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@ARTICLE{Dehestani:163360,
author = {Dehestani, Mohammad and Liu, Hui and Gasser, Thomas},
title = {{P}olygenic {R}isk {S}cores {C}ontribute to {P}ersonalized
{M}edicine of {P}arkinson's {D}isease.},
journal = {Journal of Personalized Medicine},
volume = {11},
number = {10},
issn = {2075-4426},
address = {Basel},
publisher = {MDPI},
reportid = {DZNE-2022-00123},
pages = {1030},
year = {2021},
note = {CC BY},
abstract = {Parkinson's disease (PD) is the second most common
neurodegenerative disorder characterized by the loss of
dopaminergic neurons. The vast majority of PD patients
develop the disease sporadically and it is assumed that the
cause lies in polygenic and environmental components. The
overall polygenic risk is the result of a large number of
common low-risk variants discovered by large genome-wide
association studies (GWAS). Polygenic risk scores (PRS),
generated by compiling genome-wide significant variants, are
a useful prognostic tool that quantifies the cumulative
effect of genetic risk in a patient and in this way helps to
identify high-risk patients. Although there are limitations
to the construction and application of PRS, such as
considerations of limited genetic underpinning of diseases
explained by SNPs and generalizability of PRS to other
populations, this personalized risk prediction could make a
promising contribution to stratified medicine and tailored
therapeutic interventions in the future.},
subtyp = {Review Article},
keywords = {Parkinson’s disease (Other) / personalized medicine
(Other) / polygenic risk scores (Other)},
cin = {AG Gasser / Tübingen common},
ddc = {610},
cid = {I:(DE-2719)1210000 / I:(DE-2719)6000018},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:34683174},
pmc = {pmc:PMC8539098},
doi = {10.3390/jpm11101030},
url = {https://pub.dzne.de/record/163360},
}