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Anzahl der Publikationen: 15
Zeitschriftenartikel
Brenner, David 
ORCID: https://orcid.org/0000-0002-1535-3146; Sieverding, Kirsten ORCID: https://orcid.org/0009-0006-7223-5943; Srinidhi, Jahnavi ORCID: https://orcid.org/0009-0003-8416-2276; Zellner, Susanne ORCID: https://orcid.org/0000-0002-8523-824X; Secker, Christopher ORCID: https://orcid.org/0000-0002-7222-536X; Yilmaz, Rüstem ORCID: https://orcid.org/0000-0002-4261-5236; Dyckow, Julia ORCID: https://orcid.org/0000-0003-1423-9322; Amr, Shady ORCID: https://orcid.org/0009-0000-1597-1510; Ponomarenko, Anna ORCID: https://orcid.org/0009-0009-9223-9310; Tunaboylu, Esra ORCID: https://orcid.org/0009-0002-4266-4449; Douahem, Yasmin ORCID: https://orcid.org/0009-0004-7079-7120; Schlag, Joana S. ORCID: https://orcid.org/0009-0005-2001-4121; Rodríguez Martínez, Lucía ORCID: https://orcid.org/0009-0003-3576-3702; Kislinger, Georg ORCID: https://orcid.org/0000-0002-6559-7421; Niemann, Cornelia ORCID: https://orcid.org/0009-0000-7197-6770; Nalbach, Karsten ORCID: https://orcid.org/0000-0002-3928-4026; Ruf, Wolfgang P. ORCID: https://orcid.org/0000-0002-8105-6123; Uhl, Jonathan ORCID: https://orcid.org/0009-0005-1754-173X; Hollenbeck, Johanna ORCID: https://orcid.org/0009-0009-9877-7822; Schirmer, Lucas ORCID: https://orcid.org/0000-0001-7142-4116; Catanese, Alberto ORCID: https://orcid.org/0000-0002-8266-4913; Lobsiger, Christian S. ORCID: https://orcid.org/0000-0002-4313-010X; Danzer, Karin M. ORCID: https://orcid.org/0000-0003-0133-7046; Yilmazer-Hanke, Deniz ORCID: https://orcid.org/0000-0003-1483-0286; Münch, Christian ORCID: https://orcid.org/0000-0003-3832-090X; Koch, Philipp ORCID: https://orcid.org/0000-0003-3713-8786; Freischmidt, Axel ORCID: https://orcid.org/0000-0003-1216-3790; Fetting, Martina ORCID: https://orcid.org/0000-0002-0500-8218; Behrends, Christian ORCID: https://orcid.org/0000-0002-9184-7607; Parlato, Rosanna ORCID: https://orcid.org/0000-0001-6682-9645 und Weishaupt, Jochen H. ORCID: https://orcid.org/0000-0002-3399-9784
(2024):
A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice.
In: Journal of Experimental Medicine, Bd. 221, Nr. 5, e20221190
[PDF, 7MB]
ORCID: https://orcid.org/0000-0002-1535-3146; Sieverding, Kirsten ORCID: https://orcid.org/0009-0006-7223-5943; Srinidhi, Jahnavi ORCID: https://orcid.org/0009-0003-8416-2276; Zellner, Susanne ORCID: https://orcid.org/0000-0002-8523-824X; Secker, Christopher ORCID: https://orcid.org/0000-0002-7222-536X; Yilmaz, Rüstem ORCID: https://orcid.org/0000-0002-4261-5236; Dyckow, Julia ORCID: https://orcid.org/0000-0003-1423-9322; Amr, Shady ORCID: https://orcid.org/0009-0000-1597-1510; Ponomarenko, Anna ORCID: https://orcid.org/0009-0009-9223-9310; Tunaboylu, Esra ORCID: https://orcid.org/0009-0002-4266-4449; Douahem, Yasmin ORCID: https://orcid.org/0009-0004-7079-7120; Schlag, Joana S. ORCID: https://orcid.org/0009-0005-2001-4121; Rodríguez Martínez, Lucía ORCID: https://orcid.org/0009-0003-3576-3702; Kislinger, Georg ORCID: https://orcid.org/0000-0002-6559-7421; Niemann, Cornelia ORCID: https://orcid.org/0009-0000-7197-6770; Nalbach, Karsten ORCID: https://orcid.org/0000-0002-3928-4026; Ruf, Wolfgang P. ORCID: https://orcid.org/0000-0002-8105-6123; Uhl, Jonathan ORCID: https://orcid.org/0009-0005-1754-173X; Hollenbeck, Johanna ORCID: https://orcid.org/0009-0009-9877-7822; Schirmer, Lucas ORCID: https://orcid.org/0000-0001-7142-4116; Catanese, Alberto ORCID: https://orcid.org/0000-0002-8266-4913; Lobsiger, Christian S. ORCID: https://orcid.org/0000-0002-4313-010X; Danzer, Karin M. ORCID: https://orcid.org/0000-0003-0133-7046; Yilmazer-Hanke, Deniz ORCID: https://orcid.org/0000-0003-1483-0286; Münch, Christian ORCID: https://orcid.org/0000-0003-3832-090X; Koch, Philipp ORCID: https://orcid.org/0000-0003-3713-8786; Freischmidt, Axel ORCID: https://orcid.org/0000-0003-1216-3790; Fetting, Martina ORCID: https://orcid.org/0000-0002-0500-8218; Behrends, Christian ORCID: https://orcid.org/0000-0002-9184-7607; Parlato, Rosanna ORCID: https://orcid.org/0000-0001-6682-9645 und Weishaupt, Jochen H. ORCID: https://orcid.org/0000-0002-3399-9784
(2024):
A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice.
In: Journal of Experimental Medicine, Bd. 221, Nr. 5, e20221190
[PDF, 7MB]
Siebert, Alexander; Gattringer, Vanessa; Weishaupt, Jochen H. und Behrends, Christian
(16. Dezember 2022):
ALS-linked loss of Cyclin-F function affects HSP90.
In: Life Science Alliance, Bd. 5, Nr. 12
[PDF, 4MB]
Strohm, Laura; Hu, Zehan; Suk, Yongwon; Rühmkorf, Alina; Sternburg, Erin; Gattringer, Vanessa; Riemenschneider, Henrick; Berutti, Riccardo; Graf, Elisabeth; Weishaupt, Jochen H. ORCID: https://orcid.org/0000-0002-3399-9784; Brill, Monika S.; Harbauer, Angelika B.; Dormann, Dorothee; Dengjel, Jörn; Edbauer, Dieter und Behrends, Christian
(1. Juli 2022):
Multi-omics profiling identifies a deregulated FUS-MAP1B axis in ALS/FTD–associated UBQLN2 mutants.
In: Life Science Alliance, Bd. 5, Nr. 11
[PDF, 6MB]
ORCID: https://orcid.org/0000-0002-3399-9784; Brill, Monika S.; Harbauer, Angelika B.; Dormann, Dorothee; Dengjel, Jörn; Edbauer, Dieter und Behrends, Christian
(1. Juli 2022):
Multi-omics profiling identifies a deregulated FUS-MAP1B axis in ALS/FTD–associated UBQLN2 mutants.
In: Life Science Alliance, Bd. 5, Nr. 11
[PDF, 6MB]
Barschke, Peggy; Oeckl, Patrick; Steinacker, Petra; Al Shweiki, Mhd Rami; Weishaupt, Jochen H.; Landwehrmeyer, G. Bernhard; Anderl-Straub, Sarah; Weydt, Patrick; Diehl-Schmid, Janine; Danek, Adrian; Kornhuber, Johannes; Schroeter, Matthias L.; Prudlo, Johannes; Jahn, Holger; Fassbender, Klaus; Lauer, Martin; Ende, Emma Louise van der; Swieten, John Cornelis van; Volk, Alexander E.; Ludolph, Albert C. und Otto, Markus
(2020):
Different CSF protein profiles in amyotrophic lateral sclerosis and frontotemporal dementia with C9orf72 hexanucleotide repeat expansion.
In: Journal of Neurology Neurosurgery and Psychiatry, Bd. 91, Nr. 5: S. 503-511
[PDF, 2MB]
Yilmaz, Ruestem; Mueller, Kathrin; Brenner, David; Volk, Alexander E.; Borck, Guntram; Hermann, Andreas; Meitinger, Thomas; Strom, Tim M.; Danzer, Karin M.; Ludolph, Albert C.; Andersen, Peter M. und Weishaupt, Jochen H.
(2020):
SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden.
In: Neurobiology of Aging, Bd. 87
Naumann, Marcel; Peikert, Kevin; Guenther, Rene; van der Kooi, Anneke J.; Aronica, Eleonora; Huebers, Annemarie; Danel, Veronique; Corcia, Philippe; Pan-Montojo, Francisco; Cirak, Sebahattin; Haliloglu, Goeknur; Ludolph, Albert C.; Goswami, Anand; Andersen, Peter M.; Prudlo, Johannes; Wegner, Florian; Van Damme, Philip; Weishaupt, Jochen H. und Hermann, Andreas
(2019):
Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis.
In: Annals of Clinical and Translational Neurology
[PDF, 626kB]
Grozdanov, Veselin; Bousset, Luc; Hoffmeister, Meike; Bliederhaeuser, Corinna; Meier, Christoph; Madiona, Karine; Pieri, Laura; Kiechle, Martin; McLean, Pamela J.; Kassubek, Jan; Behrends, Christian; Ludolph, Albert C.; Weishaupt, Jochen H.; Melki, Ronald und Danzer, Karin M.
(2019):
Increased Immune Activation by Pathologic alpha-Synuclein in Parkinson's Disease.
In: Annals of Neurology, Bd. 86, Nr. 4: S. 593-606
[PDF, 4MB]
Dorst, Johannes; Chen, Lu; Rosenbohm, Angela; Dreyhaupt, Jens; Huebers, Annemarie; Schuster, Joachim; Weishaupt, Jochen H.; Kassubek, Jan; Gess, Burkhard; Meyer, Thomas; Weyen, Ute; Hermann, Andreas; Winkler, Jürgen; Grehl, Torsten; Hagenacker, Tim; Lingor, Paul; Koch, Jan C.; Sperfeld, Anne; Petri, Susanne; Grosskreutz, Julian; Metelmann, Moritz; Wolf, Joachim; Winkler, Andrea S.; Klopstock, Thomas; Boentert, Matthias; Johannesen, Siw; Storch, Alexander; Schrank, Bertold; Zeller, Daniel; Liu, Xiao-lu; Tang, Lu; Fan, Dong-Sheng und Ludolph, Albert C.
(2019):
Prognostic factors in ALS: a comparison between Germany and China.
In: Journal of Neurology, Bd. 266, Nr. 6: S. 1516-1525
Oeckl, Patrick; Weydt, Patrick; Steinacker, Petra; Anderl-Straub, Sarah; Nordin, Frida; Volk, Alexander E.; Diehl-Schmid, Janine; Andersen, Peter M.; Kornhuber, Johannes; Danek, Adrian; Fassbender, Klaus; Fliessbach, Klaus; Jahn, Holger; Lauer, Martin; Müller, Kathrin; Knehr, Antje; Prudlo, Johannes; Schneider, Anja; Thal, Dietmar R.; Yilmazer-Hanke, Deniz; Weishaupt, Jochen H.; Ludolph, Albert C. und Otto, Markus
(2019):
Different neuroinflammatory profile in amyotrophic lateral sclerosis and frontotemporal dementia is linked to the clinical phase.
In: Journal of Neurology Neurosurgery and Psychiatry, Bd. 90, Nr. 1: S. 4-10
[PDF, 421kB]
Brenner, David; Rosenbohm, Angela; Yilmaz, Ruestem; Mueller, Kathrin; Grehl, Torsten; Petri, Susanne; Meyer, Thomas; Grosskreutz, Julian; Weydt, Patrick; Ruf, Wolfgang; Neuwirth, Christoph; Weber, Markus; Pinto, Susana; Claeys, Kristl G.; Schrank, Berthold; Jordan, Berit; Knehr, Antje; Guenther, Kornelia; Huebers, Annemarie; Zeller, Daniel; Kubisch, Christian; Jablonka, Sibylle; Sendtner, Michael; Klopstock, Thomas; de Carvalho, Mamede; Sperfeld, Anne; Borck, Guntram; Volk, Alexander E.; Dorst, Johannes; Weis, Joachim; Otto, Markus; Schuster, Joachim; Del Tredici, Kelly; Braak, Heiko; Danzer, Karin M.; Freischmidt, Axel; Meitinger, Thomas; Ludolph, Albert C.; Andersen, Peter M.; Weishaupt, Jochen H.; Weyen, Ute; Hermann, Andreas; Winkler, Juergen; Hagenacker, Tim; Koch, Jan Christoph; Lingor, Paul; Goericke, Bettina; Zierz, Stephan; Baum, Petra; Wolf, Joachim; Winkler, Andrea; Young, Peter; Bogdahn, Ulrich; Prudlo, Johannes und Kassubek, Jan
(2019):
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
In: Brain, Bd. 142, e67
[PDF, 190kB]
Forouhideh, Yalda; Mueller, Kathrin; Ruf, Wolfgang; Assi, Muhannad; Seker, Tuncay; Tunca, Ceren; Knehr, Antje; Strom, Tim M.; Gorges, Martin; Schradt, Falk; Meitinger, Thomas; Ludolph, Albert C.; Pinkhardt, Elmar H.; Basak, A. Nazli; Kassubek, Jan; Uttner, Ingo und Weishaupt, Jochen H.
(2019):
A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification.
In: Brain, Bd. 142
[PDF, 446kB]
Naumann, Marcel; Pal, Arun; Goswami, Anand; Lojewski, Xenia; Japtok, Julia; Vehlow, Anne; Naujock, Maximilian; Günther, Rene; Jin, Mengmeng; Stanslowsky, Nancy; Reinhardt, Peter; Sterneckert, Jared; Frickenhaus, Marie; Pan-Montojo, Francisco; Storkebaum, Erik; Poser, Ina; Freischmidt, Axel; Weishaupt, Jochen H.; Holzmann, Karlheinz; Troost, Dirk; Ludolph, Albert C.; Böckers, Tobias M.; Liebau, Stefan; Petri, Susanne; Cordes, Nils; Hyman, Anthony A.; Wegner, Florian; Grill, Stephan W.; Weis, Joachim; Storch, Alexander und Hermann, Andreas
(2018):
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation.
In: Nature Communications, Bd. 9, 335
[PDF, 6MB]
Müller, Kathrin; Brenner, David; Weydt, Patrick; Meyer, Thomas; Grehl, Torsten; Petri, Susanne; Grosskreutz, Julian; Schuster, Joachim; Volk, Alexander E.; Borck, Guntram; Kubisch, Christian; Klopstock, Thomas; Zeller, Daniel; Jablonka, Sibylle; Sendtner, Michael; Klebe, Stephan; Knehr, Antje; Günther, Kornelia; Weis, Joachim; Claeys, Kristl G.; Schrank, Berthold; Sperfeld, Anne-Dorte; Hübers, Annemarie; Otto, Markus; Dorst, Johannes; Meitinger, Thomas; Strom, Tim M.; Andersen, Peter M.; Ludolph, Albert C. und Weishaupt, Jochen H.
(2018):
Comprehensive analysis of the mutation spectrum in 301 German ALS families.
In: Journal of Neurology Neurosurgery and Psychiatry, Bd. 89, Nr. 8: S. 817-827
[PDF, 637kB]
Lehmer, Carina; Öckl, Patrick; Weishaupt, Jochen H.; Volk, Alexander E.; Diehl-Schmid, Janine; Schröter, Matthias L.; Lauer, Martin; Kornhuber, Johannes; Levin, Johannes; Fassbender, Klaus; Landwehrmeyer, Bernhard; Schludi, Martin H.; Arzberger, Thomas; Kremmer, Elisabeth; Flatley, Andrew; Feederle, Regina; Steinacker, Petra; Weydt, Patrick; Ludolph, Albert C.; Edbauer, Dieter und Otto, Markus
(2017):
Poly-GP in cerebrospinal fluid links C9orf72-associated dipeptide repeat expression to the asymptomatic phase of ALS/FTD.
In: Embo Molecular Medicine, Bd. 9, Nr. 7: S. 859-868
Auer-Grumbach, Michaela; Toegel, Stefan; Schabhüttl, Maria; Weinmann, Daniela; Chiari, Catharina; Bennett, David L. H.; Beetz, Christian; Klein, Dennis; Andersen, Peter M.; Böhme, Ilka; Fink-Puches, Regina; Gonzalez, Michael; Harms, Matthew B.; Motley, William; Reilly, Mary M.; Renner, Wilfried; Rudnik-Schoeneborn, Sabine; Schlotter-Weigel, Beate; Themistocleous, Andreas C.; Weishaupt, Jochen H.; Ludolph, Albert C.; Wieland, Thomas; Tao, Feifei; Abreu, Lisa; Windhager, Reinhard; Zitzelsberger, Manuela; Strom, Tim M.; Walther, Thomas; Scherer, Steven S.; Züchner, Stephan; Martini, Rudolf und Senderek, Jan
(2016):
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.
In: American Journal of Human Genetics, Bd. 99, Nr. 3: S. 607-623