Publications

In press

Hertel, J., Harms, A. C., Heinken, A., Baldini, F., Thinnes, C. C., Glaab, E., Vasco, D., Pietzner, M., Stewart, I. D., Wareham, N. J., Langenberg, C., Trenkwalder, C., Krüger, R., Hankemeier, T., Fleming, R. M. T., Mollenhauer, B., & Thiele, I. (in press). Integrated Analyses of Microbiome and Longitudinal Metabolome Data Reveal Microbial-Host Interactions on Sulfur Metabolism in Parkinson’s Disease. Cell Reports.
Peer reviewed

2019

Grossmann, D., Berenguer, C., Bellet, M. E., Scheibner, D., Bohler, J., Massart, F., Rapaport, D., Skupin, A., Fouquier d'Hérouël, A., Sharma, M., Ghelfi, J., Rakovic, A., Lichtner, P., Antony, P., Glaab, E., May, P., Dimmer, K. S., Fitzgerald, J. C., Grünewald, A., & Krüger, R. (2019, July 15). Mutations in RHOT1 disrupt ER-mitochondria contact sites interfering with calcium homeostasis and mitochondrial dynamics in Parkinson's disease. Antioxidants & redox signaling.
Peer reviewed
Smits, L., Magni, S., Grzyb, K., Antony, P., Krüger, R., Skupin, A., Bolognin, S., & Schwamborn, J. C. (2019). Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids. Eprint/Working paper retrieved from https://www.biorxiv.org/content/10.1101/589598v1.
Schoellmann, A., Scholten, M., Wasserka, B., Govindan, R. B., Krüger, R., Gharabaghi, A., Plewnia, C., & Weiss, D. (2019). Anodal tDCS modulates cortical activity and synchronization in Parkinson's disease depending on motor processing. NeuroImage. Clinical, 22, 101689.
Peer reviewed (verified by ORBilu)

2018

Hipp Epouse D'amico, G., Vaillant, M., Diederich, N. J., Roomp, K., Satagopam, V., Banda, P., Sandt, E., Mommaerts, K., Schmitz, S., Longhino, L., Schweicher, A., Hanff, A.-M., Nicolai, B., Kolber, P. L., Reiter, D., Pavelka, L., Binck, S., Pauly, C., Geffers, L., Betsou, F., Gantenbein, M., Klucken, J., Gasser, T., Hu, M., Balling, R., & Krüger, R. (2018). The Luxembourg Parkinson’s Study: A Comprehensive Approach for Stratification and Early Diagnosis. Frontiers in Aging Neuroscience, 10, 326.
Peer reviewed (verified by ORBilu)
Fitzgerald, J. C., Zimprich, A., Bobbili, D. R., Sharma, M., May, P., & Krüger, R. (2018, January 24). Reply: No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson’s disease. Brain : A Journal of Neurology.
Peer reviewed (verified by ORBilu)
Krüger, R., Larsen, S., & Hanss, Z. (2018, January). The genetic architecture of mitochondrial dysfunction in Parkinson's Disease. Cell and Tissue Research.
Peer reviewed
Hanci, I., Kamm, C., Scholten, M., Roncoroni, L. P., Weber, Y., Krüger, R., Plewnia, C., Gharabaghi, A., & Weiss, D. (2018). Long-Term Effect of GPi-DBS in a Patient With Generalized Dystonia Due to GLUT1 Deficiency Syndrome. Frontiers in neurology, 9, 381.
Peer reviewed (verified by ORBilu)
Harmuth, T., Prell-Schicker, C., Weber, J. J., Gellerich, F., Funke, C., Driessen, S., Magg, J. C. D., Krebiehl, G., Wolburg, H., Hayer, S. N., Hauser, S., Krüger, R., Schols, L., Riess, O., & Hubener-Schmid, J. (2018). Mitochondrial Morphology, Function and Homeostasis Are Impaired by Expression of an N-terminal Calpain Cleavage Fragment of Ataxin-3. Frontiers in molecular neuroscience, 11, 368.
Peer reviewed (verified by ORBilu)
Lhommee, E., Wojtecki, L., Czernecki, V., Witt, K., Maier, F., Tonder, L., Timmermann, L., Halbig, T. D., Pineau, F., Durif, F., Witjas, T., Pinsker, M., Mehdorn, M., Sixel-Doring, F., Kupsch, A., Krüger, R., Elben, S., Chabardes, S., Thobois, S., Brefel-Courbon, C., Ory-Magne, F., Regis, J.-M., Maltete, D., Sauvaget, A., Rau, J., Schnitzler, A., Schupbach, M., Schade-Brittinger, C., Deuschl, G., Houeto, J.-L., & Krack, P. (2018). Behavioural outcomes of subthalamic stimulation and medical therapy versus medical therapy alone for Parkinson's disease with early motor complications (EARLYSTIM trial): secondary analysis of an open-label randomised trial. The Lancet. Neurology, 17(3), 223-231.
Peer reviewed (verified by ORBilu)
Riederer, P., Jellinger, K. A., Kolber, P. L., Hipp, G., Sian-Hulsmann, J., & Krüger, R. (2018). Lateralisation in Parkinson disease. Cell and tissue research, 373(1), 297-312.
Peer reviewed (verified by ORBilu)

2017

Burbulla, L. F., Song, P., Mazzulli, J. R., Zampese, E., Wong, Y. C., Jeon, S., Santos, D. P., Blanz, J., Obermaier, C. D., Strojny, C., Savas, J. N., Kiskinis, E., Zhuang, X., Krüger, R., Surmeier, D. J., & Krainc, D. (2017). Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson's disease. Science (New York, N.Y.), 357(6357), 1255-1261.
Peer reviewed (verified by ORBilu)
Fitzgerald, J. C., Zimprich, A., Carvajal-Berrio, D. A., Schindler, K. M., Maurer, B., Schulte, C., Bus, C., Hauser, A.-K., Kübler, M., Lewin, R., Bobbili, D. R., Schwarz, L. M., Vartholomaiou, E., Brockmann, K., Wüst, R., Madlung, J., Nordheim, A., Riess, O., Martins, L. M., Glaab, E., May, P., Schenke-Layland, K., Picard, D., Sharma, M., Gasser, T., & Krüger, R. (2017). Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's disease. Brain : A Journal of Neurology, 140(9), 2444-2459.
Peer reviewed (verified by ORBilu)
Krüger, R., Lingor, P., Doskas, T., Henselmans, J. M. L., Danielsen, E. H., de Fabregues, O., Stefani, A., Sensken, S.-C., Parra, J. C., Onuk, K., Yegin, A., & Antonini, A. (2017, June 19). An Observational Study of the Effect of Levodopa-Carbidopa Intestinal Gel on Activities of Daily Living and Quality of Life in Advanced Parkinson's Disease Patients. Advances in therapy.
Peer reviewed
Bobbili, D. R., May, P., & Krüger, R. (2017). Rare variant analysis of the PPMI dataset to uncover the complex genetic architecture of Parkinson’s disease. Movement Disorders : Official Journal of the Movement Disorder Society, 322(Supplement S2), 405.
Peer reviewed (verified by ORBilu)
Seidel, K., Bouzrou, M., Heidemann, N., Krüger, R., Schols, L., den Dunnen, W. F. A., Korf, H.-W., & Rub, U. (2017). Involvement of the cerebellum in Parkinson disease and dementia with Lewy bodies. Annals of neurology, 81(6), 898-903.
Peer reviewed (verified by ORBilu)
Blauwendraat, C., Faghri, F., Pihlstrom, L., Geiger, J. T., Elbaz, A., Lesage, S., May, P., Aude, N., Abramzon, Y., Murphy, N. A., Gibbs, J. R., Ryten, M., Ferrari, R., Bras, J., Guerreiro, R., Williams, J., Sims, R., Lubbe, S., Hernandez, D. G., Mok, K. Y., Robak, L., Camphell, R. H., Rogaeva, E., Traynor, B. J., Chia, R., Chung, S. J., International Parkinson’s Disease Genomics Consortium (IPDGC), COURAGE-PD Consortium, Glaab, E., Balling, R., Hardy, J. A., Brice, A., Houlden, H., Shulman, J. M., Morris, H. R., Gasser, T., Heutink, P., Krüger, R., Sharma, M., Simon-Sanchez, J., Nalls, M. A., Singleton, A. B., & Scholz, S. W. (2017, May 17). NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases. Neurobiology of Aging.
Peer reviewed (verified by ORBilu)
Krüger, R., Klucken, J., Weiss, D., Tonges, L., Kolber, P. L., Unterecker, S., Lorrain, M., Baas, H., Muller, T., & Riederer, P. (2017). Classification of advanced stages of Parkinson's disease: translation into stratified treatments. Journal of neural transmission (Vienna, Austria : 1996), 124(124), 1015-1027.
Peer reviewed (verified by ORBilu)
Wang, L., Heckman, M. G., Aasly, J. O., Annesi, G., Bozi, M., Chung, S. J., Clarke, C., Crosiers, D., Eckstein, G., Garraux, G., Hadjigeorgiou, G. M., Hattori, N., Jeon, B., Kim, Y. J., Kubo, M., Lesage, S., Lin, J. J., Lynch, T., Lichtner, P., Mellick, G. D., Mok, V., Morrison, K. E., Quattrone, A., Satake, W., Silburn, P. A., Stefanis, L., Stockton, J. D., Tan, E. K., Toda, T., Brice, A., Van Broeckhoven, C., Uitti, R. J., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., Maraganore, D. M., Gasser, T., Krüger, R., Farrer, M. J., Ross, O. A., & Sharma, M. (2017). Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study. Neurobiology of aging, 49, 217.e1-217.e4.
Peer reviewed (verified by ORBilu)
Scholten, M., Klemt, J., Heilbronn, M., Plewnia, C., Bloem, B. R., Bunjes, F., Krüger, R., Gharabaghi, A., & Weiss, D. (2017). Effects of Subthalamic and Nigral Stimulation on Gait Kinematics in Parkinson's Disease. Frontiers in neurology, 8, 543.
Peer reviewed (verified by ORBilu)
Straniero, L., Rimoldi, V., Samarani, M., Goldwurm, S., Di Fonzo, A., Krüger, R., Deleidi, M., Aureli, M., Solda, G., Duga, S., & Asselta, R. (2017). The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. Scientific reports, 7(1), 12702.
Peer reviewed (verified by ORBilu)

2016

Casadei, N., Sood, P., Ulrich, T., Kieper, N., Helling, S., May, C., Glaab, E., Chen, J., Nuber, S., Marcus, K., Rapaport, D., Ott, T., Riess, O., Krüger, R., & Fitzgerald, J. (2016). Mitochondrial Defects and Neurodegeneration in Mice Overexpressing Wild Type or G399S Mutant HtrA2. Human Molecular Genetics, 25(3), 459-71.
Peer reviewed (verified by ORBilu)
Dams, J., Balzer-Geldsetzer, M., Siebert, U., Deuschl, G., Schuepbach, W. M., Krack, P., Timmermann, L., Schnitzler, A., Reese, J.-P., Dodel, R., Krüger, R., & EARLYSTIM-investigators. (2016). Cost-Effectiveness of Neurostimulation in Parkinson's Disease With Early Motor Complications. Movement Disorders : Official Journal of the Movement Disorder Society, 31(8), 1183-1191.
Peer reviewed (verified by ORBilu)
Heinzel, S., Roeben, B., Ben-Shlomo, Y., Lerche, S., Alves, G., Barone, P., Behnke, S., Berendse, H. W., Bloem, B. R., Burn, D., Dodel, R., Grosset, D. G., Hu, M., Kasten, M., Krüger, R., Moccia, M., Mollenhauer, B., Oertel, W., Suenkel, U., Walter, U., Wirdefeldt, K., Liepelt-Scarfone, I., Maetzler, W., & Berg, D. (2016). Prodromal Markers in Parkinson's Disease: Limitations in Longitudinal Studies and Lessons Learned. Frontiers in aging neuroscience, 8, 147.
Peer reviewed (verified by ORBilu)
Klionsky, D., Krüger, R., & et al. (2016). Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy, 12(1), 1-222.
Peer reviewed (verified by ORBilu)
Krüger, R., Hilker, R., Winkler, C., Lorrain, M., Hahne, M., Redecker, C., Lingor, P., & Jost, W. H. (2016). Advanced stages of PD: interventional therapies and related patient-centered care. Journal of neural transmission (Vienna, Austria : 1996).
Peer reviewed (verified by ORBilu)
Lerche, S., Heinzel, S., Alves, G. W., Barone, P., Behnke, S., Ben-Shlomo, Y., Berendse, H., Bloem, B. R., Burn, D., Dodel, R., Grosset, D. G., Hipp, G., Hu, M. T., Kasten, M., Krüger, R., Liepelt-Scarfone, I., Maetzler, W., Moccia, M., Mollenhauer, B., Oertel, W., Roeben, B., Walter, U., Wirdefeldt, K., & Berg, D. (2016). Aiming for Study Comparability in Parkinson's Disease: Proposal for a Modular Set of Biomarker Assessments to be Used in Longitudinal Studies. Frontiers in aging neuroscience, 8, 121.
Peer reviewed (verified by ORBilu)
Maetzler, W., Krüger, R., Muller, T., Oertel, W., Urban, P., Warnecke, T., & Klucken, J. (2016). Tragbare und aktiv vom Parkinson-Patienten genutzte Technologie im hauslichen Umfeld: Was bringt die Zukunft? Fortschritte der Neurologie-Psychiatrie, 84 Suppl 1, 48-51.
Peer reviewed (verified by ORBilu)
Meiser, J., Delcambre, S., Wegner, A., Jäger, C., Ghelfi, J., Fouquier d'Hérouël, A., Dong, X., Weindl, D., Stautner, C., Nonnenmacher, Y., Michelucci, A., Popp, O., Giesert, F., Schildknecht, S., Kraemer, L., Schneider, J. G., Woitalla, D., Wurst, W., Skupin, A., Vogt Weisenhorn, D. M., Krüger, R., Leist, M., & Hiller, K. (2016). Loss of DJ-1 impairs antioxidant response by altered glutamine and serine metabolism. Neurobiology of disease, 89, 112-125.
Peer reviewed (verified by ORBilu)
Scholten, M., Govindan, R. B., Braun, C., Bloem, B. R., Plewnia, C., Krüger, R., Gharabaghi, A., & Weiss, D. (2016). Cortical correlates of susceptibility to upper limb freezing in Parkinson's disease. Clinical Neurophysiology, 127(6), 2386-93.
Peer reviewed (verified by ORBilu)
Scholten, M., Klotz, R., Plewnia, C., Wachter, T., Mielke, C., Bloem, B. R., Braun, C., Ziemann, U., Govindan, R. B., Gharabaghi, A., Krüger, R., & Weiss, D. (2016). Neuromuscular correlates of subthalamic stimulation and upper limb freezing in Parkinson's disease. Clinical Neurophysiology.
Peer reviewed (verified by ORBilu)
Weiss, D., Herrmann, S., Wang, L., Schulte, C., Brockmann, K., Plewnia, C., Gasser, T., Sharma, M., Gharabaghi, A., & Krüger, R. (2016). Alpha-synuclein gene variants may predict neurostimulation outcome. Movement disorders : official journal of the Movement Disorder Society.
Peer reviewed (verified by ORBilu)
Wüst, R., Maurer, B., Hauser, K., Woitalla, D., Sharma, M., & Krüger, R. (2016). 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.
Peer reviewed (verified by ORBilu)

2015

Bruggemann, N., Kuhn, A., Schneider, S. A., Kamm, C., Wolters, A., Krause, P., Moro, E., Steigerwald, F., Wittstock, M., Tronnier, V., Lozano, A. M., Hamani, C., Poon, Y. Y., Zittel, S., Wachter, T., Deuschl, G., Krüger, R., Kupsch, A., Munchau, A., Lohmann, K., Volkmann, J., & Klein, C. (2015). Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia. Neurology, 84(9), 895-903.
Peer reviewed (verified by ORBilu)
Chen, J., Shinde, S., Koch, M.-H., Eisenacher, M., Galozzi, S., Lerari, T., Barkovits, K., Subedi, P., Krüger, R., Kuhlmann, K., Sellergren, B., Helling, S., & Marcus, K. (2015). Low-bias phosphopeptide enrichment from scarce samples using plastic antibodies. Scientific reports, 5, 11438.
Peer reviewed (verified by ORBilu)
Lerche, S., Liepelt-Scarfone, I., Alves, G., Barone, P., Behnke, S., Ben-Shlomo, Y., Berendse, H., Burn, D., Dodel, R., Grosset, D., Heinzel, S., Hu, M., Kasten, M., Krüger, R., Maetzler, W., Moccia, M., Mollenhauer, B., Oertel, W., Roeben, B., Sunkel, U., Walter, U., Wirdefeldt, K., & Berg, D. (2015). Methods in Neuroepidemiology Characterization of European Longitudinal Cohort Studies in Parkinson's Disease - Report of the JPND Working Group BioLoC-PD. Neuroepidemiology, 45(4), 282-297.
Peer reviewed (verified by ORBilu)
Lew, M. F., Slevin, J. T., Krüger, R., Martinez, C., Chatamra, K., Dubow, J. S., Robieson, W. Z., Benesh, J. A., & Fung, V. S. (2015). Initiation and dose optimization for levodopa-carbidopa intestinal gel: Insights from phase 3 clinical trials. Parkinsonism & related disorders, 21(7), 742-748.
Peer reviewed (verified by ORBilu)
Maus, F., Sakry, D., Biname, F., Karram, K., Rajalingam, K., Watts, C., Heywood, R., Krüger, R., Stegmuller, J., Werner, H. B., Nave, K. A., Kramer-Albers, E. M., & Trotter, J. (2015). The NG2 Proteoglycan Protects Oligodendrocyte Precursor Cells against Oxidative Stress via Interaction with OMI/HtrA2. PLoS ONE, 10(9), 0137311.
Peer reviewed (verified by ORBilu)
Nieratschker, V., Kiefer, C., Giel, K., Krüger, R., & Plewnia, C. (2015). The COMT Val/Met polymorphism modulates effects of tDCS on response inhibition. Brain stimulation, 8(2), 283-288.
Peer reviewed
Odin, P., Chaudhuri, K. R., Slevin, J. T., Volkmann, J., Dietrichs, E., Martinez-Martin, P., Krauss, J. K., Henriksen, T., Katzenschlager, R., Antonini, A., Rascol, O., Poewe, W., Krüger, R., & National Steering Committees. (2015). Collective physician perspectives on non-oral medication approaches for the management of clinically relevant unresolved issues in Parkinson's disease: Consensus from an international survey and discussion program. Parkinsonism & Related Disorders.
Peer reviewed (verified by ORBilu)
Ortega-Cubero, S., Lorenzo-Betancor, O., Lorenzo, E., Agundez, J. A., Jimenez-Jimenez, F. J., Ross, O. A., Wurster, I., Mielke, C., Lin, J. J., Coria, F., Clarimon, J., Ezquerra, M., Brighina, L., Annesi, G., Alonso-Navarro, H., Garcia-Martin, E., Gironell, A., Marti, M. J., Yueh, K. C., Wszolek, Z. K., Sharma, M., Berg, D., Krüger, R., Pastor, M. A., & Pastor, P. (2015). TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study. Parkinsonism & related disorders, 21(3), 306-309.
Peer reviewed (verified by ORBilu)
Puschmann, A., Brighina, L., Markopoulou, K., Aasly, J., Chung, S. J., Frigerio, R., Hadjigeorgiou, G., Koks, S., Krüger, R., Siuda, J., Wider, C., Zesiewicz, T. A., & Maraganore, D. M. (2015). Clinically meaningful parameters of progression and long-term outcome of Parkinson disease: An international consensus statement. Parkinsonism & related disorders, 21(7), 675-682.
Peer reviewed (verified by ORBilu)
Wang, L., Aasly, J. O., Annesi, G., Bardien, S., Bozi, M., Brice, A., Carr, J., Chung, S. J., Clarke, C., Crosiers, D., Deutschlander, A., Eckstein, G., Farrer, M. J., Goldwurm, S., Garraux, G., Hadjigeorgiou, G. M., Hicks, A. A., Hattori, N., Klein, C., Jeon, B., Kim, Y. J., Lesage, S., Lin, J. J., Lynch, T., Lichtner, P., Lang, A. E., Mok, V., Jasinska-Myga, B., Mellick, G. D., Morrison, K. E., Opala, G., Pihlstrom, L., Pramstaller, P. P., Park, S. S., Quattrone, A., Rogaeva, E., Ross, O. A., Stefanis, L., Stockton, J. D., Silburn, P. A., Theuns, J., Tan, E. K., Tomiyama, H., Toft, M., Van Broeckhoven, C., Uitti, R. J., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., Yueh, K. C., Zhao, Y., Gasser, T., Maraganore, D. M., Krüger, R., & Sharma, M. (2015). Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. Neurology, 85(15), 1283-92.
Peer reviewed (verified by ORBilu)
Weiss, D., Klotz, R., Govindan, R. B., Scholten, M., Naros, G., Ramos-Murguialday, A., Bunjes, F., Meisner, C., Plewnia, C., Krüger, R., & Gharabaghi, A. (2015). Subthalamic stimulation modulates cortical motor network activity and synchronization in Parkinson's disease. Brain : a journal of neurology, 138(Pt 3), 679-93.
Peer reviewed (verified by ORBilu)
Weiss, D., Mielke, C., Wachter, T., Bender, B., Liscic, R. M., Scholten, M., Naros, G., Plewnia, C., Gharabaghi, A., & Krüger, R. (2015). Long-term outcome of deep brain stimulation in fragile X-associated tremor/ataxia syndrome. Parkinsonism & related disorders, 21(3), 310-313.
Peer reviewed (verified by ORBilu)

2014

Jonmohamadi, Y., Poudel, Innes, C., Weiss, D., Krüger, R., & Jones, R. (2014). Comparison of beamformers for EEG source signal reconstruction. Biomedical Signal Processing and Control, 14, 175-188.
Peer reviewed (verified by ORBilu)
Burbulla, L. F., Fitzgerald, J. C., Stegen, K., Westermeier, J., Thost, A.-K., Kato, H., Mokranjac, D., Sauerwald, J., Martins, L., Woitalla, D., Rapaport, D., Riess, O., Proikas-Cezanne, T., Rasse, T. M., & Krüger, R. (2014). Mitochondrial proteolytic stress induced by loss of mortalin function is rescued by Parkin and PINK1. Cell death & disease, 5, 1180.
Peer reviewed (verified by ORBilu)
Casadei, N., Pohler, A.-M., Tomas-Zapico, C., Torres-Peraza, J., Schwedhelm, I., Witz, A., Zamolo, I., De Heer, R., Spruijt, B., Noldus, L. P. J. J., Klucken, J., Lucas, J. J., Kahle, P. J., Krüger, R., Riess, O., & Nuber, S. (2014). Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice. Human molecular genetics, 23(3), 767-81.
Peer reviewed (verified by ORBilu)
Chung, S. J., Biernacka, J. M., Armasu, S. M., Anderson, K., Frigerio, R., Aasly, J. O., Annesi, G., Bentivoglio, A. R., Brighina, L., Chartier-Harlin, M.-C., Goldwurm, S., Hadjigeorgiou, G., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Krüger, R., Lesage, S., Markopoulou, K., Mellick, G., Morrison, K. E., Puschmann, A., Tan, E.-K., Crosiers, D., Theuns, J., Van Broeckhoven, C., Wirdefeldt, K., Wszolek, Z. K., Elbaz, A., & Maraganore, D. M. (2014). Alpha-synuclein repeat variants and survival in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society.
Peer reviewed (verified by ORBilu)
Heckman, M. G., Elbaz, A., Soto-Ortolaza, A. I., Serie, D. J., Aasly, J. O., Annesi, G., Auburger, G., Bacon, J. A., Boczarska-Jedynak, M., Bozi, M., Brighina, L., Chartier-Harlin, M.-C., Dardiotis, E., Destee, A., Ferrarese, C., Ferraris, A., Fiske, B., Gispert, S., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P. A., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Krüger, R., Kyratzi, E., Lin, C.-H., Lohmann, K., Loriot, M.-A., Lynch, T., Mellick, G. D., Mutez, E., Opala, G., Park, S. S., Petrucci, S., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Tomiyama, H., Uitti, R. J., Valente, E. M., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R.-M., Xiromerisiou, G., Maraganore, D. M., Farrer, M. J., & Ross, O. A. (2014). Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants. Neurobiology of aging, 35(1), 266.e5-14.
Peer reviewed (verified by ORBilu)
Huttenlocher, J., Krüger, R., Capetian, P., Lohmann, K., Brockmann, K., Csoti, I., Klein, C., Berg, D., Gasser, T., Bonin, M., Riess, O., & Bauer, P. (2014). EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts. Journal of medical genetics, 0, 1-5.
Peer reviewed (verified by ORBilu)
Sharma, M., Krüger, R., & Gasser, T. (2014). From genome-wide association studies to next-generation sequencing: lessons from the past and planning for the future. JAMA neurology, 71(1), 5-6.
Peer reviewed (verified by ORBilu)
Sharma, M., Wenning, G., & Krüger, R. (2014). Mutant COQ2 in multiple-system atrophy. The New England journal of medicine, 371(1), 80-1.
Peer reviewed (verified by ORBilu)
Theuns, J., Verstraeten, A., Sleegers, K., Wauters, E., Gijselinck, I., Smolders, S., Crosiers, D., Corsmit, E., Elinck, E., Sharma, M., Krüger, R., Lesage, S., Brice, A., Chung, S. J., Kim, M.-J., Kim, Y. J., Ross, O. A., Wszolek, Z. K., Rogaeva, E., Xi, Z., Lang, A. E., Klein, C., Weissbach, A., Mellick, G. D., Silburn, P. A., Hadjigeorgiou, G. M., Dardiotis, E., Hattori, N., Ogaki, K., Tan, E.-K., Zhao, Y., Aasly, J., Valente, E. M., Petrucci, S., Annesi, G., Quattrone, A., Ferrarese, C., Brighina, L., Deutschlander, A., Puschmann, A., Nilsson, C., Garraux, G., LeDoux, M. S., Pfeiffer, R. F., Boczarska-Jedynak, M., Opala, G., Maraganore, D. M., Engelborghs, S., De Deyn, P. P., Cras, P., Cruts, M., & Van Broeckhoven, C. (2014). Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease. Neurology.
Peer reviewed (verified by ORBilu)
Weiss, D., Lam, J. M., Breit, S., Gharabaghi, A., Krüger, R., Luft, A. R., & Wachter, T. (2014). The subthalamic nucleus modulates the early phase of probabilistic classification learning. Experimental brain research, 232(7), 2255-62.
Peer reviewed (verified by ORBilu)

2013

Antony, P., Diederich, N., Krüger, R., & Balling, R. (2013, May 09). The hallmarks of Parkinson's disease. FEBS Journal, 13.
Peer reviewed
Grau, T., Burbulla, L. F., Engl, G., Delettre, C., Delprat, B., Oexle, K., Leo-Kottler, B., Roscioli, T., Krüger, R., Rapaport, D., Wissinger, B., & Schimpf-Linzenbold, S. (2013). A novel heterozygous OPA3 mutation located in the mitochondrial target sequence results in altered steady-state levels and fragmented mitochondrial network. Journal of medical genetics, 50(12), 848-58.
Peer reviewed (verified by ORBilu)
Heckman, M. G., Soto-Ortolaza, A. I., Aasly, J. O., Abahuni, N., Annesi, G., Bacon, J. A., Bardien, S., Bozi, M., Brice, A., Brighina, L., Carr, J., Chartier-Harlin, M.-C., Dardiotis, E., Dickson, D. W., Diehl, N. N., Elbaz, A., Ferrarese, C., Fiske, B., Gibson, J. M., Gibson, R., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P. A., Boczarska-Jedynak, M., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Krüger, R., Kyratzi, E., Lesage, S., Lin, C.-H., Lynch, T., Maraganore, D. M., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Park, S. S., Petrucci, S., Puschmann, A., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Theuns, J., Tomiyama, H., Uitti, R. J., Valente, E. M., Van Broeckhoven, C., van de Loo, S., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R.-M., Hentati, F., Farrer, M. J., & Ross, O. A. (2013). Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium. Movement disorders : official journal of the Movement Disorder Society, 28(12), 1740-4.
Peer reviewed (verified by ORBilu)
Karle, K. N., Biskup, S., Schule, R., Schweitzer, K. J., Krüger, R., Bauer, P., Bender, B., Nagele, T., & Schols, L. (2013). De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS). Neurology, 81(23), 2039-44.
Peer reviewed (verified by ORBilu)
Plewnia, C., Zwissler, B., Langst, I., Maurer, B., Giel, K., & Krüger, R. (2013). Effects of transcranial direct current stimulation (tDCS) on executive functions: influence of COMT Val/Met polymorphism. Cortex : A Journal Devoted to the Study of the Nervous System & Behavior, 49(7), 1801-7.
Peer reviewed (verified by ORBilu)
Reinhardt, P., Schmid, B., Burbulla, L. F., Schondorf, D. C., Wagner, L., Glatza, M., Hoing, S., Hargus, G., Heck, S. A., Dhingra, A., Wu, G., Muller, S., Brockmann, K., Kluba, T., Maisel, M., Krüger, R., Berg, D., Tsytsyura, Y., Thiel, C. S., Psathaki, O.-E., Klingauf, J., Kuhlmann, T., Klewin, M., Muller, H., Gasser, T., Scholer, H. R., & Sterneckert, J. (2013). Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expression. Cell Stem Cell, 12(3), 354-67.
Peer reviewed (verified by ORBilu)
Riess, A., Rossier, E., Krüger, R., Dufke, A., Beck-Woedl, S., Horber, V., Alber, M., Glaser, D., Riess, O., & Tzschach, A. (2013). Novel SLC9A6 mutations in two families with Christianson syndrome. Clinical genetics, 83(6), 596-7.
Peer reviewed (verified by ORBilu)
Schuepbach, W. M. M., Rau, J., Knudsen, K., Volkmann, J., Krack, P., Timmermann, L., Halbig, T. D., Hesekamp, H., Navarro, S. M., Meier, N., Falk, D., Mehdorn, M., Paschen, S., Maarouf, M., Barbe, M. T., Fink, G. R., Kupsch, A., Gruber, D., Schneider, G.-H., Seigneuret, E., Kistner, A., Chaynes, P., Ory-Magne, F., Brefel Courbon, C., Vesper, J., Schnitzler, A., Wojtecki, L., Houeto, J.-L., Bataille, B., Maltete, D., Damier, P., Raoul, S., Sixel-Doering, F., Hellwig, D., Gharabaghi, A., Krüger, R., Pinsker, M. O., Amtage, F., Regis, J.-M., Witjas, T., Thobois, S., Mertens, P., Kloss, M., Hartmann, A., Oertel, W. H., Post, B., Speelman, H., Agid, Y., Schade-Brittinger, C., & Deuschl, G. (2013). Neurostimulation for Parkinson's disease with early motor complications. The New England journal of medicine, 368(7), 610-22.
Peer reviewed (verified by ORBilu)
Weiss, D., Walach, M., Meisner, C., Fritz, M., Scholten, M., Breit, S., Plewnia, C., Bender, B., Gharabaghi, A., Wachter, T., & Krüger, R. (2013). Nigral stimulation for resistant axial motor impairment in Parkinson's disease? A randomized controlled trial. Brain : a journal of neurology, 136(Pt 7), 2098-108.
Peer reviewed (verified by ORBilu)
Zhu, J.-Y., Vereshchagina, N., Sreekumar, V., Burbulla, L. F., Costa, A. C., Daub, K. J., Woitalla, D., Martins, L., Krüger, R., & Rasse, T. M. (2013). Knockdown of Hsc70-5/mortalin induces loss of synaptic mitochondria in a Drosophila Parkinson's disease model. PloS one, 8(12), 83714.
Peer reviewed (verified by ORBilu)

2012

Klionsky, D. J., Abdalla, F. C., Abeliovich, H., Abraham, R. T., Acevedo-Arozena, A., Adeli, K., Agholme, L., Agnello, M., Agostinis, P., Aguirre-Ghiso, J. A., Ahn, H. J., Ait-Mohamed, O., Ait-Si-Ali, S., Akematsu, T., Akira, S., Al-Younes, H. M., Al-Zeer, M. A., Albert, M. L., Albin, R. L., Alegre-Abarrategui, J., Aleo, M. F., Alirezaei, M., Almasan, A., Almonte-Becerril, M., Amano, A., Amaravadi, R., Amarnath, S., Amer, A. O., Andrieu-Abadie, N., Anantharam, V., Ann, D. K., Anoopkumar-Dukie, S., Aoki, H., Apostolova, N., Arancia, G., Aris, J. P., Asanuma, K., Asare, N. Y. O., Ashida, H., Askanas, V., Askew, D. S., Auberger, P., Baba, M., Backues, S. K., Baehrecke, E. H., Bahr, B. A., Bai, X.-Y., Bailly, Y., Baiocchi, R., Baldini, G., Balduini, W., Ballabio, A., Bamber, B. A., Bampton, E. T. W., Banhegyi, G., Bartholomew, C. R., Bassham, D. C., Bast, R. C. J., Batoko, H., Bay, B.-H., Beau, I., Bechet, D. M., Begley, T. J., Behl, C., Behrends, C., Bekri, S., Bellaire, B., Bendall, L. J., Benetti, L., Berliocchi, L., Bernardi, H., Bernassola, F., Besteiro, S., Bhatia-Kissova, I., Bi, X., Biard-Piechaczyk, M., Blum, J. S., Boise, L. H., Bonaldo, P., Boone, D. L., Bornhauser, B. C., Bortoluci, K. R., Bossis, I., Bost, F., Bourquin, J.-P., Boya, P., Boyer-Guittaut, M., Bozhkov, P. V., Brady, N. R., Brancolini, C., Brech, A., Brenman, J. E., Brennand, A., Bresnick, E. H., Brest, P., Bridges, D., Bristol, M. L., Brookes, P. S., Brown, E. J., Brumell, J. H., Brunetti-Pierri, N., Brunk, U. T., Bulman, D. E., Bultman, S. J., Bultynck, G., Burbulla, L. F., Bursch, W., Butchar, J. P., Buzgariu, W., Bydlowski, S. P., Cadwell, K., Cahova, M., Cai, D., Cai, J., Cai, Q., Calabretta, B., Calvo-Garrido, J., Camougrand, N., Campanella, M., Campos-Salinas, J., Candi, E., Cao, L., Caplan, A. B., Carding, S. R., Cardoso, S. M., Carew, J. S., Carlin, C. R., Carmignac, V., Carneiro, L. A. M., Carra, S., Caruso, R. A., Casari, G., Casas, C., Castino, R., Cebollero, E., Cecconi, F., Celli, J., Chaachouay, H., Chae, H.-J., Chai, C.-Y., Chan, D. C., Chan, E. Y., Chang, R. C.-C., Che, C.-M., Chen, C.-C., Chen, G.-C., Chen, G.-Q., Chen, M., Chen, Q., Chen, S. S.-L., Chen, W., Chen, X., Chen, X., Chen, X., Chen, Y.-G., Chen, Y., Chen, Y., Chen, Y.-J., Chen, Z., Cheng, A., Cheng, C. H. K., Cheng, Y., Cheong, H., Cheong, J.-H., Cherry, S., Chess-Williams, R., Cheung, Z. H., Chevet, E., Chiang, H.-L., Chiarelli, R., Chiba, T., Chin, L.-S., Chiou, S.-H., Chisari, F. V., Cho, C. H., Cho, D.-H., Choi, A. M. K., Choi, D., Choi, K. S., Choi, M. E., Chouaib, S., Choubey, D., Choubey, V., Chu, C. T., Chuang, T.-H., Chueh, S.-H., Chun, T., Chwae, Y.-J., Chye, M.-L., Ciarcia, R., Ciriolo, M. R., Clague, M. J., Clark, R. S. B., Clarke, P. G. H., Clarke, R., Codogno, P., Coller, H. A., Colombo, M. I., Comincini, S., Condello, M., Condorelli, F., Cookson, M. R., Coombs, G. H., Coppens, I., Corbalan, R., Cossart, P., Costelli, P., Costes, S., Coto-Montes, A., Couve, E., Coxon, F. P., Cregg, J. M., Crespo, J. L., Cronje, M. J., Cuervo, A. M., Cullen, J. J., Czaja, M. J., D'Amelio, M., Darfeuille-Michaud, A., Davids, L. M., Davies, F. E., De Felici, M., de Groot, J. F., de Haan, C. A. M., De Martino, L., De Milito, A., De Tata, V., Debnath, J., Degterev, A., Dehay, B., Delbridge, L. M. D., Demarchi, F., Deng, Y. Z., Dengjel, J., Dent, P., Denton, D., Deretic, V., Desai, S. D., Devenish, R. J., Di Gioacchino, M., Di Paolo, G., Di Pietro, C., Diaz-Araya, G., Diaz-Laviada, I., Diaz-Meco, M. T., Diaz-Nido, J., Dikic, I., Dinesh-Kumar, S. P., Ding, W.-X., Distelhorst, C. W., Diwan, A., Djavaheri-Mergny, M., Dokudovskaya, S., Dong, Z., Dorsey, F. C., Dosenko, V., Dowling, J. J., Doxsey, S., Dreux, M., Drew, M. E., Duan, Q., Duchosal, M. A., Duff, K., Dugail, I., Durbeej, M., Duszenko, M., Edelstein, C. L., Edinger, A. L., Egea, G., Eichinger, L., Eissa, N. T., Ekmekcioglu, S., El-Deiry, W. S., Elazar, Z., Elgendy, M., Ellerby, L. M., Eng, K. E., Engelbrecht, A.-M., Engelender, S., Erenpreisa, J., Escalante, R., Esclatine, A., Eskelinen, E.-L., Espert, L., Espina, V., Fan, H., Fan, J., Fan, Q.-W., Fan, Z., Fang, S., Fang, Y., Fanto, M., Fanzani, A., Farkas, T., Farre, J.-C., Faure, M., Fechheimer, M., Feng, C. G., Feng, J., Feng, Q., Feng, Y., Fesus, L., Feuer, R., Figueiredo-Pereira, M. E., Fimia, G. M., Fingar, D. C., Finkbeiner, S., Finkel, T., Finley, K. D., Fiorito, F., Fisher, E. A., Fisher, P. B., Flajolet, M., Florez-McClure, M. L., Florio, S., Fon, E. A., Fornai, F., Fortunato, F., Fotedar, R., Fowler, D. H., Fox, H. S., Franco, R., Frankel, L. B., Fransen, M., Fuentes, J. M., Fueyo, J., Fujii, J., Fujisaki, K., Fujita, E., Fukuda, M., Furukawa, R. H., Gaestel, M., Gailly, P., Gajewska, M., Galliot, B., Galy, V., Ganesh, S., Ganetzky, B., Ganley, I. G., Gao, F.-B., Gao, G. F., Gao, J., Garcia, L., Garcia-Manero, G., Garcia-Marcos, M., Garmyn, M., Gartel, A. L., Gatti, E., Gautel, M., Gawriluk, T. R., Gegg, M. E., Geng, J., Germain, M., Gestwicki, J. E., Gewirtz, D. A., Ghavami, S., Ghosh, P., Giammarioli, A. M., Giatromanolaki, A. N., Gibson, S. B., Gilkerson, R. W., Ginger, M. L., Ginsberg, H. N., Golab, J., Goligorsky, M. S., Golstein, P., Gomez-Manzano, C., Goncu, E., Gongora, C., Gonzalez, C. D., Gonzalez, R., Gonzalez-Estevez, C., Gonzalez-Polo, R. A., Gonzalez-Rey, E., Gorbunov, N. V., Gorski, S., Goruppi, S., Gottlieb, R. A., Gozuacik, D., Granato, G. E., Grant, G. D., Green, K. N., Gregorc, A., Gros, F., Grose, C., Grunt, T. W., Gual, P., Guan, J.-L., Guan, K.-L., Guichard, S. M., Gukovskaya, A. S., Gukovsky, I., Gunst, J., Gustafsson, A. B., Halayko, A. J., Hale, A. N., Halonen, S. K., Hamasaki, M., Han, F., Han, T., Hancock, M. K., Hansen, M., Harada, H., Harada, M., Hardt, S. E., Harper, J. W., Harris, A. L., Harris, J., Harris, S. D., Hashimoto, M., Haspel, J. A., Hayashi, S.-I., Hazelhurst, L. A., He, C., He, Y.-W., Hebert, M.-J., Heidenreich, K. A., Helfrich, M. H., Helgason, G. V., Henske, E. P., Herman, B., Herman, P. K., Hetz, C., Hilfiker, S., Hill, J. A., Hocking, L. J., Hofman, P., Hofmann, T. G., Hohfeld, J., Holyoake, T. L., Hong, M.-H., Hood, D. A., Hotamisligil, G. S., Houwerzijl, E. J., Hoyer-Hansen, M., Hu, B., Hu, C.-A. A., Hu, H.-M., Hua, Y., Huang, C., Huang, J., Huang, S., Huang, W.-P., Huber, T. B., Huh, W.-K., Hung, T.-H., Hupp, T. R., Hur, G. M., Hurley, J. B., Hussain, S. N. A., Hussey, P. J., Hwang, J. J., Hwang, S., Ichihara, A., Ilkhanizadeh, S., Inoki, K., Into, T., Iovane, V., Iovanna, J. L., Ip, N. Y., Isaka, Y., Ishida, H., Isidoro, C., Isobe, K.-I., Iwasaki, A., Izquierdo, M., Izumi, Y., Jaakkola, P. M., Jaattela, M., Jackson, G. R., Jackson, W. T., Janji, B., Jendrach, M., Jeon, J.-H., Jeung, E.-B., Jiang, H., Jiang, H., Jiang, J. X., Jiang, M., Jiang, Q., Jiang, X., Jiang, X., Jimenez, A., Jin, M., Jin, S., Joe, C. O., Johansen, T., Johnson, D. E., Johnson, G. V. W., Jones, N. L., Joseph, B., Joseph, S. K., Joubert, A. M., Juhasz, G., Juillerat-Jeanneret, L., Jung, C. H., Jung, Y.-K., Kaarniranta, K., Kaasik, A., Kabuta, T., Kadowaki, M., Kagedal, K., Kamada, Y., Kaminskyy, V. O., Kampinga, H. H., Kanamori, H., Kang, C., Kang, K. B., Kang, K. I., Kang, R., Kang, Y.-A., Kanki, T., Kanneganti, T.-D., Kanno, H., Kanthasamy, A. G., Kanthasamy, A., Karantza, V., Kaushal, G. P., Kaushik, S., Kawazoe, Y., Ke, P.-Y., Kehrl, J. H., Kelekar, A., Kerkhoff, C., Kessel, D. H., Khalil, H., Kiel, J. A. K. W., Kiger, A. A., Kihara, A., Kim, D. R., Kim, D.-H., Kim, D.-H., Kim, E.-K., Kim, H.-R., Kim, J.-S., Kim, J. H., Kim, J. C., Kim, J. K., Kim, P. K., Kim, S. W., Kim, Y.-S., Kim, Y., Kimchi, A., Kimmelman, A. C., King, J. S., Kinsella, T. J., Kirkin, V., Kirshenbaum, L. A., Kitamoto, K., Kitazato, K., Klein, L., Klimecki, W. T., Klucken, J., Knecht, E., Ko, B. C. B., Koch, J. C., Koga, H., Koh, J.-Y., Koh, Y. H., Koike, M., Komatsu, M., Kominami, E., Kong, H. J., Kong, W.-J., Korolchuk, V. I., Kotake, Y., Koukourakis, M. I., Kouri Flores, J. B., Kovacs, A. L., Kraft, C., Krainc, D., Kramer, H., Kretz-Remy, C., Krichevsky, A. M., Kroemer, G., Krüger, R., Krut, O., Ktistakis, N. T., Kuan, C.-Y., Kucharczyk, R., Kumar, A., Kumar, R., Kumar, S., Kundu, M., Kung, H.-J., Kurz, T., Kwon, H. J., La Spada, A. R., Lafont, F., Lamark, T., Landry, J., Lane, J. D., Lapaquette, P., Laporte, J. F., Laszlo, L., Lavandero, S., Lavoie, J. N., Layfield, R., Lazo, P. A., Le, W., Le Cam, L., Ledbetter, D. J., Lee, A. J. X., Lee, B.-W., Lee, G. M., Lee, J., Lee, J.-H., Lee, M., Lee, M.-S., Lee, S. H., Leeuwenburgh, C., Legembre, P., Legouis, R., Lehmann, M., Lei, H.-Y., Lei, Q.-Y., Leib, D. A., Leiro, J., Lemasters, J. J., Lemoine, A., Lesniak, M. S., Lev, D., Levenson, V. V., Levine, B., Levy, E., Li, F., Li, J.-L., Li, L., Li, S., Li, W., Li, X.-J., Li, Y.-B., Li, Y.-P., Liang, C., Liang, Q., Liao, Y.-F., Liberski, P. P., Lieberman, A., Lim, H. J., Lim, K.-L., Lim, K., Lin, C.-F., Lin, F.-C., Lin, J., Lin, J. D., Lin, K., Lin, W.-W., Lin, W.-C., Lin, Y.-L., Linden, R., Lingor, P., Lippincott-Schwartz, J., Lisanti, M. P., Liton, P. B., Liu, B., Liu, C.-F., Liu, K., Liu, L., Liu, Q. A., Liu, W., Liu, Y.-C., Liu, Y., Lockshin, R. A., Lok, C.-N., Lonial, S., Loos, B., Lopez-Berestein, G., Lopez-Otin, C., Lossi, L., Lotze, M. T., Low, P., Lu, B., Lu, B., Lu, B., Lu, Z., Luciano, F., Lukacs, N. W., Lund, A. H., Lynch-Day, M. A., Ma, Y., Macian, F., MacKeigan, J. P., Macleod, K. F., Madeo, F., Maiuri, L., Maiuri, M. C., Malagoli, D., Malicdan, M. C. V., Malorni, W., Man, N., Mandelkow, E.-M., Manon, S., Manov, I., Mao, K., Mao, X., Mao, Z., Marambaud, P., Marazziti, D., Marcel, Y. L., Marchbank, K., Marchetti, P., Marciniak, S. J., Marcondes, M., Mardi, M., Marfe, G., Marino, G., Markaki, M., Marten, M. R., Martin, S. J., Martinand-Mari, C., Martinet, W., Martinez-Vicente, M., Masini, M., Matarrese, P., Matsuo, S., Matteoni, R., Mayer, A., Mazure, N. M., McConkey, D. J., McConnell, M. J., McDermott, C., McDonald, C., McInerney, G. M., McKenna, S. L., McLaughlin, B., McLean, P. J., McMaster, C. R., McQuibban, G. A., Meijer, A. J., Meisler, M. H., Melendez, A., Melia, T. J., Melino, G., Mena, M. A., Menendez, J. A., Menna-Barreto, R. F. S., Menon, M. B., Menzies, F. M., Mercer, C. A., Merighi, A., Merry, D. E., Meschini, S., Meyer, C. G., Meyer, T. F., Miao, C.-Y., Miao, J.-Y., Michels, P. A. M., Michiels, C., Mijaljica, D., Milojkovic, A., Minucci, S., Miracco, C., Miranti, C. K., Mitroulis, I., Miyazawa, K., Mizushima, N., Mograbi, B., Mohseni, S., Molero, X., Mollereau, B., Mollinedo, F., Momoi, T., Monastyrska, I., Monick, M. M., Monteiro, M. J., Moore, M. N., Mora, R., Moreau, K., Moreira, P. I., Moriyasu, Y., Moscat, J., Mostowy, S., Mottram, J. C., Motyl, T., Moussa, C. E.-H., Muller, S., Muller, S., Munger, K., Munz, C., Murphy, L. O., Murphy, M. E., Musaro, A., Mysorekar, I., Nagata, E., Nagata, K., Nahimana, A., Nair, U., Nakagawa, T., Nakahira, K., Nakano, H., Nakatogawa, H., Nanjundan, M., Naqvi, N. I., Narendra, D. P., Narita, M., Navarro, M., Nawrocki, S. T., Nazarko, T. Y., Nemchenko, A., Netea, M. G., Neufeld, T. P., Ney, P. A., Nezis, I. P., Nguyen, H. P., Nie, D., Nishino, I., Nislow, C., Nixon, R. A., Noda, T., Noegel, A. A., Nogalska, A., Noguchi, S., Notterpek, L., Novak, I., Nozaki, T., Nukina, N., Nurnberger, T., Nyfeler, B., Obara, K., Oberley, T. D., Oddo, S., Ogawa, M., Ohashi, T., Okamoto, K., Oleinick, N. L., Oliver, F. J., Olsen, L. J., Olsson, S., Opota, O., Osborne, T. F., Ostrander, G. K., Otsu, K., Ou, J.-H. J., Ouimet, M., Overholtzer, M., Ozpolat, B., Paganetti, P., Pagnini, U., Pallet, N., Palmer, G. E., Palumbo, C., Pan, T., Panaretakis, T., Pandey, U. B., Papackova, Z., Papassideri, I., Paris, I., Park, J., Park, O. K., Parys, J. B., Parzych, K. R., Patschan, S., Patterson, C., Pattingre, S., Pawelek, J. M., Peng, J., Perlmutter, D. H., Perrotta, I., Perry, G., Pervaiz, S., Peter, M., Peters, G. J., Petersen, M., Petrovski, G., Phang, J. M., Piacentini, M., Pierre, P., Pierrefite-Carle, V., Pierron, G., Pinkas-Kramarski, R., Piras, A., Piri, N., Platanias, L. C., Poggeler, S., Poirot, M., Poletti, A., Pous, C., Pozuelo-Rubio, M., Praetorius-Ibba, M., Prasad, A., Prescott, M., Priault, M., Produit-Zengaffinen, N., Progulske-Fox, A., Proikas-Cezanne, T., Przedborski, S., Przyklenk, K., Puertollano, R., Puyal, J., Qian, S.-B., Qin, L., Qin, Z.-H., Quaggin, S. E., Raben, N., Rabinowich, H., Rabkin, S. W., Rahman, I., Rami, A., Ramm, G., Randall, G., Randow, F., Rao, V. A., Rathmell, J. C., Ravikumar, B., Ray, S. K., Reed, B. H., Reed, J. C., Reggiori, F., Regnier-Vigouroux, A., Reichert, A. S., Reiners, J. J. J., Reiter, R. J., Ren, J., Revuelta, J. L., Rhodes, C. J., Ritis, K., Rizzo, E., Robbins, J., Roberge, M., Roca, H., Roccheri, M. C., Rocchi, S., Rodemann, H. P., Rodriguez de Cordoba, S., Rohrer, B., Roninson, I. B., Rosen, K., Rost-Roszkowska, M. M., Rouis, M., Rouschop, K. M. A., Rovetta, F., Rubin, B. P., Rubinsztein, D. C., Ruckdeschel, K., Rucker, E. B. R., Rudich, A., Rudolf, E., Ruiz-Opazo, N., Russo, R., Rusten, T. E., Ryan, K. M., Ryter, S. W., Sabatini, D. M., Sadoshima, J., Saha, T., Saitoh, T., Sakagami, H., Sakai, Y., Salekdeh, G. H., Salomoni, P., Salvaterra, P. M., Salvesen, G., Salvioli, R., Sanchez, A. M. J., Sanchez-Alcazar, J. A., Sanchez-Prieto, R., Sandri, M., Sankar, U., Sansanwal, P., Santambrogio, L., Saran, S., Sarkar, S., Sarwal, M., Sasakawa, C., Sasnauskiene, A., Sass, M., Sato, K., Sato, M., Schapira, A. H. V., Scharl, M., Schatzl, H. M., Scheper, W., Schiaffino, S., Schneider, C., Schneider, M. E., Schneider-Stock, R., Schoenlein, P. V., Schorderet, D. F., Schuller, C., Schwartz, G. K., Scorrano, L., Sealy, L., Seglen, P. O., Segura-Aguilar, J., Seiliez, I., Seleverstov, O., Sell, C., Seo, J. B., Separovic, D., Setaluri, V., Setoguchi, T., Settembre, C., Shacka, J. J., Shanmugam, M., Shapiro, I. M., Shaulian, E., Shaw, R. J., Shelhamer, J. H., Shen, H.-M., Shen, W.-C., Sheng, Z.-H., Shi, Y., Shibuya, K., Shidoji, Y., Shieh, J.-J., Shih, C.-M., Shimada, Y., Shimizu, S., Shintani, T., Shirihai, O. S., Shore, G. C., Sibirny, A. A., Sidhu, S. B., Sikorska, B., Silva-Zacarin, E. C. M., Simmons, A., Simon, A., Simon, H.-U., Simone, C., Simonsen, A., Sinclair, D. A., Singh, R., Sinha, D., Sinicrope, F. A., Sirko, A., Siu, P. M., Sivridis, E., Skop, V., Skulachev, V. P., Slack, R. S., Smaili, S. S., Smith, D. R., Soengas, M. S., Soldati, T., Song, X., Sood, A. K., Soong, T. W., Sotgia, F., Spector, S. A., Spies, C. D., Springer, W., Srinivasula, S. M., Stefanis, L., Steffan, J. S., Stendel, R., Stenmark, H., Stephanou, A., Stern, S. T., Sternberg, C., Stork, B., Stralfors, P., Subauste, C. S., Sui, X., Sulzer, D., Sun, J., Sun, S.-Y., Sun, Z.-J., Sung, J. J. Y., Suzuki, K., Suzuki, T., Swanson, M. S., Swanton, C., Sweeney, S. T., Sy, L.-K., Szabadkai, G., Tabas, I., Taegtmeyer, H., Tafani, M., Takacs-Vellai, K., Takano, Y., Takegawa, K., Takemura, G., Takeshita, F., Talbot, N. J., Tan, K. S. W., Tanaka, K., Tanaka, K., Tang, D., Tang, D., Tanida, I., Tannous, B. A., Tavernarakis, N., Taylor, G. S., Taylor, G. A., Taylor, J. P., Terada, L. S., Terman, A., Tettamanti, G., Thevissen, K., Thompson, C. B., Thorburn, A., Thumm, M., Tian, F., Tian, Y., Tocchini-Valentini, G., Tolkovsky, A. M., Tomino, Y., Tonges, L., Tooze, S. A., Tournier, C., Tower, J., Towns, R., Trajkovic, V., Travassos, L. H., Tsai, T.-F., Tschan, M. P., Tsubata, T., Tsung, A., Turk, B., Turner, L. S., Tyagi, S. C., Uchiyama, Y., Ueno, T., Umekawa, M., Umemiya-Shirafuji, R., Unni, V. K., Vaccaro, M. I., Valente, E. M., Van den Berghe, G., van der Klei, I. J., van Doorn, W., van Dyk, L. F., van Egmond, M., van Grunsven, L. A., Vandenabeele, P., Vandenberghe, W. P., Vanhorebeek, I., Vaquero, E. C., Velasco, G., Vellai, T., Vicencio, J. M., Vierstra, R. D., Vila, M., Vindis, C., Viola, G., Viscomi, M. T., Voitsekhovskaja, O. V., von Haefen, C., Votruba, M., Wada, K., Wade-Martins, R., Walker, C. L., Walsh, C. M., Walter, J., Wan, X.-B., Wang, A., Wang, C., Wang, D., Wang, F., Wang, F., Wang, G., Wang, H., Wang, H.-G., Wang, H.-D., Wang, J., Wang, K., Wang, M., Wang, R. C., Wang, X., Wang, X., Wang, Y.-J., Wang, Y., Wang, Z., Wang, Z. C., Wang, Z., Wansink, D. G., Ward, D. M., Watada, H., Waters, S. L., Webster, P., Wei, L., Weihl, C. C., Weiss, W. A., Welford, S. M., Wen, L.-P., Whitehouse, C. A., Whitton, J. L., Whitworth, A. J., Wileman, T., Wiley, J. W., Wilkinson, S., Willbold, D., Williams, R. L., Williamson, P. R., Wouters, B. G., Wu, C., Wu, D.-C., Wu, W. K. K., Wyttenbach, A., Xavier, R. J., Xi, Z., Xia, P., Xiao, G., Xie, Z., Xie, Z., Xu, D.-Z., Xu, J., Xu, L., Xu, X., Yamamoto, A., Yamamoto, A., Yamashina, S., Yamashita, M., Yan, X., Yanagida, M., Yang, D.-S., Yang, E., Yang, J.-M., Yang, S. Y., Yang, W., Yang, W. Y., Yang, Z., Yao, M.-C., Yao, T.-P., Yeganeh, B., Yen, W.-L., Yin, J.-J., Yin, X.-M., Yoo, O.-J., Yoon, G., Yoon, S.-Y., Yorimitsu, T., Yoshikawa, Y., Yoshimori, T., Yoshimoto, K., You, H. J., Youle, R. J., Younes, A., Yu, L., Yu, L., Yu, S.-W., Yu, W. H., Yuan, Z.-M., Yue, Z., Yun, C.-H., Yuzaki, M., Zabirnyk, O., Silva-Zacarin, E., Zacks, D., Zacksenhaus, E., Zaffaroni, N., Zakeri, Z., Zeh, H. J. R., Zeitlin, S. O., Zhang, H., Zhang, H.-L., Zhang, J., Zhang, J.-P., Zhang, L., Zhang, L., Zhang, M.-Y., Zhang, X. D., Zhao, M., Zhao, Y.-F., Zhao, Y., Zhao, Z. J., Zheng, X., Zhivotovsky, B., Zhong, Q., Zhou, C.-Z., Zhu, C., Zhu, W.-G., Zhu, X.-F., Zhu, X., Zhu, Y., Zoladek, T., Zong, W.-X., Zorzano, A., Zschocke, J., & Zuckerbraun, B. (2012). Guidelines for the use and interpretation of assays for monitoring autophagy. Autophagy, 8(4), 445-544.
Peer reviewed (verified by ORBilu)
Burbulla, L. F., & Krüger, R. (2012). The use of primary human fibroblasts for monitoring mitochondrial phenotypes in the field of Parkinson's disease. Journal of visualized experiments : JoVE, (68).
Peer reviewed
Fitzgerald, J. C., Camprubi, M. D., Dunn, L., Wu, H.-C., Ip, N. Y., Krüger, R., Martins, L., Wood, N. W., & Plun-Favreau, H. (2012). Phosphorylation of HtrA2 by cyclin-dependent kinase-5 is important for mitochondrial function. Cell death and differentiation, 19(2), 257-66.
Peer reviewed (verified by ORBilu)
Gispert, S., Kurz, A., Waibel, S., Bauer, P., Liepelt, I., Geisen, C., Gitler, A. D., Becker, T., Weber, M., Berg, D., Andersen, P. M., Krüger, R., Riess, O., Ludolph, A. C., & Auburger, G. (2012). The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. Neurobiology of disease, 45(1), 356-61.
Peer reviewed (verified by ORBilu)
Lengerer, S., Kipping, J., Rommel, N., Weiss, D., Breit, S., Gasser, T., Plewnia, C., Krüger, R., & Wachter, T. (2012). Deep-brain-stimulation does not impair deglutition in Parkinson's disease. Parkinsonism & related disorders, 18(7), 847-53.
Peer reviewed (verified by ORBilu)
Sharma, M., Ioannidis, J. P. A., Aasly, J. O., Annesi, G., Brice, A., Bertram, L., Bozi, M., Barcikowska, M., Crosiers, D., Clarke, C. E., Facheris, M. F., Farrer, M., Garraux, G., Gispert, S., Auburger, G., Vilarino-Guell, C., Hadjigeorgiou, G. M., Hicks, A. A., Hattori, N., Jeon, B. S., Jamrozik, Z., Krygowska-Wajs, A., Lesage, S., Lill, C. M., Lin, J.-J., Lynch, T., Lichtner, P., Lang, A. E., Libioulle, C., Murata, M., Mok, V., Jasinska-Myga, B., Mellick, G. D., Morrison, K. E., Meitnger, T., Zimprich, A., Opala, G., Pramstaller, P. P., Pichler, I., Park, S. S., Quattrone, A., Rogaeva, E., Ross, O. A., Stefanis, L., Stockton, J. D., Satake, W., Silburn, P. A., Strom, T. M., Theuns, J., Tan, E.-K., Toda, T., Tomiyama, H., Uitti, R. J., Van Broeckhoven, C., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., Yomono, H. S., Yueh, K.-C., Zhao, Y., Gasser, T., Maraganore, D., & Krüger, R. (2012). A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of medical genetics, 49(11), 721-6.
Peer reviewed (verified by ORBilu)
Sharma, M., Ioannidis, J. P. A., Aasly, J. O., Annesi, G., Brice, A., Van Broeckhoven, C., Bertram, L., Bozi, M., Crosiers, D., Clarke, C., Facheris, M., Farrer, M., Garraux, G., Gispert, S., Auburger, G., Vilarino-Guell, C., Hadjigeorgiou, G. M., Hicks, A. A., Hattori, N., Jeon, B., Lesage, S., Lill, C. M., Lin, J.-J., Lynch, T., Lichtner, P., Lang, A. E., Mok, V., Jasinska-Myga, B., Mellick, G. D., Morrison, K. E., Opala, G., Pramstaller, P. P., Pichler, I., Park, S. S., Quattrone, A., Rogaeva, E., Ross, O. A., Stefanis, L., Stockton, J. D., Satake, W., Silburn, P. A., Theuns, J., Tan, E.-K., Toda, T., Tomiyama, H., Uitti, R. J., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., Yueh, K.-C., Zhao, Y., Gasser, T., Maraganore, D., & Krüger, R. (2012). Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology, 79(7), 659-67.
Peer reviewed (verified by ORBilu)
Sharma, M., Krüger, R., & Gasser, T. (2012). LRRK2: Understanding the role of common and rare variants in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society, 27(4), 475.
Peer reviewed (verified by ORBilu)
Weiss, D., Breit, S., Hoppe, J., Hauser, A.-K., Freudenstein, D., Krüger, R., Sauseng, P., Govindan, R. B., & Gerloff, C. (2012). Subthalamic nucleus stimulation restores the efferent cortical drive to muscle in parallel to functional motor improvement. The European journal of neuroscience, 35(6), 896-908.
Peer reviewed (verified by ORBilu)
Weiss, D., Brockmann, K., Srulijes, K., Meisner, C., Klotz, R., Reinbold, S., Hauser, A.-K., Schulte, C., Berg, D., Gasser, T., Plewnia, C., Gharabaghi, A., Breit, S., Wachter, T., & Krüger, R. (2012). Long-term follow-up of subthalamic nucleus stimulation in glucocerebrosidase-associated Parkinson's disease. Journal of neurology, 259(9), 1970-2.
Peer reviewed (verified by ORBilu)

2011

Bruck, C., Wildgruber, D., Kreifelts, B., Krüger, R., & Wachter, T. (2011). Effects of subthalamic nucleus stimulation on emotional prosody comprehension in Parkinson's disease. PloS one, 6(4), 19140.
Peer reviewed (verified by ORBilu)
Burbulla, L. F., & Krüger, R. (2011). Converging environmental and genetic pathways in the pathogenesis of Parkinson's disease. Journal of the neurological sciences, 306(1-2), 1-8.
Peer reviewed
Elbaz, A., Ross, O. A., Ioannidis, J. P. A., Soto-Ortolaza, A. I., Moisan, F., Aasly, J., Annesi, G., Bozi, M., Brighina, L., Chartier-Harlin, M.-C., Destee, A., Ferrarese, C., Ferraris, A., Gibson, J. M., Gispert, S., Hadjigeorgiou, G. M., Jasinska-Myga, B., Klein, C., Krüger, R., Lambert, J.-C., Lohmann, K., van de Loo, S., Loriot, M.-A., Lynch, T., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Puschmann, A., Quattrone, A., Sharma, M., Silburn, P. A., Stefanis, L., Uitti, R. J., Valente, E. M., Vilarino-Guell, C., Wirdefeldt, K., Wszolek, Z. K., Xiromerisiou, G., Maraganore, D. M., & Farrer, M. J. (2011). Independent and joint effects of the MAPT and SNCA genes in Parkinson disease. Annals of neurology, 69(5), 778-92.
Peer reviewed (verified by ORBilu)
Krüger, R., Sharma, M., Riess, O., Gasser, T., Van Broeckhoven, C., Theuns, J., Aasly, J., Annesi, G., Bentivoglio, A. R., Brice, A., Djarmati, A., Elbaz, A., Farrer, M., Ferrarese, C., Gibson, J. M., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P. A., Jasinska-Myga, B., Klein, C., Lambert, J.-C., Lesage, S., Lin, J.-J., Lynch, T., Mellick, G. D., de Nigris, F., Opala, G., Prigione, A., Quattrone, A., Ross, O. A., Satake, W., Silburn, P. A., Tan, E. K., Toda, T., Tomiyama, H., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., & Maraganore, D. M. (2011). A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease. Neurobiology of aging, 32(3), 548.e9-18.
Peer reviewed (verified by ORBilu)
Nuber, S., Petrasch-Parwez, E., Arias-Carrion, O., Koch, L., Kohl, Z., Schneider, J., Calaminus, C., Dermietzel, R., Samarina, A., Boy, J., Nguyen, H. P., Teismann, P., Velavan, T. P., Kahle, P. J., von Horsten, S., Fendt, M., Krüger, R., & Riess, O. (2011). Olfactory neuron-specific expression of A30P alpha-synuclein exacerbates dopamine deficiency and hyperactivity in a novel conditional model of early Parkinson's disease stages. Neurobiology of disease, 44(2), 192-204.
Peer reviewed (verified by ORBilu)
Ross, O. A., Soto-Ortolaza, A. I., Heckman, M. G., Aasly, J. O., Abahuni, N., Annesi, G., Bacon, J. A., Bardien, S., Bozi, M., Brice, A., Brighina, L., Van Broeckhoven, C., Carr, J., Chartier-Harlin, M.-C., Dardiotis, E., Dickson, D. W., Diehl, N. N., Elbaz, A., Ferrarese, C., Ferraris, A., Fiske, B., Gibson, J. M., Gibson, R., Hadjigeorgiou, G. M., Hattori, N., Ioannidis, J. P. A., Jasinska-Myga, B., Jeon, B. S., Kim, Y. J., Klein, C., Krüger, R., Kyratzi, E., Lesage, S., Lin, C.-H., Lynch, T., Maraganore, D. M., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Park, S. S., Puschmann, A., Quattrone, A., Sharma, M., Silburn, P. A., Sohn, Y. H., Stefanis, L., Tadic, V., Theuns, J., Tomiyama, H., Uitti, R. J., Valente, E. M., van de Loo, S., Vassilatis, D. K., Vilarino-Guell, C., White, L. R., Wirdefeldt, K., Wszolek, Z. K., Wu, R.-M., & Farrer, M. J. (2011). Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study. Lancet neurology, 10(10), 898-908.
Peer reviewed (verified by ORBilu)
Rzesnitzek, L., Wachter, T., Krüger, R., Gharabaghi, A., & Plewnia, C. (2011). Suppression of extrapyramidal side effects of doxepin by thalamic deep brain stimulation for Tourette syndrome. Neurology, 77(18), 1708-9.
Peer reviewed (verified by ORBilu)
Sharma, M., Maraganore, D. M., Ioannidis, J. P. A., Riess, O., Aasly, J. O., Annesi, G., Abahuni, N., Bentivoglio, A. R., Brice, A., Van Broeckhoven, C., Chartier-Harlin, M.-C., Destee, A., Djarmati, A., Elbaz, A., Farrer, M., Ferrarese, C., Gibson, J. M., Gispert, S., Hattori, N., Jasinska-Myga, B., Klein, C., Lesage, S., Lynch, T., Lichtner, P., Lambert, J.-C., Lang, A. E., Mellick, G. D., De Nigris, F., Opala, G., Quattrone, A., Riva, C., Rogaeva, E., Ross, O. A., Satake, W., Silburn, P. A., Theuns, J., Toda, T., Tomiyama, H., Uitti, R. J., Wirdefeldt, K., Wszolek, Z., Gasser, T., & Krüger, R. (2011). Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. Neurobiology of aging, 32(11), 2108.e1-5.
Peer reviewed (verified by ORBilu)
Wachter, T., Engeholm, M., Bisdas, S., Schittenhelm, J., Gasser, T., & Krüger, R. (2011). Slowly progressive Parkinson syndrome due to thalamic butterfly astrocytoma. Neurology, 77(4), 404-5.
Peer reviewed (verified by ORBilu)
Weiss, D., Brockmann, K., Nagele, T., Gasser, T., & Krüger, R. (2011). Rapid emergence of temporal and pulvinar lesions in MELAS mimicking Creutzfeldt-Jakob disease. Neurology, 77(9), 914.
Peer reviewed (verified by ORBilu)
Weiss, D., Breit, S., Wachter, T., Plewnia, C., Gharabaghi, A., & Krüger, R. (2011). Combined stimulation of the substantia nigra pars reticulata and the subthalamic nucleus is effective in hypokinetic gait disturbance in Parkinson's disease. Journal of neurology, 258(6), 1183-5.
Peer reviewed (verified by ORBilu)
Weiss, D., Govindan, R. B., Rilk, A., Wachter, T., Breit, S., Zizlsperger, L., Haarmeier, T., Plewnia, C., Krüger, R., & Gharabaghi, A. (2011). Central oscillators in a patient with neuropathic tremor: evidence from intraoperative local field potential recordings. Movement disorders : official journal of the Movement Disorder Society, 26(2), 323-7.
Peer reviewed (verified by ORBilu)
Weiss, D., Wachter, T., Meisner, C., Fritz, M., Gharabaghi, A., Plewnia, C., Breit, S., & Krüger, R. (2011). Combined STN/SNr-DBS for the treatment of refractory gait disturbances in Parkinson's disease: study protocol for a randomized controlled trial. Trials, 12, 222.
Peer reviewed (verified by ORBilu)

2010

Breit, S., Wachter, T., Schmid-Bielenberg, D., Weiss, D., Leitner, P., Nagele, T., Freudenstein, D., Gasser, T., & Krüger, R. (2010). Effective long-term subthalamic stimulation in PARK8 positive Parkinson's disease. Journal of neurology, 257(7), 1205-7.
Peer reviewed (verified by ORBilu)
Burbulla, L. F., Krebiehl, G., & Krüger, R. (2010). Balance is the challenge--the impact of mitochondrial dynamics in Parkinson's disease. European journal of clinical investigation, 40(11), 1048-60.
Peer reviewed (verified by ORBilu)
Burbulla, L. F., Schelling, C., Kato, H., Rapaport, D., Woitalla, D., Schiesling, C., Schulte, C., Sharma, M., Illig, T., Bauer, P., Jung, S., Nordheim, A., Schols, L., Riess, O., & Krüger, R. (2010). Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasis. Human molecular genetics, 19(22), 4437-52.
Peer reviewed (verified by ORBilu)
Kieper, N., Holmstrom, K. M., Ciceri, D., Fiesel, F. C., Wolburg, H., Ziviani, E., Whitworth, A. J., Martins, L., Kahle, P. J., & Krüger, R. (2010). Modulation of mitochondrial function and morphology by interaction of Omi/HtrA2 with the mitochondrial fusion factor OPA1. Experimental cell research, 316(7), 1213-24.
Peer reviewed (verified by ORBilu)
Krebiehl, G., Ruckerbauer, S., Burbulla, L. F., Kieper, N., Maurer, B., Waak, J., Wolburg, H., Gizatullina, Z., Gellerich, F. N., Woitalla, D., Riess, O., Kahle, P. J., Proikas-Cezanne, T., & Krüger, R. (2010). Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1. PloS one, 5(2), 9367.
Peer reviewed (verified by ORBilu)
Nuber, S., Franck, T., Wolburg, H., Schumann, U., Casadei, N., Fischer, K., Calaminus, C., Pichler, B. J., Chanarat, S., Teismann, P., Schulz, J. B., Luft, A. R., Tomiuk, J., Wilbertz, J., Bornemann, A., Krüger, R., & Riess, O. (2010). Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in mice. Neurogenetics, 11(1), 107-20.
Peer reviewed (verified by ORBilu)
Seidel, K., Schols, L., Nuber, S., Petrasch-Parwez, E., Gierga, K., Wszolek, Z., Dickson, D., Gai, W. P., Bornemann, A., Riess, O., Rami, A., Den Dunnen, W. F. A., Deller, T., Rub, U., & Krüger, R. (2010). First appraisal of brain pathology owing to A30P mutant alpha-synuclein. Annals of neurology, 67(5), 684-9.
Peer reviewed (verified by ORBilu)
Soehn, A. S., Franck, T., Biskup, S., Giaime, E., Melle, C., Rott, R., Cebo, D., Kalbacher, H., Ott, E., Pahnke, J., Meitinger, T., Krüger, R., Gasser, T., Berg, D., von Eggeling, F., Engelender, S., da Costa, C. A., & Riess, O. (2010). Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease. Neurogenetics, 11(2), 203-15.
Peer reviewed (verified by ORBilu)
Synofzik, M., Schule, R., Schulte, C., Krüger, R., Lindig, T., Schols, L., & Asmus, F. (2010). Complex hyperkinetic movement disorders associated with POLG mutations. Movement disorders : official journal of the Movement Disorder Society, 25(14), 2472-5.
Peer reviewed (verified by ORBilu)
Synofzik, M., Weiss, D., Erharhaghen, J., Krüger, R., & Schols, L. (2010). Severe orthostatic dysregulation associated with Wolfram syndrome. Journal of neurology, 257(10), 1751-3.
Peer reviewed (verified by ORBilu)
Weiss, D., Wachter, T., Breit, S., Jacob, S. N., Pomper, J. K., Asmus, F., Valls-Sole, J., Plewnia, C., Gasser, T., Gharabaghi, A., & Krüger, R. (2010). Involuntary eyelid closure after STN-DBS: evidence for different pathophysiological entities. Journal of neurology, neurosurgery, and psychiatry, 81(9), 1002-7.
Peer reviewed (verified by ORBilu)

2009

Breit, S., Wachter, T., Schols, L., Gasser, T., Nagele, T., Freudenstein, D., & Krüger, R. (2009). Effective thalamic deep brain stimulation for neuropathic tremor in a patient with severe demyelinating neuropathy. Journal of neurology, neurosurgery, and psychiatry, 80(2), 235-6.
Peer reviewed (verified by ORBilu)
Elstner, M., Morris, C. M., Heim, K., Lichtner, P., Bender, A., Mehta, D., Schulte, C., Sharma, M., Hudson, G., Goldwurm, S., Giovanetti, A., Zeviani, M., Burn, D. J., McKeith, I. G., Perry, R. H., Jaros, E., Krüger, R., Wichmann, H.-E., Schreiber, S., Campbell, H., Wilson, J. F., Wright, A. F., Dunlop, M., Pistis, G., Toniolo, D., Chinnery, P. F., Gasser, T., Klopstock, T., Meitinger, T., Prokisch, H., & Turnbull, D. M. (2009). Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene. Annals of neurology, 66(6), 792-8.
Peer reviewed (verified by ORBilu)
Sharma, M., Lichtner, P., Krüger, R., Berg, D., Schulte, C., Illig, T., Riess, O., & Gasser, T. (2009). Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease. Neurobiology of aging, 30(10), 1706-9.
Peer reviewed (verified by ORBilu)
Simon-Sanchez, J., Schulte, C., Bras, J. M., Sharma, M., Gibbs, J. R., Berg, D., Paisan-Ruiz, C., Lichtner, P., Scholz, S. W., Hernandez, D. G., Krüger, R., Federoff, M., Klein, C., Goate, A., Perlmutter, J., Bonin, M., Nalls, M. A., Illig, T., Gieger, C., Houlden, H., Steffens, M., Okun, M. S., Racette, B. A., Cookson, M. R., Foote, K. D., Fernandez, H. H., Traynor, B. J., Schreiber, S., Arepalli, S., Zonozi, R., Gwinn, K., van der Brug, M., Lopez, G., Chanock, S. J., Schatzkin, A., Park, Y., Hollenbeck, A., Gao, J., Huang, X., Wood, N. W., Lorenz, D., Deuschl, G., Chen, H., Riess, O., Hardy, J. A., Singleton, A. B., & Gasser, T. (2009). Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nature genetics, 41(12), 1308-12.
Peer reviewed (verified by ORBilu)
Wachter, T., Weiss, D., Breit, S., Gasser, T., Krüger, R., & Gharabaghi, A. (2009). Severe muscular fasciculations as an uncommon side-effect due to microdefect of an extension wire in deep brain stimulation. Movement disorders : official journal of the Movement Disorder Society, 24(14), 2161-2.
Peer reviewed (verified by ORBilu)

2008

Bonin, M., Marx, F. P., Kautzmann, S., Riess, O., & Krüger, R. (2008). Microarray expression analysis reveals genetic pathways implicated in C621 synphilin-1-mediated toxicity. Journal of neural transmission (Vienna, Austria : 1996), 115(7), 941-58.
Peer reviewed (verified by ORBilu)
Kamm, C., Fogel, W., Wachter, T., Schweitzer, K., Berg, D., Krüger, R., Freudenstein, D., & Gasser, T. (2008). Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation. Neurology, 70(16 Pt 2), 1501-3.
Peer reviewed (verified by ORBilu)
Krüger, R. (2008). LRRK2 in Parkinson's disease - drawing the curtain of penetrance: a commentary. BMC medicine, 6, 33.
Peer reviewed (verified by ORBilu)
Plewnia, C., Schober, F., Rilk, A., Buchkremer, G., Reimold, M., Wachter, T., Breit, S., Weiss, D., Krüger, R., & Freudenstein, D. (2008). Sustained improvement of obsessive-compulsive disorder by deep brain stimulation in a woman with residual schizophrenia. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP), 11(8), 1181-3.
Peer reviewed (verified by ORBilu)
Radke, S., Chander, H., Schafer, P., Meiss, G., Krüger, R., Schulz, J. B., & Germain, D. (2008). Mitochondrial protein quality control by the proteasome involves ubiquitination and the protease Omi. The Journal of biological chemistry, 283(19), 12681-5.
Peer reviewed (verified by ORBilu)
Schiesling, C., Kieper, N., Seidel, K., & Krüger, R. (2008). Review: Familial Parkinson's disease--genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease. Neuropathology and applied neurobiology, 34(3), 255-71.
Peer reviewed (verified by ORBilu)
Tabatabai, G., Schober, W., Ernemann, U., Weller, M., & Krüger, R. (2008). Vertebral artery dissection presenting with ispilateral acute C5 and C6 sensorimotor radiculopathy: A case report. Cases journal, 1(1), 139.
Peer reviewed
Wahl, C., Kautzmann, S., Krebiehl, G., Strauss, K., Woitalla, D., Muller, T., Bauer, P., Riess, O., & Krüger, R. (2008). A comprehensive genetic study of the proteasomal subunit S6 ATPase in German Parkinson's disease patients. Journal of neural transmission (Vienna, Austria : 1996), 115(8), 1141-8.
Peer reviewed (verified by ORBilu)

2007

Abahuni, N., Gispert, S., Bauer, P., Riess, O., Krüger, R., Becker, T., & Auburger, G. (2007). Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease. Neuroscience letters, 414(2), 126-9.
Peer reviewed (verified by ORBilu)
Exner, N., Treske, B., Paquet, D., Holmstrom, K., Schiesling, C., Gispert, S., Carballo-Carbajal, I., Berg, D., Hoepken, H.-H., Gasser, T., Krüger, R., Winklhofer, K. F., Vogel, F., Reichert, A. S., Auburger, G., Kahle, P. J., Schmid, B., & Haass, C. (2007). Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin. The Journal of neuroscience : the official journal of the Society for Neuroscience, 27(45), 12413-8.
Peer reviewed (verified by ORBilu)
Matzler, W., Nagele, T., Gasser, T., & Krüger, R. (2007). Acute parkinsonism with corresponding lesions in the basal ganglia after heroin abuse. Neurology, 68(6), 414.
Peer reviewed (verified by ORBilu)
Schweitzer, K. J., Brussel, T., Leitner, P., Krüger, R., Bauer, P., Woitalla, D., Tomiuk, J., Gasser, T., & Berg, D. (2007). Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease. Journal of neurology, 254(5), 613-6.
Peer reviewed (verified by ORBilu)

2006

Elbaz, A., Nelson, L. M., Payami, H., Ioannidis, J. P. A., Fiske, B. K., Annesi, G., Carmine Belin, A., Factor, S. A., Ferrarese, C., Hadjigeorgiou, G. M., Higgins, D. S., Kawakami, H., Krüger, R., Marder, K. S., Mayeux, R. P., Mellick, G. D., Nutt, J. G., Ritz, B., Samii, A., Tanner, C. M., Van Broeckhoven, C., Van Den Eeden, S. K., Wirdefeldt, K., Zabetian, C. P., Dehem, M., Montimurro, J. S., Southwick, A., Myers, R. M., & Trikalinos, T. A. (2006). Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study. Lancet neurology, 5(11), 917-23.
Peer reviewed (verified by ORBilu)
Maraganore, D. M., de Andrade, M., Elbaz, A., Farrer, M. J., Ioannidis, J. P., Krüger, R., Rocca, W. A., Schneider, N. K., Lesnick, T. G., Lincoln, S. J., Hulihan, M. M., Aasly, J. O., Ashizawa, T., Chartier-Harlin, M.-C., Checkoway, H., Ferrarese, C., Hadjigeorgiou, G., Hattori, N., Kawakami, H., Lambert, J.-C., Lynch, T., Mellick, G. D., Papapetropoulos, S., Parsian, A., Quattrone, A., Riess, O., Tan, E.-K., & Van Broeckhoven, C. (2006). Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. JAMA : the journal of the American Medical Association, 296(6), 661-70.
Peer reviewed (verified by ORBilu)
Riess, O., Krüger, R., Hochstrasser, H., Soehn, A. S., Nuber, S., Franck, T., & Berg, D. (2006). Genetic causes of Parkinson's disease: extending the pathway. Journal of neural transmission. Supplementum, (70), 181-9.
Peer reviewed (verified by ORBilu)

2005

Hochstrasser, H., Tomiuk, J., Walter, U., Behnke, S., Spiegel, J., Krüger, R., Becker, G., Riess, O., & Berg, D. (2005). Functional relevance of ceruloplasmin mutations in Parkinson's disease. FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 19(13), 1851-3.
Peer reviewed (verified by ORBilu)
Hofer, A., Berg, D., Asmus, F., Niwar, M., Ransmayr, G., Riemenschneider, M., Bonelli, S.-B., Steffelbauer, M., Ceballos-Baumann, A., Haussermann, P., Behnke, S., Krüger, R., Prestel, J., Sharma, M., Zimprich, A., Riess, O., & Gasser, T. (2005). The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodies. Journal of neural transmission (Vienna, Austria : 1996), 112(9), 1249-54.
Peer reviewed (verified by ORBilu)
Strauss, K. M., Martins, L., Plun-Favreau, H., Marx, F. P., Kautzmann, S., Berg, D., Gasser, T., Wszolek, Z., Muller, T., Bornemann, A., Wolburg, H., Downward, J., Riess, O., Schulz, J. B., & Krüger, R. (2005). Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease. Human molecular genetics, 14(15), 2099-111.
Peer reviewed (verified by ORBilu)

2004

Glass, A. S., Huynh, D. P., Franck, T., Woitalla, D., Muller, T., Pulst, S. M., Berg, D., Krüger, R., & Riess, O. (2004). Screening for mutations in synaptotagmin XI in Parkinson's disease. Journal of neural transmission. Supplementum, (68), 21-8.
Peer reviewed (verified by ORBilu)
Hering, R., Petrovic, S., Mietz, E.-M., Holzmann, C., Berg, D., Bauer, P., Woitalla, D., Muller, T., Berger, K., Krüger, R., & Riess, O. (2004). Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease. Neurology, 62(7), 1231-2.
Peer reviewed (verified by ORBilu)
Hering, R., Strauss, K. M., Tao, X., Bauer, A., Woitalla, D., Mietz, E.-M., Petrovic, S., Bauer, P., Schaible, W., Muller, T., Schols, L., Klein, C., Berg, D., Meyer, P. T., Schulz, J. B., Wollnik, B., Tong, L., Krüger, R., & Riess, O. (2004). Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7). Human mutation, 24(4), 321-9.
Peer reviewed (verified by ORBilu)
Krüger, R. (2004). Genes in familial parkinsonism and their role in sporadic Parkinson's disease. Journal of neurology, 251 Suppl 6, 2-6.
Peer reviewed (verified by ORBilu)
Krüger, R. (2004). The role of synphilin-1 in synaptic function and protein degradation. Cell and Tissue Research, 318(1), 195-9.
Peer reviewed
Maraganore, D. M., Lesnick, T. G., Elbaz, A., Chartier-Harlin, M.-C., Gasser, T., Krüger, R., Hattori, N., Mellick, G. D., Quattrone, A., Satoh, J.-I., Toda, T., Wang, J., Ioannidis, J. P. A., de Andrade, M., & Rocca, W. A. (2004). UCHL1 is a Parkinson's disease susceptibility gene. Annals of neurology, 55(4), 512-21.
Peer reviewed (verified by ORBilu)
Muller, T., Przuntek, H., Krüger, R., & Mackowiak, A. (2004). Antiapoptotic effects of budipine. Journal of neural transmission (Vienna, Austria : 1996), 111(10-11), 1365-73.
Peer reviewed (verified by ORBilu)
Storch, A., Hofer, A., Krüger, R., Schulz, J. B., Winkler, J., & Gerlach, M. (2004). New developments in diagnosis and treatment of Parkinson's disease--from basic science to clinical applications. Journal of neurology, 251 Suppl 6, 33-8.
Peer reviewed (verified by ORBilu)

2003

Holzmann, C., Krüger, R., Saecker, A. M. M. V., Schmitt, I., Schols, L., Berger, K., & Riess, O. (2003). Polymorphisms of the alpha-synuclein promoter: expression analyses and association studies in Parkinson's disease. Journal of neural transmission (Vienna, Austria : 1996), 110(1), 67-76.
Peer reviewed (verified by ORBilu)
Kobayashi, H., Krüger, R., Markopoulou, K., Wszolek, Z., Chase, B., Taka, H., Mineki, R., Murayama, K., Riess, O., Mizuno, Y., & Hattori, N. (2003). Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease. Brain : a journal of neurology, 126(Pt 1), 32-42.
Peer reviewed (verified by ORBilu)
Krüger, R., Fischer, C., Schulte, T., Strauss, K. M., Muller, T., Woitalla, D., Berg, D., Hungs, M., Gobbele, R., Berger, K., Epplen, J. T., Riess, O., & Schols, L. (2003). Mutation analysis of the neurofilament M gene in Parkinson's disease. Neuroscience letters, 351(2), 125-9.
Peer reviewed (verified by ORBilu)
Marx, F. P., Holzmann, C., Strauss, K. M., Li, L., Eberhardt, O., Gerhardt, E., Cookson, M. R., Hernandez, D., Farrer, M. J., Kachergus, J., Engelender, S., Ross, C. A., Berger, K., Schols, L., Schulz, J. B., Riess, O., & Krüger, R. (2003). Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease. Human molecular genetics, 12(11), 1223-31.
Peer reviewed (verified by ORBilu)
Riess, O., Berg, D., Krüger, R., & Schulz, J. B. (2003). Therapeutic strategies for Parkinson's disease based on data derived from genetic research. Journal of neurology, 250 Suppl 1, 3-10.
Peer reviewed (verified by ORBilu)
Schulte, T., Bohringer, S., Schols, L., Muller, T., Fischer, C., Riess, O., Przuntek, H., Berger, K., Epplen, J. T., & Krüger, R. (2003). Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease. Journal of neural transmission (Vienna, Austria : 1996), 110(7), 749-55.
Peer reviewed (verified by ORBilu)
Thiex, R., Krüger, R., Friese, S., Gronewaller, E., & Kuker, W. (2003). Giant cavernoma of the brain stem: value of delayed MR imaging after contrast injection. European radiology, 13 Suppl 6, 219-25.
Peer reviewed (verified by ORBilu)

2002

Krüger, R., Eberhardt, O., Riess, O., & Schulz, J. B. (2002). Parkinson's disease: one biochemical pathway to fit all genes? Trends in molecular medicine, 8(5), 236-40.
Peer reviewed (verified by ORBilu)
Rahner, N., Holzmann, C., Krüger, R., Schols, L., Berger, K., & Riess, O. (2002). Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's disease. Brain research, 951(1), 82-6.
Peer reviewed (verified by ORBilu)
Riess, O., Krüger, R., & Schulz, J. B. (2002). Spectrum of phenotypes and genotypes in Parkinson's disease. Journal of neurology, 249 Suppl 3, 15-20.
Peer reviewed (verified by ORBilu)
Schulte, T., Schols, L., Muller, T., Woitalla, D., Berger, K., & Krüger, R. (2002). Polymorphisms in the interleukin-1 alpha and beta genes and the risk for Parkinson's disease. Neuroscience letters, 326(1), 70-2.
Peer reviewed (verified by ORBilu)
Ubl, A., Berg, D., Holzmann, C., Krüger, R., Berger, K., Arzberger, T., Bornemann, A., & Riess, O. (2002). 14-3-3 protein is a component of Lewy bodies in Parkinson's disease-mutation analysis and association studies of 14-3-3 eta. Molecular Brain Research, 108(1-2), 33-9.
Peer reviewed
Wintermeyer, P., Riess, O., Schols, L., Przuntek, H., Miterski, B., Epplen, J. T., & Krüger, R. (2002). Mutation analysis and association studies of nuclear factor-kappaB1 in sporadic Parkinson's disease patients. Journal of neural transmission (Vienna, Austria : 1996), 109(9), 1181-8.
Peer reviewed (verified by ORBilu)

2001

Krüger, R., Kuhn, W., Leenders, K. L., Sprengelmeyer, R., Muller, T., Woitalla, D., Portman, A. T., Maguire, R. P., Veenma, L., Schroder, U., Schols, L., Epplen, J. T., Riess, O., & Przuntek, H. (2001). Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers. Neurology, 56(10), 1355-62.
Peer reviewed (verified by ORBilu)
Krüger, R., Schols, L., Muller, T., Kuhn, W., Woitalla, D., Przuntek, H., Epplen, J. T., & Riess, O. (2001). Evaluation of the gamma-synuclein gene in German Parkinson's disease patients. Neuroscience letters, 310(2-3), 191-3.
Peer reviewed (verified by ORBilu)

2000

Krüger, R., Hardt, C., Tschentscher, F., Jackel, S., Kuhn, W., Muller, T., Werner, J., Woitalla, D., Berg, D., Kuhnl, N., Fuchs, G. A., Santos, E. J., Przuntek, H., Epplen, J. T., Schols, L., & Riess, O. (2000). Genetic analysis of immunomodulating factors in sporadic Parkinson's disease. Journal of neural transmission (Vienna, Austria : 1996), 107(5), 553-62.
Peer reviewed (verified by ORBilu)
Krüger, R., Menezes-Saecker, A. M., Schols, L., Kuhn, W., Muller, T., Woitalla, D., Berg, D., Berger, K., Przuntek, H., Epplen, J. T., & Riess, O. (2000). Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease. Neuroreport, 11(11), 2439-42.
Peer reviewed (verified by ORBilu)
Krüger, R., Muller, T., & Riess, O. (2000). Involvement of alpha-synuclein in Parkinson's disease and other neurodegenerative disorders. Journal of neural transmission (Vienna, Austria : 1996), 107(1), 31-40.
Peer reviewed (verified by ORBilu)
Miterski, B., Krüger, R., Wintermeyer, P., & Epplen, J. T. (2000). PCR/SSCP detects reliably and efficiently DNA sequence variations in large scale screening projects. Combinatorial chemistry & high throughput screening, 3(3), 211-8.
Peer reviewed (verified by ORBilu)
Riess, O., Kuhn, W., & Krüger, R. (2000). Genetic influence on the development of Parkinson's disease. Journal of neurology, 247 Suppl 2, 69-74.
Peer reviewed (verified by ORBilu)
Schols, L., Peters, S., Szymanski, S., Krüger, R., Lange, S., Hardt, C., Riess, O., & Przuntek, H. (2000). Extrapyramidal motor signs in degenerative ataxias. Archives of neurology, 57(10), 1495-500.
Peer reviewed (verified by ORBilu)
Wintermeyer, P., Krüger, R., Kuhn, W., Muller, T., Woitalla, D., Berg, D., Leroy, E., Polymeropoulos, M., Berger, K., Przuntek, H., Schols, L., Epplen, J. T., & Riess, O. (2000). Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients. Neuroreport, 11(10), 2079-82.
Peer reviewed (verified by ORBilu)

1999

Grasbon-Frodl, E. M., Egensperger, R., Kosel, S., Krüger, R., Riess, O., Mehraein, P., & Graeber, M. B. (1999). The alpha1-antichymotrypsin A-allele in German Parkinson disease patients. Journal of neural transmission (Vienna, Austria : 1996), 106(7-8), 729-36.
Peer reviewed (verified by ORBilu)
Krüger, R., Vieira-Sacker, A. M., Kuhn, W., Muller, T., Woitalla, D., Schols, L., Przuntek, H., Epplen, J. T., & Riess, O. (1999). Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communication. Journal of neural transmission (Vienna, Austria : 1996), 106(2), 159-63.
Peer reviewed (verified by ORBilu)
Krüger, R., Vieira-Saecker, A. M., Kuhn, W., Berg, D., Muller, T., Kuhnl, N., Fuchs, G. A., Storch, A., Hungs, M., Woitalla, D., Przuntek, H., Epplen, J. T., Schols, L., & Riess, O. (1999). Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype. Annals of neurology, 45(5), 611-7.
Peer reviewed (verified by ORBilu)

1998

Krüger, R., Kuhn, W., Muller, T., Woitalla, D., Graeber, M., Kosel, S., Przuntek, H., Epplen, J. T., Schols, L., & Riess, O. (1998). Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. Nature genetics, 18(2), 106-8.
Peer reviewed (verified by ORBilu)
Muller, T., Kuhn, W., Krüger, R., & Przuntek, H. (1998). Selegiline as immunostimulant--a novel mechanism of action? Journal of neural transmission. Supplementum, 52, 321-8.
Peer reviewed (verified by ORBilu)
Riess, O., Jakes, R., & Krüger, R. (1998). Genetic dissection of familial Parkinson's disease. Molecular medicine today, 4(10), 438-44.
Peer reviewed (verified by ORBilu)
Schols, L., Krüger, R., Amoiridis, G., Przuntek, H., Epplen, J. T., & Riess, O. (1998). Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds. Journal of neurology, neurosurgery, and psychiatry, 64(1), 67-73.
Peer reviewed (verified by ORBilu)

1996

Wilfried, K., Muller, T., Krüger, R., & Horst, P. (1996). Selegiline stimulates biosynthesis of cytokines interleukin-1 beta and interleukin-6. Neuroreport, 7(18), 2847-8.
Peer reviewed (verified by ORBilu)