Browsing Universitätsbibliographie by Author "Gasser, Thomas"

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Browsing Universitätsbibliographie by Author "Gasser, Thomas"

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  • LRRK2 functions as a scaffolding kinase of ASK1-mediated neuronal cell death
    Yoon, Ji-Hye; Mo, Jung-Soon; Kim, Mi-Yeon; Ann, Eun-Jung; Ahn, Ji-Seon; Jo, Eun-Hye; Lee, Hye-Jin; Lee, Young Chul; Seol, Wongi; Yarmoluk, Sergiy M.; Gasser, Thomas; Kahle, Philipp J.; Liu, Guang-Hui; Belmonte, Juan Carlos Izpisua; Park, Hee-Sae (2017)
  • LRRK2: Understanding the role of common and rare variants in Parkinson's disease
    Sharma, Manu; Krüger, Rejko; Gasser, Thomas (2012)
  • MAPT p.V363I mutation A rare cause of corticobasal degeneration
    Ahmed, Sarah; Fairen, Monica Diez; Sabir, Marya S.; Pastor, Pau; Ding, Jinhui; Ispierto, Lourdes; Butala, Ankur; Morris, Christopher M.; Schulte, Claudia; Gasser, Thomas; Jabbari, Edwin; Pletnikova, Olga; Morris, Huw R.; Troncoso, Juan; Gelpi, Ellen; Pantelyat, Alexander; Scholz, Sonja W. (2019)
  • MDS clinical diagnostic criteria for Parkinson's disease
    Postuma, Ronald B.; Berg, Daniela; Stern, Matthew; Poewe, Werner; Olanow, C. Warren; Oertel, Wolfgang; Obeso, Jose; 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 (2015)
  • MDS research criteria for prodromal Parkinson's disease
    Berg, Daniela; Postuma, Ronald B.; Adler, Charles H.; Bloem, Bastiaan R.; Chan, Piu; Dubois, Bruno; Gasser, Thomas; Goetz, Christopher G.; Halliday, Glenda; Joseph, Lawrence; Lang, Anthony E.; Liepelt-Scarfone, Inga; Litvan, Irene; Marek, Kenneth; Obeso, Jose; Oertel, Wolfgang; Olanow, C. Warren; Poewe, Werner; Stern, Matthew; Deuschl, Guenther (2015)
  • Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease
    Domenighetti, Cloe; Sugier, Pierre-Emmanuel; Sreelatha, Ashwin Ashok Kumar; Schulte, Claudia; Grover, Sandeep; Mohamed, Oceane; Portugal, Berta; May, Patrick; Bobbili, Dheeraj R.; Radivojkov-Blagojevic, Milena; Lichtner, Peter; Singleton, Andrew B.; Hernandez, Dena G.; Edsall, Connor; Mellick, George D.; Zimprich, Alexander; Pirker, Walter; Rogaeva, Ekaterina; Lang, Anthony E.; Koks, Sulev; Taba, Pille; Lesage, Suzanne; Brice, Alexis; Corvol, Jean-Christophe; Chartier-Harlin, Marie-Christine; Mutez, Eugenie; Brockmann, Kathrin; Deutschlaender, Angela B.; Hadjigeorgiou, Georges M.; Dardiotis, Efthimos; Stefanis, Leonidas; Simitsi, Athina Maria; Valente, Enza Maria; Petrucci, Simona; Duga, Stefano; Straniero, Letizia; Zecchinelli, Anna; Pezzoli, Gianni; Brighina, Laura; Ferrarese, Carlo; Annesi, Grazia; Quattrone, Andrea; Gagliardi, Monica; Matsuo, Hirotaka; Kawamura, Yusuke; Hattori, Nobutaka; Nishioka, Kenya; Chung, Sun Ju; Kim, Yun Joong; Kolber, Pierre; van de Warrenburg, Bart Pc; Bloem, Bastiaan R.; Aasly, Jan; Toft, Mathias; Pihlstrom, Lasse; Guedes, Leonor Correia; Ferreira, Joaquim J.; Bardien, Soraya; Carr, Jonathan; Tolosa, Eduardo; Ezquerra, Mario; Pastor, Pau; Diez-Fairen, Monica; Wirdefeldt, Karin; Pedersen, Nancy L.; Ran, Caroline; Belin, Andrea C.; Puschmann, Andreas; Hellberg, Clara; Clarke, Carl E.; Morrison, Karen E.; Tan, Manuela; Krainc, Dimitri; Burbulla, Lena F.; Farrer, Matt J.; Krueger, Rejko; Gasser, Thomas; Sharma, Manu; Elbaz, Alexis (2022)
  • Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's disease
    Fitzgerald, Julia C.; Zimprich, Alexander; Berrio, Daniel A. Carvajal; Schindler, Kevin M.; Maurer, Brigitte; Schulte, Claudia; Bus, Christine; Hauser, Anne-Kathrin; Kuebler, Manuela; Lewin, Rahel; Bobbili, Dheeraj Reddy; Schwarz, Lisa M.; Vartholomaiou, Evangelia; Brockmann, Kathrin; Wuest, Richard; Madlung, Johannes; Nordheim, Alfred; Riess, Olaf; Martins, L. Miguel; Glaab, Enrico; May, Patrick; Schenke-Layland, Katja; Picard, Didier; Sharma, Manu; Gasser, Thomas; Krueger, Rejko (2017)
  • Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset
    Billingsley, Kimberley J.; Barbosa, Ines A.; Bandres-Ciga, Sara; Quinn, John P.; Bubb, Vivien J.; Deshpande, Charu; Botia, Juan A.; Reynolds, Regina H.; Zhang, David; Simpson, Michael A.; Blauwendraat, Cornelis; Gan-Or, Ziv; Gibbs, J. Raphael; Nalls, Mike A.; Singleton, Andrew; Ryten, Mina; Koks, Sulev; Noyce, A.; Tucci, A.; Middlehurst, B.; Kia, D.; Tan, M.; Houlden, H.; Morris, H. R.; Plun-Favreau, H.; Holmans, P.; Hardy, J.; Trabzuni, D.; Bras, J.; Mok, K.; Kinghorn, K.; Wood, N.; Lewis, P.; Guerreiro, R.; Loverin, R.; R'Bibo, L.; Rizig, M.; Escott-Price, V; Chelban, V; Foltynie, T.; Williams, N.; Brice, A.; Danjou, F.; Lesage, S.; Martinez, M.; Giri, A.; Schulte, C.; Brockmann, K.; Simon-Sanchez, J.; Heutink, P.; Rizzu, P.; Sharma, M.; Gasser, T.; Nicolas, A.; Cookson, M.; Faghri, F.; Hernandez, D.; Shulman, J.; Robak, L.; Lubbe, S.; Finkbeiner, S.; Mencacci, N.; Lungu, C.; Scholz, S.; Reed, X.; Leonard, H.; Rouleau, G.; Krohan, L.; van Hilten, J.; Marinus, J.; Adarmes-Gomez, A.; Aguilar, M.; Alvarez, I; Alvarez, V; Javier Barrero, F.; Bergareche Yarza, J.; Bernal-Bernal, I; Blazquez, M.; Bonilla-Toribio Bernal, M.; Boungiorne, M.; Buiza-Rueda, Dolores; Camara, A.; Carcel, M.; Carrillo, F.; Carrion-Claro, M.; Cerdan, D.; Clarimon, J.; Compta, Y.; Diez-Fairen, M.; Dols-Icardo, O.; Duarte, J.; Duran, R., I; Escamilla-Sevilla, F.; Ezquerra, M.; Fernandez, M.; Fernandez-Santiago, R.; Garcia, C.; Garcia-Ruiz, P.; Gomez-Garre, P.; Gomez Heredia, M.; Gonzalez-Aramburu, I (2019)
  • Mitochondrial and autophagy-lysosomal pathway polygenic risk scores predict Parkinson's disease
    Dehestani, Mohammad; Liu, Hui; Sreelatha, Ashwin Ashok Kumar; Schulte, Claudia; Bansal, Vikas; Gasser, Thomas (2022)
  • Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism
    Borsche, Max; Koenig, Inke R.; Delcambre, Sylvie; Petrucci, Simona; Balck, Alexander; Brueggemann, Norbert; Zimprich, Alexander; Wasner, Kobi; Pereira, Sandro L.; Avenali, Micol; Deuschle, Christian; Badanjak, Katja; Ghelfi, Jenny; Gasser, Thomas; Kasten, Meike; Rosenstiel, Philip; Lohmann, Katja; Brockmann, Kathrin; Valente, Enza Maria; Youle, Richard J.; Gruenewald, Anne; Klein, Christine (2020)
  • Molekulargenetische Diagnostik und Gentherapie
    Gasser, Thomas (2012)
  • Movement disorder society criteria for clinically established early Parkinson's disease
    Berg, Daniela; Adler, Charles H.; Bloem, Bastiaan R.; Chan, Piu; Gasser, Thomas; Goetz, Christopher G.; Halliday, Glenda; Lang, Anthony E.; Lewis, Simon; Li, Yuan; Liepelt-Scarfone, Inga; Litvan, Irene; Marek, Kenneth; Maetzler, Corina; Mi, Taomian; Obeso, Jose; Oertel, Wolfgang; Olanow, C. Warren; Poewe, Werner; Rios-Romenets, Silvia; Schaeffer, Eva; Seppi, Klaus; Heim, Beatrice; Slow, Elizabeth; Stern, Matthew; Bledsoe, Ian O.; Deuschl, Guenther; Postuma, Ronald B. (2018)
  • Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability
    Reynolds, Regina H.; Botia, Juan; Nalls, Mike A.; Hardy, John; Taliun, Sarah A. Gagliano; Ryten, Mina; Noyce, Alastair J.; Nicolas, Aude; Cookson, Mark R.; Bandres-Ciga, Sara; Gibbs, J. Raphael; Hernandez, Dena G.; Singleton, Andrew B.; Reed, Xylena; Leonard, Hampton; Blauwendraat, Cornelis; Faghri, Faraz; Bras, Jose; Guerreiro, Rita; Tucci, Arianna; Kia, Demis A.; Houlden, Henry; Plun-Favreau, Helene; Mok, Kin Y.; Wood, Nicholas W.; Lovering, Ruth; R'Bibo, Lea; Rizig, Mie; Chelban, Viorica; Trabzuni, Daniah; Tan, Manuela; Morris, Huw R.; Middlehurst, Ben; Quinn, John; Billingsley, Kimberley; Holmans, Peter; Kinghorn, Kerri J.; Lewis, Patrick; Escott-Price, Valentina; Williams, Nigel; Foltynie, Thomas; Brice, Alexis; Danjou, Fabrice; Lesage, Suzanne; Corvol, Jean-Christophe; Martinez, Maria; Giri, Anamika; Schulte, Claudia; Brockmann, Kathrin; Simon-Sanchez, Javier; Heutink, Peter; Gasser, Thomas; Rizzu, Patrizia; Sharma, Manu; Shulman, Joshua M.; Robak, Laurie; Lubbe, Steven; Mencacci, Niccolo E.; Finkbeiner, Steven; Lungu, Codrin; Scholz, Sonja W.; Gan-Or, Ziv; Rouleau, Guy A.; Krohan, Lynne; van Hilten, Jacobus J.; Marinus, Johan; Adarmes-Gomez, Astrid D.; Bernal-Bernal, Inmaculada; Bonilla-Toribio, Marta; Buiza-Rueda, Dolores; Carrillo, Fatima; Carrion-Claro, Mario; Mir, Pablo; Gomez-Garre, Pilar; Jesus, Silvia; Labrador-Espinosa, Miguel A.; Macias, Daniel; Vargas-Gonzalez, Laura; Mendez-del-Barrio, Carlota; Perinan-Tocino, Teresa; Tejera-Parrado, Cristina; Diez-Fairen, Monica; Aguilar, Miquel; Alvarez, Ignacio; Teresa Boungiorno, Mara; Carcel, Maria; Pastor, Pau; Pablo Tartari, Juan; Alvarez, Victoria; Menendez Gonzalez, Manuel; Blazquez, Marta; Garcia, Ciara; Suarez-Sanmartin, Esther; Javier Barrero, Francisco; Mondragon Rezola, Elisabet; Bergareche Yarza, Jesus Alberto; Gorostidi Pagola, Ana; de Munain Arregui, Adolfo Lopez; Ruiz-Martinez, Javier; Cerdan, Debora; Duarte, Jacinto (2019)
  • Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
    Kim, Jonggeol Jeffrey; Vitale, Dan; Otani, Diego Veliz; Lian, Michelle Mulan; Heilbron, Karl; Aslibekyan, Stella; Auton, Adam; Babalola, Elizabeth; Bell, Robert K.; Bielenberg, Jessica; Bryc, Katarzyna; Bullis, Emily; Cannon, Paul; Coker, Daniella; Partida, Gabriel Cuellar; Dhamija, Devika; Das, Sayantan; Elson, Sarah L.; Eriksson, Nicholas; Filshtein, Teresa; Fitch, Alison; Fletez-Brant, Kipper; Fontanillas, Pierre; Freyman, Will; Granka, Julie M.; Hernandez, Alejandro; Hicks, Barry; Hinds, David A.; Jewett, Ethan M.; Jiang, Yunxuan; Kukar, Katelyn; Kwong, Alan; Lin, Keng-Han; Llamas, Bianca A.; Lowe, Maya; McCreight, Jey C.; McIntyre, Matthew H.; Micheletti, Steven J.; Moreno, Meghan E.; Nandakumar, Priyanka; Nguyen, Dominique T.; Noblin, Elizabeth S.; O'Connell, Jared; Petrakovitz, Aaron A.; Poznik, G. David; Reynoso, Alexandra; Schloetter, Madeleine; Schumacher, Morgan; Shastri, Anjali J.; Shelton, Janie F.; Shi, Jingchunzi; Shringarpure, Suyash; Su, Qiaojuan Jane; Tat, Susana A.; Tchakoute, Christophe Toukam; Tran, Vinh; Tung, Joyce Y.; Wang, Xin; Wang, Wei; Weldon, Catherine H.; Wilton, Peter; Wong, Corinna D.; Iwaki, Hirotaka; Lake, Julie; Solsberg, Caroline Warly; Leonard, Hampton; Makarious, Mary B.; Tan, Eng-King; Singleton, Andrew B.; Bandres-Ciga, Sara; Noyce, Alastair J.; Gatto, Emilia M.; Kauffman, Marcelo; Khachatryan, Samson; Tavadyan, Zaruhi; Shepherd, Claire E.; Hunter, Julie; Kumar, Kishore; Ellis, Melina; Renteria, Miguel E.; Koks, Sulev; Zimprich, Alexander; Schumacher-Schuh, Artur F.; Rieder, Carlos; Awad, Paula Saffie; Tumas, Vitor; Camargos, Sarah; Fon, Edward A.; Monchi, Oury; Fon, Ted; Galleguillos, Benjamin Pizarro; Miranda, Marcelo; Bustamante, Maria Leonor; Olguin, Patricio; Chana, Pedro; Tang, Beisha; Shang, Huifang; Guo, Jifeng; Chan, Piu; Luo, Wei; Arboleda, Gonzalo (2024)
  • Needs and requirements of modern biobanks on the example of dystonia syndromes
    Lohmann, Ebba; Gasser, Thomas; Grundmann, Kathrin (2017)
  • NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
    Blauwendraat, Cornelis; Faghri, Faraz; Pihlstrom, Lasse; Geiger, Joshua T.; Elbaz, Alexis; Lesage, Suzanne; Corvol, Jean-Christophe; May, Patrick; Nicolas, Aude; Abramzon, Yevgeniya; Murphy, Natalie A.; Gibbs, J. Raphael; Ryten, Mina; Ferrari, Raffaele; Bras, Jose; Guerreiro, Rita; Williams, Julie; Sims, Rebecca; Lubbe, Steven; Hernandez, Dena G.; Mok, Kin Y.; Robak, Laurie; Campbell, Roy H.; Rogaeva, Ekaterina; Traynor, Bryan J.; Chia, Ruth; Chung, Sun Ju; Hardy, John A.; Brice, Alexis; Wood, NicholasW.; Houlden, Henry; Shulman, Joshua M.; Morris, Huw R.; Gasser, Thomas; Krueger, Rejko; Heutink, Peter; Sharma, Manu; Simon-Sanchez, Javier; Nalls, Mike A.; Singleton, Andrew B.; Scholz, SonjaW. (2017)
  • Neurodegenerative CSF markers in genetic and sporadic PD: Classification and prediction in a longitudinal study
    Brockmann, Kathrin; Schulte, Claudia; Deuschle, Christian; Hauser, Ann-Kathrin; Heger, Tanja; Gasser, Thomas; Maetzler, Walter; Berg, Daniela (2015)
  • NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis
    Blauw, Hylke M.; van Rheenen, Wouter; Koppers, Max; Van Damme, Philip; Waibel, Stefan; Lemmens, Robin; van Vught, Paul W. J.; Meyer, Thomas; Schulte, Claudia; Gasser, Thomas; Cuppen, Edwin; Pasterkamp, R. Jeroen; Robberecht, Wim; Ludolph, Albert C.; Veldink, Jan H.; van den Berg, Leonard H. (2012)
  • No association between NOD2 variants and Parkinson's disease
    Appenzeller, Silke; Thier, Sandra; Papengut, Frank; Klein, Christine; Berg, Daniela; Srulijes, Karin; Gasser, Thomas (2012)
  • No Dopamine Cell Loss or Changes in Cytoskeleton Function in Transgenic Mice Expressing Physiological Levels of Wild Type or G2019S Mutant LRRK2 and in Human Fibroblasts
    Garcia-Miralles, Marta; Coomaraswamy, Janaky; Haebig, Karina; Herzig, Martin C.; Funk, Natalja; Gillardon, Frank; Maisel, Martina; Jucker, Mathias; Gasser, Thomas; Galter, Dagmar; Biskup, Saskia (2015)