Auflistung Universitätsbibliographie nach Autor "Heutink, Peter"

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Auflistung Universitätsbibliographie nach Autor "Heutink, Peter"

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  • Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
    Lesage, Suzanne; Drouet, Valerie; Majounie, Elisa; Deramecourt, Vincent; Jacoupy, Maxime; Nicolas, Aude; Cormier-Dequaire, Florence; Hassoun, Sidi Mohamed; Pujol, Claire; Ciura, Sorana; Erpapazoglou, Zoi; Usenko, Tatiana; Maurage, Claude-Alain; Sahbatou, Mourad; Liebau, Stefan; Ding, Jinhui; Bilgic, Basar; Emre, Murat; Erginel-Unaltuna, Nihan; Guven, Gamze; Tison, Francois; Tranchant, Christine; Vidailhet, Marie; Corvol, Jean-Christophe; Krack, Paul; Leutenegger, Anne-Louise; Nalls, Michael A.; Hernandez, Dena G.; Heutink, Peter; Gibbs, J. Raphael; Hardy, John; Wood, Nicholas W.; Gasser, Thomas; Durr, Alexandra; Deleuze, Jean-Francois; Tazir, Meriem; Destee, Alain; Lohmann, Ebba; Kabashi, Edor; Singleton, Andrew; Corti, Olga; Brice, Alexis (2016)
  • Medin co-aggregates with vascular amyloid-beta in Alzheimer's disease
    Wagner, Jessica; Degenhardt, Karoline; Veit, Marleen; Louros, Nikolaos; Konstantoulea, Katerina; Skodras, Angelos; Wild, Katleen; Liu, Ping; Obermueller, Ulrike; Bansal, Vikas; Dalmia, Anupriya; Haesler, Lisa M.; Lambert, Marius; De Vleeschouwer, Matthias; Davies, Hannah A.; Madine, Jillian; Kronenberg-Versteeg, Deborah; Feederle, Regina; Del Turco, Domenico; Nilsson, K. Peter R.; Lashley, Tammaryn; Deller, Thomas; Gearing, Marla; Walker, Lary C.; Heutink, Peter; Rousseau, Frederic; Schymkowitz, Joost; Jucker, Mathias; Neher, Jonas J. (2022)
  • Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis
    Gao, Yixin; Wang, Ting; Yu, Xinghao; Zhao, Huashuo; Zeng, Ping; Ferrari, Raffaele; Hernandez, Dena G.; Nails, Michael A.; Rohrers, Jonathan D.; Ramasamys, 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; Borronils, Barbara; Padovani, Alessandro; Cruchaga, Carlos; Cairns, Nigel J.; Benussi, Luisa; Binetti, Giuliano; Ghidoni, Roberta; Forloni, Gianluigi; Albani, Diego; Galimberti, Daniela; Fenoglio, Chiara; Serpente, Maria; Scarpini, Elio; Clarim, Jordi; Lie, 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, Pietro; 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; Giacconen, Giorgio; Rowe, James B.; Schlachetzki, Johannes C. M.; Uphill, James; Collinge, John; Mead, Simon; Danek, Adrian; Van Deerlin, Vivienne M.; Grossman, Murray; Trojanowski, John Q.; van der Zee, Julie; Cruts, Marc; Van Broeckhoven, Christine; Cappa, Stefano F.; Leber, Isabelle; Hannequin, Didier; Golfier, Veronique; Vercelletto, Martine; Brice, Alexis; Nacmias, Benedetta; Sorbi, Sandro; Bagnoli, Silvia; Piaceri, Irene; Nielsen, Jorgen E.; Hjermind, Lena E.; Riemenschneider, Matthias; Mayhaus, Manuel; Ibach, Bernd; Gasparoni, Gilles (2020)
  • 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)
  • 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)
  • Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
    Guven, Gamze; Lohmann, Ebba; Bras, Jose; Gibbs, J. Raphael; Gurvit, Hakan; Bilgic, Basar; Hanagasi, Hasmet; Rizzu, Patrizia; Heutink, Peter; Emre, Murat; Erginel-Unaltuna, Nihan; Just, Walter; Hardy, John; Singleton, Andrew; Guerreiro, Rita (2016)
  • 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)
  • No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
    Baradaran-Heravi, Yalda; Dillen, Lubina; Hung Phuoc Nguyen; Van Mossevelde, Sara; Baets, Jonathan; De Jonghe, Peter; Engelborghs, Sebastiaan; De Deyn, Peter P.; Vandenbulcke, Mathieu; Vandenberghe, Rik; Van Damme, Philip; Cras, Patrick; Salmon, Eric; Synofzik, Matthis; Heutink, Peter; Wilke, Carlo; Simon-Sanchez, Javier; Rojas-Garcia, Ricard; Turon-Sans, Janina; Lleo, Alberto; Illan-Gala, Ignacio; Clarimon, Jordi; Borroni, Barbara; Padovani, Alessandro; Pastor, Pau; Diez-Fairen, Monica; Aguilar, Miquel; Gelpi, Ellen; Sanchez-Valle, Raquel; Borrego-Ecija, Sergi; Matej, Radoslav; Parobkova, Eva; Nacmias, Benedetta; Sorbi, Sandro; Bagnoli, Silvia; de Mendonca, Alexandre; Ferreira, Catarina; Fraidakis, Matthew J.; Diehl-Schmid, Janine; Alexopoulos, Panagiotis; Almeida, Maria Rosario; Santana, Isabel; Van Broeckhoven, Christine; van der Zee, Julie (2018)
  • Non-invasive and high-throughput interrogation of exon-specific isoform expression
    Truong, Dong-Jiunn Jeffery; Phlairaharn, Teeradon; Esswein, Bianca; Gruber, Christoph; Tuemen, Deniz; Baligacs, Eniko; Armbrust, Niklas; Vaccaro, Francesco Leandro; Lederer, Eva-Maria; Beck, Eva Magdalena; Geilenkeuser, Julian; Goeppert, Simone; Krumwiede, Luisa; Graetz, Christian; Raffl, Gerald; Schwarz, Dominic; Zirngibl, Martin; Zivanic, Milica; Beyer, Maren; Koerner, Johann Dietmar; Santl, Tobias; Evsyukov, Valentin; Strauss, Tabea; Schwarz, Sigrid C.; Hoeglinger, Guenter U.; Heutink, Peter; Doll, Sebastian; Conrad, Marcus; Giesert, Florian; Wurst, Wolfgang; Westmeyer, Gil Gregor (2021)
  • Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencing
    Raposo, Mafalda; Bettencourt, Conceicao; Melo, Ana Rosa Vieira; Ferreira, Ana F.; Alonso, Isabel; Silva, Paulo; Vasconcelos, Joao; Kay, Teresa; Saraiva-Pereira, Maria Luiza; Costa, Marta D.; Vilasboas-Campos, Daniela; Bettencourt, Bruno Filipe; Bruges-Armas, Jacome; Houlden, Henry; Heutink, Peter; Jardim, Laura Bannach; Sequeiros, Jorge; Maciel, Patricia; Lima, Manuela (2022)
  • Novel regulators of PrP(C) biosynthesis revealed by genome-wide RNA interference
    Heinzer, Daniel; Avar, Merve; Pease, Daniel Patrick; Dhingra, Ashutosh; Yin, Jiang-An; Schaper, Elke; Dogancay, Berre; Emmenegger, Marc; Spinelli, Anna; Maggi, Kevin; Chincisan, Andra; Mead, Simon; Hornemann, Simone; Heutink, Peter; Aguzzi, Adriano (2021)
  • Parkinson's disease age at onset genome-wide association study: defining heritability, genetic loci, and α-synuclein mechanisms
    Blauwendraat, Cornelis; Heilbron, Karl; Vallerga, Costanza L.; Bandres-Ciga, Sara; von Coelln, Rainer; Pihlstrom, Lasse; Simon-Sanchez, Javier; Schulte, Claudia; Sharma, Manu; Krohn, Lynne; Siitonen, Ari; Iwaki, Hirotaka; Leonard, Hampton; Noyce, Alastair J.; Tan, Manuela; Gibbs, J. Raphael; Hernandez, Dena G.; Scholz, Sonja W.; Jankovic, Joseph; Shulman, Lisa M.; Lesage, Suzanne; Corvol, Jean-Christophe; Brice, Alexis; van Hilten, Jacobus J.; Marinus, Johan; Eerola-Rautio, Johanna; Tienari, Pentti; Majamaa, Kari; Toft, Mathias; Grosset, Donald G.; Gasser, Thomas; Heutink, Peter; Shulman, Joshua M.; Wood, Nicolas; Hardy, John; Morris, Huw R.; Hinds, David A.; Gratten, Jacob; Visscher, Peter M.; Gan-Or, Ziv; Nalls, Mike A.; Singleton, Andrew B. (2019)
  • Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
    Mencacci, Niccolo E.; Isaias, Ioannis U.; Reich, Martin M.; Ganos, Christos; Plagnol, Vincent; Polke, James M.; Bras, Jose; Hersheson, Joshua; Stamelou, Maria; Pittman, Alan M.; Noyce, Alastair J.; Mok, Kin Y.; Opladen, Thomas; Kunstmann, Erdmute; Hodecker, Sybille; Muenchau, Alexander; Volkmann, Jens; Samnick, Samuel; Sidle, Katie; Nanji, Tina; Sweeney, Mary G.; Houlden, Henry; Batla, Amit; Zecchinelli, Anna L.; Pezzoli, Gianni; Marotta, Giorgio; Lees, Andrew; Alegria, Paulo; Krack, Paul; Cormier-Dequaire, Florence; Lesage, Suzanne; Brice, Alexis; Heutink, Peter; Gasser, Thomas; Lubbe, Steven J.; Morris, Huw R.; Taba, Pille; Koks, Sulev; Majounie, Elisa; Gibbs, Raphael; Singleton, Andrew; Hardy, John; Klebe, Stephan; Bhatia, Kailash P.; Wood, Nicholas W. (2014)
  • Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture
    Davis, Lea K.; Yu, Dongmei; Keenan, Clare L.; Gamazon, Eric R.; Konkashbaev, Anuar I.; Derks, Eske M.; Neale, Benjamin M.; Yang, Jian; Lee, S. Hong; Evans, Patrick; Barr, Cathy L.; Bellodi, Laura; Benarroch, Fortu; Berrio, Gabriel Bedoya; Bienvenu, Oscar J.; Bloch, Michael H.; Blom, Rianne M.; Bruun, Ruth D.; Budman, Cathy L.; Camarena, Beatriz; Campbell, Desmond; Cappi, Carolina; Silgado, Julio C. Cardona; Cath, Danielle C.; Cavallini, Maria C.; Chavira, Denise A.; Chouinard, Sylvain; Conti, David V.; Cook, Edwin H.; Coric, Vladimir; Cullen, Bernadette A.; Deforce, Dieter; Delorme, Richard; Dion, Yves; Edlund, Christopher K.; Egberts, Karin; Falkai, Peter; Fernandez, Thomas V.; Gallagher, Patience J.; Garrido, Helena; Geller, Daniel; Girard, Simon L.; Grabe, Hans J.; Grados, Marco A.; Greenberg, Benjamin D.; Gross-Tsur, Varda; Haddad, Stephen; Heiman, Gary A.; Hemmings, Sian M. J.; Hounie, Ana G.; Illmann, Cornelia; Jankovic, Joseph; Jenike, Michael A.; Kennedy, James L.; King, Robert A.; Kremeyer, Barbara; Kurlan, Roger; Lanzagorta, Nuria; Leboyer, Marion; Leckman, James F.; Lennertz, Leonhard; Liu, Chunyu; Lochner, Christine; Lowe, Thomas L.; Macciardi, Fabio; McCracken, James T.; McGrath, Lauren M.; Restrepo, Sandra C. Mesa; Moessner, Rainald; Morgan, Jubel; Muller, Heike; Murphy, Dennis L.; Naarden, Allan L.; Ochoa, William Cornejo; Ophoff, Roel A.; Osiecki, Lisa; Pakstis, Andrew J.; Pato, Michele T.; Pato, Carlos N.; Piacentini, John; Pittenger, Christopher; Pollak, Yehuda; Rauch, Scott L.; Renner, Tobias J.; Reus, Victor I.; Richter, Margaret A.; Riddle, Mark A.; Robertson, Mary M.; Romero, Roxana; Rosario, Maria C.; Rosenberg, David; Rouleau, Guy A.; Ruhrmann, Stephan; Ruiz-Linares, Andres; Sampaio, Aline S.; Samuels, Jack; Sandor, Paul; Sheppard, Brooke; Singer, Harvey S.; Smit, Jan H.; Stein, Dan J. (2013)
  • Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants
    Blauwendraat, Cornelis; Wilke, Carlo; Jansen, Iris E.; Schulte, Claudia; Simon-Sanchez, Javier; Metzger, Florian G.; Bender, Benjamin; Gasser, Thomas; Maetzler, Walter; Rizzu, Patrizia; Heutink, Peter; Synofzik, Matthis (2016)
  • Polygenic Risk of Parkinson Disease Is Correlated with Disease Age at Onset
    Escott-Price, Valentina; Nalls, Mike A.; Morris, Huw R.; Lubbe, Steven; Brice, Alexis; Gasser, Thomas; Heutink, Peter; Wood, Nicholas W.; Hardy, John; Singleton, Andrew B.; Williams, Nigel M. (2015)
  • Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
    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; van Blitterswijk, Marka; 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 (2018)
  • Prediction of cognition in Parkinson's disease with a clinical-genetic score: a longitudinal analysis of nine cohorts
    Liu, Ganqiang; Locascio, Joseph J.; Corvol, Jean-Christophe; Boot, Brendon; Liao, Zhixiang; Page, Kara; Franco, Daly; Burke, Kyle; Jansen, Iris E.; Trisini-Lipsanopoulos, Ana; Winder-Rhodes, Sophie; Tanner, Caroline M.; Lang, Anthony E.; Eberly, Shirley; Elbaz, Alexis; Brice, Alexis; Mangone, Graziella; Ravina, Bernard; Shoulson, Ira; Cormier-Dequaire, Florence; Heutink, Peter; van Hilten, Jacobus J.; Barker, Roger A.; Williams-Gray, Caroline H.; Marinus, Johan; Scherzer, Clemens R. (2017)
  • Reassessing the Evolutionary History of the 17q21 Inversion Polymorphism
    Alves, Joao M.; Lima, Ana C.; Pais, Isa A.; Amir, Nadir; Celestino, Ricardo; Piras, Giovanna; Monne, Maria; Comas, David; Heutink, Peter; Chikhi, Lounes; Amorim, Antonio; Lopes, Alexandra M. (2015)
  • Serum Levels of Progranulin Do Not Reflect Cerebrospinal Fluid Levels in Neurodegenerative Disease
    Wilke, Carlo; Gillardon, Frank; Deuschle, Christian; Dubois, Evelyn; Hobert, Markus A.; vom Hagen, Jennifer Mueller; Krueger, Stefanie; Biskup, Saskia; Blauwendraat, Cornelis; Hruscha, Michael; Kaeser, Stephan A.; Heutink, Peter; Maetzler, Walter; Synofzik, Matthis (2016)