Auflistung Universitätsbibliographie nach Autor "Heutink, Peter"

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Auflistung Universitätsbibliographie nach Autor "Heutink, Peter"

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  • A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia
    Seixas, Ana I.; Loureiro, Joana R.; Costa, Cristina; Ordonez-Ugalde, Andres; Marcelino, Hugo; Oliveira, Claudia L.; Loureiro, Jose L.; Dhingra, Ashutosh; Brandao, Eva; Cruz, Vitor T.; Timoteo, Angela; Quintans, Beatriz; Rouleau, Guy A.; Rizzu, Patrizia; Carracedo, Angel; Bessa, Jose; Heutink, Peter; Sequeiros, Jorge; Sobrido, Maria J.; Coutinho, Paula; Silveira, Isabel (2017)
  • 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)
  • An atlas of human long non-coding RNAs with accurate 5 ' ends
    Hon, Chung-Chau; Ramilowski, Jordan A.; Harshbarger, Jayson; Bertin, Nicolas; Rackham, Owen J. L.; Gough, Julian; Denisenko, Elena; Schmeier, Sebastian; Poulsen, Thomas M.; Severin, Jessica; Lizio, Marina; Kawaji, Hideya; Kasukawa, Takeya; Itoh, Masayoshi; Burroughs, A. Maxwell; Noma, Shohei; Djebali, Sarah; Alam, Tanvir; Medvedeva, Yulia A.; Testa, Alison C.; Lipovich, Leonard; Yip, Chi-Wai; Abugessaisa, Imad; Mendez, Mickael; Hasegawa, Akira; Tang, Dave; Lassmann, Timo; Heutink, Peter; Babina, Magda; Wells, Christine A.; Kojima, Soichi; Nakamura, Yukio; Suzuki, Harukazu; Daub, Carsten O.; de Hoon, Michiel J. L.; Arner, Erik; Hayashizaki, Yoshihide; Carninci, Piero; Forrest, Alistair R. R. (2017)
  • Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases
    Zucchelli, Silvia; Fedele, Stefania; Vatta, Paolo; Calligaris, Raffaella; Heutink, Peter; Rizzu, Patrizia; Itoh, Masayoshi; Persichetti, Francesca; Santoro, Claudio; Kawaji, Hideya; Lassmann, Timo; Hayashizaki, Yoshihide; Carninci, Piero; Forrest, Alistair R. R.; Gustincich, Stefano (2019)
  • Automated Production of Human Induced Pluripotent Stem Cell-Derived Cortical and Dopaminergic Neurons with Integrated Live-Cell Monitoring
    Dhingra, Ashutosh; Taeger, Joachim; Bressan, Elisangela; Rodriguez-Nieto, Salvador; Bedi, Manmeet-Sakshi; Broeer, Stefanie; Sadikoglou, Eldem; Fernandes, Noemia; Castillo-Lizardo, Melissa; Rizzu, Patrizia; Heutink, Peter (2020)
  • C9orf72; abnormal RNA expression is the key
    Heutink, Peter; Jansen, Iris E.; Lynes, Emily M. (2014)
  • CAGE-defined promoter regions of the genes implicated in Rett Syndrome
    Vitezic, Morana; Bertin, Nicolas; Andersson, Robin; Lipovich, Leonard; Kawaji, Hideya; Lassmann, Timo; Sandelin, Albin; Heutink, Peter; Goldowitz, Dan; Ha, Thomas; Zhang, Peter; Patrizi, Annarita; Fagiolini, Michela; Forrest, Alistair R. R.; Carninci, Piero; Saxena, Alka (2014)
  • Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia
    Wilke, Carlo; Gillardon, Frank; Deuschle, Christian; Hobert, Markus A.; Jansen, Iris E.; Metzger, Florian G.; Heutink, Peter; Gasser, Thomas; Maetzler, Walter; Blauwendraat, Cornelis; Synofzik, Matthis (2017)
  • Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe
    Blauwendraat, Cornelis; Francescatto, Margherita; Gibbs, J. Raphael; Jansen, Iris E.; Simon-Sanchez, Javier; Hernandez, Dena G.; Dillman, Allissa A.; Singleton, Andrew B.; Cookson, Mark R.; Rizzu, Patrizia; Heutink, Peter (2016)
  • Concomitant gain and loss of function pathomechanisms in C9ORF72 amyotrophic lateral sclerosis
    Pal, Arun; Kretner, Benedikt; Abo-Rady, Masin; Glass, Hannes; Dash, Banaja P.; Naumann, Marcel; Japtok, Julia; Kreiter, Nicole; Dhingra, Ashutosh; Heutink, Peter; Bockers, Tobias M.; Gunther, Rene; Sterneckert, Jared; Hermann, Andreas (2021)
  • Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome
    Kelmemi, W.; Teeuw, M. E.; Bochdanovits, Z.; Ouburg, S.; Jonker, M. A.; Alkuraya, F.; Hashem, M.; Kayserili, H.; van Haeringen, A.; Sheridan, E.; Masri, A.; Cobben, J. M.; Rizzu, P.; Kostense, P. J.; Dommering, C. J.; Henneman, L.; Bouhamed-Chaabouni, H.; Heutink, P.; ten Kate, L. P.; Cornel, M. C. (2015)
  • Differences in the Presentation and Progression of Parkinson's Disease by Sex
    Iwaki, Hirotaka; Blauwendraat, Cornelis; Leonard, Hampton L.; Makarious, Mary B.; Kim, Jonggeol J.; Liu, Ganqiang; Maple-Grodem, Jodi; Corvol, Jean-Christophe; Pihlstrom, Lasse; van Nimwegen, Marlies; Smolensky, Luba; Amondikar, Ninad; Hutten, Samantha J.; Frasier, Mark; 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, Raphael J.; 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 A.; 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. (2021)
  • 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)
  • Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)
    Lange, Lara; Avenali, Micol; Ellis, Melina; Illarionova, Anastasia J.; Sarmiento, Ignacio Keller; Tan, Ai-Huey; Madoev, Harutyun; Galandra, Caterina; Junker, Johanna; Roopnarain, Karisha; Solle, Justin; Wegel, Claire; Fang, Zih-Hua; Heutink, Peter R.; Kumar, Kishore; Lim, Shen-Yang; Valente, Enza Maria; Nalls, Mike; Blauwendraat, Cornelis; Singleton, Andrew; Mencacci, Niccolo; Lohmann, Katja; Klein, Christine (2023)
  • Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease
    Dong, Xianjun; Liao, Zhixiang; Gritsch, David; Hadzhiev, Yavor; Bai, Yunfei; Locascio, Joseph J.; Guennewig, Boris; Liu, Ganqiang; Blauwendraat, Cornelis; Wang, Tao; Adler, Charles H.; Hedreen, John C.; Faull, Richard L. M.; Frosch, Matthew P.; Nelson, Peter T.; Rizzu, Patrizia; Cooper, Antony A.; Heutink, Peter; Beach, Thomas G.; Mattick, John S.; Mueller, Ferenc; Scherzer, Clemens R. (2018)
  • 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)
  • 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)
  • 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)