Universität zu Köln

2019

Jiang, Xueyan, Faber, J., Giordano, I, Machts, J., Kindler, Ch, Dudesek, A., Speck, O., Kamm, Ch, Duezel, E., Jessen, F., Spottke, A., Boecker, H., Klockgether, T. and Scheef, L. (2019). Characterization of Cerebellar Atrophy and Resting State Functional Connectivity Patterns in Sporadic Adult-Onset Ataxia of Unknown Etiology (SAOA). Cerebellum, 18 (5). S. 873 - 882. NEW YORK: SPRINGER. ISSN 1473-4230

2017

Neri, M., Scotton, C., Gualandi, F., Wirth, B., Schoels, L., Klockgether, T., Lochmuller, H., Muntoni, F., D'amico, A., Bertini, E., Pane, M., Mercuri, E. and Ferlini, A. (2017). Genetic landscapes in neuromuscular disorders: The influence of next-generation sequencing analysis. Eur. J. Neurol., 24. S. 500 - 501. HOBOKEN: WILEY. ISSN 1468-1331

Neri, M., Scotton, C., Selvatici, R., Gualandi, F., Wirth, B., Schols, L., Klockgether, T., Lochmuller, H., Muntoni, F., D'Amico, A., Bertini, E., Pane, M., Mercuri, E. and Ferlini, A. (2017). The success of whole exome sequencing analysis in neuromuscular diseases patients: the UNIFE experience within neuromics project. Neuromusc. Disord., 27. S. S194 - 1. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364

2016

Neri, M., Scotton, C., Gualandi, F., Wirth, B., Schols, L., Klockgether, T., Lochmuller, H., Muntoni, F., D'Amico, A., Bertini, E., Pane, M., Mercuri, E. and Ferlini, A. (2016). Genetic landscapes in neuromuscular disorders: The influence of next-generation sequencing analysis. Neuromusc. Disord., 26. S. S162 - 1. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364

2015

Hessler, N., Geise, M. H., I, Coassin, S., Moskau-Hartmannt, S., Nuernberg, G., Hennig, F., Bauer, M., Moehlenkamp, S., Mahabadi, A. A., Moebus, S., Erbel, R., Karl-Heinz, J., Hoffmann, B., Nuemberg, P., Klockgether, T., Kronenberg, F., Scherag, A. and Ziegler, A. (2015). Linkage and Association Analyses of Carotid Intima Media Thickness for Common Genomic Variants: Results from the Bonn IMT Family Study and The Heinz Nixdorf Recall Study. Hum. Hered., 79 (1). S. 37 - 38. BASEL: KARGER. ISSN 1423-0062

Turner, C., Brice, A., Bushby, K., Riess, O., Hanna, M., van Ommen, G., Muntoni, F., Klockgether, T., Wirth, B., Lochmueller, H., Timmerman, V., Schoells, L., Straub, V. and Tabrizi, S. (2015). NeurOmics: EU-funded-omics research for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases. Neuromusc. Disord., 25. S. S298 - 2. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364