Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Sclerosis and SMN2[original query] |
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| Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis. Annals of neurology 2002 Feb 51 (2): 243-6. Corcia Philippe, Mayeux-Portas Véronique, Khoris Jawad, de Toffol Bertrand, Autret Alain, Müh Jean-Pierre, Camu William, Andres Christian, |
| SMN1 gene, but not SMN2, is a risk factor for sporadic ALS. Neurology 2006 Oct 67 (7): 1147-50. Corcia P, Camu W, Halimi J-M, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres C R, |
| Association between survivor motor neuron 2 (SMN2) gene homozygous deletion and sporadic lower motor neuron disease in a Korean population. Annals of clinical and laboratory science 2010 40 (4): 368-74. Kim Juwon, Lee Sang-Guk, Choi Young-Chul, Kang Seong-Woong, Lee Jun-Beom, Choi Jong Rak, Lee Kyung |
| Homozygous SMN2 deletion is a major risk factor among twenty-five Korean sporadic amyotrophic lateral sclerosis patients. Yonsei medical journal 2012 Jan 53 (1): 1. Lee JB, Lee KA, Hong JM, Suh GI, Choi YC |
| SMN1 gene duplications are associated with sporadic ALS. Neurology 2012 Feb . Blauw HM, Barnes CP, van Vught PW, van Rheenen W, Verheul M, Cuppen E, Veldink JH, van den Berg LH |
| Homozygous SMN2 deletion is a protective factor in the Swedish ALS population. European journal of human genetics : EJHG 2012 May 20 (5): 588-91. Corcia Philippe, Ingre Caroline, Blasco Helene, Press Rayomand, Praline Julien, Antar Catherine, Veyrat-Durebex Charlotte, Guettard Yves-Olivier, Camu William, Andersen Peter M, Vourc'h Patrick, Andres Christian |
| SMN1 gene duplications are more frequent in patients with progressive muscular atrophy. Amyotrophic lateral sclerosis & frontotemporal degeneration 2013 Sep 14 (5-6): 457-62. Ku?ma-Kozakiewicz Magdalena, J?drzejowska Maria, Ka?mierczak Bea |
| Analysis of the C9orf72 gene in spinal muscular atrophy patients. Amyotrophic lateral sclerosis & frontotemporal degeneration 2014 Dec 15 (7-8): 563-8. Alías Laura, Bernal Sara, Barceló Maria J, Martínez-Hernández Rebeca, Martínez Elisabeth, Baiget Montserrat, Tizzano Eduardo |
| SMN1 duplications contribute to sporadic amyotrophic lateral sclerosis susceptibility: evidence from a meta-analysis. Journal of the neurological sciences 2014 May 340 (1-2): 63-8. Wang Xue-Bin, Cui Ning-Hua, Gao Jia-Jia, Qiu Xue-Ping, Zheng Fa |
| SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis. Neurology. Genetics 2021 6 7 (4): e598. Bos Jeroen W, Groen Ewout J N, Wadman Renske I, Curial Chantall A D, Molleman Naomi N, Zegers Marinka, van Vught Paul W J, Snetselaar Reinier, Vijzelaar Raymon, van der Pol W Ludo, van den Berg Leonard |
| Re-analysis of the Hungarian amyotrophic lateral sclerosis population and evaluation of novel ALS genetic risk variants. Neurobiology of aging 2022 Aug 116 1-11. Nagy Zsófia Flóra, Pál Margit, Salamon András, Kafui Esi Zodanu Gloria, Füstös Dalma, Klivényi Péter, Széll Már |
| Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in Africans. Neurology. Genetics 2023 6 9 (4): e200077. Nomakhosazana R Monnakgotla, Amokelani C Mahungu, Jeannine M Heckmann, Gerrit Botha, Nicola J Mulder, Gang Wu, Evadnie Rampersaud, Jason Myers, Marka Van Blitterswijk, Rosa Rademakers, J Paul Taylor, Joanne Wuu, Michael Benatar, Melissa N |
| SMN2 gene copy number affects the incidence and prognosis of motor neuron diseases in Japan. BMC medical genomics 2024 11 17 (1): 263. Tomohiko Ishihara, Akihide Koyama, Naoki Atsuta, Mari Tada, Saori Toyoda, Kenta Kashiwagi, Sachiko Hirokawa, Yuya Hatano, Akio Yokoseki, Ryoichi Nakamura, Genki Tohnai, Yuishin Izumi, Ryuji Kaji, Mitsuya Morita, Asako Tamura, Osamu Kano, Masashi Aoki, Satoshi Kuwabara, Akiyoshi Kakita, Gen Sobue, Osamu Onode |
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