255 related articles for article (PubMed ID: 35042540)
1. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1.
Restuadi R; Steyn FJ; Kabashi E; Ngo ST; Cheng FF; Nabais MF; Thompson MJ; Qi T; Wu Y; Henders AK; Wallace L; Bye CR; Turner BJ; Ziser L; Mathers S; McCombe PA; Needham M; Schultz D; Kiernan MC; van Rheenen W; van den Berg LH; Veldink JH; Ophoff R; Gusev A; Zaitlen N; McRae AF; Henderson RD; Wray NR; Giacomotto J; Garton FC
Genome Med; 2022 Jan; 14(1):7. PubMed ID: 35042540
[TBL] [Abstract][Full Text] [Related]
2. Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
Benyamin B; He J; Zhao Q; Gratten J; Garton F; Leo PJ; Liu Z; Mangelsdorf M; Al-Chalabi A; Anderson L; Butler TJ; Chen L; Chen XD; Cremin K; Deng HW; Devine M; Edson J; Fifita JA; Furlong S; Han YY; Harris J; Henders AK; Jeffree RL; Jin ZB; Li Z; Li T; Li M; Lin Y; Liu X; Marshall M; McCann EP; Mowry BJ; Ngo ST; Pamphlett R; Ran S; Reutens DC; Rowe DB; Sachdev P; Shah S; Song S; Tan LJ; Tang L; van den Berg LH; van Rheenen W; Veldink JH; Wallace RH; Wheeler L; Williams KL; Wu J; Wu X; Yang J; Yue W; Zhang ZH; Zhang D; Noakes PG; Blair IP; Henderson RD; McCombe PA; Visscher PM; Xu H; Bartlett PF; Brown MA; Wray NR; Fan D
Nat Commun; 2017 Sep; 8(1):611. PubMed ID: 28931804
[TBL] [Abstract][Full Text] [Related]
3. Shared genetic risk loci between Alzheimer's disease and related dementias, Parkinson's disease, and amyotrophic lateral sclerosis.
Wainberg M; Andrews SJ; Tripathy SJ
Alzheimers Res Ther; 2023 Jun; 15(1):113. PubMed ID: 37328865
[TBL] [Abstract][Full Text] [Related]
4. Genome-wide genetic links between amyotrophic lateral sclerosis and autoimmune diseases.
Li CY; Yang TM; Ou RW; Wei QQ; Shang HF
BMC Med; 2021 Feb; 19(1):27. PubMed ID: 33541344
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.
Diekstra FP; Saris CG; van Rheenen W; Franke L; Jansen RC; van Es MA; van Vught PW; Blauw HM; Groen EJ; Horvath S; Estrada K; Rivadeneira F; Hofman A; Uitterlinden AG; Robberecht W; Andersen PM; Melki J; Meininger V; Hardiman O; Landers JE; Brown RH; Shatunov A; Shaw CE; Leigh PN; Al-Chalabi A; Ophoff RA; van den Berg LH; Veldink JH
PLoS One; 2012; 7(4):e35333. PubMed ID: 22509407
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Shared Genetics and Comorbid Genes of Amyotrophic Lateral Sclerosis and Parkinson's Disease.
Tian Y; Ma G; Li H; Zeng Y; Zhou S; Wang X; Shan S; Xu Y; Xiong J; Cheng G
Mov Disord; 2023 Oct; 38(10):1813-1821. PubMed ID: 37534731
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Identifying Candidate Genes Associated with Sporadic Amyotrophic Lateral Sclerosis via Integrative Analysis of Transcriptome-Wide Association Study and Messenger RNA Expression Profile.
Li P; Cheng S; Wen Y; Cheng B; Liu L; Wu X; Ao X; Huang Z; Liao C; Li S; Zhang F; Zhang Z
Cell Mol Neurobiol; 2023 Jan; 43(1):327-338. PubMed ID: 35038056
[TBL] [Abstract][Full Text] [Related]
11. A Powerful Approach to Estimating Annotation-Stratified Genetic Covariance via GWAS Summary Statistics.
Lu Q; Li B; Ou D; Erlendsdottir M; Powles RL; Jiang T; Hu Y; Chang D; Jin C; Dai W; He Q; Liu Z; Mukherjee S; Crane PK; Zhao H
Am J Hum Genet; 2017 Dec; 101(6):939-964. PubMed ID: 29220677
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. TBK1, a prioritized drug repurposing target for amyotrophic lateral sclerosis: evidence from druggable genome Mendelian randomization and pharmacological verification in vitro.
Duan QQ; Wang H; Su WM; Gu XJ; Shen XF; Jiang Z; Ren YL; Cao B; Li GB; Wang Y; Chen YP
BMC Med; 2024 Mar; 22(1):96. PubMed ID: 38443977
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis.
Sha Q; Zhang Z; Schymick JC; Traynor BJ; Zhang S
BMC Med Genet; 2009 Sep; 10():86. PubMed ID: 19740415
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics.
Iacoangeli A; Lin T; Al Khleifat A; Jones AR; Opie-Martin S; Coleman JRI; Shatunov A; Sproviero W; Williams KL; Garton F; Restuadi R; Henders AK; Mather KA; Needham M; Mathers S; Nicholson GA; Rowe DB; Henderson R; McCombe PA; Pamphlett R; Blair IP; Schultz D; Sachdev PS; Newhouse SJ; Proitsi P; Fogh I; Ngo ST; Dobson RJB; Wray NR; Steyn FJ; Al-Chalabi A
Cell Rep; 2020 Oct; 33(4):108323. PubMed ID: 33113361
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia.
Restuadi R; Garton FC; Benyamin B; Lin T; Williams KL; Vinkhuyzen A; van Rheenen W; Zhu Z; Laing NG; Mather KA; Sachdev PS; Ngo ST; Steyn FJ; Wallace L; Henders AK; Visscher PM; Needham M; Mathers S; Nicholson G; Rowe DB; Henderson RD; McCombe PA; Pamphlett R; Blair IP; Wray NR; McRae AF
Eur J Hum Genet; 2022 May; 30(5):532-539. PubMed ID: 33907316
[TBL] [Abstract][Full Text] [Related]
19. Causal Inference of Genetic Variants and Genes in Amyotrophic Lateral Sclerosis.
Pan S; Liu X; Liu T; Zhao Z; Dai Y; Wang YY; Jia P; Liu F
Front Genet; 2022; 13():917142. PubMed ID: 35812739
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
