Genome wide assessment of young onset Parkinson's disease from Finland.
Genome wide assessment of young onset Parkinson's disease from Finland.
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DOI:
10.1371/journal.pone.0041859
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发表时间:
2012
期刊:
影响因子:
3.7
通讯作者:
Singleton AB
中科院分区:
文献类型:
--
作者:
Hernandez DG;Nalls MA;Ylikotila P;Keller M;Hardy JA;Majamaa K;Singleton AB
In the current study we undertook a series of experiments to test the hypothesis that a monogenic cause of disease may be detectable within a cohort of Finnish young onset Parkinson’s disease patients. In the first instance we performed standard genome wide association analyses, and subsequent risk profile analysis. In addition we performed a series of analyses that involved testing measures of global relatedness within the cases compared to controls, searching for excess homozygosity in the cases, and examining the cases for signs of excess local genomic relatedness using a sliding window approach. This work suggested that the previously identified common, low risk alleles, and the risk models associated with these alleles, were generalizable to the Finnish Parkinson’s disease population. However, we found no evidence that would suggest a single common high penetrance mutation exists in this cohort of young onset patients.
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影响因子:
4.5
作者:
Do CB;Tung JY;Dorfman E;Kiefer AK;Drabant EM;Francke U;Mountain JL;Goldman SM;Tanner CM;Langston JW;Wojcicki A;Eriksson N
通讯作者:
Eriksson N
影响因子:
48
作者:
Laaksovirta, Hannu;Peuralinna, Terhi;Schymick, Jennifer C.;Scholz, Sonja W.;Lai, Shaoi-Lin;Myllykangas, Liisa;Sulkava, Raimo;Jansson, Lilja;Hernandez, Dena G.;Gibbs, J. Raphael;Nalls, Michael A.;Heckerman, David;Tienari, Pentti J.;Traynor, Bryan J.
通讯作者:
Traynor, Bryan J.
DOI:
10.1056/nejmra0808700
发表时间:
2009-04-23
期刊:
The New England journal of medicine
影响因子:
--
作者:
Hardy J;Singleton A
通讯作者:
Singleton A
影响因子:
30.8
作者:
Satake, Wataru;Nakabayashi, Yuko;Toda, Tatsushi
通讯作者:
Toda, Tatsushi
影响因子:
30.8
作者:
Skol, AD;Scott, LJ;Boehnke, M
通讯作者:
Boehnke, M