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Anzahl der Publikationen: 6
Zeitschriftenartikel
Ullrich Gavilanes, Emily M. 
ORCID: https://orcid.org/0009-0009-9811-1019; Bartos, Laura M. ORCID: https://orcid.org/0009-0007-6158-319X; Gernert, Jonathan A. ORCID: https://orcid.org/0000-0002-6655-5557; Carral, Carla Ares ORCID: https://orcid.org/0009-0007-9605-4992; Ruiz Navarro, Diego ORCID: https://orcid.org/0009-0007-4825-8624; Havla, Joachim ORCID: https://orcid.org/0000-0002-4386-1340; Gerdes, Lisa-Ann ORCID: https://orcid.org/0000-0002-7053-3924; Gnörich, Johannes S. ORCID: https://orcid.org/0000-0003-1554-7765; Kunze, Lea H. ORCID: https://orcid.org/0000-0003-4669-2113; Dorneich, Julia S.; Pakula, Vanessa; Tagnin, Lisa ORCID: https://orcid.org/0009-0000-9116-4497; Zimmermann, Hanna ORCID: https://orcid.org/0000-0002-1476-3477; Seelos, Klaus ORCID: https://orcid.org/0009-0009-0350-1293; Franzmeier, Nicolai ORCID: https://orcid.org/0000-0001-9736-2283; Frontzkowski, Lukas ORCID: https://orcid.org/0000-0001-9321-956X; Pedrosa de Barros, Nuno ORCID: https://orcid.org/0000-0003-2403-6705; Ribbens, Annemie ORCID: https://orcid.org/0000-0002-5732-5389; Zwergal, Rachel Maria ORCID: https://orcid.org/0009-0006-5083-6182; Zwergal, Andreas ORCID: https://orcid.org/0000-0002-3839-8398; Vollmar, Christian ORCID: https://orcid.org/0000-0002-4630-7484; Remi, Jan ORCID: https://orcid.org/0000-0003-1527-9350; Picon, Carmen; Reynolds, Richard ORCID: https://orcid.org/0000-0003-4622-4694; Merkler, Doron ORCID: https://orcid.org/0000-0002-0247-2007; Wattjes, Mike P.; Kümpfel, Tania ORCID: https://orcid.org/0000-0001-7509-5268; Brendel, Matthias ORCID: https://orcid.org/0000-0002-9247-2843 und Kerschensteiner, Martin ORCID: https://orcid.org/0000-0003-4898-9383
(2025):
SV2A-PET imaging uncovers cortical synapse loss in multiple sclerosis.
In: Science Translational Medicine, Bd. 17, Nr. 818, eadt5585
ORCID: https://orcid.org/0009-0009-9811-1019; Bartos, Laura M. ORCID: https://orcid.org/0009-0007-6158-319X; Gernert, Jonathan A. ORCID: https://orcid.org/0000-0002-6655-5557; Carral, Carla Ares ORCID: https://orcid.org/0009-0007-9605-4992; Ruiz Navarro, Diego ORCID: https://orcid.org/0009-0007-4825-8624; Havla, Joachim ORCID: https://orcid.org/0000-0002-4386-1340; Gerdes, Lisa-Ann ORCID: https://orcid.org/0000-0002-7053-3924; Gnörich, Johannes S. ORCID: https://orcid.org/0000-0003-1554-7765; Kunze, Lea H. ORCID: https://orcid.org/0000-0003-4669-2113; Dorneich, Julia S.; Pakula, Vanessa; Tagnin, Lisa ORCID: https://orcid.org/0009-0000-9116-4497; Zimmermann, Hanna ORCID: https://orcid.org/0000-0002-1476-3477; Seelos, Klaus ORCID: https://orcid.org/0009-0009-0350-1293; Franzmeier, Nicolai ORCID: https://orcid.org/0000-0001-9736-2283; Frontzkowski, Lukas ORCID: https://orcid.org/0000-0001-9321-956X; Pedrosa de Barros, Nuno ORCID: https://orcid.org/0000-0003-2403-6705; Ribbens, Annemie ORCID: https://orcid.org/0000-0002-5732-5389; Zwergal, Rachel Maria ORCID: https://orcid.org/0009-0006-5083-6182; Zwergal, Andreas ORCID: https://orcid.org/0000-0002-3839-8398; Vollmar, Christian ORCID: https://orcid.org/0000-0002-4630-7484; Remi, Jan ORCID: https://orcid.org/0000-0003-1527-9350; Picon, Carmen; Reynolds, Richard ORCID: https://orcid.org/0000-0003-4622-4694; Merkler, Doron ORCID: https://orcid.org/0000-0002-0247-2007; Wattjes, Mike P.; Kümpfel, Tania ORCID: https://orcid.org/0000-0001-7509-5268; Brendel, Matthias ORCID: https://orcid.org/0000-0002-9247-2843 und Kerschensteiner, Martin ORCID: https://orcid.org/0000-0003-4898-9383
(2025):
SV2A-PET imaging uncovers cortical synapse loss in multiple sclerosis.
In: Science Translational Medicine, Bd. 17, Nr. 818, eadt5585
Mulazzani, Elisabeth; Wagner, Danny; Havla, Joachim; Schlueter, Miriam; Meinl, Ingrid; Gerdes, Lisa-Ann und Kuempfel, Tania
(2020):
Neurological phenotypes in patients with NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants.
In: Journal of Neuroinflammation, Bd. 17, Nr. 1, 196
[PDF, 1MB]
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]
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]
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]
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]