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Anzahl der Publikationen: 7
Zeitschriftenartikel
Lahrouchi, Najim; Tadros, Rafik; Crotti, Lia; Mizusawa, Yuka; Postema, Pieter G.; Beekman, Leander; Walsh, Roddy; Hasegawa, Kanae; Barc, Julien; Ernsting, Marko; Turkowski, Kari L.; Mazzanti, Andrea; Beckmann, Britt M.; Shimamoto, Keiko; Diamant, Ulla-Britt; Wijeyeratne, Yanushi D.; Kucho, Yu; Robyns, Tomas; Ishikawa, Taisuke; Arbelo, Elena; Christiansen, Michael; Winbo, Annika; Jabbari, Reza; Lubitz, Steven A.; Steinfurt, Johannes; Rudic, Boris; Loeys, Bart; Shoemaker, M. Ben; Weeke, Peter E.; Pfeiffer, Ryan; Davies, Brianna; Andorin, Antoine; Hofman, Nynke; Dagradi, Federica; Pedrazzini, Matteo; Tester, David J.; Bos, J. Martijn; Sarquella-Brugada, Georgia; Campuzano, Oscar; Platonov, Pyotr G.; Stallmeyer, Birgit; Zumhagen, Sven; Nannenberg, Eline A.; Veldink, Jan H.; Berg, Leonard H. van den; Al-Chalabi, Ammar; Shaw, Christopher E.; Shaw, Pamela J.; Morrison, Karen E.; Andersen, Peter M.; Müller-Nurasyid, Martina; Cusi, Daniele; Barlassina, Cristina; Galan, Pilar; Lathrop, Mark; Munter, Markus; Werge, Thomas; Ribases, Marta; Aung, Tin; Khor, Chiea C.; Ozaki, Mineo; Lichtner, Peter; Meitinger, Thomas; Tintelen, J. Peter van; Hoedemaekers, Yvonne; Denjoy, Isabelle; Leenhardt, Antoine; Napolitano, Carlo; Shimizu, Wataru; Schott, Jean-Jacques; Gourraud, Jean-Baptiste; Makiyama, Takeru; Ohno, Seiko; Itoh, Hideki; Krahn, Andrew D.; Antzelevitch, Charles; Roden, Dan M.; Saenen, Johan; Borggrefe, Martin; Odening, Katja E.; Ellinor, Patrick T.; Tfelt-Hansen, Jacob; Skinner, Jonathan R.; Berg, Maarten P. van den; Olesen, Morten Salling; Brugada, Josep; Brugada, Ramon; Makita, Naomasa; Breckpot, Jeroen; Yoshinaga, Masao; Behr, Elijah R.; Rydberg, Annika; Aiba, Takeshi; Kaeaeb, Stefan; Priori, Silvia G.; Guicheney, Pascale; Tan, Hanno L.; Newton-Cheh, Christopher; Ackerman, Michael J.; Schwartz, Peter J.; Schulze-Bahr, Eric; Probst, Vincent; Horie, Minoru; Wilde, Arthur A.; Tanck, Michael W. T. und Bezzina, Connie R.
(2020):
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
In: Circulation, Bd. 142, Nr. 4: S. 324-338
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]
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]
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]
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