https://doi.org/10.1038/ng.803
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study
The Lancet Neurology · 2011 · https://doi.org/10.1016/s1474-4422(11)70175-2
Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2
Neurology · 2010 · 10.1212/wnl.0b013e3181ff9685
Cerebrospinal fluid biomarkers for Parkinson disease diagnosis and progression
Annals of Neurology · 2010 · 10.1002/ana.22311
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
New England Journal of Medicine · 2009 · https://doi.org/10.1056/nejmoa0901281
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
The Lancet Neurology · 2008 · https://doi.org/10.1016/s1474-4422(08)70117-0
APOE ε4 lowers age at onset and is a high risk factor for Alzheimer's disease; A case control study from central Norway
BMC Neurology · 2008 · https://doi.org/10.1186/1471-2377-8-9
Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations
The American Journal of Human Genetics · 2005 · 10.1086/429256
Lrrk2 pathogenic substitutions in Parkinson's disease
Neurogenetics · 2005 · 10.1007/s10048-005-0005-1
Current projects
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