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Publications While At HealthPartners

selected publications

Journal Article

A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. 

Parkinsonism & Related Disorders. 2008

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. 

BMC Medicine. 2008

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families. 

Movement Disorders. 2007

Association study of Parkin gene polymorphisms with idiopathic Parkinson disease. 

Archives of Neurology. 2003

Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease. 

Neurology. 2003

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease. 

Human Molecular Genetics. 2003

Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. 

American Journal of Human Genetics. 2003

Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. 

Annals of Neurology. 2003

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R. L. Watts

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