Anzahl der Publikationen: 7
Zeitschriftenartikel
Manzoni, Claudia
ORCID: https://orcid.org/0000-0001-5367-4023; Kia, Demis A.; Ferrari, Raffaele; Leonenko, Ganna; Costa, Beatrice; Saba, Valentina; Jabbari, Edwin; Tan, Manuela MX.; Albani, Diego; Alvarez, Victoria; Alvarez, Ignacio; Andreassen, Ole A.; Angiolillo, Antonella; Arighi, Andrea; Baker, Matt; Benussi, Luisa; Bessi, Valentina; Binetti, Giuliano; Blackburn, Daniel J.; Boada, Merce; Boeve, Bradley F.; Borrego-Ecija, Sergi; Borroni, Barbara; Bråthen, Geir; Brooks, William S.; Bruni, Amalia C.; Caroppo, Paola; Bandres-Ciga, Sara; Clarimon, Jordi; Colao, Rosanna; Cruchaga, Carlos; Danek, Adrian
ORCID: https://orcid.org/0000-0001-8857-5383; Boer, Sterre CM. de; Rojas, Itziar de; di Costanzo, Alfonso; Dickson, Dennis W.; Diehl-Schmid, Janine; Dobson-Stone, Carol; Dols-Icardo, Oriol; Donizetti, Aldo; Dopper, Elise; Durante, Elisabetta; Ferrari, Camilla; Forloni, Gianluigi; Frangipane, Francesca; Fratiglioni, Laura; Kramberger, Milica G.; Galimberti, Daniela; Gallucci, Maurizio; García-González, Pablo; Ghidoni, Roberta; Giaccone, Giorgio; Graff, Caroline; Graff-Radford, Neill R.; Grafman, Jordan; Halliday, Glenda M.; Hernandez, Dena G.; Hjermind, Lena E.; Hodges, John R.; Holloway, Guy; Huey, Edward D.; Illán-Gala, Ignacio; Josephs, Keith A.; Knopman, David S.; Kristiansen, Mark; Kwok, John B.; Leber, Isabelle; Leonard, Hampton L.; Libri, Ilenia; Lleo, Alberto; Mackenzie, Ian R.; Madhan, Gaganjit K.; Maletta, Raffaele; Marquié, Marta; Maver, Ales; Menendez-Gonzalez, Manuel; Milan, Graziella; Miller, Bruce L.; Morris, Christopher M.; Morris, Huw R.; Nacmias, Benedetta; Newton, Judith; Nielsen, Jørgen E.; Nilsson, Christer; Novelli, Valeria; Padovani, Alessandro; Pal, Suvankar; Pasquier, Florence; Pastor, Pau; Perneczky, Robert
ORCID: https://orcid.org/0000-0003-1981-7435; Peterlin, Borut; Petersen, Ronald C.; Piguet, Olivier; Pijnenburg, Yolande AL.; Puca, Annibale A.; Rademakers, Rosa; Rainero, Innocenzo; Reus, Lianne M.; Richardson, Anna MT.; Riemenschneider, Matthias; Rogaeva, Ekaterina; Rogelj, Boris; Rollinson, Sara; Rosen, Howard; Rossi, Giacomina; Rowe, James B.; Rubino, Elisa; Ruiz, Agustin; Salvi, Erika; Sanchez-Valle, Raquel; Sando, Sigrid Botne; Santillo, Alexander F.; Saxon, Jennifer A.; Schlachetzki, Johannes CM.; Scholz, Sonja W.; Seelaar, Harro; Seeley, William W.; Serpente, Maria; Sorbi, Sandro; Sordon, Sabrina; St George-Hyslop, Peter; Thompson, Jennifer C.; Broeckhoven, Christine Van; Deerlin, Vivianna M. Van; Lee, Sven J. Van der; Swieten, John Van; Tagliavini, Fabrizio; Zee, Julie van der; Veronesi, Arianna; Vitale, Emilia; Waldo, Maria Landqvist; Yokoyama, Jennifer S.; Nalls, Mike A.; Momeni, Parastoo; Singleton, Andrew B.; Hardy, John und Escott-Price, Valentina
(2024):
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia.
In: The American Journal of Human Genetics, Bd. 111, Nr. 7: S. 1316-1329
[PDF, 2MB]
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; Deerlin, Vivienne M. van; Grossman, Murray; Trojanowski, John Q.; Zee, Julie van der; Cruts, Marc; Broeckhoven, Christine van; 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; Pichler, Sabrina; Gu, Wei; Rossor, Martin N.; Fox, Nick C.; Warren, Jason D.; Spillantini, Maria Grazia; Morris, Huw R.; Rizzu, Patrizia; Heutink, Peter; Snowden, Julie S.; Rollinson, Sara; Richardson, Anna; Gerhard, Alexander; Bruni, Amalie C.; Maletta, Raffaele; Frangipane, Francesca; Cupidi, Chiara; Bernardi, Livia; Anfossi, Maria; Gallo, Maura; Conidi, Maria Elena; Smirne, Nicoletta; Rademakers, Rosa; Baker, Matt; Dickson, Dennis W.; Graff-Radford, Neill R.; Petersen, Ronald C.; Knopman, David; Josephs, Keith A.; Boeve, Bradley F.; Parisi, Joseph E.; Seeley, William W.; Miller, Bruce L.; Karydas, Anna M.; Rosen, Howard; Swieten, John C. van; Dopper, Elise G. P.; Seelaar, Harro; Pijnenburg, Yolande A. L.; Scheltens, Philip; Logroscino, Giancarlo; Capozzo, Rosa; Novelli, Valeria; Puca, Annibale A.; Franceschi, Massimo; Postiglione, Alfredo; Milan, Graziella; Sorrentino, Paolo; Kristiansen, Mark; Huei-Hsin, G.; Graff, Chian Caroline; Pasquier, Florence; Rollin, Adeline; Deramecourt, Vincent; Lebouvier, Thibaud; Ferrucci, Luigi; Pickering-Brown, Stuart; Singleton, Andrew B.; Hardy, John und Momeni, Parastoo
(2020):
Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis.
In: Scientific Reports, Bd. 10, Nr. 1, 12184
[PDF, 1MB]
Lehmer, Carina; Schludi, Martin H.; Ransom, Linnea; Greiling, Johanna; Junghaenel, Michaela; Exner, Nicole; Riemenschneider, Henrick; Zee, Julie van der; Broeckhoven, Christine van; Weydt, Patrick; Heneka, Michael T. und Edbauer, Dieter
(2018):
A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALS.
In: EMBO Molecular Medicine, Bd. 10, Nr. 6
[PDF, 2MB]
Zhang, Ming; Ferrari, Raffaele; Tartaglia, Maria Carmela; Keith, Julia; Surace, Ezequiel I.; Wolf, Uri; Sato, Christine; Grinberg, Mark; Liang, Yan; Xi, Zhengrui; Dupont, Kyle; McGoldrick, Philip; Weichert, Anna; McKeever, Paul M.; Schneider, Raphael; McCorkindale, Michael D.; Manzoni, Claudia; Rademakers, Rosa; Graff-Radford, Neill R.; Dickson, Dennis W.; Parisi, Joseph E.; Boeve, Bradley F.; Petersen, Ronald C.; Miller, Bruce L.; Seeley, William W.; Swieten, John C. van; Rooij, Jeroen van; Pijnenburg, Yolande; Zee, Julie van der; Broeckhoven, Christine van; Le Ber, Isabelle; Deerlin, Vivianna van; Suh, EunRan; Rohrer, Jonathan D.; Mead, Simon; Graff, Caroline; Oijerstedt, Linn; Pickering-Brown, Stuart; Rollinson, Sara; Rossi, Giacomina; Tagliavini, Fabrizio; Brooks, William S.; Dobson-Stone, Carol; Halliday, Glenda M.; Hodges, John R.; Piguet, Olivier; Binetti, Giuliano; Benussi, Luisa; Ghidoni, Roberta; Nacmias, Benedetta; Sorbi, Sandro; Bruni, Amalia C.; Galimberti, Daniela; Scarpini, Elio; Rainero, Innocenzo; Rubino, Elisa; Clarimon, Jordi; Lleo, Alberto; Ruiz, Agustin; Hernandez, Isabel; Pastor, Pau; Diez-Fairen, Monica; Borroni, Barbara; Pasquier, Florence; Deramecourt, Vincent; Lebouvier, Thibaud; Perneczky, Robert; Diehl-Schmid, Janine; Grafman, Jordan; Huey, Edward D.; Mayeux, Richard; Nalls, Michael A.; Hernandez, Dena; Singleton, Andrew; Momeni, Parastoo; Zeng, Zhen; Hardy, John; Robertson, Janice; Zinman, Lorne und Rogaeva, Ekaterina
(2018):
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.
In: Brain, Bd. 141: S. 2895-2907
Zee, Julie van der; Gijselinck, Ilse; Mossevelde, Sara van; Perrone, Federica; Dillen, Lubina; Heeman, Bavo; Bäumer, Veerle; Engelborghs, Sebastiaan; Bleecker, Jan de; Baets, Jonathan; Gelpi, Ellen; Rojas-Garcia, Ricardo; Clarimon, Jordi; Lleo, Alberto; Diehl-Schmid, Janine; Alexopoulos, Panagiotis; Perneczky, Robert; Synofzik, Matthis; Just, Jennifer; Schöls, Ludger; Graff, Caroline; Thonberg, Håkan; Borroni, Barbara; Padovani, Alessandro; Jordanova, Albena; Sarafov, Stayko; Tournev, Ivailo; Mendonca, Alexandre de; Miltenberger-Miltenyi, Gabriel; Simoes do Couto, Frederico; Ramirez, Alfredo; Jessen, Frank; Heneka, Michael T.; Gomez-Tortosa, Estrella; Danek, Adrian; Cras, Patrick; Vandenberghe, Rik; Jonghe, Peter de; Deyn, Peter P. de; Sleegers, Kristel; Cruts, Marc und Broeckhoven, Christine van
(2017):
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
In: Human Mutation, Bd. 38, Nr. 3: S. 297-309
Gijselinck, Ilse; Mossevelde, Sara van; Zee, Julie van der; Sieben, Anne; Engelborghs, Sebastiaan; Bleecker, Jan de; Ivanoiu, Adrian; Deryck, O.; Edbauer, Dieter; Zhang, M.; Heeman, Bavo; Bäumer, Veerle; Broeck, M. van den; Mattheijssens, Maria; Peeters, K.; Rogaeva, E.; Jonghe, Peter de; Cras, Patrick; Martin, Jean-Jacques; Deyn, Peter Paul de; Cruts, Marc und Broeckhoven, Christine van
(2016):
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter.
In: Molecular Psychiatry, Bd. 21, Nr. 8: S. 1112-1124
Janssens, Jonathan; Philtjens, Stephanie; Kleinberger, Gernot; Mossevelde, Sara van; Zee, Julie van der; Cacace, Rita; Engelborghs, Sebastiaan; Sieben, Anne; Banzhaf-Strathmann, Julia; Dillen, Lubina; Merlin, Celine; Cuijt, Ivy; Robberecht, Caroline; Schmid, Bettina; Santens, Patrick; Ivanoiu, Adrian; Vandenbulcke, Mathieu; Vandenberghe, Rik; Cras, Patrick; De Deyn, Peter P.; Martin, Jean-Jacques; Maudsley, Stuart; Haass, Christian
ORCID: https://orcid.org/0000-0002-4869-1627; Cruts, Marc und Broeckhoven, Christine van
(2015):
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.
In: Acta Neuropathologica Communications
3:68
[PDF, 3MB]
Diese Liste wurde am
Sat Mar 8 21:45:11 2025 CET
erstellt.