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1 Ergebnisse
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Genome-wide association analyses identify new risk variants..:
van Rheenen, Wouter
;
Shatunov, Aleksey
;
Dekker, Annelot M
...
qt22r175sv. , 2016
Link:
https://escholarship.org/uc/item/22r175sv
RT Journal T1
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt22r175sv&Exemplar=1&LAN=DE A1 van Rheenen, Wouter A1 Shatunov, Aleksey A1 Dekker, Annelot M A1 McLaughlin, Russell L A1 Diekstra, Frank P A1 Pulit, Sara L A1 van der Spek, Rick AA A1 Võsa, Urmo A1 de Jong, Simone A1 Robinson, Matthew R A1 Yang, Jian A1 Fogh, Isabella A1 van Doormaal, Perry Tc A1 Tazelaar, Gijs HP A1 Koppers, Max A1 Blokhuis, Anna M A1 Sproviero, William A1 Jones, Ashley R A1 Kenna, Kevin P A1 van Eijk, Kristel R A1 Harschnitz, Oliver A1 Schellevis, Raymond D A1 Brands, William J A1 Medic, Jelena A1 Menelaou, Androniki A1 Vajda, Alice A1 Ticozzi, Nicola A1 Lin, Kuang A1 Rogelj, Boris A1 Vrabec, Katarina A1 Ravnik-Glavač, Metka A1 Koritnik, Blaž A1 Zidar, Janez A1 Leonardis, Lea A1 Grošelj, Leja Dolenc A1 Millecamps, Stéphanie A1 Salachas, François A1 Meininger, Vincent A1 de Carvalho, Mamede A1 Pinto, Susana A1 Mora, Jesus S A1 Rojas-García, Ricardo A1 Polak, Meraida A1 Chandran, Siddharthan A1 Colville, Shuna A1 Swingler, Robert A1 Morrison, Karen E A1 Shaw, Pamela J A1 Hardy, John A1 Orrell, Richard W A1 Pittman, Alan A1 Sidle, Katie A1 Fratta, Pietro A1 Malaspina, Andrea A1 Topp, Simon A1 Petri, Susanne A1 Abdulla, Susanne A1 Drepper, Carsten A1 Sendtner, Michael A1 Meyer, Thomas A1 Ophoff, Roel A A1 Staats, Kim A A1 Wiedau-Pazos, Martina A1 Lomen-Hoerth, Catherine A1 Van Deerlin, Vivianna M A1 Trojanowski, John Q A1 Elman, Lauren A1 McCluskey, Leo A1 Basak, A Nazli A1 Tunca, Ceren A1 Hamzeiy, Hamid A1 Parman, Yesim A1 Meitinger, Thomas A1 Lichtner, Peter A1 Radivojkov-Blagojevic, Milena A1 Andres, Christian R A1 Maurel, Cindy A1 Bensimon, Gilbert A1 Landwehrmeyer, Bernhard A1 Brice, Alexis A1 Payan, Christine AM A1 Saker-Delye, Safaa A1 Dürr, Alexandra A1 Wood, Nicholas W A1 Tittmann, Lukas A1 Lieb, Wolfgang A1 Franke, Andre A1 Rietschel, Marcella A1 Cichon, Sven A1 Nöthen, Markus M A1 Amouyel, Philippe A1 Tzourio, Christophe A1 Dartigues, Jean-François A1 Uitterlinden, Andre G A1 Rivadeneira, Fernando A1 Estrada, Karol A1 Hofman, Albert A1 Curtis, Charles A1 Blauw, Hylke M PB eScholarship, University of California YR 2016 K1 PARALS Registry K1 SLALOM Group K1 SLAP Registry K1 FALS Sequencing Consortium K1 SLAGEN Consortium K1 NNIPPS Study Group K1 Humans K1 Amyotrophic Lateral Sclerosis K1 Genetic Predisposition to Disease K1 Proteins K1 Cytoskeletal Proteins K1 Myelin Proteins K1 Case-Control Studies K1 Cohort Studies K1 Mutation K1 Netherlands K1 Munc18 Proteins K1 Genome-Wide Association Study K1 Neurosciences K1 Rare Diseases K1 Brain Disorders K1 Biotechnology K1 Prevention K1 Human Genome K1 Neurodegenerative K1 Genetics K1 ALS K1 Aetiology K1 2.1 Biological and endogenous factors K1 Biological Sciences K1 Medical and Health Sciences K1 Developmental Biology JF qt22r175sv LK http://dx.doi.org/https://escholarship.org/uc/item/22r175sv DO https://escholarship.org/uc/item/22r175sv SF ELIB - SuUB Bremen
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