Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Neurodegenerative Diseases and SOD1[original query] |
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| Increased incidence of the Hfe mutation in amyotrophic lateral sclerosis and related cellular consequences. Journal of the neurological sciences 2004 Dec 227 (1): 27-33. Wang Xin-Sheng, Lee Sang, Simmons Zachary, Boyer Philip, Scott Kevin, Liu Wenlei, Connor Jam |
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.
The Lancet. Neurology 2010 Oct 9 (10): 978-85. Laaksovirta Hannu, Peuralinna Terhi, Schymick Jennifer C, Scholz Sonja W, Lai Shaoi-Lin, Myllykangas Liisa, Sulkava Raimo, Jansson Lilja, Hernandez Dena G, Gibbs J Raphael, Nalls Michael A, Heckerman David, Tienari Pentti J, Traynor Bryan |
| Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS. Neuropathology : official journal of the Japanese Society of Neuropathology 2015 Aug . Bury Joanna J, Highley J Robin, Cooper-Knock Johnathan, Goodall Emily F, Higginbottom Adrian, McDermott Christopher J, Ince Paul G, Shaw Pamela J, Kirby Jani |
| Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort. Frontiers in molecular neuroscience 2016 9 92. Krüger Stefanie, Battke Florian, Sprecher Andrea, Munz Marita, Synofzik Matthis, Schöls Ludger, Gasser Thomas, Grehl Torsten, Prudlo Johannes, Biskup Sask |
| Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum. JAMA neurology 2018 Jul 75 (7): 860-875. Karch Celeste M, Wen Natalie, Fan Chun C, Yokoyama Jennifer S, Kouri Naomi, Ross Owen A, Höglinger Gunter, Müller Ulrich, Ferrari Raffaele, Hardy John, Schellenberg Gerard D, Sleiman Patrick M, Momeni Parastoo, Hess Christopher P, Miller Bruce L, Sharma Manu, Van Deerlin Vivianna, Smeland Olav B, Andreassen Ole A, Dale Anders M, Desikan Rahul S, |
| Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis. Clinical epigenetics 2020 9 12 (1): 137. Stoccoro Andrea, Smith Adam R, Mosca Lorena, Marocchi Alessandro, Gerardi Francesca, Lunetta Christian, Cereda Cristina, Gagliardi Stella, Lunnon Katie, Migliore Lucia, Coppedè Fab |
| Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum. Journal of neurology 2021 Mar . Bartoletti-Stella Anna, Vacchiano Veria, De Pasqua Silvia, Mengozzi Giacomo, De Biase Dario, Bartolomei Ilaria, Avoni Patrizia, Rizzo Giovanni, Parchi Piero, Donadio Vincenzo, Chiò Adriano, Pession Annalisa, Oppi Federico, Salvi Fabrizio, Liguori Rocco, Capellari Sabina, |
| A molecular view of amyotrophic lateral sclerosis through the lens of interaction network modules. PloS one 2022 5 17 (5): e0268159. Jensen Klaus Højgaard, Stalder Anna Katharina, Wernersson Rasmus, Roloff-Handschin Tim-Christoph, Hansen Daniel Hvidberg, Groenen Peter M |
| Elevated serum circulating cell-free mitochondrial DNA in amyotrophic lateral sclerosis. European journal of neurology 2024 9 e16493. Jieyu Li, Chao Gao, Qingqing Wang, Jing Liu, Zhiying Xie, Yawen Zhao, Meng Yu, Yiming Zheng, He Lv, Wei Zhang, Yun Yuan, Lingchao Meng, Jianwen Deng, Zhaoxia Wa |
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