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- Publications
- Influence
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
- Laurie A Robak, I. Jansen, +134 authors A. Singleton
- Biology, Medicine
- Brain : a journal of neurology
- 18 April 2017
Mutations in the glucocerebrosidase gene (GBA), which cause Gaucher disease, are also potent risk factors for Parkinson's disease. We examined whether a genetic burden of variants in other lysosomal… Expand
A susceptibility gene for late‐onset idiopathic Parkinson's disease
- A. Hicks, H. Pétursson, +8 authors S. Sveinbjörnsdóttir
- Medicine
- Annals of neurology
- 1 November 2002
Eight regions of the genome (PARK1‐8) have been implicated in autosomal dominant and autosomal recessive forms of early‐onset Parkinson's disease. These forms constitute a few of all cases. However,… Expand
Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype
- T. Li, H. Stefánsson, +11 authors D. Collier
- Medicine
- Molecular Psychiatry
- 1 July 2004
To determine if neuregulin 1 (NRG1) is associated with schizophrenia in Asian populations, we investigated a Han Chinese population using both a family trio design and a case–control design. A total… Expand
Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing
- I. Jansen, H. Ye, +164 authors P. Heutink
- Biology, Medicine
- Genome Biology
- 30 January 2017
BackgroundWhole-exome sequencing (WES) has been successful in identifying genes that cause familial Parkinson’s disease (PD). However, until now this approach has not been deployed to study large… Expand
Atypical juvenile parkinsonism in a consanguineous SPG15 family
- J. Schicks, M. Synofzik, +4 authors P. Bauer
- Medicine
- Movement disorders : official journal of the…
- 15 February 2011