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Comment
. 2006 Jun;78(6):1090-2; author reply 1092-4.
doi: 10.1086/504725.

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan

Yonghong Li, Charles Rowland, Steven Schrodi, Walter Laird, Kristina Tacey, David Ross, Diane Leong, Joseph Catanese, John Sninsky, Andrew Grupe
Comment

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan

Yonghong Li et al. Am J Hum Genet. 2006 Jun.
No abstract available

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References

Web Resources

    1. dbSNP, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=snp
    1. International HapMap Project, http://www.hapmap.org/
    1. NINDS Human Genetics Resources at the Coriell Institute, http://locus.umdnj.edu/ninds
    1. Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/ (for PD, LRRK2, PARK10, ELMO1, and SEMA5A)

References

    1. Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PVK, Frazer KA, Cox DR, Ballinger DG (2005) High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 77:685–693 - PMC - PubMed
    1. Hughes AJ, Daniel SE, Kilford L, Lees AJ (1992) Accuracy of clinical diagnosis of idiopathic Parkinson’s disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 55:181–184 - PMC - PubMed
    1. Gilks WP, Abou-Sleiman PM, Gandhi S, Jain S, Singleton A, Lees AJ, Shaw K, Bhatia KP, Bonifati V, Quinn NP, Lynch J, Healy DG, Holton JL, Revesz T, Wood NW (2005) A common LRRK2 mutation in idiopathic Parkinson’s disease. Lancet 365:415–416 - PubMed
    1. Li Y, Nowotny P, Holmans P, Smemo S, Kauwe JS, Hinrichs AL, Tacey K, et al (2004) Association of late-onset Alzheimer’s disease with genetic variation in multiple members of the GAPD gene family. Proc Natl Acad Sci USA 101:15688–1569310.1073/pnas.0403535101 - DOI - PMC - PubMed
    1. Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T (2003) Significant linkage of Parkinson disease to chromosome 2q36-37. Am J Hum Genet 72:1053–1057 - PMC - PubMed