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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 3

Zeitschriftenartikel

Luo, Jiao; Thomassen, Jesper Qvist; Bellenguez, Céline; Grenier-Boley, Benjamin; de Rojas, Itziar; Castillo, Atahualpa; Parveen, Kayenat; Küçükali, Fahri; Nicolas, Aude; Peters, Oliver; Schneider, Anja; Dichgans, Martin ORCID logoORCID: https://orcid.org/0000-0002-0654-387X; Rujescu, Dan; Scherbaum, Norbert; Jürgen, Deckert; Riedel-Heller, Steffi; Hausner, Lucrezia; Porcel, Laura Molina; Düzel, Emrah; Grimmer, Timo; Wiltfang, Jens; Heilmann-Heimbach, Stefanie; Moebus, Susanne; Tegos, Thomas; Scarmeas, Nikolaos; Clarimon, Jordi; Moreno, Fermin; Pérez-Tur, Jordi; Bullido, María J.; Pastor, Pau; Sánchez-Valle, Raquel; Álvarez, Victoria; Boada, Mercè; García-González, Pablo; Puerta, Raquel; Mir, Pablo; Real, Luis M.; Piñol-Ripoll, Gerard; García-Alberca, Jose María; Royo, Jose Luís; Rodriguez-Rodriguez, Eloy; Soininen, Hilkka; Kuulasmaa, Teemu; de Mendonça, Alexandre; Mehrabian, Shima; Hort, Jakub; Vyhnalek, Martin; van der Lee, Sven; Graff, Caroline; Papenberg, Goran; Giedraitis, Vilmantas; Boland, Anne; Bacq-Daian, Delphine; Deleuze, Jean-François; Nicolas, Gael; Dufouil, Carole; Pasquier, Florence; Hanon, Olivier; Debette, Stéphanie; Grünblatt, Edna; Popp, Julius; Benussi, Luisa; Galimberti, Daniela; Arosio, Beatrice; Mecocci, Patrizia; Solfrizzi, Vincenzo; Parnetti, Lucilla; Squassina, Alessio; Tremolizzo, Lucio; Borroni, Barbara; Nacmias, Benedetta; Sorbi, Sandro; Caffarra, Paolo; Seripa, Davide; Rainero, Innocenzo; Daniele, Antonio; Masullo, Carlo; Spalletta, Gianfranco; Williams, Julie; Amouyel, Philippe; Jessen, Frank; Kehoe, Patrick; Tsolaki, Magda; Rossi, Giacomina; Sánchez-Juan, Pascual; Sleegers, Kristel; Ingelsson, Martin; Andreassen, Ole A.; Hiltunen, Mikko; Van Duijn, Cornelia; Sims, Rebecca; van der Flier, Wiesje; Ruiz, Agustín; Ramirez, Alfredo; Lambert, Jean-Charles und Frikke-Schmidt, Ruth (2023): Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease. In: JAMA Network Open, Bd. 6, Nr. 5, e2313734 [PDF, 1MB]

Sugier, Pierre-Emmanuel; Lucotte, Elise A.; Domenighetti, Cloe; Law, Matthew H.; Iles, Mark M.; Brown, Kevin; Amos, Christopher; McKay, James D.; Hung, Rayjean J.; Karimi, Mojgan; Bacq-Daian, Delphine; Boland-Auge, Anne; Olaso, Robert; Deleuze, Jean-francois; Lesueur, Fabienne; Ostroumova, Evgenia; Kesminiene, Ausrele; de Vathaire, Florent; Guenel, Pascal; Sreelatha, Ashwin Ashok Kumar; Schulte, Claudia; Grover, Sandeep; May, Patrick; Bobbili, Dheeraj R.; Radivojkov-Blagojevic, Milena; Lichtner, Peter; Singleton, Andrew B.; Hernandez, Dena G.; Edsall, Connor; Mellick, George D.; Zimprich, Alexander; Pirker, Walter; Rogaeva, Ekaterina; Lang, Anthony E.; Koks, Sulev; Taba, Pille; Lesage, Suzanne; Brice, Alexis; Corvol, Jean-Christophe; Chartier-Harlin, Marie-Christine; Mutez, Eugenie; Brockmann, Kathrin; Deutschlaender, Angela B.; Hadjigeorgiou, Georges M.; Dardiotis, Efthimios; Stefanis, Leonidas; Simitsi, Athina Maria; Valente, Enza Maria; Petrucci, Simona; Straniero, Letizia; Zecchinelli, Anna; Pezzoli, Gianni; Brighina, Laura; Ferrarese, Carlo; Annesi, Grazia; Quattrone, Andrea; Gagliardi, Monica; Matsuo, Hirotaka; Nakayama, Akiyoshi; Hattori, Nobutaka; Nishioka, Kenya; Chung, Sun Ju; Kim, Yun Joong; Kolber, Pierre; van de Warrenburg, Bart P. C.; Bloem, Bastiaan R.; Aasly, Jan; Toft, Mathias; Pihlstrom, Lasse; Guedes, Leonor Correia; Ferreira, Joaquim J.; Bardien, Soraya; Carr, Jonathan; Tolosa, Eduardo; Ezquerra, Mario; Pastor, Pau; Diez-Fairen, Monica; Wirdefeldt, Karin; Pedersen, Nancy; Ran, Caroline; Belin, Andrea C.; Puschmann, Andreas; Roedstroem, Emil Ygland; Clarke, Carl E.; Morrison, Karen E.; Tan, Manuela; Krainc, Dimitri; Burbulla, Lena F.; Farrer, Matt J.; Kruger, Rejko; Gasser, Thomas; Sharma, Manu; Truong, Therese und Elbaz, Alexis (2023): Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. In: Movement Disorders, Bd. 38, Nr. 4: S. 604-615 [PDF, 757kB]

Garnier, Sophie; Harakalova, Magdalena; Weiss, Stefan; Mokry, Michal; Regitz-Zagrosek, Vera; Hengstenberg, Christian; Cappola, Thomas P.; Isnard, Richard; Arbustini, Eloisa; Cook, Stuart A.; Setten, Jessica van; Calis, Jorg J. A.; Hakonarson, Hakon; Morley, Michael P.; Stark, Klaus; Prasad, Sanjay K.; Li, Jin; O'Regan, Declan P.; Grasso, Maurizia; Müller-Nurasyid, Martina; Meitinger, Thomas; Empana, Jean-Philippe; Strauch, Konstantin; Waldenberger, Melanie; Marguiles, Kenneth B.; Seidman, Christine E.; Kararigas, Georgios; Meder, Benjamin; Haas, Jan; Boutouyrie, Pierre; Lacolley, Patrick; Jouven, Xavier; Erdmann, Jeanette; Blankenberg, Stefan; Wichter, Thomas; Ruppert, Volker; Tavazzi, Luigi; Dubourg, Olivier; Roizes, Gerard; Dorent, Richard; Groote, Pascal de; Fauchier, Laurent; Trochu, Jean-Noel; Aupetit, Jean-Francois; Bilinska, Zofia T.; Germain, Marine; Völker, Uwe; Hemerich, Daiane; Raji, Ibticem; Bacq-Daian, Delphine; Proust, Carole; Remior, Paloma; Gomez-Bueno, Manuel; Lehnert, Kristin; Maas, Renee; Olaso, Robert; Saripella, Ganapathi Varma; Felix, Stephan B.; McGinn, Steven; Duboscq-Bidot, Laetitia; Mil, Alain van; Besse, Celine; Fontaine, Vincent; Blanche, Helene; Ader, Flavie; Keating, Brendan; Curjol, Angelique; Boland, Anne; Komajda, Michel; Cambien, Francois; Deleuze, Jean-Francois; Dörr, Marcus; Asselbergs, Folkert W.; Villard, Eric; Tregoueet, David-Alexandre und Charron, Philippe (2021): Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23. In: European Heart Journal, Bd. 42, Nr. 20: S. 2000-2011

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