Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: Sarcoma and FUS[original query] |
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The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS. European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 May 17 (5): 754-6. Damme P Van, Goris A, Race V, Hersmus N, Dubois B, Bosch L Van Den, Matthijs G, Robberecht |
Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis. Muscle & nerve 2010 Aug 42 (2): 170-6. Rademakers Rosa, Stewart Heather, Dejesus-Hernandez Mariely, Krieger Charles, Graff-Radford Neill, Fabros Marife, Briemberg Hannah, Cashman Neil, Eisen Andrew, Mackenzie Ian R |
FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration. Journal of Alzheimer's disease : JAD 2010 19 (4): 1317-22. Cantoni Claudia, Fenoglio Chiara, Cortini Francesca, Venturelli Eliana, Villa Chiara, Clerici Francesca, Marcone Alessandra, Benussi Luisa, Ghidoni Roberta, Gallone Salvatore, Scalabrini Diego, Franceschi Massimo, Cappa Stefano, Binetti Giuliano, Mariani Claudio, Rainero Innocenzo, Giordana Maria Teresa, Bresolin Nereo, Scarpini Elio, Galimberti Danie |
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene. Acta neuropathologica 2011 Jul 122 (1): 99-110. Snowden Julie S, Hu Quan, Rollinson Sara, Halliwell Nicola, Robinson Andrew, Davidson Yvonne S, Momeni Parastoo, Baborie Atik, Griffiths Timothy D, Jaros Evelyn, Perry Robert H, Richardson Anna, Pickering-Brown Stuart M, Neary David, Mann David M |
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. Neurobiology of aging 2012 Apr 33 (4): 837.e1-5. Sproviero William, La Bella Vincenzo, Mazzei Rosalucia, Valentino Paola, Rodolico Carmelo, Simone Isabella Laura, Logroscino Giancarlo, Ungaro Carmine, Magariello Angela, Patitucci Alessandra, Tedeschi Gioacchino, Spataro Rossella, Condino Francesca, Bono Francesco, Citrigno Luigi, Monsurrò Maria Rosaria, Muglia Maria, Gambardella Antonio, Quattrone Aldo, Conforti Francesca Lui |
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.
![]() Nature genetics 2012 Mar 44 (3): 323-7. Postel-Vinay Sophie, Véron Amélie S, Tirode Franck, Pierron Gaelle, Reynaud Stéphanie, Kovar Heinrich, Oberlin Odile, Lapouble Eve, Ballet Stelly, Lucchesi Carlo, Kontny Udo, González-Neira Anna, Picci Piero, Alonso Javier, Patino-Garcia Ana, de Paillerets Brigitte Bressac, Laud Karine, Dina Christian, Froguel Philippe, Clavel-Chapelon Françoise, Doz Francois, Michon Jean, Chanock Stephen J, Thomas Gilles, Cox David G, Delattre Olivi |
Genetic analysis of the FUS/TLS gene in essential tremor. European journal of neurology : the official journal of the European Federation of Neurological Societies 2013 Mar 20 (3): 534-9. Parmalee N, Mirzozoda K, Kisselev S, Merner N, Dion P, Rouleau G, Clark L, Louis E |
Genetic overlap between apparently sporadic motor neuron diseases. PloS one 2012 7 (11): 11. van Blitterswijk M, Vlam L, van Es MA, van der Pol WL, Hennekam EA, Dooijes D, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH |
Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis. Human molecular genetics 2013 Dec 22 (23): 4748-55. Sabatelli Mario, Moncada Alice, Conte Amelia, Lattante Serena, Marangi Giuseppe, Luigetti Marco, Lucchini Matteo, Mirabella Massimiliano, Romano Angela, Del Grande Alessandra, Bisogni Giulia, Doronzio Paolo Niccolo', Rossini Paolo Maria, Zollino Marcel |
Identification of FUS p.R377W in essential tremor. European journal of neurology : the official journal of the European Federation of Neurological Societies 2014 Feb 21 (2): 361-3. Rajput A, Rajput A H, Rajput M L, Encarnacion M, Bernales C Q, Ross J P, Farrer M J, Vilariño-Güell |
Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS. Neurobiology of aging 2013 Sep 34 (9): 2235.e11-3. Ravenscroft Thomas A, Baker Matt C, Rutherford Nicola J, Neumann Manuela, Mackenzie Ian R, Josephs Keith A, Boeve Bradley F, Petersen Ronald, Halliday Glenda M, Kril Jillian, van Swieten John C, Seeley William W, Dickson Dennis W, Rademakers Ro |
Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor. Neurobiology of aging 2013 Aug 34 (8): 2078.e3-4. Zheng Wen, Deng Xiong, Liang Hui, Song Zhi, Gao Kai, Yang Yan, Deng H |
Genetic analysis of the fused in sarcoma gene in Chinese Han patients with Parkinson's disease. Parkinsonism & related disorders 2014 Jan 20 (1): 119-21. Gao Kai, Zheng Wen, Deng Xiong, Xiong Wei, Song Zhi, Yang Yan, Deng H |
The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation. PLoS genetics 2014 Jul 10 (7): e1004475. Brohl Andrew S, Solomon David A, Chang Wendy, Wang Jianjun, Song Young, Sindiri Sivasish, Patidar Rajesh, Hurd Laura, Chen Li, Shern Jack F, Liao Hongling, Wen Xinyu, Gerard Julia, Kim Jung-Sik, Lopez Guerrero Jose Antonio, Machado Isidro, Wai Daniel H, Picci Piero, Triche Timothy, Horvai Andrew E, Miettinen Markku, Wei Jun S, Catchpool Daniel, Llombart-Bosch Antonio, Waldman Todd, Khan Jav |
Genetics of essential tremor: meta-analysis and review. Neurology 2014 Mar 82 (11): 1000-7. Kuhlenbäumer Gregor, Hopfner Franziska, Deuschl Günth |
De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients. Neurobiology of aging 2015 Aug . Hübers Annemarie, Just Walter, Rosenbohm Angela, Müller Kathrin, Marroquin Nicolai, Goebel Ingrid, Högel Josef, Thiele Holger, Altmüller Janine, Nürnberg Peter, Weishaupt Jochen H, Kubisch Christian, Ludolph Albert C, Volk Alexander |
Rare variants at 16p11.2 are associated with common variable immunodeficiency. The Journal of allergy and clinical immunology 2015 Jun 135 (6): 1569-77. Maggadottir S Melkorka, Li Jin, Glessner Joseph T, Li Yun Rose, Wei Zhi, Chang Xiao, Mentch Frank D, Thomas Kelly A, Kim Cecilia E, Zhao Yan, Hou Cuiping, Wang Fengxiang, Jørgensen Silje F, Perez Elena E, Sullivan Kathleen E, Orange Jordan S, Karlsen Tom H, Chapel Helen, Cunningham-Rundles Charlotte, Hakonarson Hak |
Rare variants in ?-Amyloid precursor protein (APP) and Parkinson's disease. European journal of human genetics : EJHG 2015 Oct 23 (10): 1328-33. Schulte Eva C, Fukumori Akio, Mollenhauer Brit, Hor Hyun, Arzberger Thomas, Perneczky Robert, Kurz Alexander, Diehl-Schmid Janine, Hüll Michael, Lichtner Peter, Eckstein Gertrud, Zimprich Alexander, Haubenberger Dietrich, Pirker Walter, Brücke Thomas, Bereznai Benjamin, Molnar Maria J, Lorenzo-Betancor Oswaldo, Pastor Pau, Peters Annette, Gieger Christian, Estivill Xavier, Meitinger Thomas, Kretzschmar Hans A, Trenkwalder Claudia, Haass Christian, Winkelmann Julia |
Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis. Annals of clinical and translational neurology 2019 11 6 (12): 2384-2394. Naumann Marcel, Peikert Kevin, Günther Rene, van der Kooi Anneke J, Aronica Eleonora, Hübers Annemarie, Danel Veronique, Corcia Philippe, Pan-Montojo Francisco, Cirak Sebahattin, Haliloglu Göknur, Ludolph Albert C, Goswami Anand, Andersen Peter M, Prudlo Johannes, Wegner Florian, Van Damme Philip, Weishaupt Jochen H, Hermann Andre |
Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophy. Neurology. Genetics 2020 2 6 (1): e386. Wadman Renske I, Jansen Marc D, Curial Chantall A D, Groen Ewout J N, Stam Marloes, Wijngaarde Camiel A, Medic Jelena, Sodaar Peter, van Eijk Kristel R, Huibers Manon M H, van Kuik Joyce, Lemmink Henny H, van Rheenen Wouter, Veldink Jan Herman, van den Berg Leonard H, van der Pol W Lu |
Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11. Stem cell research 2021 2 52 102246. Hedges Erin C, Topp Simon, Shaw Christopher E, Nishimura Agnes |
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis. Neurology. Genetics 2022 9 8 (5): e200011. Grassano Maurizio, Brodini Giorgia, De Marco Giovanni, Casale Federico, Fuda Giuseppe, Salamone Paolina, Brunetti Maura, Sbaiz Luca, Gallone Salvatore, Cugnasco Paolo, Bombaci Alessandro, Vasta Rosario, Manera Umberto, Canosa Antonio, Moglia Cristina, Calvo Andrea, Traynor Bryan J, Chio Adria |
FUS-P525L Juvenile Amyotrophic Lateral Sclerosis and Intellectual Disability: Evidence for Association and Oligogenic Inheritance. Neurology. Genetics 2022 7 8 (4): e200009. Goldstein Orly, Inbar Talya, Kedmi Merav, Gana-Weisz Mali, Abramovich Beatrice, Orr-Urtreger Avi, Drory Vivian |
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