256 related articles for article (PubMed ID: 37528491)
1. Genetic Modifiers of Age at Onset for Amyotrophic Lateral Sclerosis: A Genome-Wide Association Study.
Li C; Lin J; Jiang Q; Yang T; Xiao Y; Huang J; Hou Y; Wei Q; Cui Y; Wang S; Zheng X; Ou R; Liu K; Chen X; Song W; Zhao B; Shang H
Ann Neurol; 2023 Nov; 94(5):933-941. PubMed ID: 37528491
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide analyses identify NEAT1 as genetic modifier of age at onset of amyotrophic lateral sclerosis.
Li C; Wei Q; Hou Y; Lin J; Ou R; Zhang L; Jiang Q; Xiao Y; Liu K; Chen X; Yang T; Song W; Zhao B; Wu Y; Shang H
Mol Neurodegener; 2023 Oct; 18(1):77. PubMed ID: 37872557
[TBL] [Abstract][Full Text] [Related]
3. Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study.
Li C; Ou R; Chen Y; Gu X; Wei Q; Cao B; Zhang L; Hou Y; Liu K; Chen X; Song W; Zhao B; Wu Y; Li T; Dong X; Shang H
Mov Disord; 2021 Sep; 36(9):2077-2084. PubMed ID: 33884653
[TBL] [Abstract][Full Text] [Related]
4. An association study between SCFD1 rs10139154 variant and amyotrophic lateral sclerosis in a Chinese cohort.
Chen Y; Zhou Q; Gu X; Wei Q; Cao B; Liu H; Hou Y; Shang H
Amyotroph Lateral Scler Frontotemporal Degener; 2018 Aug; 19(5-6):413-418. PubMed ID: 29260601
[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. Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.
Laaksovirta H; Peuralinna T; Schymick JC; Scholz SW; Lai SL; Myllykangas L; Sulkava R; Jansson L; Hernandez DG; Gibbs JR; Nalls MA; Heckerman D; Tienari PJ; Traynor BJ
Lancet Neurol; 2010 Oct; 9(10):978-85. PubMed ID: 20801718
[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. Lack of an association between SCFD1 rs10139154 polymorphism and amyotrophic lateral sclerosis.
Siokas V; Aloizou AM; Liampas I; Bakirtzis C; Nasios G; Paterakis K; Sgantzos M; Bogdanos DP; Spandidos DA; Tsatsakis A; Mitsias PD; Dardiotis E
Mol Med Rep; 2022 Apr; 25(4):. PubMed ID: 35234271
[TBL] [Abstract][Full Text] [Related]
9. Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
Fogh I; Lin K; Tiloca C; Rooney J; Gellera C; Diekstra FP; Ratti A; Shatunov A; van Es MA; Proitsi P; Jones A; Sproviero W; Chiò A; McLaughlin RL; Sorarù G; Corrado L; Stahl D; Del Bo R; Cereda C; Castellotti B; Glass JD; Newhouse S; Dobson R; Smith BN; Topp S; van Rheenen W; Meininger V; Melki J; Morrison KE; Shaw PJ; Leigh PN; Andersen PM; Comi GP; Ticozzi N; Mazzini L; D'Alfonso S; Traynor BJ; Van Damme P; Robberecht W; Brown RH; Landers JE; Hardiman O; Lewis CM; van den Berg LH; Shaw CE; Veldink JH; Silani V; Al-Chalabi A; Powell J
JAMA Neurol; 2016 Jul; 73(7):812-20. PubMed ID: 27244217
[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. Genome-wide association analysis reveals potential genetic correlation and causality between circulating inflammatory proteins and amyotrophic lateral sclerosis.
Shen J; Gu X; Xiao C; Yan H; Feng Y; Li X
Aging (Albany NY); 2024 May; 16(11):9470-9484. PubMed ID: 38819224
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Identifying novel genes for amyotrophic lateral sclerosis by integrating human brain proteomes with genome-wide association data.
Gu XJ; Su WM; Dou M; Jiang Z; Duan QQ; Wang H; Ren YL; Cao B; Wang Y; Chen YP
J Neurol; 2023 Aug; 270(8):4013-4023. PubMed ID: 37148340
[TBL] [Abstract][Full Text] [Related]
14. Smoking and amyotrophic lateral sclerosis: A mendelian randomization study.
Zhan Y; Fang F
Ann Neurol; 2019 Apr; 85(4):482-484. PubMed ID: 30786056
[TBL] [Abstract][Full Text] [Related]
15. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis.
Bandres-Ciga S; Noyce AJ; Hemani G; Nicolas A; Calvo A; Mora G; ; ; Tienari PJ; Stone DJ; Nalls MA; Singleton AB; Chiò A; Traynor BJ
Ann Neurol; 2019 Apr; 85(4):470-481. PubMed ID: 30723964
[TBL] [Abstract][Full Text] [Related]
16. Associations of the circulating levels of cytokines with risk of amyotrophic lateral sclerosis: a Mendelian randomization study.
Liu B; Lyu L; Zhou W; Song J; Ye D; Mao Y; Chen GB; Sun X
BMC Med; 2023 Feb; 21(1):39. PubMed ID: 36737740
[TBL] [Abstract][Full Text] [Related]
17. Bidirectional Mendelian randomization to explore the causal relationships between Sleep traits, Parkinson's disease and Amyotrophic lateral sclerosis.
Di H; Zhu Y; Xia W; Meng X; Zhang M; Xu M; Feng J; Tian Q; He Y; Cao S; Lu Z
Sleep Med; 2022 Aug; 96():42-49. PubMed ID: 35594779
[TBL] [Abstract][Full Text] [Related]
18. Genetically predicted coffee consumption and amyotrophic lateral sclerosis.
Zhang Z; Wang M; Liu X
Amyotroph Lateral Scler Frontotemporal Degener; 2022 Nov; 23(7-8):575-579. PubMed ID: 35254179
[No Abstract] [Full Text] [Related]
19. Alcohol Drinking and Amyotrophic Lateral Sclerosis: An Instrumental Variable Causal Inference.
Yu X; Wang T; Chen Y; Shen Z; Gao Y; Xiao L; Zheng J; Zeng P
Ann Neurol; 2020 Jul; 88(1):195-198. PubMed ID: 32196748
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]