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selected publications

Journal Article

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12. 

Neurogenetics. 2006

Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. 

American Journal of Human Genetics. 2006

Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations. 

Neurogenetics. 2004

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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full name

M. A. Pericak-Vance

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