R. L. Watts
Publications While At Healthpartners
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease
Parkinsonism & Related Disorders.
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families
Association study of Parkin gene polymorphisms with idiopathic Parkinson disease
Archives of Neurology.
Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease
Human Molecular Genetics.
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
American Journal of Human Genetics.
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease
Annals of Neurology.
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