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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 13
2022
Monroe, J. Grey; Srikant, Thanvi; Carbonell-Bejerano, Pablo; Becker, Claude; Lensink, Mariele; Exposito-Alonso, Moises; Klein, Marie; Hildebrandt, Julia; Neumann, Manuela; Kliebenstein, Daniel; Weng, Mao-Lun; Imbert, Eric; Agren, Jon; Rutter, Matthew T.; Fenster, Charles B. und Weigel, Detlef
(2022):
Mutation bias reflects natural selection in Arabidopsis thaliana.
In: Nature, Bd. 602, Nr. 7895: S. 101-105
Hopfner, Franziska; Tietz, Anja K.; Ruf, Viktoria C.; Ross, Owen A.; Koga, Shunsuke; Dickson, Dennis; Aguzzi, Adriano; Attems, Johannes; Beach, Thomas; Beller, Allison; Cheshire, William P.; Deerlin, Vivianna van; Desplats, Paula; Deuschl, Guenther; Duyckaerts, Charles; Ellinghaus, David; Evsyukov, Valentin; Flanagan, Margaret Ellen; Franke, Andre; Frosch, Matthew P.; Gearing, Marla; Gelpi, Ellen; Gerpen, Jay A. van; Ghetti, Bernardino; Glass, Jonathan D.; Grinberg, Lea T.; Halliday, Glenda; Helbig, Ingo; Hollerhage, Matthias; Huitinga, Inge; Irwin, David John; Keene, Dirk C.; Kovacs, Gabor G.; Lee, Edward B.; Levin, Johannes; Marti, Maria J.; Mackenzie, Ian; McKeith, Ian; Mclean, Catriona; Mollenhauer, Brit; Neumann, Manuela; Newell, Kathy L.; Pantelyat, Alex; Pendziwiat, Manuela; Peters, Annette; Porcel, Laura Molina; Rabano, Alberto; Matej, Radoslav; Rajput, Alex; Rajput, Ali; Reimann, Regina; Scott, William K.; Seeley, William; Selvackadunco, Sashika; Simuni, Tanya; Stadelmann, Christine; Svenningsson, Per; Thomas, Alan; Trenkwalder, Claudia; Troakes, Claire; Trojanowski, John Q.; Uitti, Ryan J.; White, Charles L.; Wszolek, Zbigniew K.; Xie, Tao; Ximelis, Teresa; Yebenes, Justo; Mueller, Ulrich; Schellenberg, Gerard D.; Herms, Jochen; Kuhlenbaumer, Gregor und Hoeglinger, Gunter
(2022):
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy.
In: Movement Disorders, Bd. 37, Nr. 10: S. 2110-2121
[PDF, 2MB]
2021
Liu, Shu; Hossinger, Andre; Heumuller, Stefanie-Elisabeth; Hornberger, Annika; Buravlova, Oleksandra; Konstantoulea, Katerina; Muller, Stephan A.; Paulsen, Lydia; Rousseau, Frederic; Schymkowitz, Joost; Lichtenthaler, Stefan F.; Neumann, Manuela; Denner, Philip und Vorberg, Ina M.
(2021):
Highly efficient intercellular spreading of protein misfolding mediated by viral ligand-receptor interactions.
In: Nature Communications, Bd. 12, Nr. 1, 5739
[PDF, 6MB]
2020
LaClair, Katherine D.; Zhou, Qihui; Michaelsen, Meike; Wefers, Benedikt; Brill, Monika S.; Janjic, Aleksandar; Rathkolb, Birgit; Farny, Daniel; Cygan, Mikolaj; de Angelis, Martin Hrabe; Wurst, Wolfgang; Neumann, Manuela; Enard, Wolfgang; Misgeld, Thomas; Arzberger, Thomas und Edbauer, Dieter
(2020):
Congenic expression of poly-GA but not poly-PR in mice triggers selective neuron loss and interferon responses found in C9orf72 ALS.
In: Acta Neuropathologica, Bd. 140, Nr. 2: S. 121-142
[PDF, 8MB]
2019
Pottier, Cyril; Ren, Yingxue; Perkerson, Ralph B.; Baker, Matt; Jenkins, Gregory D.; Blitterswijk, Marka van; DeJesus-Hernandez, Mariely; van Rooij, Jeroen G. J.; Murray, Melissa E.; Christopher, Elizabeth; McDonnell, Shannon K.; Fogarty, Zachary; Batzler, Anthony; Tian, Shulan; Vicente, Cristina T.; Matchett, Billie; Karydas, Anna M.; Hsiung, Ging-Yuek Robin; Seelaar, Harro; Mol, Merel O.; Finger, Elizabeth C.; Graff, Caroline; Oijerstedt, Linn; Neumann, Manuela; Heutink, Peter; Synofzik, Matthis; Wilke, Carlo; Prudlo, Johannes; Rizzu, Patrizia; Simon-Sanchez, Javier; Edbauer, Dieter; Roeber, Sigrun; Diehl-Schmid, Janine; Evers, Bret M.; King, Andrew; Mesulam, M. Marsel; Weintraub, Sandra; Geula, Changiz; Bieniek, Kevin F.; Petrucelli, Leonard; Ahern, Geoffrey L.; Reiman, Eric M.; Woodruff, Bryan K.; Caselli, Richard J.; Huey, Edward D.; Farlow, Martin R.; Grafman, Jordan; Mead, Simon; Grinberg, Lea T.; Spina, Salvatore; Grossman, Murray; Irwin, David J.; Lee, Edward B.; Suh, EunRan; Snowden, Julie; Mann, David; Ertekin-Taner, Nilufer; Uitti, Ryan J.; Wszolek, Zbigniew K.; Josephs, Keith A.; Parisi, Joseph E.; Knopman, David S.; Petersen, Ronald C.; Hodges, John R.; Piguet, Olivier; Geier, Ethan G.; Yokoyama, Jennifer S.; Rissman, Robert A.; Rogaeva, Ekaterina; Keith, Julia; Zinman, Lorne; Tartaglia, Maria Carmela; Cairns, Nigel J.; Cruchaga, Carlos; Ghetti, Bernardino; Kofler, Julia; Lopez, Oscar L.; Beach, Thomas G.; Arzberger, Thomas; Herms, Jochen; Honig, Lawrence S.; Vonsattel, Jean Paul; Halliday, Glenda M.; Kwok, John B.; White, Charles L.; Gearing, Marla; Glass, Jonathan; Rollinson, Sara; Pickering-Brown, Stuart; Rohrer, Jonathan D.; Trojanowski, John Q.; Van Deerlin, Vivianna; Bigio, Eileen H.; Troakes, Claire; Al-Sarraj, Safa; Asmann, Yan; Miller, Bruce L.; Graff-Radford, Neill R.; Boeve, Bradley F.; Seeley, William W.; Mackenzie, Ian R. A.; van Swieten, John C.; Dickson, Dennis W.; Biernacka, Joanna M. und Rademakers, Rosa
(2019):
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.
In: Acta Neuropathologica, Bd. 137, Nr. 6: S. 879-899
[PDF, 1MB]
2018
Pottier, Cyril; Zhou, Xiaolai; Perkerson, Ralph B. III; Baker, Matt; Jenkins, Gregory D.; Serie, Daniel J.; Ghidoni, Roberta; Benussi, Luisa; Binetti, Giuliano; de Munain, Adolfo Lopez; Zulaica, Miren; Moreno, Fermin; Le Ber, Isabelle; Pasquier, Florence; Hannequin, Didier; Sanchez-Valle, Raquel; Antonell, Anna; Llado, Albert; Parsons, Tammee M.; Finch, Nicole A.; Finger, Elizabeth C.; Lippa, Carol F.; Huey, Edward D.; Neumann, Manuela; Heutink, Peter; Synofzik, Matthis; Wilke, Carlo; Rissman, Robert A.; Slawek, Jaroslaw; Sitek, Emilia; Johannsen, Peter; Nielsen, Jorgen E.; Ren, Yingxue; Blitterswijk, Marka van; DeJesus-Hernandez, Mariely; Christopher, Elizabeth; Murray, Melissa E.; Bieniek, Kevin F.; Evers, Bret M.; Ferrari, Camilla; Rollinson, Sara; Richardson, Anna; Scarpini, Elio; Fumagalli, Giorgio G.; Padovani, Alessandro; Hardy, John; Momeni, Parastoo; Ferrari, Raffaele; Frangipane, Francesca; Maletta, Raffaele; Anfossi, Maria; Gallo, Maura; Petrucelli, Leonard; Suh, EunRan; Lopez, Oscar L.; Wong, Tsz H.; van Rooij, Jeroen G. J.; Seelaar, Harro; Mead, Simon; Caselli, Richard J.; Reiman, Eric M.; Sabbagh, Marwan Noel; Kjolby, Mads; Nykjaer, Anders; Karydas, Anna M.; Boxer, Adam L.; Grinberg, Lea T.; Grafman, Jordan; Spina, Salvatore; Oblak, Adrian; Mesulam, M-Marsel; Weintraub, Sandra; Geula, Changiz; Hodges, John R.; Piguet, Olivier; Brooks, William S.; Irwin, David J.; Trojanowski, John Q.; Lee, Edward B.; Josephs, Keith A.; Parisi, Joseph E.; Ertekin-Taner, Nilufer; Knopman, David S.; Nacmias, Benedetta; Piaceri, Irene; Bagnoli, Silvia; Sorbi, Sandro; Gearing, Marla; Glass, Jonathan; Beach, Thomas G.; Black, Sandra E.; Masellis, Mario; Rogaeva, Ekaterina; Vonsattel, Jean-Paul; Honig, Lawrence S.; Kofler, Julia; Bruni, Amalia C.; Snowden, Julie; Mann, David; Pickering-Brown, Stuart; Diehl-Schmid, Janine; Winkelmann, Juliane; Galimberti, Daniela; Graff, Caroline; Oijerstedt, Linn; Troakes, Claire; Al-Sarraj, Safa; Cruchaga, Carlos; Cairns, Nigel J.; Rohrer, Jonathan D.; Halliday, Glenda M.; Kwok, John B.; Swieten, John C. van; White, Charles L. III; Ghetti, Bernardino; Murell, Jill R.; Mackenzie, Ian R. A.; Hsiung, Ging-Yuek R.; Borroni, Barbara; Rossi, Giacomina; Tagliavini, Fabrizio; Wszolek, Zbigniew K.; Petersen, Ronald C.; Bigio, Eileen H.; Grossman, Murray; Deerlin, Vivianna M. van; Seeley, William W.; Miller, Bruce L.; Graff-Radford, Neill R.; Boeve, Bradley F.; Dickson, Dennis W.; Biernacka, Joanna M. und Rademakers, Rosa
(2018):
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
In: Lancet Neurology, Bd. 17, Nr. 6: S. 548-558
Frick, Petra; Sellier, Chantal; Mackenzie, Ian R. A.; Cheng, Chieh-Yu; Tahraoui-Bories, Julie; Martinat, Cecile; Pasterkamp, R. Jeroen; Prudlo, Johannes; Edbauer, Dieter; Oulad-Abdelghani, Mustapha; Feederle, Regina; Charlet-Berguerand, Nicolas und Neumann, Manuela
(2018):
Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriers.
In: Acta Neuropathologica Communications
6:72
[PDF, 3MB]
2016
Haass, Christian 
ORCID: https://orcid.org/0000-0002-4869-1627 und Neumann, Manuela
(2016):
Frontotemporal dementias: From molecular mechanisms to therapy PREFACE.
In: Journal of Neurochemistry, Bd. 138: S. 3-5
ORCID: https://orcid.org/0000-0002-4869-1627 und Neumann, Manuela
(2016):
Frontotemporal dementias: From molecular mechanisms to therapy PREFACE.
In: Journal of Neurochemistry, Bd. 138: S. 3-5
Suárez-Calvet, Marc; Neumann, Manuela; Arzberger, Thomas; Abou-Ajram, Claudia; Funk, Eva; Hartmann, Hannelore; Edbauer, Dieter; Kremmer, Elisabeth; Göbl, Christoph; Resch, Moritz; Bourgeois, Benjamin; Madl, Tobias; Reber, Stefan; Jutzi, Daniel; Ruepp, Marc-David; Mackenzie, Ian R. A.; Ansorge, Olaf; Dormann, Dorothee und Haass, Christian ORCID: https://orcid.org/0000-0002-4869-1627
(2016):
Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUS.
In: Acta Neuropathologica, Bd. 131, Nr. 4: S. 587-604
ORCID: https://orcid.org/0000-0002-4869-1627
(2016):
Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUS.
In: Acta Neuropathologica, Bd. 131, Nr. 4: S. 587-604
2013
Kragh, Christine L.; Fillon, Gwenaëlle; Gysbers, Amanda; Hansen, Hanne D.; Neumann, Manuela; Richter-Landsberg, Christiane; Haass, Christian ORCID: https://orcid.org/0000-0002-4869-1627; Zalc, Bernard; Lubetzki, Catherine; Gai, Wei-Ping; Halliday, Glenda M.; Kahle, Philipp J. und Jensen, Poul H.
(2013):
FAS-dependent cell death in α-synuclein transgenic oligodendrocyte models of multiple system atrophy.
In: PLOS ONE 8(1), e55243 [PDF, 849kB]
ORCID: https://orcid.org/0000-0002-4869-1627; Zalc, Bernard; Lubetzki, Catherine; Gai, Wei-Ping; Halliday, Glenda M.; Kahle, Philipp J. und Jensen, Poul H.
(2013):
FAS-dependent cell death in α-synuclein transgenic oligodendrocyte models of multiple system atrophy.
In: PLOS ONE 8(1), e55243 [PDF, 849kB]
2012
Jesse, Sarah; Lehnert, Stefan; Jahn, Olaf; Parnetti, Lucilla; Soininen, Hilkka; Herukka, Sanna-Kaisa; Steinacker, Petra; Tawfik, Saskia; Tumani, Hayrettin; Arnim, Christine A. F. von; Neumann, Manuela; Kretzschmar, Hans A.; Kulaksiz, Hasan; Lenter, Martin; Wiltfang, Jens; Ferger, Boris; Hengerer, Bastian und Otto, Markus
(2012):
Differential sialylation of serpin A1 in the early diagnosis of Parkinson's disease dementia.
In: PLOS ONE 7(11), e48783 [PDF, 775kB]
In: PLOS ONE 7(11), e48783 [PDF, 775kB]
2009
Wüllner, U.; Schmitt, I.; Kammal, M.; Kretzschmar, Hans A. und Neumann, Manuela
(2009):
Definite multiple system atrophy in a German family.
In: Journal of Neurology, Neurosurgery & Psychiatry, Bd. 80, Nr. 4: S. 449-450
[PDF, 636kB]
2005
Mollenhauer, Brit; Cepek, Lukas; Bibl, Mirko; Wiltfang, Jens; Schulz-Schaeffer, Walter J.; Ciesielczyk, Barbara; Neumann, Manuela; Steinacker, Petra; Kretzschmar, Hans A.; Poser, Sigrid; Trenkwalder, Claudia und Otto, Markus
(2005):
Tau protein, A beta 42 and S-100B protein in cerebrospinal fluid of patients with dementia with Lewy bodies.
In: Dementia and Geriatric Cognitive Disorders, Nr. 2-3: S. 164-170
[PDF, 111kB]