Auflistung Universitätsbibliographie nach Autor "Gasser, Thomas"

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Auflistung Universitätsbibliographie nach Autor "Gasser, Thomas"

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  • A genome-wide association study in multiple system atrophy
    Sailer, Anna; Scholz, Sonja W.; Nalls, Michael A.; Schulte, Claudia; Federoff, Monica; Price, T. Ryan; Lees, Andrew; Ross, Owen A.; Dickson, Dennis W.; Mok, Kin; Mencacci, Niccolo E.; Schottlaender, Lucia; Chelban, Viorica; Ling, Helen; O'Sullivan, Sean S.; Wood, Nicholas W.; Traynor, Bryan J.; Ferrucci, Luigi; Federoff, Howard J.; Mhyre, Timothy R.; Morris, Huw R.; Deuschl, Gunther; Quinn, Niall; Widner, Hakan; Albanese, Alberto; Infante, Jon; Bhatia, Kailash P.; Poewe, Werner; Oertel, Wolfgang; Hoglinger, Gunter U.; Wullner, Ullrich; Goldwurm, Stefano; Pellecchia, Maria Teresa; Ferreira, Joaquim; Tolosa, Eduardo; Bloem, Bastiaan R.; Rascol, Olivier; Meissner, Wassilios G.; Hardy, John A.; Revesz, Tamas; Holton, Janice L.; Gasser, Thomas; Wenning, Gregor K.; Singleton, Andrew B.; Houlden, Henry (2016)
  • A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia
    Mencacci, Niccolo E.; Rubio-Agusti, Ignacio; Zdebik, Anselm; Asmus, Friedrich; Ludtmann, Marthe H. R.; Ryten, Mina; Plagnol, Vincent; Hauser, Ann-Kathrin; Bandres-Ciga, Sara; Bettencourt, Conceicao; Forabosco, Paola; Hughes, Deborah; Soutar, Marc M. P.; Peall, Kathryn; Morris, Huw R.; Trabzuni, Daniah; Tekman, Mehmet; Stanescu, Horia C.; Kleta, Robert; Carecchio, Miryam; Zorzi, Giovanna; Nardocci, Nardo; Garavaglia, Barbara; Lohmann, Ebba; Weissbach, Anne; Klein, Christine; Hardy, John; Pittman, Alan M.; Foltynie, Thomas; Abramov, Andrey Y.; Gasser, Thomas; Bhatia, Kailash P.; Wood, Nicholas W. (2015)
  • A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
    Sharma, Manu; Ioannidis, John P. A.; Aasly, Jan O.; Annesi, Grazia; Brice, Alexis; Bertram, Lars; Bozi, Maria; Barcikowska, Maria; Crosiers, David; Clarke, Carl E.; Facheris, Maurizio F.; Farrer, Matthew; Garraux, Gaetan; Gispert, Suzana; Auburger, Georg; Vilarino-Guell, Carles; Hadjigeorgiou, Georgios M.; Hicks, Andrew A.; Hattori, Nobutaka; Jeon, Beom S.; Jamrozik, Zygmunt; Krygowska-Wajs, Anna; Lesage, Suzanne; Lill, Christina M.; Lin, Juei-Jueng; Lynch, Timothy; Lichtner, Peter; Lang, Anthony E.; Libioulle, Cecile; Murata, Miho; Mok, Vincent; Jasinska-Myga, Barbara; Mellick, George D.; Morrison, Karen E.; Meitnger, Thomas; Zimprich, Alexander; Opala, Grzegorz; Pramstaller, Peter P.; Pichler, Irene; Park, Sung Sup; Quattrone, Aldo; Rogaeva, Ekaterina; Ross, Owen A.; Stefanis, Leonidas; Stockton, Joanne D.; Satake, Wataru; Silburn, Peter A.; Strom, Tim M.; Theuns, Jessie; Tan, Eng-King; Toda, Tatsushi; Tomiyama, Hiroyuki; Uitti, Ryan J.; Van Broeckhoven, Christine; Wirdefeldt, Karin; Wszolek, Zbigniew; Xiromerisiou, Georgia; Yomono, Harumi S.; Yueh, Kuo-Chu; Zhao, Yi; Gasser, Thomas; Maraganore, Demetrius; Krueger, Rejko (2012)
  • A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies
    Nalls, Michael A.; Duran, Raquel; Lopez, Grisel; Kurzawa-Akanbi, Marzena; McKeith, Ian G.; Chinnery, Patrick F.; Morris, Christopher M.; Theuns, Jessie; Crosiers, David; Cras, Patrick; Engelborghs, Sebastiaan; De Deyn, Peter Paul; Van Broeckhoven, Christine; Mann, David M. A.; Snowden, Julie; Pickering-Brown, Stuart; Halliwell, Nicola; Davidson, Yvonne; Gibbons, Linda; Harris, Jenny; Sheerin, Una-Marie; Bras, Jose; Hardy, John; Clark, Lorraine; Marder, Karen; Honig, Lawrence S.; Berg, Daniela; Maetzler, Walter; Brockmann, Kathrin; Gasser, Thomas; Novellino, Fabiana; Quattrone, Aldo; Annesi, Grazia; De Marco, Elvira Valeria; Rogaeva, Ekaterina; Masellis, Mario; Black, Sandra E.; Bilbao, Juan M.; Foroud, Tatiana; Ghetti, Bernardino; Nichols, William C.; Pankratz, Nathan; Halliday, Glenda; Lesage, Suzanne; Klebe, Stephan; Durr, Alexandra; Duyckaerts, Charles; Brice, Alexis; Giasson, Benoit I.; Trojanowski, John Q.; Hurtig, Howard I.; Tayebi, Nahid; Landazabal, Claudia; Knight, Melanie A.; Keller, Margaux; Singleton, Andrew B.; Wolfsberg, Tyra G.; Sidransky, Ellen (2013)
  • A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
    van der Lee, Sven J.; Conway, Olivia J.; Jansen, Iris; Carrasquillo, Minerva M.; Kleineidam, Luca; van den Akker, Erik; Hernandez, Isabel; van Eijk, Kristel R.; Stringa, Najada; Chen, Jason A.; Zettergren, Anna; Andlauer, Till F. M.; Diez-Fairen, Monica; Simon-Sanchez, Javier; Lleo, Alberto; Zetterberg, Henrik; Nygaard, Marianne; Blauwendraat, Cornelis; Savage, Jeanne E.; Mengel-From, Jonas; Moreno-Grau, Sonia; Wagner, Michael; Fortea, Juan; Keogh, Michael J.; Blennow, Kaj; Skoog, Ingmar; Friese, Manuel A.; Pletnikova, Olga; Zulaica, Miren; Lage, Carmen; de Rojas, Itziar; Riedel-Heller, Steffi; Illan-Gala, Ignacio; Wei, Wei; Jeune, Bernard; Orellana, Adelina; Bergh, Florian Then; Wang, Xue; Hulsman, Marc; Beker, Nina; Tesi, Niccolo; Morris, Christopher M.; Indakoetxea, Begona; Collij, Lyduine E.; Scherer, Martin; Morenas-Rodriguez, Estrella; Ironside, James W.; van Berckel, Bart N. M.; Alcolea, Daniel; Wiendl, Heinz; Strickland, Samantha L.; Pastor, Pau; Rodriguez Rodriguez, Eloy; Boeve, Bradley F.; Petersen, Ronald C.; Ferman, Tanis J.; van Gerpen, Jay A.; Reinders, Marcel J. T.; Uitti, Ryan J.; Tarraga, Lluis; Maier, Wolfgang; Dols-Icardo, Oriol; Kawalia, Amit; Dalmasso, Maria Carolina; Boada, Merce; Zettl, Uwe K.; van Schoor, Natasja M.; Beekman, Marian; Allen, Mariet; Masliah, Eliezer; Lopez de Munain, Adolfo; Pantelyat, Alexander; Wszolek, Zbigniew K.; Ross, Owen A.; Dickson, Dennis W.; Graff-Radford, Neill R.; Knopman, David; Rademakers, Rosa; Lemstra, Afina W.; Pijnenburg, Yolande A. L.; Scheltens, Philip; Gasser, Thomas; Chinnery, Patrick F.; Hemmer, Bernhard; Huisman, Martijn A.; Troncoso, Juan; Moreno, Fermin; Nohr, Ellen A.; Sorensen, Thorkild I. A.; Heutink, Peter; Sanchez-Juan, Pascual; Posthuma, Danielle; Clarimon, Jordi; Christensen, Kaare; Ertekin-Taner, Nilufer; Scholz, Sonja W.; Ramirez, Alfredo; Ruiz, Agustin; Slagboom, Eline; van der Flier, Wiesje M.; Holstege, Henne (2019)
  • A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family
    Hanagasi, Hasmet A.; Giri, Anamika; Kartal, Ece; Guven, Gamze; Bilgic, Basar; Hauser, Ann-Kathrin; Emre, Murat; Heutink, Peter; Basak, Nazh; Gasser, Thomas; Simon-Sanchez, Javier; Lohmann, Ebba (2016)
  • A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritance
    Engeholm, Maik; Sekler, Julia; Schoendorf, David C.; Arora, Vineet; Schittenhelm, Jens; Biskup, Saskia; Schell, Caroline; Gasser, Thomas (2014)
  • A Novel SNCA A30G Mutation Causes Familial Parkinson's Disease
    Liu, Hui; Koros, Christos; Strohaeker, Timo; Schulte, Claudia; Bozi, Maria; Varvaresos, Stefanos; Ibanez de Opakua, Alain; Simitsi, Athina Maria; Bougea, Anastasia; Voumvourakis, Konstantinos; Maniati, Matina; Papageorgiou, Sokratis G.; Hauser, Ann-Kathrin; Becker, Stefan; Zweckstetter, Markus; Stefanis, Leonidas; Gasser, Thomas (2021)
  • A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinsons disease
    Holmans, Peter; Moskvina, Valentina; Jones, Lesley; Sharma, Manu; Vedernikov, Alexey; Buchel, Finja; Sadd, Mohamad; Bras, Jose M.; Bettella, Francesco; Nicolaou, Nayia; Simon-Sanchez, Javier; Mittag, Florian; Gibbs, J. Raphael; Schulte, Claudia; Durr, Alexandra; Guerreiro, Rita; Hernandez, Dena; Brice, Alexis; Stefansson, Hreinn; Majamaa, Kari; Gasser, Thomas; Heutink, Peter; Wood, Nicholas W.; Martinez, Maria; Singleton, Andrew B.; Nalls, Michael A.; Hardy, John; Morris, Huw R.; Williams, Nigel M. (2013)
  • A patient-based model of RNA mis-splicing uncovers treatment targets in Parkinson's disease
    Boussaad, Ibrahim; Obermaier, Carolin D.; Hanss, Zoe; Bobbili, Dheeraj R.; Bolognin, Silvia; Glaab, Enrico; Wolynska, Katarzyna; Weisschuh, Nicole; De Conti, Laura; May, Caroline; Giesert, Florian; Grossmann, Dajana; Lambert, Annika; Kirchen, Susanne; Biryukov, Maria; Burbulla, Lena F.; Massart, Francois; Bohler, Jill; Cruciani, Gerald; Schmid, Benjamin; Kurz-Drexler, Annerose; May, Patrick; Duga, Stefano; Klein, Christine; Schwamborn, Jens C.; Marcus, Katrin; Woitalla, Dirk; Weisenhorn, Daniela M. Vogt; Wurst, Wolfgang; Baralle, Marco; Krainc, Dimitri; Gasser, Thomas; Wissinger, Bernd; Krueger, Rejko (2020)
  • Abolishing the 1-year rule: How much evidence will be enough?
    Postuma, Ronald B.; Berg, Daniela; Stern, Matthew; Poewe, Werner; Olanow, C. Warren; Oertel, Wolfgang; Marek, Kenneth; Litvan, Irene; Lang, Anthony E.; Halliday, Glenda; Goetz, Christopher G.; Gasser, Thomas; Dubois, Bruno; Chan, Piu; Bloem, Bastiaan R.; Adler, Charles H.; Deuschl, Guenther (2016)
  • Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
    Lubbe, Steven J.; Escott-Price, Valentina; Gibbs, J. Raphael; Nalls, Mike A.; Bras, Jose; Price, T. Ryan; Nicolas, Aude; Jansen, Iris E.; Mok, Kin Y.; Pittman, Alan M.; Tomkins, James E.; Lewis, Patrick A.; Noyce, Alastair J.; Lesage, Suzanne; Sharma, Manu; Schiff, Elena R.; Levine, Adam P.; Brice, Alexis; Gasser, Thomas; Hardy, John; Heutink, Peter; Wood, NicholasW.; Singleton, Andrew B.; Williams, Nigel M.; Morris, Huw R. (2016)
  • Alpha-synuclein gene variants may predict neurostimulation outcome
    Weiss, Daniel; Herrmann, Sonja; Wang, Lisa; Schulte, Claudia; Brockmann, Kathrin; Plewina, Christian; Gasser, Thomas; Sharma, Manu; Gharabaghi, Alireza; Krüger, Rejko (2016)
  • Alpha-synuclein research: defining strategic moves in the battle against Parkinson's disease
    Oliveira, Luis M. A.; Gasser, Thomas; Edwards, Robert; Zweckstetter, Markus; Melki, Ronald; Stefanis, Leonidas; Lashuel, Hilal A.; Sulzer, David; Vekrellis, Kostas; Halliday, Glenda M.; Tomlinson, Julianna J.; Schlossmacher, Michael; Jensen, Poul Henning; Schulze-Hentrich, Julia; Riess, Olaf; Hirst, Warren D.; El-Agnaf, Omar; Mollenhauer, Brit; Lansbury, Peter; Outeiro, Tiago F. (2021)
  • Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease
    Brown, Emmeline E.; Blauwendraat, Cornelis; Trinh, Joanne; Rizig, Mie; Nalls, Mike A.; Leveille, Etienne; Ruskey, Jennifer A.; Jonvik, Hallgeir; Tan, Manuela M. X.; Bandres-Ciga, Sara; Hassin-Baer, Sharon; Brockmann, Kathrin; Infante, Jon; Tolosa, Eduardo; Ezquerra, Mario; Ben Romdhan, Sawssan; Benmahdjoub, Mustapha; Arezki, Mohamed; Mhiri, Chokri; Hardy, John; Singleton, Andrew B.; Alcalay, Roy N.; Gasser, Thomas; Grosset, Donald G.; Williams, Nigel M.; Pittman, Alan; Gan-Or, Ziv; Fernandez-Santiago, Ruben; Brice, Alexis; Lesage, Suzanne; Farrer, Matthew; Wood, Nicholas; Morris, Huw R. (2021)
  • Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
    Moskvina, Valentina; Harold, Denise; Russo, GianCarlo; Vedemikov, Alexey; Sharma, Manu; Saad, Mohamad; Holmans, Peter; Bras, Jose M.; Bettella, Francesco; Keller, Margaux F.; Nicolaou, Nayia; Simon-Sanchez, Javier; Gibbs, J. Raphael; Schulte, Claudia; Durr, Alexandra; Guerreiro, Rita; Hernandez, Dena; Brice, Alexis; Stefansson, Hreinn; Majamaa, Kari; Gasser, Thomas; Heutink, Peter; Wood, Nick; Martinez, Maria; Singleton, Andrew B.; Nalls, Michael A.; Hardy, John; Owen, Michael J.; O'Donovan, Michael C.; Williams, Julie; Morris, Huw R.; Williams, Nigel M. (2013)
  • Analysis of shared heritability in common disorders of the brain
    Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K.; Walters, Raymond K.; Bras, Jose; Duncan, Laramie; Escott-Price, Valentina; Falcone, Guido J.; Gormley, Padhraig; Malik, Rainer; Patsopoulos, Nikolaos A.; Ripke, Stephan; Wei, Zhi; Yu, Dongmei; Lee, Phil H.; Turley, Patrick; Grenier-Boley, Benjamin; Chouraki, Vincent; Kamatani, Yoichiro; Berr, Claudine; Letenneur, Luc; Hannequin, Didier; Amouyel, Philippe; Boland, Anne; Deleuze, Jean-Francois; Duron, Emmanuelle; Vardarajan, Badri N.; Reitz, Christiane; Goate, Alison M.; Huentelman, Matthew J.; Kamboh, M. Ilyas; Larson, Eric B.; Rogaeva, Ekaterina; St George-Hyslop, Peter; Hakonarson, Hakon; Kukull, Walter A.; Farrer, Lindsay A.; Barnes, Lisa L.; Beach, Thomas G.; Demirci, F. Yesim; Head, Elizabeth; Hulette, Christine M.; Jicha, Gregory A.; Kauwe, John S. K.; Kaye, Jeffrey A.; Leverenz, James B.; Levey, Allan I.; Lieberman, Andrew P.; Pankratz, Vernon S.; Poon, Wayne W.; Quinn, Joseph F.; Saykin, Andrew J.; Schneider, Lon S.; Smith, Amanda G.; Sonnen, Joshua A.; Stern, Robert A.; Van Deerlin, Vivianna M.; Van Eldik, Linda J.; Harold, Denise; Russo, Giancarlo; Rubinsztein, David C.; Bayer, Anthony; Tsolaki, Magda; Proitsi, Petra; Fox, Nick C.; Hampel, Harald; Owen, Michael J.; Mead, Simon; Passmore, Peter; Morgan, Kevin; Noethen, Markus M.; Rossor, Martin; Lupton, Michelle K.; Hoffmann, Per; Kornhuber, Johannes; Lawlor, Brian; McQuillin, Andrew; Al-Chalabi, Ammar; Bis, Joshua C.; Ruiz, Agustin; Boada, Merce; Seshadri, Sudha; Beiser, Alexa; Rice, Kenneth; van der Lee, Sven J.; De Jager, Philip L.; Geschwind, Daniel H.; Riemenschneider, Matthias; Riedel-Heller, Steffi; Rotter, Jerome I.; Ransmayr, Gerhard; Hyman, Bradley T.; Cruchaga, Carlos; Alegret, Montserrat; Winsvold, Bendik; Palta, Priit; Farh, Kai-How; Cuenca-Leon, Ester; Furlotte, Nicholas; Kurth, Tobias; Ligthart, Lannie (2018)
  • Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson's disease and dementia with Lewy bodies
    Brockmann, Kathrin; Quadalti, Corinne; Lerche, Stefanie; Rossi, Marcello; Wurster, Isabel; Baiardi, Simone; Roeben, Benjamin; Mammana, Angela; Zimmermann, Milan; Hauser, Ann-Kathrin; Deuschle, Christian; Schulte, Claudia; Waniek, Katharina; Lachmann, Ingolf; Sjodin, Simon; Brinkmalm, Ann; Blennow, Kaj; Zetterberg, Henrik; Gasser, Thomas; Parchi, Piero (2021)
  • Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia
    Mencacci, Niccolo E.; Brockmann, Marisa M.; Dai, Jinye; Pajusalu, Sander; Atasu, Burcu; Campos, Joaquin; Pino, Gabriela; Gonzalez-Latapi, Paulina; Patzke, Christopher; Schwake, Michael; Tucci, Arianna; Pittman, Alan; Simon-Sanchez, Javier; Carvill, Gemma L.; Balint, Bettina; Wiethoff, Sarah; Warner, Thomas T.; Papandreou, Apostolos; Soo, Audrey; Rein, Reet; Kadastik-Eerme, Liis; Puusepp, Sanna; Reinson, Karit; Tomberg, Tiiu; Hanagasi, Hasmet; Gasser, Thomas; Bhatia, Kailash P.; Kurian, Manju A.; Lohmann, Ebba; Ounap, Katrin; Rosenmund, Christian; Sudhof, Thomas C.; Wood, Nicholas W.; Krainc, Dimitri; Acuna, Claudio (2021)
  • Case Report: Deep brain stimulation improves tremor in FGF-14 associated spinocerebellar ataxia
    Loeffler, Moritz A. A.; Synofzik, Matthis; Cebi, Idil; Klocke, Philipp; Hormozi, Mohammad; Gasser, Thomas; Gharabaghi, Alireza; Weiss, Daniel (2022)