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Nature Reviews Genetics, ISSN 1471-0056, 2019
The genetic correlation describes the genetic relationship between two traits and can contribute to a better understanding of the shared biological pathways... 
Journal Article
European Neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S1083 - S1083
Journal Article
Journal Article
Journal Article
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 07/2019, Volume 20, Issue 5-6, pp. 432 - 440
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive fatal neurodegenerative disease affecting one in 350 people. The aim of Project MinE is to... 
Databrowser | open-access | amyotrophic lateral sclerosis | whole-genome sequencing
Journal Article
JOURNAL OF NEUROLOGY, ISSN 0340-5354, 04/2017, Volume 264, Issue 4, pp. 694 - 700
To examine evidence for a role of gluten sensitivity (GS) or celiac disease (CD) in ALS etiology, we included participants from a population-based case-control... 
Journal Article
Nature Communications [E], ISSN 2041-1723, 2017, Volume 8
We have previously shown higher-than-expected rates of schizophrenia in relatives of patients with amyotrophic lateral sclerosis (ALS), suggesting an... 
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/2016, Volume 80, Issue 1, p. 71
OBJECTIVE: We investigated the pathogenicity of immunoglobulin M (IgM) anti-GM1 antibodies in serum from patients with multifocal motor neuropathy (MMN) using... 
Journal Article
Journal of Neurology, ISSN 0340-5354, 02/2017, Volume 264, Issue 4, p. 694
To examine evidence for a role of gluten sensitivity (GS) or celiac disease (CD) in ALS etiology, we included participants from a population-based case-control... 
Journal Article
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
by Smith, Bradley N and Ticozzi, Nicola and Fallini, Claudia and Gkazi, Athina Soragia and Topp, Simon and Kenna, Kevin P and Scotter, Emma L and Kost, Jason and Keagle, Pamela and Miller, Jack W and Calini, Daniela and Vance, Caroline and Danielson, Eric W and Troakes, Claire and Tiloca, Cinzia and Al-Sarraj, Safa and Lewis, Elizabeth A and King, Andrew and Colombrita, Claudia and Pensato, Viviana and Castellotti, Barbara and de Belleroche, Jacqueline and Baas, Frank and ten Asbroek, Anneloor LMA and Sapp, Peter C and McKenna-Yasek, Diane and McLaughlin, Russell L and Polak, Meraida and Asress, Seneshaw and Esteban-Pérez, Jesús and Muñoz-Blanco, José Luis and Simpson, Michael and D’Alfonso, Sandra and Mazzini, Letizia and Comi, Giacomo P and Del Bo, Roberto and Ceroni, Mauro and Gagliardi, Stella and Querin, Giorgia and Bertolin, Cinzia and van Rheenen, Wouter and Diekstra, Frank P and Lauria, Giuseppe and Duga, Stefano and Corti, Stefania and Cereda, Cristina and Corrado, Lucia and Sorarù, Gianni and Morrison, Karen E and Williams, Kelly L and Nicholson, Garth A and Blair, Ian P and Dion, Patrick A and Leblond, Claire S and Rouleau, Guy A and Hardiman, Orla and Veldink, Jan H and van den Berg, Leonard H and Al-Chalabi, Ammar and Pall, Hardev and Shaw, Christopher E and Shaw, Pamela J and Turner, Martin R and Talbot, Kevin and Taroni, Franco and García-Redondo, Alberto and Wu, Zheyang and Glass, Jonathan D and Gellera, Cinzia and Ratti, Antonia and Brown, Robert H and Silani, Vincenzo and Landers, John E and SLAGEN Consortium
Neuron, ISSN 0896-6273, 10/2014, Volume 84, Issue 2, pp. 324 - 331
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2012, Volume 7, Issue 4
Amyotrophic lateral sclerosis (ALS) is a progressive, neurodegenerative disease characterized by loss of upper and lower motor neurons. ALS is considered to be... 
Journal Article
by McCarthy, Shane and Das, Sayantan and Kretzschmar, Warren and Delaneau, Olivier and Wood, Anew R and Teumer, Alexander and Kang, Hyun Min and Fuchsberger, Christian and Danecek, Petr and Sharp, Kevin and Luo, Yang and Sidorel, Carlo and Kwong, Alan and Timpson, Nicholas and Koskinen, Seppo and Vrieze, Scott and Scott, Laura J and Zhang, He and Mahajan, Anubha and Veldink, Jan and Peters, Ulrike and Pato, Carlos and van Duijn, Cornelia M and Gillies, Christopher E and Gandin, Ilaria and Mezzavilla, Massimo and Gilly, Arthur and Cocca, Massimiliano and Traglia, Michela and Angius, Anea and Barrett, Jeffrey C and Boomsma, Dorrett and Branham, Kari and Breen, Gerome and Brummett, Chad M and Busonero, Fabio and Campbell, Harry and Chan, Anew and Che, Sai and Chew, Emily and Collins, Francis S and Corbin, Laura J and Smith, George Davey and Dedoussis, George and Dorr, Marcus and Farmaki, Aliki-Eleni and Ferrucci, Luigi and Forer, Lukas and Fraser, Ross M and Gabriel, Stacey and Levy, Shawn and Groop, Leif and Harrison, Tabitha and Hattersley, Anew and Holmen, Oddgeir L and Hveem, Kristian and Kretzler, Matthias and Lee, James C and McGue, Matt and Meitinger, Thomas and Melzer, David and Min, Josine L and Mohlke, Karen L and Vincent, John B and Nauck, Matthias and Nickerson, Deborah and Palotie, Aarno and Pato, Michele and Pirastu, Nicola and McInnis, Melvin and Richards, J. Brent and Sala, Cinzia and Salomaa, Veikko and Schlessinger, David and Schoenherr, Sebastian and Slagboom, P. Eline and Small, Kerrin and Spector, Timothy and Stambolian, Dwight and Tuke, Marcus and Tuomilehto, Jaakko and van den Berg, Leonard H and Van Rheenen, Wouter and Volker, Uwe and Wijmenga, Cisca and Toniolo, Daniela and Zeggini, Eleftheria and Gasparini, Paolo and Sampson, Matthew G and Wilson, James F and Frayling, Timothy and de Bakker, Paul I. W and Swertz, Morris A and McCarroll, Steven and Kooperberg, Charles and Dekker, Annelot and Altshuler, David and Willer, Cristen and Iacono, William and Ripatti, Samuli and ... and Haplotype Reference Consortium and the Haplotype Reference Consortium and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1279 - 1283
Journal Article