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Replication of association between ELAVL4 and Parkinson disease: the GenePD study
Authors:Anita L. DeStefano  Jeanne Latourelle  Mark F. Lew  Oksana Suchowersky  Christine Klein  Lawrence I. Golbe  Margery H. Mark  John H. Growdon  G. Fredrick Wooten  Ray Watts  Mark Guttman  Brad A. Racette  Joel S. Perlmutter  Lynn Marlor  Holly A. Shill  Carlos Singer  Stefano Goldwurm  Gianni Pezzoli  Marie H. Saint-Hilaire  Audrey E. Hendricks  Adam Gower  Sally Williamson  Michael W. Nagle  Jemma B. Wilk  Tiffany Massood  Karen W. Huskey  Kenneth B. Baker  Ilia Itin  Irene Litvan  Garth Nicholson  Alastair Corbett  Martha Nance  Edward Drasby  Stuart Isaacson  David J. Burn  Patrick F. Chinnery  Peter P. Pramstaller  Jomana Al-hinti  Anette T. Moller  Karen Ostergaard  Scott J. Sherman  Richard Roxburgh  Barry Snow  John T. Slevin  Franca Cambi  James F. Gusella  Richard H. Myers
Affiliation:Department of Biostatistics, Boston University School of Public Health, 715 Albany Street, Crosstown Center, 3rd floor, Boston, MA 02118, USA. adestef@bu.edu
Abstract:Genetic variants in embryonic lethal, abnormal vision, Drosophila-like 4 (ELAVL4) have been reported to be associated with onset age of Parkinson disease (PD) or risk for PD affection in Caucasian populations. In the current study we genotyped three single nucleotide polymorphisms in ELAVL4 in a Caucasian study sample consisting of 712 PD patients and 312 unrelated controls from the GenePD study. The minor allele of rs967582 was associated with increased risk of PD (odds ratio = 1.46, nominal P value = 0.011) in the GenePD population. The minor allele of rs967582 was also the risk allele for PD affection or earlier onset age in the previously studied populations. This replication of association with rs967582 in a third cohort further implicates ELAVL4 as a PD susceptibility gene.
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