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amyotrophic lateral sclerosis (5) 5
index medicus (4) 4
als (3) 3
clinical neurology (3) 3
humans (3) 3
medical and health sciences (3) 3
medicin och hälsovetenskap (3) 3
neurodegeneration (3) 3
amyotrophic lateral sclerosis - genetics (2) 2
amyotrophic-lateral-sclerosis (2) 2
basic medicine (2) 2
case-control studies (2) 2
genetics and genomics of als (2) 2
medicinska och farmaceutiska grundvetenskaper (2) 2
neurodegenerative disease (2) 2
neurology (2) 2
neurosciences (2) 2
retrotransposons (2) 2
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activates microglia (1) 1
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als, atxn2, age of onset, amyotrophic lateral sclerosis, cag, expansion, exponential risk, intermediate expansion, risk, sca2, trinucleotide repeat, triplet (1) 1
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dk/atira/pure/subjectarea/asjc/2700/2717 (1) 1
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by van Rheenen, Wouter and Shatunov, Aleksey and Dekker, Annelot M and McLaughlin, Russell L and Diekstra, Frank P and Pulit, Sara L and van der Spek, Rick A. A and Võsa, Urmo and de Jong, Simone and Robinson, Matthew R and Yang, Jian and Fogh, Isabella and van Doormaal, Perry Tc and Tazelaar, Gijs H. P and Koppers, Max and Blokhuis, Anna M and Sproviero, William and Jones, Ashley R and Kenna, Kevin P and van Eijk, Kristel R and Harschnitz, Oliver and Schellevis, Raymond D and Brands, William J and Medic, Jelena and Menelaou, Anoniki and Vajda, Alice and Ticozzi, Nicola and Lin, Kuang and Rogelj, Boris and Vrabec, Katarina and Ravnik-Glavač, Metka and Koritnik, Blaž and Zidar, Janez and Leonardis, Lea and Grošelj, Leja Dolenc and Millecamps, Stéphanie and Salachas, François and Meininger, Vincent and de Carvalho, Mamede and Pinto, Susana and Mora, Jesus S and Rojas-García, Ricardo and Polak, Meraida and Chanan, Siddharthan and Colville, Shuna and Swingler, Robert and Morrison, Karen E and Shaw, Pamela J and Hardy, John and Orrell, Richard W and Pittman, Alan and Sidle, Katie and Fratta, Pietro and Malaspina, Anea and Topp, Simon and Petri, Susanne and Abdulla, Susanne and pper, Carsten and Sendtner, Michael and Meyer, Thomas and Ophoff, Roel A and Staats, Kim A and Wiedau-Pazos, Martina and Lomen-Hoerth, Catherine and van Deerlin, Vivianna M and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Basak, A. Nazli and Tunca, Ceren and Hamzeiy, Hamid and Parman, Yesim and Meitinger, Thomas and Lichtner, Peter and Radivojkov-Blagojevic, Milena and Anes, Christian R and Maurel, Cindy and Bensimon, Gilbert and Landwehrmeyer, Bernhard and Brice, Alexis and Payan, Christine A. M and Saker-Delye, Safaa and Dürr, Alexana and Wood, Nicholas W and Tittmann, Lukas and Lieb, Wolfgang and Franke, Ane and Rietschel, Marcella and Cichon, Sven and Nöthen, Markus M and Amouyel, Philippe and Tzourio, Christophe and Dartigues, Jean-François and Uitterlinden, Ane G and Rivadeneira, Fernando and Estrada, Karol and Hofman, Albert and Curtis, Charles and Blauw, Hylke M and van der Kooi, Anneke J and ... and PARALS Registry and FALS Sequencing Consortium and SLALOM Grp and SLAGEN Consortium and NNIPPS Study Grp and SLAP Registry and SLALOM Group and NNIPPS Study Group and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk neurovetenskap and Umeå universitet
Nature genetics, ISSN 1061-4036, 2016, Volume 48, Issue 9, pp. 1043 - 1048
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2016, Volume 51, pp. 178.e1 - 178.e9
Journal Article
Cell Reports, ISSN 2211-1247, 10/2019, Volume 29, Issue 5, pp. 1164 - 1177.e5
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the progressive loss of motor neurons. While several pathogenic... 
neurodegenerative disease | genetics and genomics of ALS | TDP-43 | neurodegeneration | retrotransposons | transposable elements | amyotrophic lateral sclerosis | yes | GENE | TRANSCRIPTOME | RNA TARGETS | MICROGLIA | TRANSPOSABLE ELEMENTS | SITES | NEURODEGENERATION | FRONTOTEMPORAL LOBAR DEGENERATION | CLIP | CELL BIOLOGY
Journal Article
by Bridel, Claire and van Wieringen, Wessel N and Zetterberg, Henrik and Tijms, Betty M and Teunissen, Charlotte E and Alvarez-Cermeño, José C and Aneasson, Ulf and Axelsson, Markus and Bäckström, David C and Bartos, Ales and Bjerke, Maria and Blennow, Kaj and Boxer, Adam and Brundin, Lou and Burman, Joachim and Christensen, Tove and Fialová, Lenká and Forsgren, Lars and Frederiksen, Jette L and Gisslén, Magnus and Gray, Elizabeth and Gunnarsson, Martin and Hall, Sara and Hansson, Oskar and Herbert, Megan K and Jakobsson, Joel and Jessen-Krut, Jan and Janelidze, Shorena and Johannsson, Gudmundur and Jonsson, Michael and Kappos, Ludwig and Khademi, Mohsen and Khalil, Michael and Kuhle, Jens and Landén, Mikael and Leinonen, Ville and Logroscino, Giancarlo and Lu, Ching-Hua and Lycke, Jan and Magdalinou, Nadia K and Malaspina, Anea and Mattsson, Niklas and Meeter, Lieke H and Mehta, Sanjay R and Modvig, Signe and Olsson, Tomas and Paterson, Ross W and Pérez-Santiago, Josué and Piehl, Freik and Pijnenburg, Yolande A. L and Pyykkö, Okko T and Ragnarsson, Oskar and Rojas, Julio C and Romme Christensen, Jeppe and Sandberg, Linda and Scherling, Carole S and Schott, Jonathan M and Sellebjerg, Finn T and Simone, Isabella L and Skillbäck, Tobias and Stilund, Morten and Sundström, Peter and Svenningsson, Anders and Tortelli, Rosanna and Tortorella, Carla and Trentini, Alessano and Troiano, Maria and Turner, Martin R and van Swieten, John C and Vågberg, Mattias and Verbeek, Marcel M and Villar, Luisa M and Visser, Pieter Jelle and Wallin, Anders and Weiss, Aneas and Wikkelsø, Carsten and Wild, Edward J and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Landtblom: Neurologi and Institutionen för neurovetenskap
JAMA Neurology, ISSN 2168-6149, 09/2019, Volume 76, Issue 9, pp. 1035 - 1048
Importance: Neurofilament light protein (NfL) is elevated in cerebrospinal fluid (CSF) of a number of neurological conditions compared with healthy controls... 
Clinical Neurology | Clinical Medicine | Neurology | Neurologi | Medical and Health Sciences | Medicin och hälsovetenskap | Psykiatri | Klinisk medicin | Psychiatry
Journal Article
Cell Reports, ISSN 2211-1247, 10/2019, Volume 29, Issue 5, pp. 1164 - 1177.e5
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the progressive loss of motor neurons. While several pathogenic... 
genetics and genomics of ALS | neurodegenerative disease | TDP-43 | neurodegeneration | Biochemistry, Genetics and Molecular Biology(all) | retrotransposons | transposable elements | amyotrophic lateral sclerosis
Journal Article
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