Auflistung Universitätsbibliographie nach Autor "Heutink, Peter"

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Auflistung Universitätsbibliographie nach Autor "Heutink, Peter"

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  • Functional annotation of human long noncoding RNAs via molecular phenotyping
    Ramilowski, Jordan A.; Yip, Chi Wai; Agrawal, Saumya; Chang, Jen-Chien; Ciani, Yari; Kulakovskiy, Ivan V.; Mendez, Mickael; Ooi, Jasmine Li Ching; Ouyang, John F.; Parkinson, Nick; Petri, Andreas; Roos, Leonie; Severin, Jessica; Yasuzawa, Kayoko; Abugessaisa, Imad; Akalin, Altuna; Antonov, Ivan V.; Arner, Erik; Bonetti, Alessandro; Bono, Hidemasa; Borsari, Beatrice; Brombacher, Frank; Cameron, Chris J. F.; Cannistraci, Carlo Vittorio; Cardenas, Ryan; Cardon, Melissa; Chang, Howard; Dostie, Josee; Ducoli, Luca; Favorov, Alexander; Fort, Alexandre; Garrido, Diego; Gil, Noa; Gimenez, Juliette; Guler, Reto; Handoko, Lusy; Harshbarger, Jayson; Hasegawa, Akira; Hasegawa, Yuki; Hashimoto, Kosuke; Hayatsu, Norihito; Heutink, Peter; Hirose, Tetsuro; Imada, Eddie L.; Itoh, Masayoshi; Kaczkowski, Bogumil; Kanhere, Aditi; Kawabata, Emily; Kawaji, Hideya; Kawashima, Tsugumi; Kelly, S. Thomas; Kojima, Miki; Kondo, Naoto; Koseki, Haruhiko; Kouno, Tsukasa; Kratz, Anton; Kurowska-Stolarska, Mariola; Kwon, Andrew Tae Jun; Leek, Jeffrey; Lennartsson, Andreas; Lizio, Marina; Lopez-Redondo, Fernando; Luginbuhl, Joachim; Maeda, Shiori; Makeev, Vsevolod J.; Marchionni, Luigi; Medvedeva, Yulia A.; Minoda, Aki; Mueller, Ferenc; Munoz-Aguirre, Manuel; Murata, Mitsuyoshi; Nishiyori, Hiromi; Nitta, Kazuhiro R.; Noguchi, Shuhei; Noro, Yukihiko; Nurtdinov, Ramil; Okazaki, Yasushi; Orlando, Valerio; Paquette, Denis; Parr, Callum J. C.; Rackham, Owen J. L.; Rizzu, Patrizia; Martinez, Diego Fernando Sanchez; Sandelin, Albin; Sanjana, Pillay; Semple, Colin A. M.; Shibayama, Youtaro; Sivaraman, Divya M.; Suzuki, Takahiro; Szumowski, Suzannah C.; Tagami, Michihira; Taylor, Martin S.; Terao, Chikashi; Thodberg, Malte; Thongjuea, Supat; Tripathi, Vidisha; Ulitsky, Igor; Verardo, Roberto; Vorontsov, Ilya E.; Yamamoto, Chinatsu; Young, Robert S. (2020)
  • Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia
    Mishra, Aniket; Ferrari, Raffaele; Heutink, Peter; Hardy, John; Pijnenburg, Yolande; Posthuma, Danielle (2017)
  • Genetic comorbidities in Parkinson's disease
    Nalls, Mike A.; Saad, Mohamad; Noyce, Alastair J.; Keller, Margaux F.; Schrag, Anette; Bestwick, Jonathan P.; Traynor, Bryan J.; Gibbs, J. Raphael; Hernandez, Dena G.; Cookson, Mark R.; Morris, Huw R.; Williams, Nigel; Gasser, Thomas; Heutink, Peter; Wood, Nick; Hardy, John; Martinez, Maria; Singleton, Andrew B. (2014)
  • Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
    Blauwendraat, Cornelis; Reed, Xylena; Krohn, Lynne; Heilbron, Karl; Bandres-Ciga, Sara; Tan, Manuela; Gibbs, J. Raphael; Hernandez, Dena G.; Kumaran, Ravindran; Langston, Rebekah; Bonet-Ponce, Luis; Alcalay, Roy N.; Hassin-Baer, Sharon; Greenbaum, Lior; Iwaki, Hirotaka; Leonard, Hampton L.; Grenn, Francis P.; Ruskey, Jennifer A.; Sabir, Marya; Ahmed, Sarah; Makarious, Mary B.; Pihlstrom, Lasse; Toft, Mathias; van Hilten, Jacobus J.; Marinus, Johan; Schulte, Claudia; Brockmann, Kathrin; Sharma, Manu; Siitonen, Ari; Majamaa, Kari; Eerola-Rautio, Johanna; Tienari, Pentti J.; Pantelyat, Alexander; Hillis, Argye E.; Dawson, Ted M.; Rosenthal, Liana S.; Albert, Marilyn S.; Resnick, Susan M.; Ferrucci, Luigi; Morris, Christopher M.; Pletnikova, Olga; Troncoso, Juan; Grosset, Donald; Lesage, Suzanne; Corvol, Jean-Christophe; Brice, Alexis; Noyce, Alastair J.; Masliah, Eliezer; Wood, Nick; Hardy, John; Shulman, Lisa M.; Jankovic, Joseph; Shulman, Joshua M.; Heutink, Peter; Gasser, Thomas; Cannon, Paul; Scholz, Sonja W.; Morris, Huw; Cookson, Mark R.; Nalls, Mike A.; Gan-Or, Ziv; Singleton, Andrew B. (2020)
  • Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus
    Desikan, R. S.; Schork, A. J.; Wang, Y.; Witoelar, A.; Sharma, M.; McEvoy, L. K.; Holland, D.; Brewer, J. B.; Chen, C-H; Thompson, W. K.; Harold, D.; Williams, J.; Owen, M. J.; O'Donovan, M. C.; Pericak-Vance, M. A.; Mayeux, R.; Haines, J. L.; Farrer, L. A.; Schellenberg, G. D.; Heutink, P.; Singleton, A. B.; Brice, A.; Wood, N. W.; Hardy, J.; Martinez, M.; Choi, S. H.; DeStefano, A.; Ikram, M. A.; Bis, J. C.; Smith, A.; Fitzpatrick, A. L.; Launer, L.; van Duijn, C.; Seshadri, S.; Ulstein, I. D.; Aarsland, D.; Fladby, T.; Djurovic, S.; Hyman, B. T.; Snaedal, J.; Stefansson, H.; Stefansson, K.; Gasser, T.; Andreassen, O. A.; Dale, A. M. (2015)
  • Genetic risk of Parkinson disease and progression : An analysis of 13 longitudinal cohorts
    Iwaki, Hirotaka; Blauwendraat, Cornelis; Leonard, Hampton L.; Liu, Ganqiang; Maple-Grodem, Jodi; Corvol, Jean-Christophe; Pihlstrom, Lasse; van Nimwegen, Marlies; Hutten, Samantha J.; Nguyen, Khanh-Dung H.; Rick, Jacqueline; Eberly, Shirley; Faghri, Faraz; Auinger, Peggy; Scott, Kirsten M.; Wijeyekoon, Ruwani; Van Deerlin, Vivianna M.; Hernandez, Dena G.; Day-Williams, Aaron G.; Brice, Alexis; Alves, Guido; Noyce, Alastair J.; Tysnes, Ole-Bjorn; Evans, Jonathan R.; Breen, David P.; Estrada, Karol; Wegel, Claire E.; Danjou, Fabrice; Simon, David K.; Ravina, Bernard; Toft, Mathias; Heutink, Peter; Bloem, Bastiaan R.; Weintraub, Daniel; Barker, Roger A.; Williams-Gray, Caroline H.; van de Warrenburg, Bart P.; Van Hilten, Jacobus J.; Scherzer, Clemens R.; Singleton, Andrew B.; Nalls, Mike A. (2019)
  • Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
    Bonham, Luke W.; Steele, Natasha Z. R.; Karch, Celeste M.; Broce, Iris; Geier, Ethan G.; Wen, Natalie L.; Momeni, Parastoo; Hardy, John; Miller, Zachary A.; Gorno-Tempini, Maria Luisa; Hess, Christopher P.; Lewis, Patrick; Miller, Bruce L.; Seeley, William W.; Manzoni, Claudia; Desikan, Rahul S.; Baranzini, Sergio E.; Ferraris, Raffaele; Yokoyama, Jennifer S.; Hernandez, D. G.; Nalls, M. A.; Rohrer, J. D.; Ramasamy, A.; Kwok, J. B. J.; Dobson-Stone, C.; Schofield, P. R.; Halliday, G. M.; Hodges, J. R.; Piguet, O.; Bartley, L.; Thompson, E.; Haan, E.; Hernandez, I; Ruiz, A.; Boada, M.; Borroni, B.; Padovani, A.; Cruchaga, C.; Cairns, N. J.; Benussi, L.; Binetti, G.; Ghidoni, R.; Forloni, G.; Albani, D.; Galimberti, D.; Fenoglio, C.; Serpente, M.; Scarpini, E.; Clarimon, J.; Lleo, A.; Blesa, R.; Waldo, M. Landqvist; Nilsson, K.; Nilsson, C.; Mackenzie, I. R. A.; Hsiung, G-Y R.; Mann, D. M. A.; Grafman, J.; Morris, C. M.; Attems, J.; Griffiths, T. D.; McKeith, I. G.; Thomas, A. J.; Pietrini, P.; Huey, E. D.; Wassermann, E. M.; Baborie, A.; Jaros, E.; Tierney, M. C.; Pastor, P.; Razquin, C.; Ortega-Cubero, S.; Alonso, E.; Perneczky, R.; Diehl-Schmid, J.; Alexopoulos, P.; Kurz, A.; Rainero, I; Rubino, E.; Pinessi, L.; Rogaeva, E.; St George-Hyslop, P.; Rossi, G.; Tagliavini, F.; Giaccone, G.; Rowe, J. B.; Schlachetzki, J. C. M.; Uphill, J.; Collinge, J.; Mead, S.; Danek, A.; Van Deerlin, V. M.; Grossman, M.; Trojanowski, J. Q.; van der Zee, J.; Cruts, M.; Van Broeckhoven, C.; Cappa, S. F.; Leber, I; Hannequin, D.; Golfier, V (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
    Pottier, Cyril; Ren, Yingxue; Perkerson, Ralph B., III; Baker, Matt; Jenkins, Gregory D.; van Blitterswijk, Marka; 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., III; 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. (2019)
  • Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases
    Witoelar, Aree; Jansen, Iris E.; Wang, Yunpeng; Desikan, Rahul S.; Gibbs, J. Raphael; Blauwendraat, Cornelis; Thompson, Wesley K.; Hernandez, Dena G.; Djurovic, Srdjan; Schork, Andrew J.; Bettella, Francesco; Ellinghaus, David; Franke, Andre; Lie, Benedicte A.; McEvoy, Linda K.; Karlsen, Tomh.; Lesage, Suzanne; Morris, Huw R.; Brice, Alexis; Wood, Nicholas W.; Heutink, Peter; Hardy, John; Singleton, Andrew B.; Dale, Anders M.; Gasser, Thomas; Andreassen, Ole A.; Sharma, Manu (2017)
  • Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease
    Liu, Ganqiang; Peng, Jiajie; Liao, Zhixiang; Locascio, Joseph J.; Corvol, Jean-Christophe; Zhu, Frank; Dong, Xianjun; Maple-Grodem, Jodi; Campbell, Meghan C.; Elbaz, Alexis; Lesage, Suzanne; Brice, Alexis; Mangone, Graziella; Growdon, John H.; Hung, Albert Y.; Schwarzschild, Michael A.; Hayes, Michael T.; Wills, Anne-Marie; Herrington, Todd M.; Ravina, Bernard; Shoulson, Ira; Taba, Pille; Koks, Sulev; Beach, Thomas G.; Cormier-Dequaire, Florence; Alves, Guido; Tysnes, Ole-Bjorn; Perlmutter, Joel S.; Heutink, Peter; Amr, Sami S.; van Hilten, Jacobus J.; Kasten, Meike; Mollenhauer, Brit; Trenkwalder, Claudia; Klein, Christine; Barker, Roger A.; Williams-Gray, Caroline H.; Marinus, Johan; Scherzer, Clemens R. (2021)
  • Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
    Iwaki, Hirotaka; Blauwendraat, Cornelis; Leonard, Hampton L.; Kim, Jonggeol J.; Liu, Ganqiang; Maple-Grodem, Jodi; Corvol, Jean-Christophe; Pihlstrom, Lasse; van Nimwegen, Marlies; Hutten, Samantha J.; Nguyen, Khanh-Dung H.; Rick, Jacqueline; Eberly, Shirley; Faghri, Faraz; Auinger, Peggy; Scott, Kirsten M.; Wijeyekoon, Ruwani; Van Deerlin, Vivianna M.; Hernandez, Dena G.; Gibbs, J. Raphael; Chitrala, Kumaraswamy Naidu; Day-Williams, Aaron G.; Brice, Alexis; Alves, Guido; Noyce, Alastair J.; Tysnes, Ole-Bjorn; Evans, Jonathan R.; Breen, David P.; Estrada, Karol; Wegel, Claire E.; Danjou, Fabrice; Simon, David K.; Andreassen, Ole; Ravina, Bernard; Toft, Mathias; Heutink, Peter; Bloem, Bastiaan R.; Weintraub, Daniel; Barker, Roger A.; Williams-Gray, Caroline H.; van de Warrenburg, Bart P.; Van Hilten, Jacobus J.; Scherzer, Clemens R.; Singleton, Andrew B.; Nalls, Mike A. (2019)
  • HPCA Confirmed as a Genetic Cause of DYT2-Like Dystonia Phenotype
    Atasu, Burcu; Hanagasi, Hasmet; Bilgic, Basar; Pak, Meltem; Erginel-Unaltuna, Nihan; Hauser, Ann-Kathrin; Guven, Gamze; Simon-Sanchez, Javier; Heutink, Peter; Gasser, Thomas; Lohmann, Ebba (2018)
  • Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia
    Swarup, Vivek; Hinz, Flora I.; Rexach, Jessica E.; Noguchi, Ken-ichi; Toyoshiba, Hiroyoshi; Oda, Akira; Hirai, Keisuke; Sarkar, Arjun; Seyfried, Nicholas T.; Cheng, Chialin; Haggarty, Stephen J.; Ferrari, Raffaele; Rohrer, Jonathan D.; Ramasamy, Adaikalavan; Hardy, John; Hernandez, Dena G.; Nalls, Michael A.; Singleton, Andrew B.; Kwok, John B. J.; Dobson-Stone, Carol; Brooks, William S.; Schofield, Peter R.; Halliday, Glenda M.; Hodges, John R.; Piguet, Olivier; Bartley, Lauren; Thompson, Elizabeth; Haan, Eric; Hernandez, Isabel; Ruiz, Agustin; Boada, Merce; Borroni, Barbara; Padovani, Alessandro; Cairns, Nigel J.; Cruchaga, Carlos; Binetti, Giuliano; Ghidoni, Roberta; Benussi, Luisa; Forloni, Gianluigi; Albani, Diego; Galimberti, Daniela; Fenoglio, Chiara; Serpente, Maria; Scarpini, Elio; Clarimon, Jordi; Lleo, Alberto; Blesa, Rafael; Waldo, Maria Landqvist; Nilsson, Karin; Nilsson, Christer; Mackenzie, Ian R. A.; Hsiung, Ging-Yuek R.; Mann, David M. A.; Grafman, Jordan; Morris, Christopher M.; Attems, Johannes; Griffiths, Timothy D.; McKeith, Ian G.; Thomas, Alan J.; Jaros, Evelyn; Pietrini, Pietro; Huey, Edward D.; Wassermann, Eric M.; Tierney, Michael C.; Baborie, Atik; Pastor, Pau; Ortega-Cubero, Sara; Razquin, Cristina; Alonso, Elena; Perneczky, Robert; Diehl-Schmid, Janine; Alexopoulos, Panagiotis; Kurz, Alexander; Rainero, Innocenzo; Rubino, Elisa; Pinessi, Lorenzo; Rogaeva, Ekaterina; St George-Hyslop, Peter; Rossi, Giacomina; Tagliavini, Fabrizio; Giaccone, Giorgio; Rowe, James B.; Schlachetzki, Johannes C. M.; Uphill, James; Collinge, John; Mead, Simon; Danek, Adrian; Van Deerlin, Vivianna M.; Grossman, Murray; Trojanowski, John Q.; Pickering-Brown, Stuart; Momeni, Parastoo; van der Zee, Julie; Cruts, Marc; Van Broeckhoven, Christine; Cappa, Stefano F.; Leber, Isabelle; Brice, Alexis; Hannequin, Didier; Golfier, Veronique; Vercelletto, Martine (2019)
  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
    Nalls, Mike A.; Blauwendraat, Cornelis; Vallerga, Costanza L.; Heilbron, Karl; Bandres-Ciga, Sara; Chang, Diana; Tan, Manuela; Kia, Demis A.; Noyce, Alastair J.; Xue, Angli; Bras, Jose; Young, Emily; von Coelln, Rainer; Simon-Sanchez, Javier; Schulte, Claudia; Sharma, Manu; Krohn, Lynne; Pihlstrom, Lasse; Siitonen, Ari; Iwaki, Hirotaka; Leonard, Hampton; Faghri, Faraz; Gibbs, J. Raphael; Hernandez, Dena G.; Scholz, Sonja W.; Botia, Juan A.; Martinez, Maria; Corvol, Jean-Christophe; Lesage, Suzanne; Jankovic, Joseph; Shulman, Lisa M.; Sutherland, Margaret; Tienari, Pentti; Majamaa, Kari; Toft, Mathias; Andreassen, Ole A.; Bangale, Tushar; Brice, Alexis; Yang, Jian; Gan-Or, Ziv; Gasser, Thomas; Heutink, Peter; Shulman, Joshua M.; Wood, Nicholas W.; Hinds, David A.; Hardy, John A.; Morris, Huw R.; Gratten, Jacob; Visscher, Peter M.; Graham, Robert R.; Singleton, Andrew B. (2019)
  • In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment
    Rosa, Filip; Dhingra, Ashutosh; Uysal, Betuel; Mendis, G. Dulini C.; Loeffler, Heidi; Elsen, Gina; Mueller, Stephan; Schwarz, Niklas; Castillo-Lizardo, Melissa; Cuddy, Claire; Becker, Felicitas; Heutink, Peter; Reid, Christopher A.; Petrou, Steven; Lerche, Holger; Maljevic, Snezana (2020)
  • Integrated, automated maintenance, expansion and differentiation of 2D and 3D patient-derived cellular models for high throughput drug screening
    Boussaad, Ibrahim; Cruciani, Gerald; Bolognin, Silvia; Antony, Paul; Dording, Claire M.; Kwon, Yong-Jun; Heutink, Peter; Fava, Eugenio; Schwamborn, Jens C.; Krueger, Rejko (2021)
  • Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains
    Haenig, Christian; Atias, Nir; Taylor, Alexander K.; Mazza, Arnon; Schaefer, Martin H.; Russ, Jenny; Riechers, Sean-Patrick; Jain, Shushant; Coughlin, Maura; Fontaine, Jean-Fred; Freibaum, Brian D.; Brusendorf, Lydia; Zenkner, Martina; Porras, Pablo; Stroedicke, Martin; Schnoegl, Sigrid; Arnsburg, Kristin; Boeddrich, Annett; Pigazzini, Lucia; Heutink, Peter; Taylor, J. Paul; Kirstein, Janine; Andrade-Navarro, Miguel A.; Sharan, Roded; Wanker, Erich E. (2020)
  • Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease
    Blauwendraat, Cornelis; Iwaki, Hirotaka; Makarious, Mary B.; Bandres-Ciga, Sara; Leonard, Hampton L.; Grenn, Francis P.; Lake, Julie; Krohn, Lynne; Tan, Manuela; Kim, Jonggeol J.; Gibbs, Jesse R.; Hernandez, Dena G.; Ruskey, Jennifer A.; Pihlstrom, Lasse; Toft, Mathias; van Hilten, Jacobus J.; Marinus, Johan; Schulte, Claudia; Brockmann, Kathrin; Sharma, Manu; Siitonen, Ari; Majamaa, Kari; Eerola-Rautio, Johanna; Tienari, Pentti J.; Grosset, Donald G.; Lesage, Suzanne; Corvol, Jean-Christophe; Brice, Alexis; Wood, Nick; Hardy, John; Gan-Or, Ziv; Heutink, Peter; Gasser, Thomas; Morris, Huw R.; Noyce, Alastair J.; Nalls, Mike A.; Singleton, Andrew B. (2021)
  • iPS Cell-Based Model for MAPT Haplotype as a Risk Factor for Human Tauopathies Identifies No Major Differences in TAU Expression
    Strauss, Tabea; Marvian-Tayaranian, Amir; Sadikoglou, Eldem; Dhingra, Ashutosh; Wegner, Florian; Truembach, Dietrich; Wurst, Wolfgang; Heutink, Peter; Schwarz, Sigrid C.; Hoeglinger, Guenter U. (2021)
  • Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
    Nalls, Mike A.; Pankratz, Nathan; Lill, Christina M.; Do, Chuong B.; Hernandez, Dena G.; Saad, Mohamad; DeStefano, Anita L.; Kara, Eleanna; Bras, Jose; Sharma, Manu; Schulte, Claudia; Keller, Margaux F.; Arepalli, Sampath; Letson, Christopher; Edsall, Connor; Stefansson, Hreinn; Liu, Xinmin; Pliner, Hannah; Lee, Joseph H.; Cheng, Rong; Ikram, M. Arfan; Ioannidis, John P. A.; Hadjigeorgiou, Georgios M.; Bis, Joshua C.; Martinez, Maria; Perlmutter, Joel S.; Goate, Alison; Marder, Karen; Fiske, Brian; Sutherland, Margaret; Xiromerisiou, Georgia; Myers, Richard H.; Clark, Lorraine N.; Stefansson, Kari; Hardy, John A.; Heutink, Peter; Chen, Honglei; Wood, Nicholas W.; Houlden, Henry; Payami, Haydeh; Brice, Alexis; Scott, William K.; Gasser, Thomas; Bertram, Lars; Eriksson, Nicholas; Foroud, Tatiana; Singleton, Andrew B. (2014)