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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Springe zu: 2025 | 2024 | 2020 | 2016 | 2015 | 2013 | 2012
Anzahl der Publikationen: 9

2025

Fissolo, Nicolás; Schaedelin, Sabine; Villar, Luisa M.; Lünemann, Jan D.; Correale, Jorge; Rejdak, Konrad; Schwab, Nicholas; Vilaseca, Andreu; Held, Friederike; García-Merino, Antonio; Bittner, Stefan; Trojano, María; Furlan, Roberto; Tumani, Hayrettin; Pérez-Miralles, Francisco; Rosenstein, Igal; Galimberti, Daniela; Álvarez-Bravo, Gary; Thouvenot, Eric; Llufriu, Sara; Khoury, Samia J.; Hoepner, Robert; Martínez-Yélamos, Sergio; Hegen, Harald; Drulovic, Jelena; Téllez-Lara, Neus; Khalil, Michael; Oechtering, Johanna; Pérez-Sempere, Ángel; Rodríguez-Antigüedad, Alfredo; Enrique-Martínez, José; Strijbis, Eva; Killestein, Joep; Eichau, Sara; Colombo, Elena; Schaller-Nagengast, Jonas; Midaglia, Luciana; Sánchez-López, Antonio J.; Monreal, Enric; Chan, Andrew; Paul, Friedemann; Rovira, Àlex; Tintoré, Mar; Lycke, Jan; Zipp, Frauke; Hemmer, Bernhard; Kuhle, Jens; Montalban, Xavier und Comabella, Manuel (2025): Prognostic Factors for Multiple Sclerosis Symptoms in Radiologically Isolated Syndrome. In: JAMA Neurology, Bd. 82, Nr. 7, 722

Abdelhak, Ahmed ORCID logoORCID: https://orcid.org/0000-0001-9731-4169; Bachhuber, Franziska; Ning, Kiarra; Benkert, Pascal; John Boscardin, W; Maleska Maceski, Aleksandra; Schaedelin, Sabine; Achtnichts, Lutz; Finkener, Sebastian; Lalive, Patrice H; Uginet, Marjolaine; Pot, Caroline; Du Pasquier, Renaud; Hoepner, Robert ORCID logoORCID: https://orcid.org/0000-0002-0115-7021; Chan, Andrew; Gobbi, Claudio; Zecca, Chiara ORCID logoORCID: https://orcid.org/0000-0002-9990-3431; Müller, Stefanie; Roth, Patrick; Granziera, Cristina ORCID logoORCID: https://orcid.org/0000-0002-4917-8761; Chitnis, Tanuja; Madill, Evan; Weiner, Howard L; Green, Ari J; Hauser, Stephen L; Cree, Bruce AC; Kümpfel, Tania ORCID logoORCID: https://orcid.org/0000-0001-7509-5268; Havla, Joachim ORCID logoORCID: https://orcid.org/0000-0002-4386-1340; Skripuletz, Thomas ORCID logoORCID: https://orcid.org/0000-0001-8550-335X; Gingele, Stefan ORCID logoORCID: https://orcid.org/0000-0002-6055-5695; Senel, Makbule ORCID logoORCID: https://orcid.org/0000-0002-2737-7495; Vardakas, Ioannis; Taranu, Daniela; Ziemann, Ulf; Kowarik, Markus C; Kleiter, Ingo ORCID logoORCID: https://orcid.org/0000-0002-8249-4408; Hoshi, Muna-Miriam; Zettl, Uwe K; Haarmann, Axel; Thebault, Simon; Freedman, Mark S ORCID logoORCID: https://orcid.org/0000-0003-1255-9701; Bergman, Hailey P; Iacobaeus, Ellen; Khademi, Mohsen; Ferraro, Diana ORCID logoORCID: https://orcid.org/0000-0003-4818-3806; Cardi, Martina; Mariotto, Sara ORCID logoORCID: https://orcid.org/0000-0002-7806-3103; Comabella, Manuel ORCID logoORCID: https://orcid.org/0000-0002-2373-6657; Montalban, Xavier; Vilaseca-Jolonch, Andreu; Strijbis, Eva M ORCID logoORCID: https://orcid.org/0000-0001-6705-5864; Wessels, Mark HJ ORCID logoORCID: https://orcid.org/0000-0003-2324-0499; Killestein, Joep; Hemmer, Bernhard ORCID logoORCID: https://orcid.org/0000-0001-5985-6784; Held, Friederike; Sellebjerg, Finn ORCID logoORCID: https://orcid.org/0000-0002-1333-9623; Højsgaard Chow, Helene ORCID logoORCID: https://orcid.org/0000-0003-2032-2755; Alvarez-Lafuente, Roberto ORCID logoORCID: https://orcid.org/0000-0002-3132-1486; Domínguez-Mozo, Maria Inmaculada; Hegen, Harald ORCID logoORCID: https://orcid.org/0000-0002-2833-6337; Berek, Klaus; Deisenhammer, Florian ORCID logoORCID: https://orcid.org/0000-0003-4541-8841; Thouvenot, Eric; Agherbi, Hanane; Rejdak, Konrad; Gąsior, Magda; Tzanetakos, Dimitrios; Tzartos, John S; Sormani, Maria Pia ORCID logoORCID: https://orcid.org/0000-0001-6892-104X; Dujmovic Basuroski, Irena; Arrambide, Georgina ORCID logoORCID: https://orcid.org/0000-0002-2657-5510; Khalil, Michael ORCID logoORCID: https://orcid.org/0000-0002-5350-3328; Piehl, Fredrik ORCID logoORCID: https://orcid.org/0000-0001-8329-5219; Teunissen, Charlotte E; Kuhle, Jens ORCID logoORCID: https://orcid.org/0000-0002-6963-8892 und Tumani, Hayrettin ORCID logoORCID: https://orcid.org/0000-0002-1647-6201 (2025): Blood biomarkers for predicting disability worsening in progressive multiple sclerosis: a multinational, individual participant-level analysis. In: Journal of Neurology, Neurosurgery & Psychiatry, Bd. 96, Nr. 11: S. 1046-1052

2024

Perneczky, Robert; Dom, Geert; Chan, Andrew; Falkai, Peter und Bassetti, Claudio (2024): Anti-amyloid antibody treatments for Alzheimer's disease. In: European Journal of Neurology, Bd. 31, Nr. 2 [PDF, 793kB]

2020

Gomez-Fernandez, Paloma; de Lapuente Portilla, Aitzkoa Lopez; Astobiza, Ianire; Mena, Jorge; Urtasun, Andoni; Altmann, Vivian; Matesanz, Fuencisla; Otaegui, David; Urcelay, Elena; Antiguedad, Alfredo; Malhotra, Sunny; Montalban, Xavier; Castillo-Trivino, Tamara; Espino-Paisan, Laura; Aktas, Orhan; Buttmann, Mathias; Chan, Andrew; Fontaine, Bertrand; Gourraud, Pierre-Antoine; Hecker, Michael; Hoffjan, Sabine; Kubisch, Christian; Kuempfel, Tania; Luessi, Felix; Zettl, Uwe K.; Zipp, Frauke; Alloza, Iraide; Comabella, Manuel; Lill, Christina M. und Vandenbroeck, Koen (2020): The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1,-2 and-3 and Is Associated with Risk for Multiple Sclerosis. In: Cells, Bd. 9, Nr. 1, 175

2016

Sadovnick, A. Dessa; Traboulsee, Anthony L.; Bernales, Cecily Q.; Ross, Jay P.; Forwell, Amanda L.; Yee, Irene M.; Guillot-Noel, Lena; Fontaine, Bertrand; Cournu-Rebeix, Isabelle; Alcina, Antonio; Fedetz, Maria; Izquierdo, Guillermo; Matesanz, Fuencisla; Hilven, Kelly; Dubois, Benedicte; Goris, An; Astobiza, Ianire; Alloza, Iraide; Antigüedad, Alfredo; Vandenbroeck, Koen; Akkad, Denis A.; Aktas, Orhan; Blaschke, Paul; Buttmann, Mathias; Chan, Andrew; Epplen, Joerg T.; Gerdes, Lisa-Ann; Kroner, Antje; Kubisch, Christian; Kümpfel, Tania; Lohse, Peter; Rieckmann, Peter; Zettl, Uwe K.; Zipp, Frauke; Bertram, Lars; Lill, Christina M.; Fernandez, Oscar; Urbaneja, Patricia; Leyva, Laura; Carlos Alvarez-Cermeno, Jose; Arroyo, Rafael; Garagorri, Aroa M.; Garcia-Martinez, Angel; Villar, Luisa M.; Urcelay, Elena; Malhotra, Sunny; Montalban, Xavier; Comabella, Manuel; Berger, Thomas; Fazekas, Franz; Reindl, Markus; Schmied, Mascha C.; Zimprich, Alexander und Vilarino-Güell, Carles (2016): Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients. In: G3 - Genes Genomes Genetics, Bd. 6, Nr. 7: S. 2073-2079 [PDF, 1MB]

Andlauer, Till F. M.; Buck, Dorothea; Antony, Gisela; Bayas, Antonios; Bechmann, Lukas; Berthele, Achim; Chan, Andrew; Gasperi, Christiane; Gold, Ralf; Graetz, Christiane; Haas, Jürgen; Hecker, Michael; Infante-Duarte, Carmen; Knop, Matthias; Kümpfel, Tania; Limmroth, Volker; Linker, Ralf A.; Loleit, Verena; Luessi, Felix; Meuth, Sven G.; Mühlau, Mark; Nischwitz, Sandra; Paul, Friedemann; Pütz, Michael; Ruck, Tobias; Salmen, Anke; Stangel, Martin; Stellmann, Jan-Patrick; Stürner, Klarissa H.; Tackenberg, Björn; Bergh, Florian Then; Tumani, Hayrettin; Warnke, Clemens; Weber, Frank; Wiendl, Heinz; Wildemann, Brigitte; Zettl, Uwe K.; Ziemann, Ulf; Zipp, Frauke; Arloth, Janine; Weber, Peter; Radivojkov-Blagojevic, Milena; Scheinhardt, Markus O.; Dankowski, Theresa; Bettecken, Thomas; Lichtner, Peter; Czamara, Darina; Carrillo-Roa, Tania; Binder, Elisabeth B.; Berger, Klaus; Bertram, Lars; Franke, Andre; Gieger, Christian; Herms, Stefan; Homuth, Georg; Ising, Marcus; Jöckel, Karl-Heinz; Kacprowski, Tim; Kloiber, Stefan; Laudes, Matthias; Lieb, Wolfgang; Lill, Christina M.; Lucae, Susanne; Meitinger, Thomas; Moebus, Susanne; Müller-Nurasyid, Martina; Nöthen, Markus M.; Petersmann, Astrid; Rawal, Rajesh; Schminke, Ulf; Strauch, Konstantin; Völzke, Henry; Waldenberger, Melanie; Wellmann, Jürgen; Porcu, Eleonora; Mulas, Antonella; Pitzalis, Maristella; Sidore, Carlo; Zara, Ilenia; Cucca, Francesco; Zoledziewska, Magdalena; Ziegler, Andreas; Hemmer, Bernhard und Müller-Myhsok, Bertram (2016): Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. In: Science Advances, Bd. 2, Nr. 6, e1501678 [PDF, 678kB]

2015

Lill, Christina M.; Luessi, Felix; Alcina, Antonio; Sokolova, Ekaterina A.; Ugidos, Nerea; La Hera, Belen de; Guillot-Noel, Lena; Malhotra, Sunny; Reinthaler, Eva; Schjeide, Brit-Maren M.; Mescheriakova, Julia Y.; Mashychev, Andriy; Wohlers, Inken; Akkad, Denis A.; Aktas, Orhan; Alloza, Iraide; Antigüedad, Alfredo; Arroyo, Rafa; Astobiza, Ianire; Blaschke, Paul; Boyko, Alexei N.; Buttmann, Mathias; Chan, Andrew; Dörner, Thomas; Epplen, Joerg T.; Favorova, Olga O.; Fedetz, Maria; Fernandez, Oscar; Garcia-Martinez, Angel; Gerdes, Lisa-Ann; Graetz, Christiane; Hartung, Hans-Peter; Hoffjan, Sabine; Izquierdo, Guillermo; Korobko, Denis S.; Kroner, Antje; Kubisch, Christian; Kümpfel, Tania; Leyva, Laura; Lohse, Peter; Malkova, Nadezhda A.; Montalban, Xavier; Popova, Ekaterina V.; Rieckmann, Peter; Rozhdestvenskii, Alexei S.; Schmied, Christiane; Smagina, Inna V.; Tsareva, Ekaterina Y.; Winkelmann, Alexander; Zettl, Uwe K.; Binder, Harald; Cournu-Rebeix, Isabelle; Hintzen, Rogier; Zimprich, Alexander; Comabella, Manuel; Fontaine, Bertrand; Urcelay, Elena; Vandenbroeck, Koen; Filipenko, Maxim; Matesanz, Fuencisla; Zipp, Frauke und Bertram, Lars (2015): Genome-wide significant association with seven novel multiple sclerosis risk loci. In: Journal of medical genetics, Bd. 52, Nr. 12: S. 848-855 [PDF, 524kB]

2013

Lill, Christina M.; Schjeide, Brit-Maren M.; Graetz, Christiane; Liu, Tian; Damotte, Vincent; Akkad, Denis A.; Blaschke, Paul; Gerdes, Lisa-Ann; Kroner, Antje; Luessi, Felix; Cournu-Rebeix, Isabelle; Hoffjan, Sabine; Winkelmann, Alexander; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Otaegui, David; Antigueedad, Alfredo; Alcina, Antonio; Comabella, Manuel; Montalban, Xavier; Olascoaga, Javier; Matesanz, Fuencisla; Dörner, Thomas; Li, Shu-Chen; Steinhagen-Thiessen, Elisabeth; Lindenberger, Ulman; Chan, Andrew; Rieckmann, Peter; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Buttmann, Mathias; Kümpfel, Tania; Kubisch, Christian; Zettl, Uwe K.; Epplen, Joerg T.; Fontaine, Bertrand; Zipp, Frauke; Vandenbroeck, Koen und Bertram, Lars (März 2013): Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. In: Journal of Medical Genetics, Bd. 50, Nr. 3: S. 140-143 [PDF, 127kB]

2012

Lill, Christina M.; Liu, Tian; Schjeide, Brit-Maren M.; Roehr, Johannes T.; Akkad, Denis A.; Damotte, Vincent; Alcina, Antonio; Ortiz, Miguel A.; Arroyo, Rafa; Lopez de Lapuente, Aitzkoa; Blaschke, Paul; Winkelmann, Alexander; Gerdes, Lisa-Ann; Luessi, Felix; Fernadez, Oscar; Izquierdo, Guillermo; Antigüedad, Alfredo; Hoffjan, Sabine; Cournu-Rebeix, Isabelle; Gromöller, Silvana; Faber, Hans; Liebsch, Maria; Meissner, Esther; Chanvillard, Coralie; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Dörner, Thomas; Steinhagen-Thiessen, Elisabeth; Baeckman, Lars; Heekeren, Hauke R.; Li, Shu-Chen; Lindenberger, Ulman; Chan, Andrew; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Kümpfel, Tania; Kubisch, Christian; Epplen, Jörg T.; Zettl, Uwe K.; Fontaine, Bertrand; Vandenbroeck, Koen; Matesanz, Fuencisla; Urcelay, Elena; Bertram, Lars und Zipp, Frauke (September 2012): Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. In: Journal of medical genetics, Bd. 49, Nr. 9: S. 558-562 [PDF, 217kB]

Diese Liste wurde am Sat Nov 22 23:24:20 2025 CET erstellt.