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JAMA neurology, ISSN 2168-6149, 07/2019
Heritability describes the proportion of variance in the risk of developing a condition that is explained by genetic factors. Although amyotrophic lateral... 
Journal Article
Neurology, ISSN 0028-3878, 12/2013, Volume 81, Issue 24, pp. 2107 - 2115
Journal Article
by Cirulli, Elizabeth T and Lasseigne, Brittany N and Petrovski, Slavé and Sapp, Peter C and Dion, Patrick A and Leblond, Claire S and Couthouis, Julien and Lu, Yi-Fan and Wang, Quanli and Krueger, Brian J and Ren, Zhong and Keebler, Jonathan and Han, Yujun and Levy, Shawn E and Boone, Braden E and Wimbish, Jack R and Waite, Lindsay L and Jones, Angela L and Carulli, John P and Day-Williams, Aaron G and Staropoli, John F and Xin, Winnie W and Chesi, Alessana and Raphael, Alya R and McKenna-Yasek, Diane and Cady, Janet and de Jong, J. M. B. Vianney and Kenna, Kevin P and Smith, Bradley N and Topp, Simon and Miller, Jack and Gkazi, Athina and Al-Chalabi, Ammar and van den Berg, Leonard H and Veldink, Jan and Silani, Vincenzo and Ticozzi, Nicola and Shaw, Christopher E and Baloh, Robert H and Appel, Stanley and Simpson, Ericka and Lagier-Tourenne, Clotilde and Pulst, Stefan M and Gibson, Summer and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Grossman, Murray and Shneider, Neil A and Chung, Wendy K and Ravits, John M and Glass, Jonathan D and Sims, Katherine B and van Deerlin, Vivianna M and Maniatis, Tom and Hayes, Sebastian D and Ordureau, Alban and Swarup, Sharan and Landers, John and Baas, Frank and Allen, Anew S and Bedlack, Richard S and Harper, J. Wade and Gitler, Aaron D and Rouleau, Guy A and Brown, Robert and Harms, Matthew B and Cooper, Gregory M and Harris, Tim and Myers, Richard M and Goldstein, David B and Hardiman, Orla and McLaughlin, Russell L and Mazzini, Letizia and Blair, Ian P and Williams, Kelly L and Nicholson, Garth A and Al-Sarraj, Safa and King, Anew and Scotter, Emma L and Troakes, Claire and Vance, Caroline and D'alfonso, Sana and Duga, Stefano and Corrado, Lucia and ten Asbroek, Anneloor L. M. A and Calini, Daniela and Colombrita, Claudia and Ratti, Antonia and Tiloca, Cinzia and Wu, Zheyang and Asress, Seneshaw and Polak, Meraida and Diekstra, Frank and van Rheenen, Wouter and Danielson, Eric W and Fallini, Claudia and Keagle, Pamela and Lewis, Elizabeth A and Kost, Jason and ... and FALS Sequencing Consortium
Science, ISSN 0036-8075, 2015, Volume 347, Issue 6229, pp. 1436 - 1441
Journal Article
PLoS genetics, 01/2018, Volume 14, Issue 1, p. e1007152
Previous studies of the genetic landscape of Ireland have suggested homogeneity, with population substructure undetectable using single-marker methods. Here we... 
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2012, Volume 11, Issue 3, pp. 232 - 240
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 2013, Volume 50, Issue 11, pp. 776 - 783
Background Over 100 genes have been implicated in the aetiology of amyotrophic lateral sclerosis (ALS). A detailed understanding of their independent and... 
PROTEIN | VARIANTS | FORM | AMYOTROPHIC-LATERAL-SCLEROSIS | SOD1 | Motor Neurone Disease | JUVENILE | GENETICS & HEREDITY | FUS MUTATIONS | TARDBP | ASSOCIATION | Genetic Epidemiology | TOOL | Screening | 1506
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