Author Tittmann, Lukas
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2017 | Journal Article |
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Schormair, B.; Zhao, C.; Bell, S.; Tilch, E.; Salminen, A. V; Pütz, B. & Dauvilliers, Y. et al. (2017)
The Lancet Neurology, 16(11) pp. 898-907. DOI: https://doi.org/10.1016/S1474-4422(17)30327-7
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2019 | Journal Article |
Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery – a sub-analysis of the RIPHeart-Study
Westphal, S.; Stoppe, C.; Gruenewald, M.; Bein, B.; Renner, J.; Cremer, J. & Coburn, M. et al. (2019)
BMC Cardiovascular Disorders, 19(1) art. 26. DOI: https://doi.org/10.1186/s12872-019-1002-x
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2019 | Journal Article |
No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors
Hopfner, F.; Müller, S. H.; Steppat, D.; Miller, J.; Schmidt, N.; Wandinger, K.-P. & Leypoldt, F. et al. (2019)
Translational Neurodegeneration, 8(1) art. 11. DOI: https://doi.org/10.1186/s40035-019-0153-0
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2020 | Journal Article
Private variants in PRKN are associated with late-onset Parkinson's disease
Hopfner, F.; Mueller, S. H.; Szymczak, S.; Junge, O.; Tittmann, L.; May, S. & Lohmann, K. et al. (2020)
Parkinsonism & Related Disorders, 75 pp. 24-26. DOI: https://doi.org/10.1016/j.parkreldis.2020.05.003
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2020 | Journal Article
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease
Hopfner, F.; Mueller, S. H.; Szymczak, S.; Junge, O.; Tittmann, L.; May, S. & Lohmann, K. et al. (2020)
Movement Disorders, 35(7) pp. 1245-1248. DOI: https://doi.org/10.1002/mds.28037
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