Auflistung 4 Medizinische Fakultät nach Autor "Heutink, Peter"

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Auflistung 4 Medizinische Fakultät nach Autor "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 dataset for the analysis of frontotemporal dementia genetic subtypes
    Menden, Kevin; Francescatto, Margherita; Nyima, Tenzin; Blauwendraat, Cornelis; Dhingra, Ashutosh; Castillo-Lizardo, Melissa; Fernandes, Noemia; Kaurani, Lalit; Kronenberg-Versteeg, Deborah; Atasu, Burcu; Sadikoglou, Eldem; Borroni, Barbara; Rodriguez-Nieto, Salvador; Simon-Sanchez, Javier; Fischer, Andre; Craig, David Wesley; Neumann, Manuela; Bonn, Stefan; Rizzu, Patrizia; Heutink, Peter (2023)
  • A multimodal 3D neuro-microphysiological system with neurite-trapping microelectrodes
    Molina-Martinez, Beatriz; Jentsch, Laura-Victoria; Ersoy, Fulya; van der Moolen, Matthijs; Donato, Stella; Ness, Torbjorn, V; Heutink, Peter; Jones, Peter D.; Cesare, Paolo (2022)
  • A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
    van der Lee, Sven J.; Conway, Olivia J.; Jansen, Iris; Carrasquillo, Minerva M.; Kleineidam, Luca; van den Akker, Erik; Hernandez, Isabel; van Eijk, Kristel R.; Stringa, Najada; Chen, Jason A.; Zettergren, Anna; Andlauer, Till F. M.; Diez-Fairen, Monica; Simon-Sanchez, Javier; Lleo, Alberto; Zetterberg, Henrik; Nygaard, Marianne; Blauwendraat, Cornelis; Savage, Jeanne E.; Mengel-From, Jonas; Moreno-Grau, Sonia; Wagner, Michael; Fortea, Juan; Keogh, Michael J.; Blennow, Kaj; Skoog, Ingmar; Friese, Manuel A.; Pletnikova, Olga; Zulaica, Miren; Lage, Carmen; de Rojas, Itziar; Riedel-Heller, Steffi; Illan-Gala, Ignacio; Wei, Wei; Jeune, Bernard; Orellana, Adelina; Bergh, Florian Then; Wang, Xue; Hulsman, Marc; Beker, Nina; Tesi, Niccolo; Morris, Christopher M.; Indakoetxea, Begona; Collij, Lyduine E.; Scherer, Martin; Morenas-Rodriguez, Estrella; Ironside, James W.; van Berckel, Bart N. M.; Alcolea, Daniel; Wiendl, Heinz; Strickland, Samantha L.; Pastor, Pau; Rodriguez Rodriguez, Eloy; Boeve, Bradley F.; Petersen, Ronald C.; Ferman, Tanis J.; van Gerpen, Jay A.; Reinders, Marcel J. T.; Uitti, Ryan J.; Tarraga, Lluis; Maier, Wolfgang; Dols-Icardo, Oriol; Kawalia, Amit; Dalmasso, Maria Carolina; Boada, Merce; Zettl, Uwe K.; van Schoor, Natasja M.; Beekman, Marian; Allen, Mariet; Masliah, Eliezer; Lopez de Munain, Adolfo; Pantelyat, Alexander; Wszolek, Zbigniew K.; Ross, Owen A.; Dickson, Dennis W.; Graff-Radford, Neill R.; Knopman, David; Rademakers, Rosa; Lemstra, Afina W.; Pijnenburg, Yolande A. L.; Scheltens, Philip; Gasser, Thomas; Chinnery, Patrick F.; Hemmer, Bernhard; Huisman, Martijn A.; Troncoso, Juan; Moreno, Fermin; Nohr, Ellen A.; Sorensen, Thorkild I. A.; Heutink, Peter; Sanchez-Juan, Pascual; Posthuma, Danielle; Clarimon, Jordi; Christensen, Kaare; Ertekin-Taner, Nilufer; Scholz, Sonja W.; Ramirez, Alfredo; Ruiz, Agustin; Slagboom, Eline; van der Flier, Wiesje M.; Holstege, Henne (2019)
  • A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family
    Hanagasi, Hasmet A.; Giri, Anamika; Kartal, Ece; Guven, Gamze; Bilgic, Basar; Hauser, Ann-Kathrin; Emre, Murat; Heutink, Peter; Basak, Nazh; Gasser, Thomas; Simon-Sanchez, Javier; Lohmann, Ebba (2016)
  • 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)
  • 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)
  • 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-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)
  • C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers
    Rizzu, Patrizia; Blauwendraat, Cornelis; Heetveld, Sasja; Lynes, Emily M.; Castillo-Lizardo, Melissa; Dhingra, Ashutosh; Pyz, Elwira; Hobert, Markus; Synofzik, Matthis; Simon-Sanchez, Javier; Francescatto, Margherita; Heutink, Peter (2016)
  • 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)
  • 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)
  • DGEclust: differential expression analysis of clustered count data
    Vavoulis, Dimitrios V.; Francescatto, Margherita; Heutink, Peter; Gough, Julian (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)