selected publications
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Journal Article
- Huntington disease 2015
- Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics. 2013
- CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012
- Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. American Journal of Human Genetics. 2012
- Population stratification may bias analysis of PGC-1alpha as a modifier of age at Huntington disease motor onset. Human Genetics. 2012
- TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochemical and Biophysical Research Communications. 2012
- Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Human Genetics. 2009
- Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology. 2008
- Replication of association between ELAVL4 and Parkinson disease: the GenePD study. Human Genetics. 2008
- The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. BMC Medicine. 2008
- Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study. BMC Medical Genetics. 2006
- A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study. American Journal of Human Genetics. 2003
- Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease. American Journal of Medical Genetics. Part A. 2003