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A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.
Ann Neurol. 2018 Jul;84(1):117-129. doi: 10.1002/ana.25274. Epub 2018 Aug 26.
Ann Neurol. 2018.
PMID: 30146727
Free PMC article.
The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal.
Berge-Seidl V, Pihlstrøm L, Maple-Grødem J, Forsgren L, Linder J, Larsen JP, Tysnes OB, Toft M.
Berge-Seidl V, et al.
Neurosci Lett. 2017 Sep 29;658:48-52. doi: 10.1016/j.neulet.2017.08.040. Epub 2017 Aug 19.
Neurosci Lett. 2017.
PMID: 28830825
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No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease.
Berge-Seidl V, Pihlstrøm L, Wszolek ZK, Ross OA, Toft M.
Berge-Seidl V, et al.
Neurobiol Aging. 2019 Feb;74:236.e1-236.e5. doi: 10.1016/j.neurobiolaging.2018.09.022. Epub 2018 Sep 22.
Neurobiol Aging. 2019.
PMID: 30340792
Free PMC article.
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Integrative analysis identifies bHLH transcription factors as contributors to Parkinson's disease risk mechanisms.
Berge-Seidl V, Pihlstrøm L, Toft M.
Berge-Seidl V, et al.
Sci Rep. 2021 Feb 10;11(1):3502. doi: 10.1038/s41598-021-83087-2.
Sci Rep. 2021.
PMID: 33568722
Free PMC article.
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