Auflistung 4 Medizinische Fakultät nach Autor "Heutink, Peter"

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Auflistung 4 Medizinische Fakultät nach Autor "Heutink, Peter"

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  • Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
    Jansen, Iris E.; Ye, Hui; Heetveld, Sasja; Lechler, Marie C.; Michels, Helen; Seinstra, Renee I.; Lubbe, Steven J.; Drouet, Valerie; Lesage, Suzanne; Majounie, Elisa; Gibbs, J. Raphael; Nalls, Mike A.; Ryten, Mina; Botia, Juan A.; Vandrovcova, Jana; Simon-Sanchez, Javier; Castillo-Lizardo, Melissa; Rizzu, Patrizia; Blauwendraat, Cornelis; Chouhan, Amit K.; Li, Yarong; Yogi, Puja; Amin, Najaf; van Duijn, Cornelia M.; Morris, Huw R.; Brice, Alexis; Singleton, Andrew B.; David, Della C.; Nollen, Ellen A.; Jain, Shushant; Shulman, Joshua M.; Heutink, Peter (2017)
  • Dominant negative effect of polyglutamine expansion perturbs normal function of ataxin-3 in neuronal cells
    Neves-Carvalho, Andreia; Logarinho, Elsa; Freitas, Ana; Duarte-Silva, Sara; Costa, Maria do Carmo; Silva-Fernandes, Anabela; Martins, Margarida; Serra, Sofia Cravino; Lopes, Andre T.; Paulson, Henry L.; Heutink, Peter; Relvas, Joao B.; Maciel, Patricia (2015)
  • Drug screen in iPSC-Neurons identifies nucleoside analogs as inhibitors of (G(4)C(2))(n) expression in C9orf72 ALS/FTD
    Czuppa, Mareike; Dhingra, Ashutosh; Zhou, Qihui; Schludi, Carina; Koenig, Laura; Scharf, Elisabeth; Farny, Daniel; Dalmia, Anupriya; Taeger, Joachim; Castillo-Lizardo, Melissa; Katona, Eszter; Mori, Kohji; Aumer, Tina; Schelter, Florian; Mueller, Markus; Carell, Thomas; Kalliokoski, Tuomo; Messinger, Josef; Rizzu, Patrizia; Heutink, Peter; Edbauer, Dieter (2022)
  • Establishing the role of rare coding variants in known Parkinson's disease risk loci
    Jansen, Iris E.; Gibbs, J. Raphael; Nalls, Mike A.; Price, T. Ryan; Lubbe, Steven; van Rooij, Jeroen; Uitterlinden, Andre G.; Kraaij, Robert; Williams, Nigel M.; Brice, Alexis; Hardy, John; Wood, Nicholas W.; Morris, Huw R.; Gasser, Thomas; Singleton, Andrew B.; Heutink, Peter; Sharma, Manu (2017)
  • Evidence for Immune Response, Axonal Dysfunction and Reduced Endocytosis in the Substantia Nigra in Early Stage Parkinson's Disease
    Dijkstra, Anke A.; Ingrassia, Angela; de Menezes, Renee X.; van Kesteren, Ronald E.; Rozemuller, Annemieke J. M.; Heutink, Peter; van de Berg, Wilma D. J. (2015)
  • Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease
    Robak, Laurie A.; Jansen, Iris E.; van Rooij, Jeroen; Uitterlinden, Andre G.; Kraaij, Robert; Jankovic, Joseph; Heutink, Peter; Shulman, Joshua M. (2017)
  • Frontotemporal dementia and its subtypes: a genome-wide association study
    Ferrari, Raffaele; Hernandez, Dena G.; Nalls, Michael A.; Rohrer, Jonathan D.; Ramasamy, Adaikalavan; 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; Cruchaga, Carlos; Cairns, Nigel J.; Benussi, Luisa; Binetti, Giuliano; Ghidoni, Roberta; Forloni, Gianluigi; 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.; Pietrini, P.; Huey, Edward D.; Wassermann, Eric M.; Baborie, Atik; Jaros, Evelyn; Tierney, Michael C.; Pastor, Pau; Razquin, Cristina; Ortega-Cubero, Sara; 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.; van der Zee, Julie; Deschamps, William; Van Langenhove, Tim; Cruts, Marc; Van Broeckhoven, Christine; Cappa, Stefano F.; Le Ber, Isabelle; Hannequin, Didier; Golfier, Veronique; Vercelletto, Martine; Brice, Alexis; Nacmias, Benedetta; Sorbi, Sandra; Bagnoli, Silvia; Piaceri, Irene; Nielsen, Jorgen E.; Hjermind, Lena E.; Riemenschneider, Matthias; Mayhaus, Manuel; Ibach, Bernd; Gasparoni, Gilles; Pichler, Sabrina; Gu, Wei; Rossor, Martin N.; Fox, Nick C. (2014)
  • 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)
  • 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 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)