Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Amyotrophic Lateral 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 |
| 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 |
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