Genome-Wide Association Study of Parkinson Disease

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson’s disease

T. Hamza, C. Zabetian, A. Tenesa, et al.. (2010). Nature genetics. Cited 753 times. https://doi.org/10.1038/ng.642

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease

C. Zabetian, C. Hutter, S. Factor, et al.. (2007). Annals of Neurology. Cited 165 times. https://doi.org/10.1002/ana.21157

Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk

K. Powers, Denise M. Kay, S. Factor, et al.. (2008). Movement Disorders. Cited 151 times. https://doi.org/10.1002/mds.21782

Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients

Denise M. Kay, D. Moran, Lina M. Moses, et al.. (2007). Annals of Neurology. Cited 134 times. https://doi.org/10.1002/ana.21039

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

C. Zabetian, C. Hutter, Dora Yearout, et al.. (2006). American journal of human genetics. Cited 131 times. https://doi.org/10.1086/508025

Exploring gene-environment interactions in Parkinson’s disease

C. McCulloch, Denise M. Kay, S. Factor, et al.. (2008). Human Genetics. Cited 96 times. https://doi.org/10.1007/s00439-008-0466-z

Familial aggregation of Parkinson disease: a comparative study of early-onset and late-onset disease.

H. Payami, S. Zareparsi, D. James, et al.. (2002). Archives of neurology. Cited 95 times. https://doi.org/10.1001/ARCHNEUR.59.5.848

The heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factors

T. Hamza, H. Payami. (2010). Journal of Human Genetics. Cited 77 times. https://doi.org/10.1038/jhg.2010.13

Genetic association between α‐synuclein and idiopathic parkinson's disease

Denise M. Kay, S. Factor, A. Samii, et al.. (2008). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. Cited 62 times. https://doi.org/10.1002/ajmg.b.30758

Segregation analysis of Parkinson disease.

S. Zareparsi, T. Taylor, E. Harris, et al.. (1998). American journal of medical genetics. Cited 23 times. https://doi.org/10.1002/(SICI)1096-8628(19981204)80:4<410::AID-AJMG21>3.0.CO;2-2

Validity and Utility of a LRRK2 G2019S Mutation Test for the Diagnosis of Parkinson's Disease

Denise M. Kay, T. Bird, C. Zabetian, et al.. (2006). Genetic Testing. Cited 21 times. https://doi.org/10.1089/gte.2006.10.221