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Ext HIH
Ext Hertie-Institut für klinische Hirnforschung Also known as:Ext HIHID | I:(DE-2719)5000057 |
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Journal Article
Polygenic resilience modulates the penetrance of Parkinson's disease genetic risk factors.
Annals of neurology 92(2), 270-278 (2022) [10.1002/ana.26416]
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Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's disease.
Brain 140(9), 2444-2459 (2017) [10.1093/brain/awx202]
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Journal Article
Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients.
Annals of neurology 79(4), 646-658 (2016) [10.1002/ana.24611]
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Journal Article
Mutation analyses and association studies to assess the role of the presenilin-associated rhomboid-like gene in Parkinson's disease.
Neurobiology of aging 39, 217.e13-217.e15 (2016) [10.1016/j.neurobiolaging.2015.11.025]
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Journal Article (Review Article)
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.
Molecular psychiatry 20(5), 647-656 (2014) [10.1038/mp.2014.107]
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Journal Article
Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations.
Journal of neurology 262(8), 1961-1971 (2015) [10.1007/s00415-015-7791-7]
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Journal Article
Subthalamic stimulation modulates cortical motor network activity and synchronization in Parkinson's disease.
Brain 138(3), 679-693 (2015) [10.1093/brain/awu380]
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Journal Article
TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study.
Parkinsonism & related disorders 21(3), 306-309 (2015) [10.1016/j.parkreldis.2014.12.010]
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Journal Article
AP5Z1/SPG48 frequency in autosomal recessive and sporadic spastic paraplegia.
Molecular genetics & genomic medicine 2(5), 379-382 (2014) [10.1002/mgg3.87]
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Journal Article
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.
Neurology 83(21), 1906-1913 (2014) [10.1212/WNL.0000000000001012]
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All known publications ...
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