Ext HIH

Ext Hertie-Institut für klinische Hirnforschung Also known as:Ext HIH
IDI:(DE-2719)5000057

TÜ DZNE

Recent Publications

All known publications ...
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Polygenic resilience modulates the penetrance of Parkinson's disease genetic risk factors.
Annals of neurology 92(2), 270-278 () [10.1002/ana.26416] OpenAccess  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's disease.
Brain 140(9), 2444-2459 () [10.1093/brain/awx202] BibTeX | EndNote: XML, Text | RIS

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Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients.
Annals of neurology 79(4), 646-658 () [10.1002/ana.24611] BibTeX | EndNote: XML, Text | RIS

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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 () [10.1016/j.neurobiolaging.2015.11.025]  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.
Molecular psychiatry 20(5), 647-656 () [10.1038/mp.2014.107] pmc   Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations.
Journal of neurology 262(8), 1961-1971 () [10.1007/s00415-015-7791-7]  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Subthalamic stimulation modulates cortical motor network activity and synchronization in Parkinson's disease.
Brain 138(3), 679-693 () [10.1093/brain/awu380] pmc  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study.
Parkinsonism & related disorders 21(3), 306-309 () [10.1016/j.parkreldis.2014.12.010] pmc  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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AP5Z1/SPG48 frequency in autosomal recessive and sporadic spastic paraplegia.
Molecular genetics & genomic medicine 2(5), 379-382 () [10.1002/mgg3.87] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.
Neurology 83(21), 1906-1913 () [10.1212/WNL.0000000000001012] pmc   Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

All known publications ...
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 Record created 2020-05-04, last modified 2024-08-16



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