Whole-exome sequencing of 228 patients with sporadic Parkinson’s disease-Reference-Cited by-同舟云学术

Whole-exome sequencing of 228 patients with sporadic Parkinson’s disease

Published:2017-01-24 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Sandor Cynthia,Honti Frantisek,Haerty Wilfried,Szewczyk-Krolikowski Konrad,Tomlinson Paul,Evetts Sam,Millin Stephanie,Keane Thomas,McCarthy Shane A.,Durbin Richard,Talbot Kevin,Hu Michele,Webber Caleb,Ponting Chris P.,Wade-Martins Richard

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep41188.pdf

Reference34 articles.

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2. Verstraeten, A., Theuns, J. & Van Broeckhoven, C. Progress in unraveling the genetic etiology of Parkinson disease in a genomic era. Trends Genet 31, 140–149, doi: 10.1016/j.tig.2015.01.004 (2015).

3. Nalls, M. A. et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease. Nat Genet 46, 989–993, doi: 10.1038/ng.3043 (2014).

4. Finucane, H. K. et al. Partitioning heritability by functional annotation using genome-wide association summary statistics. Nat Genet 47, 1228–1235, doi: 10.1038/ng.3404 (2015).

5. Kiezun, A. et al. Exome sequencing and the genetic basis of complex traits. Nat Genet 44, 623–630, doi: 10.1038/ng.2303 (2012).

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