![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach:
Dokumententyp
| Veröffentlichungsdatum
Springe zu: Zeitschriftenartikel
Anzahl der Publikationen: 6
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]
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]
Fanciulli, Alessandra; Leys, Fabian; Lehner, Fabienne; Sidoroff, Victoria; Ruf, Viktoria C.; Raccagni, Cecilia; Mahlknecht, Philipp; Kuipers, Demy J. S.; IJcken, Wilfred F. J. van; Stockner, Heike; Musacchio, Thomas; Volkmann, Jens; Monoranu, Camelia Maria; Stankovic, Iva; Breedveld, Guido; Ferraro, Federico; Fevga, Christina; Windl, Otto; Herms, Jochen; Kiechl, Stefan; Poewe, Werner; Seppi, Klaus; Stefanova, Nadia; Scholz, Sonja W.; Bonifati, Vincenzo und Wenning, Gregor K.
(2022):
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementia.
In: Brain Communications, Bd. 4, Nr. 4, fcac175
Pantazis, Caroline B.; Yang, Andrian; Lara, Erika; McDonough, Justin A.; Blauwendraat, Cornelis; Peng, Lirong; Oguro, Hideyuki; Kanaujiya, Jitendra; Zou, Jizhong; Sebesta, David; Pratt, Gretchen; Cross, Erin; Blockwick, Jeffrey; Buxton, Philip; Kinner-Bibeau, Lauren; Medura, Constance; Tompkins, Christopher; Hughes, Stephen; Santiana, Marianita; Faghri, Faraz; Nalls, Mike A.; Vitale, Daniel; Ballard, Shannon; Qi, Yue A.; Ramos, Daniel M.; Anderson, Kailyn M.; Stadler, Julia; Narayan, Priyanka; Papademetriou, Jason; Reilly, Luke; Nelson, Matthew P.; Aggarwal, Sanya; Rosen, Leah U.; Kirwan, Peter; Pisupati, Venkat; Coon, Steven L.; Scholz, Sonja W.; Priebe, Theresa; Ottl, Miriam; Dong, Jian; Meijer, Marieke; Janssen, Lara J. M.; Lourenco, Vanessa S.; Kant, Rik van der; Crusius, Dennis; Paquet, Dominik; Raulin, Ana-Caroline; Bu, Guojun; Held, Aaron; Wainger, Brian J.; Gabriele, Rebecca M. C.; Casey, Jackie M.; Wray, Selina; Abu-Bonsrah, Dad; Parish, Clare L.; Beccari, Melinda S.; Cleveland, Don W.; Li, Emmy; Rose, Indigo V. L.; Kampmann, Martin; Aristoy, Carles Calatayud; Verstreken, Patrik; Heinrich, Laurin; Chen, Max Y.; Schule, Birgitt; Dou, Dan; Holzbaur, Erika L. F.; Zanellati, Maria Clara; Basundra, Richa; Deshmukh, Mohanish; Cohen, Sarah; Khanna, Richa; Raman, Malavika; Nevin, Zachary S.; Matia, Madeline; Lent, Jonas; Timmerman, Vincent; Conklin, Bruce R.; Chase, Katherine Johnson; Zhang, Ke; Funes, Salome; Bosco, Daryl A.; Erlebach, Lena; Welzer, Marc; Kronenberg-Versteeg, Deborah; Lyu, Guochang; Arenas, Ernest; Coccia, Elena; Sarrafha, Lily; Ahfeldt, Tim; Marioni, John C. van; Skarnes, William C.; Cookson, Mark R.; Ward, Michael E. und Merkle, Florian T.
(2022):
A reference human induced pluripotent stem cell line for collaborative studies.
In: Cell Stem Cell, Bd. 29, Nr. 12, E22: S. 1685-1702
[PDF, 5MB]
Shadrin, Alexey A.; Mucha, Sören; Ellinghaus, David; Makarious, Mary B.; Blauwendraat, Cornelis; Sreelatha, Ashwin A. K.; Heras-Garvin, Antonio; Ding, Jinhui; Hammer, Monia; Foubert-Samier, Alexandra; Meissner, Wassilios G.; Rascol, Olivier; Pavy-Le Traon, Anne; Frei, Oleksandr; O'Connell, Kevin S.; Bahrami, Shahram; Schreiber, Stefan; Lieb, Wolfgang; Müller-Nurasyid, Martina; Schminke, Ulf; Homuth, Georg; Schmidt, Carsten O.; Nöthen, Markus M.; Hoffmann, Per; Gieger, Christian; Wenning, Gregor; Gibbs, J. Raphael; Franke, Andre; Hardy, John; Stefanova, Nadia; Gasser, Thomas; Singleton, Andrew; Houlden, Henry; Scholz, Sonja W.; Andreassen, Ole A. und Sharma, Manu
(2020):
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease.
In: Movement Disorders, Bd. 36, Nr. 2: S. 449-459
Stankovic, Iva; Quinn, Niall; Vignatelli, Luca; Antonini, Angelo; Berg, Daniela; Coon, Elizabeth; Cortelli, Pietro; Fanciulli, Alessandra; Ferreira, Joaquim J.; Freeman, Roy; Halliday, Glenda; Hoglinger, Gunter U.; Iodice, Valeria; Kaufmann, Horacio; Klockgether, Thomas; Kostic, Vladimir; Krismer, Florian; Lang, Anthony; Levin, Johannes; Low, Phillip; Mathias, Christopher; Meissner, Wassillios G.; Kaufmann, Lucy Norcliffe; Palma, Jose-Alberto; Panicker, Jalesh N.; Pellecchia, Maria Teresa; Sakakibara, Ryuji; Schmahmann, Jeremy; Scholz, Sonja W.; Singer, Wolfgang; Stamelou, Maria; Tolosa, Eduardo; Tsuji, Shoji; Seppi, Klaus; Poewe, Werner und Wenning, Gregor K.
(2019):
A critique of the second consensus criteria for multiple system atrophy.
In: Movement Disorders, Bd. 34, Nr. 7: S. 975-984
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. und Holstege, Henne
(2019):
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.
In: Acta Neuropathologica, Bd. 138, Nr. 2: S. 237-250
[PDF, 1MB]