232 related articles for article (PubMed ID: 31201598)
1. UNC13A variant rs12608932 is associated with increased risk of amyotrophic lateral sclerosis and reduced patient survival: a meta-analysis.
Yang B; Jiang H; Wang F; Li S; Wu C; Bao J; Zhu Y; Xu Z; Liu B; Ren H; Yang X
Neurol Sci; 2019 Nov; 40(11):2293-2302. PubMed ID: 31201598
[TBL] [Abstract][Full Text] [Related]
2. UNC13A is a modifier of survival in amyotrophic lateral sclerosis.
Diekstra FP; van Vught PW; van Rheenen W; Koppers M; Pasterkamp RJ; van Es MA; Schelhaas HJ; de Visser M; Robberecht W; Van Damme P; Andersen PM; van den Berg LH; Veldink JH
Neurobiol Aging; 2012 Mar; 33(3):630.e3-8. PubMed ID: 22118904
[TBL] [Abstract][Full Text] [Related]
3. UNC13A confers risk for sporadic ALS and influences survival in a Spanish cohort.
Vidal-Taboada JM; Lopez-Lopez A; Salvado M; Lorenzo L; Garcia C; Mahy N; Rodríguez MJ; Gamez J
J Neurol; 2015 Oct; 262(10):2285-92. PubMed ID: 26162714
[TBL] [Abstract][Full Text] [Related]
4. UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study.
Chiò A; Mora G; Restagno G; Brunetti M; Ossola I; Barberis M; Ferrucci L; Canosa A; Manera U; Moglia C; Fuda G; Traynor BJ; Calvo A
Neurobiol Aging; 2013 Jan; 34(1):357.e1-5. PubMed ID: 22921269
[TBL] [Abstract][Full Text] [Related]
5. UNC13A polymorphism contributes to frontotemporal disease in sporadic amyotrophic lateral sclerosis.
Placek K; Baer GM; Elman L; McCluskey L; Hennessy L; Ferraro PM; Lee EB; Lee VMY; Trojanowski JQ; Van Deerlin VM; Grossman M; Irwin DJ; McMillan CT
Neurobiol Aging; 2019 Jan; 73():190-199. PubMed ID: 30368160
[TBL] [Abstract][Full Text] [Related]
6. Lithium carbonate in amyotrophic lateral sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A: protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial.
Willemse SW; Roes KCB; Van Damme P; Hardiman O; Ingre C; Povedano M; Wray NR; Gijzen M; de Pagter MS; Demaegd KC; Janse AFC; Vink RG; Sleutjes BTHM; Chiò A; Corcia P; Reviers E; Al-Chalabi A; Kiernan MC; van den Berg LH; van Es MA; van Eijk RPA
Trials; 2022 Dec; 23(1):978. PubMed ID: 36471413
[TBL] [Abstract][Full Text] [Related]
7. The Distinct Traits of the UNC13A Polymorphism in Amyotrophic Lateral Sclerosis.
Tan HHG; Westeneng HJ; van der Burgh HK; van Es MA; Bakker LA; van Veenhuijzen K; van Eijk KR; van Eijk RPA; Veldink JH; van den Berg LH
Ann Neurol; 2020 Oct; 88(4):796-806. PubMed ID: 32627229
[TBL] [Abstract][Full Text] [Related]
8. Association of the risk factor
Manini A; Casiraghi V; Brusati A; Maranzano A; Gentile F; Colombo E; Bonetti R; Peverelli S; Invernizzi S; Gentilini D; Messina S; Verde F; Poletti B; Fogh I; Morelli C; Silani V; Ratti A; Ticozzi N
Front Aging Neurosci; 2023; 15():1067954. PubMed ID: 36819716
[TBL] [Abstract][Full Text] [Related]
9.
Willemse SW; Harley P; van Eijk RPA; Demaegd KC; Zelina P; Pasterkamp RJ; van Damme P; Ingre C; van Rheenen W; Veldink JH; Kiernan MC; Al-Chalabi A; van den Berg LH; Fratta P; van Es MA
J Neurol Neurosurg Psychiatry; 2023 Aug; 94(8):649-656. PubMed ID: 36737245
[TBL] [Abstract][Full Text] [Related]
10. Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis.
Su WM; Gu XJ; Duan QQ; Jiang Z; Gao X; Shang HF; Chen YP
BMC Med; 2022 Jun; 20(1):209. PubMed ID: 35754054
[TBL] [Abstract][Full Text] [Related]
11. Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population.
Chen X; Huang R; Chen Y; Zheng Z; Chen K; Song W; Zhao B; Yang Y; Yuan L; Shang H
Neurol Sci; 2014 Jul; 35(7):1089-95. PubMed ID: 24493373
[TBL] [Abstract][Full Text] [Related]
12. Clinical and Metabolic Signature of
Calvo A; Canosa A; Moglia C; Manera U; Grassano M; Vasta R; Palumbo F; Cugnasco P; Gallone S; Brunetti M; De Marchi F; Arena V; Pagani M; Dalgard C; Scholz SW; Chia R; Corrado L; Dalfonso S; Mazzini L; Traynor BJ; Chio A
Neurol Genet; 2022 Dec; 8(6):e200033. PubMed ID: 36313067
[TBL] [Abstract][Full Text] [Related]
13. Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis.
Chiò A; Moglia C; Canosa A; Manera U; Grassano M; Vasta R; Palumbo F; Gallone S; Brunetti M; Barberis M; De Marchi F; Dalgard C; Chia R; Mora G; Iazzolino B; Peotta L; Traynor BJ; Corrado L; D'Alfonso S; Mazzini L; Calvo A
Neurology; 2023 Jul; 101(1):e83-e93. PubMed ID: 37202167
[TBL] [Abstract][Full Text] [Related]
14. Lack of association between the Angiogenin (ANG) rs11701 polymorphism and amyotrophic lateral sclerosis risk: a meta-analysis.
Pan LS; Deng XB; Wang Z; Leng HL; Zhu XP; Ding D
Neurol Sci; 2016 May; 37(5):655-62. PubMed ID: 26753798
[TBL] [Abstract][Full Text] [Related]
15. Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis.
Gaastra B; Shatunov A; Pulit S; Jones AR; Sproviero W; Gillett A; Chen Z; Kirby J; Fogh I; Powell JF; Leigh PN; Morrison KE; Shaw PJ; Shaw CE; van den Berg LH; Veldink JH; Lewis CM; Al-Chalabi A
Amyotroph Lateral Scler Frontotemporal Degener; 2016; 17(7-8):593-599. PubMed ID: 27584932
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
van Es MA; Veldink JH; Saris CG; Blauw HM; van Vught PW; Birve A; Lemmens R; Schelhaas HJ; Groen EJ; Huisman MH; van der Kooi AJ; de Visser M; Dahlberg C; Estrada K; Rivadeneira F; Hofman A; Zwarts MJ; van Doormaal PT; Rujescu D; Strengman E; Giegling I; Muglia P; Tomik B; Slowik A; Uitterlinden AG; Hendrich C; Waibel S; Meyer T; Ludolph AC; Glass JD; Purcell S; Cichon S; Nöthen MM; Wichmann HE; Schreiber S; Vermeulen SH; Kiemeney LA; Wokke JH; Cronin S; McLaughlin RL; Hardiman O; Fumoto K; Pasterkamp RJ; Meininger V; Melki J; Leigh PN; Shaw CE; Landers JE; Al-Chalabi A; Brown RH; Robberecht W; Andersen PM; Ophoff RA; van den Berg LH
Nat Genet; 2009 Oct; 41(10):1083-7. PubMed ID: 19734901
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Association between C677T polymorphism of MTHFR gene and risk of amyotrophic lateral sclerosis: Polish population study and a meta-analysis.
Żur-Wyrozumska K; Pera J; Dziubek A; Sado M; Golenia A; Słowik A; Dziedzic T
Neurol Neurochir Pol; 2017; 51(2):135-139. PubMed ID: 28187987
[TBL] [Abstract][Full Text] [Related]
19. Meta-analysis of the association between CHCHD10 Pro34Ser variant and the risk of amyotrophic lateral sclerosis.
Yang B; Yang C; Ren J; Zhong C; Liu K; Zhao L; Li L; Wang H; Zhu M; Lin Z
Neurol Sci; 2021 Feb; 42(2):625-631. PubMed ID: 32651855
[TBL] [Abstract][Full Text] [Related]
20. Lack of association between the P413L variant of chromogranin B and ALS risk or age at onset: a meta-analysis.
Yang X; Li S; Xing D; Li P; Li C; Qi L; Xu Y; Ren H
Amyotroph Lateral Scler Frontotemporal Degener; 2018 Feb; 19(1-2):80-86. PubMed ID: 28795874
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]