Browsing Universitätsbibliographie by Author "Heutink, Peter"

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Browsing Universitätsbibliographie by Author "Heutink, Peter"

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  • 17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson's disease are associated with LRRC37A/2 expression in astrocytes
    Bowles, Kathryn R.; Pugh, Derian A.; Liu, Yiyuan; Patel, Tulsi; Renton, Alan E.; Bandres-Ciga, Sara; Gan-Or, Ziv; Heutink, Peter; Siitonen, Ari; Bertelsen, Sarah; Cherry, Jonathan D.; Karch, Celeste M.; Frucht, Steven J.; Kopell, Brian H.; Peter, Inga; Park, Y. J.; Charney, Alexander; Raj, Towfique; Crary, John F.; Goate, A. M. (2022)
  • A Multi-omics Data Resource for Frontotemporal Dementia Research
    Heutink, Peter; Menden, Kevin; Dalmia, Anupriya (2021)
  • A role for astrocytic miR-129-5p in frontotemporal dementia
    Kaurani, Lalit; Pradhan, Ranjit; Schroeder, Sophie; Burkhardt, Susanne; Schuetz, Anna-Lena; Krueger, Dennis M.; Pena, Tonatiuh; Heutink, Peter; Sananbenesi, Farahnaz; Fischer, Andre (2025)
  • 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)
  • An integrated expression atlas of miRNAs and their promoters in human and mouse
    de Rie, Derek; Abugessaisa, Imad; Alam, Tanvir; Arner, Erik; Arner, Peter; Ashoor, Haitham; Astrom, Gaby; Babina, Magda; Bertin, Nicolas; Burroughs, A. Maxwell; Carlisle, Ailsa J.; Daub, Carsten O.; Detmar, Michael; Deviatiiarov, Ruslan; Fort, Alexandre; Gebhard, Claudia; Goldowitz, Daniel; Guhl, Sven; Ha, Thomas J.; Harshbarger, Jayson; Hasegawa, Akira; Hashimoto, Kosuke; Herlyn, Meenhard; Heutink, Peter; Hitchens, Kelly J.; Hon, Chung Chau; Huang, Edward; Ishizu, Yuri; Kai, Chieko; Kasukawa, Takeya; Klinken, Peter; Lassmann, Timo; Lecellier, Charles-Henri; Lee, Weonju; Lizio, Marina; Makeev, Vsevolod; Mathelier, Anthony; Medvedeva, Yulia A.; Mejhert, Niklas; Mungall, Christopher J.; Noma, Shohei; Ohshima, Mitsuhiro; Okada-Hatakeyama, Mariko; Persson, Helena; Rizzu, Patrizia; Roudnicky, Filip; Saetrom, Pal; Sato, Hiroki; Severin, Jessica; Shin, Jay W.; Swoboda, Rolf K.; Tarui, Hiroshi; Toyoda, Hiroo; Vitting-Seerup, Kristoffer; Winteringham, Louise; Yamaguchi, Yoko; Yasuzawa, Kayoko; Yoneda, Misako; Yumoto, Noriko; Zabierowski, Susan; Zhang, Peter G.; Wells, Christine A.; Summers, Kim M.; Kawaji, Hideya; Sandelin, Albin; Rehli, Michael; Hayashizaki, Yoshihide; Carninci, Piero; Forrest, Alistair R. R.; de Hoon, Michiel J. L. (2017)
  • Analysis of shared heritability in common disorders of the brain
    Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K.; Walters, Raymond K.; Bras, Jose; Duncan, Laramie; Escott-Price, Valentina; Falcone, Guido J.; Gormley, Padhraig; Malik, Rainer; Patsopoulos, Nikolaos A.; Ripke, Stephan; Wei, Zhi; Yu, Dongmei; Lee, Phil H.; Turley, Patrick; Grenier-Boley, Benjamin; Chouraki, Vincent; Kamatani, Yoichiro; Berr, Claudine; Letenneur, Luc; Hannequin, Didier; Amouyel, Philippe; Boland, Anne; Deleuze, Jean-Francois; Duron, Emmanuelle; Vardarajan, Badri N.; Reitz, Christiane; Goate, Alison M.; Huentelman, Matthew J.; Kamboh, M. Ilyas; Larson, Eric B.; Rogaeva, Ekaterina; St George-Hyslop, Peter; Hakonarson, Hakon; Kukull, Walter A.; Farrer, Lindsay A.; Barnes, Lisa L.; Beach, Thomas G.; Demirci, F. Yesim; Head, Elizabeth; Hulette, Christine M.; Jicha, Gregory A.; Kauwe, John S. K.; Kaye, Jeffrey A.; Leverenz, James B.; Levey, Allan I.; Lieberman, Andrew P.; Pankratz, Vernon S.; Poon, Wayne W.; Quinn, Joseph F.; Saykin, Andrew J.; Schneider, Lon S.; Smith, Amanda G.; Sonnen, Joshua A.; Stern, Robert A.; Van Deerlin, Vivianna M.; Van Eldik, Linda J.; Harold, Denise; Russo, Giancarlo; Rubinsztein, David C.; Bayer, Anthony; Tsolaki, Magda; Proitsi, Petra; Fox, Nick C.; Hampel, Harald; Owen, Michael J.; Mead, Simon; Passmore, Peter; Morgan, Kevin; Noethen, Markus M.; Rossor, Martin; Lupton, Michelle K.; Hoffmann, Per; Kornhuber, Johannes; Lawlor, Brian; McQuillin, Andrew; Al-Chalabi, Ammar; Bis, Joshua C.; Ruiz, Agustin; Boada, Merce; Seshadri, Sudha; Beiser, Alexa; Rice, Kenneth; van der Lee, Sven J.; De Jager, Philip L.; Geschwind, Daniel H.; Riemenschneider, Matthias; Riedel-Heller, Steffi; Rotter, Jerome I.; Ransmayr, Gerhard; Hyman, Bradley T.; Cruchaga, Carlos; Alegret, Montserrat; Winsvold, Bendik; Palta, Priit; Farh, Kai-How; Cuenca-Leon, Ester; Furlotte, Nicholas; Kurth, Tobias; Ligthart, Lannie (2018)
  • 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)
  • Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypes
    Fodder, Katherine; Murthy, Megha; Rizzu, Patrizia; Toomey, Christina E. E.; Hasan, Rahat; Humphrey, Jack; Raj, Towfique; Lunnon, Katie; Mill, Jonathan; Heutink, Peter; Lashley, Tammaryn; Bettencourt, Conceicao (2023)
  • Brain-specific noncoding RNAs are likely to originate in repeats and may play a role in up-regulating genes in cis
    Francescatto, Margherita; Vitezic, Morana; Heutink, Peter; Saxena, Alka (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)
  • Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
    Mok, Kin Y.; Sheerin, Una; Simon-Sanchez, Javier; Salaka, Afnan; Chester, Lucy; Escott-Price, Valentina; Mantripragada, Kiran; Doherty, Karen M.; Noyce, Alastair J.; Mencacci, Niccolo E.; Lubbe, Steven J.; Williams-Gray, Caroline H.; Barker, Roger A.; Van Dijk, Karin D.; Berendse, Henk W.; Heutink, Peter; Corvol, Jean-Christophe; Cormier, Florence; Lesage, Suzanne; Brice, Alexis; Brockmann, Kathrin; Schulte, Claudia; Gasser, Thomas; Foltynie, Thomas; Limousin, Patricia; Morrison, Karen E.; Clarke, Carl E.; Sawcer, Stephen; Warner, Tom T.; Lees, Andrew J.; Morris, Huw R.; Nalls, Mike A.; Singleton, Andrew B.; Hardy, John; Abramov, Andrey Y.; Plagnol, Vincent; Williams, Nigel M.; Wood, Nicholas W. (2016)
  • 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)
  • Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study
    Nalls, Mike A.; McLean, Cory Y.; Rick, Jacqueline; Eberly, Shirley; Hutten, Samantha J.; Gwinn, Katrina; Sutherland, Margaret; Martinez, Maria; Heutink, Peter; Williams, Nigel M.; Hardy, John; Gasser, Thomas; Brice, Alexis; Price, T. Ryan; Nicolas, Aude; Keller, Margaux F.; Molony, Cliona; Gibbs, J. Raphael; Chen-Plotkin, Alice; Suh, Eunran; Letson, Christopher; Fiandaca, Massimo S.; Mapstone, Mark; Federoff, Howard J.; Noyce, Alastair J.; Morris, Huw; Van Deerlin, Vivianna M.; Weintraub, Daniel; Zabetian, Cyrus; Hernandez, Dena G.; Lesage, Suzanne; Mullins, Meghan; Conley, Emily Drabant; Northover, Carrie A. M.; Frasier, Mark; Marek, Ken; Day-Williams, Aaron G.; Stone, David J.; Ioannidis, John P. A.; Singleton, Andrew B. (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)
  • Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia
    Miedema, Suzanne S. M.; Mol, Merel O.; Koopmans, Frank T. W.; Hondius, David C.; van Nierop, Pim; Menden, Kevin; Mestdagh, Christina F. de Veij; van Rooij, Jeroen; Ganz, Andrea B.; Paliukhovich, Iryna; Melhem, Shamiram; Li, Ka Wan; Holstege, Henne; Rizzu, Patrizia; van Kesteren, Ronald E.; van Swieten, John C.; Heutink, Peter; Smit, August B. (2022)