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Comment
. 2006 Jun;78(6):1081-2.
doi: 10.1086/504730.

Considerations for genomewide association studies in Parkinson disease

Comment

Considerations for genomewide association studies in Parkinson disease

Richard H Myers. Am J Hum Genet. 2006 Jun.
No abstract available

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Comment on

References

Web Resources

    1. Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/entrez/Omim/ (for PD and LRRK2)

References

    1. Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, Kachergus J, Hulihan H, Uitti RJ, Calne DB, et al (2004) Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 44:601–607 10.1016/j.neuron.2004.11.005 - DOI - PubMed
    1. Clarimon J, Scholz S, Fung H-C, Hardy J, Eerola J, Hellström O, Chen C-M, Wu Y-R, Tienari PJ, Singleton A (2006) Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. Am J Hum Genet 78:1082–1084 (in this issue) - PMC - PubMed
    1. Farrer MJ, Haugarvoll K, Ross OA, Stone JT, Milkovic NM, Cobb SA, Whittle AJ, Lincoln SJ, Hulihan MM, Heckman MG, White LR, Aasly JO, Gibson JM, Gosal D, Lynch T, Wszolek ZK, Uitti RJ, Toft M (2006) Genomewide association, Parkinson disease, and PARK10. Am J Hum Genet 78:1084–1088 (in this issue) - PMC - PubMed
    1. Goris A, Williams-Gray CH, Foltynie T, Compston DAS, Barker RA, Sawcer SJ (2006) No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening. Am J Hum Genet 78:1088–1090 (in this issue) - PMC - PubMed
    1. Li Y, Rowland C, Schrodi S, Laird W, Tacey K, Ross D, Leong D, Catanese J, Sninsky J, Grupe A (2006) A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan. Am J Hum Genet 78:1090–1092 (in this issue) - PMC - PubMed