These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
158 related articles for article (PubMed ID: 32732921)
1. Functional fine-mapping of noncoding risk variants in amyotrophic lateral sclerosis utilizing convolutional neural network. Yousefian-Jazi A; Sung MK; Lee T; Hong YH; Choi JK; Choi J Sci Rep; 2020 Jul; 10(1):12872. PubMed ID: 32732921 [TBL] [Abstract][Full Text] [Related]
2. Replication analysis of genetic variants on 17q11.2 and 9p21.2 with sporadic amyotrophic lateral sclerosis and Parkinson's disease in a Chinese population. Chen X; Chen Y; Guo X; Cao B; Wei Q; Ou R; Zhao B; Song W; Wu Y; Shang HF Neurobiol Aging; 2015 Nov; 36(11):3116.e1-3116.e3. PubMed ID: 26304631 [TBL] [Abstract][Full Text] [Related]
4. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. Fogh I; Ratti A; Gellera C; Lin K; Tiloca C; Moskvina V; Corrado L; Sorarù G; Cereda C; Corti S; Gentilini D; Calini D; Castellotti B; Mazzini L; Querin G; Gagliardi S; Del Bo R; Conforti FL; Siciliano G; Inghilleri M; Saccà F; Bongioanni P; Penco S; Corbo M; Sorbi S; Filosto M; Ferlini A; Di Blasio AM; Signorini S; Shatunov A; Jones A; Shaw PJ; Morrison KE; Farmer AE; Van Damme P; Robberecht W; Chiò A; Traynor BJ; Sendtner M; Melki J; Meininger V; Hardiman O; Andersen PM; Leigh NP; Glass JD; Overste D; Diekstra FP; Veldink JH; van Es MA; Shaw CE; Weale ME; Lewis CM; Williams J; Brown RH; Landers JE; Ticozzi N; Ceroni M; Pegoraro E; Comi GP; D'Alfonso S; van den Berg LH; Taroni F; Al-Chalabi A; Powell J; Silani V; Hum Mol Genet; 2014 Apr; 23(8):2220-31. PubMed ID: 24256812 [TBL] [Abstract][Full Text] [Related]
5. Genome-wide analysis of the heritability of amyotrophic lateral sclerosis. Keller MF; Ferrucci L; Singleton AB; Tienari PJ; Laaksovirta H; Restagno G; Chiò A; Traynor BJ; Nalls MA JAMA Neurol; 2014 Sep; 71(9):1123-34. PubMed ID: 25023141 [TBL] [Abstract][Full Text] [Related]
6. A Genome-wide Expression Association Analysis Identifies Genes and Pathways Associated with Amyotrophic Lateral Sclerosis. Du Y; Wen Y; Guo X; Hao J; Wang W; He A; Fan Q; Li P; Liu L; Liang X; Zhang F Cell Mol Neurobiol; 2018 Apr; 38(3):635-639. PubMed ID: 28639078 [TBL] [Abstract][Full Text] [Related]
7. Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis. McLaughlin RL; Kenna KP; Vajda A; Bede P; Elamin M; Cronin S; Donaghy CG; Bradley DG; Hardiman O Neurobiol Aging; 2015 Feb; 36(2):1221.e7-13. PubMed ID: 25442119 [TBL] [Abstract][Full Text] [Related]
8. Difficulty in determining the association of a single nucleotide polymorphism in the ZNF512B gene with the risk and prognosis of amyotrophic lateral sclerosis. Tetsuka S Rinsho Shinkeigaku; 2017 Aug; 57(8):417-424. PubMed ID: 28740063 [TBL] [Abstract][Full Text] [Related]
9. Using the structure of genome data in the design of deep neural networks for predicting amyotrophic lateral sclerosis from genotype. Yin B; Balvert M; van der Spek RAA; Dutilh BE; Bohté S; Veldink J; Schönhuth A Bioinformatics; 2019 Jul; 35(14):i538-i547. PubMed ID: 31510706 [TBL] [Abstract][Full Text] [Related]
10. Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. Shatunov A; Mok K; Newhouse S; Weale ME; Smith B; Vance C; Johnson L; Veldink JH; van Es MA; van den Berg LH; Robberecht W; Van Damme P; Hardiman O; Farmer AE; Lewis CM; Butler AW; Abel O; Andersen PM; Fogh I; Silani V; Chiò A; Traynor BJ; Melki J; Meininger V; Landers JE; McGuffin P; Glass JD; Pall H; Leigh PN; Hardy J; Brown RH; Powell JF; Orrell RW; Morrison KE; Shaw PJ; Shaw CE; Al-Chalabi A Lancet Neurol; 2010 Oct; 9(10):986-94. PubMed ID: 20801717 [TBL] [Abstract][Full Text] [Related]
11. A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS. Wills AM; Cronin S; Slowik A; Kasperaviciute D; Van Es MA; Morahan JM; Valdmanis PN; Meininger V; Melki J; Shaw CE; Rouleau GA; Fisher EM; Shaw PJ; Morrison KE; Pamphlett R; Van den Berg LH; Figlewicz DA; Andersen PM; Al-Chalabi A; Hardiman O; Purcell S; Landers JE; Brown RH Neurology; 2009 Jul; 73(1):16-24. PubMed ID: 19321847 [TBL] [Abstract][Full Text] [Related]
12. Genome-wide pathway analysis in amyotrophic lateral sclerosis. Lee YH; Song GG Genet Mol Res; 2015 Jun; 14(2):6429-38. PubMed ID: 26125848 [TBL] [Abstract][Full Text] [Related]
13. Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach. Morello G; Guarnaccia M; Spampinato AG; La Cognata V; D'Agata V; Cavallaro S Mol Neurobiol; 2018 Feb; 55(2):1299-1322. PubMed ID: 28120152 [TBL] [Abstract][Full Text] [Related]
14. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. Goris A; van Setten J; Diekstra F; Ripke S; Patsopoulos NA; Sawcer SJ; ; van Es M; ; Andersen PM; Melki J; Meininger V; Hardiman O; Landers JE; Brown RH; Shatunov A; Leigh N; Al-Chalabi A; Shaw CE; Traynor BJ; Chiò A; Restagno G; Mora G; Ophoff RA; Oksenberg JR; Van Damme P; Compston A; Robberecht W; Dubois B; van den Berg LH; De Jager PL; Veldink JH; de Bakker PI Hum Mol Genet; 2014 Apr; 23(7):1916-22. PubMed ID: 24234648 [TBL] [Abstract][Full Text] [Related]
15. No association between DNA repair gene XRCC1 and amyotrophic lateral sclerosis. Fang F; Umbach DM; Xu Z; Ye W; Sandler DP; Taylor JA; Kamel F Neurobiol Aging; 2012 May; 33(5):1015.e25-6. PubMed ID: 20719408 [TBL] [Abstract][Full Text] [Related]
16. Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis. Meltz Steinberg K; Nicholas TJ; Koboldt DC; Yu B; Mardis E; Pamphlett R Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(5-6):385-92. PubMed ID: 25960086 [TBL] [Abstract][Full Text] [Related]
17. An Integrative Transcriptome-Wide Analysis of Amyotrophic Lateral Sclerosis for the Identification of Potential Genetic Markers and Drug Candidates. Park S; Kim D; Song J; Joo JWJ Int J Mol Sci; 2021 Mar; 22(6):. PubMed ID: 33809961 [TBL] [Abstract][Full Text] [Related]
18. The relationship between four GWAS-identified loci in Alzheimer's disease and the risk of Parkinson's disease, amyotrophic lateral sclerosis, and multiple system atrophy. Chen Y; Cao B; Chen X; Ou R; Wei Q; Zhao B; Wu Y; Yuan L; Shang HF Neurosci Lett; 2018 Nov; 686():205-210. PubMed ID: 30144538 [TBL] [Abstract][Full Text] [Related]
19. Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Ahmeti KB; Ajroud-Driss S; Al-Chalabi A; Andersen PM; Armstrong J; Birve A; Blauw HM; Brown RH; Bruijn L; Chen W; Chio A; Comeau MC; Cronin S; Diekstra FP; Soraya Gkazi A; Glass JD; Grab JD; Groen EJ; Haines JL; Hardiman O; Heller S; Huang J; Hung WY; ; Jaworski JM; Jones A; Khan H; Landers JE; Langefeld CD; Leigh PN; Marion MC; McLaughlin RL; Meininger V; Melki J; Miller JW; Mora G; Pericak-Vance MA; Rampersaud E; Robberecht W; Russell LP; Salachas F; Saris CG; Shatunov A; Shaw CE; Siddique N; Siddique T; Smith BN; Sufit R; Topp S; Traynor BJ; Vance C; van Damme P; van den Berg LH; van Es MA; van Vught PW; Veldink JH; Yang Y; Zheng JG; Neurobiol Aging; 2013 Jan; 34(1):357.e7-19. PubMed ID: 22959728 [TBL] [Abstract][Full Text] [Related]
20. Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Gijselinck I; Engelborghs S; Maes G; Cuijt I; Peeters K; Mattheijssens M; Joris G; Cras P; Martin JJ; De Deyn PP; Kumar-Singh S; Van Broeckhoven C; Cruts M Arch Neurol; 2010 May; 67(5):606-16. PubMed ID: 20457961 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]