BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

301 related articles for article (PubMed ID: 22959728)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.
    Gijselinck I; Van Langenhove T; van der Zee J; Sleegers K; Philtjens S; Kleinberger G; Janssens J; Bettens K; Van Cauwenberghe C; Pereson S; Engelborghs S; Sieben A; De Jonghe P; Vandenberghe R; Santens P; De Bleecker J; Maes G; Bäumer V; Dillen L; Joris G; Cuijt I; Corsmit E; Elinck E; Van Dongen J; Vermeulen S; Van den Broeck M; Vaerenberg C; Mattheijssens M; Peeters K; Robberecht W; Cras P; Martin JJ; De Deyn PP; Cruts M; Van Broeckhoven C
    Lancet Neurol; 2012 Jan; 11(1):54-65. PubMed ID: 22154785
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East Asians.
    Iida A; Takahashi A; Deng M; Zhang Y; Wang J; Atsuta N; Tanaka F; Kamei T; Sano M; Oshima S; Tokuda T; Morita M; Akimoto C; Nakajima M; Kubo M; Kamatani N; Nakano I; Sobue G; Nakamura Y; Fan D; Ikegawa S
    Neurobiol Aging; 2011 Apr; 32(4):757.e13-4. PubMed ID: 21295378
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment bias.
    Mehta PR; Jones AR; Opie-Martin S; Shatunov A; Iacoangeli A; Al Khleifat A; Smith BN; Topp S; Morrison KE; Shaw PJ; Shaw CE; Morgan S; Pittman A; Al-Chalabi A
    J Neurol Neurosurg Psychiatry; 2019 Mar; 90(3):268-271. PubMed ID: 30270202
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.
    Cady J; Allred P; Bali T; Pestronk A; Goate A; Miller TM; Mitra RD; Ravits J; Harms MB; Baloh RH
    Ann Neurol; 2015 Jan; 77(1):100-13. PubMed ID: 25382069
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.
    Diekstra FP; Van Deerlin VM; van Swieten JC; Al-Chalabi A; Ludolph AC; Weishaupt JH; Hardiman O; Landers JE; Brown RH; van Es MA; Pasterkamp RJ; Koppers M; Andersen PM; Estrada K; Rivadeneira F; Hofman A; Uitterlinden AG; van Damme P; Melki J; Meininger V; Shatunov A; Shaw CE; Leigh PN; Shaw PJ; Morrison KE; Fogh I; Chiò A; Traynor BJ; Czell D; Weber M; Heutink P; de Bakker PI; Silani V; Robberecht W; van den Berg LH; Veldink JH
    Ann Neurol; 2014 Jul; 76(1):120-33. PubMed ID: 24931836
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis.
    Deng M; Wei L; Zuo X; Tian Y; Xie F; Hu P; Zhu C; Yu F; Meng Y; Wang H; Zhang F; Ma H; Ye R; Cheng H; Du J; Dong W; Zhou S; Wang C; Wang Y; Wang J; Chen X; Sun Z; Zhou N; Jiang Y; Liu X; Li X; Zhang N; Liu N; Guan Y; Han Y; Han Y; Lv X; Fu Y; Yu H; Xi C; Xie D; Zhao Q; Xie P; Wang X; Zhang Z; Shen L; Cui Y; Yin X; Cheng H; Liang B; Zheng X; Lee TM; Chen G; Zhou F; Veldink JH; Robberecht W; Landers JE; Andersen PM; Al-Chalabi A; Shaw C; Liu C; Tang B; Xiao S; Robertson J; Zhang F; van den Berg LH; Sun L; Liu J; Yang S; Ju X; Wang K; Zhang X
    Nat Genet; 2013 Jun; 45(6):697-700. PubMed ID: 23624525
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association analysis of SNP rs11868035 in SREBF1 with sporadic Parkinson's disease, sporadic amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.
    Yuan X; Cao B; Wu Y; Chen Y; Wei Q; Ou R; Yang J; Chen X; Zhao B; Song W; Shang H
    Neurosci Lett; 2018 Jan; 664():128-132. PubMed ID: 29128630
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Whole-genome analysis of sporadic amyotrophic lateral sclerosis.
    Dunckley T; Huentelman MJ; Craig DW; Pearson JV; Szelinger S; Joshipura K; Halperin RF; Stamper C; Jensen KR; Letizia D; Hesterlee SE; Pestronk A; Levine T; Bertorini T; Graves MC; Mozaffar T; Jackson CE; Bosch P; McVey A; Dick A; Barohn R; Lomen-Hoerth C; Rosenfeld J; O'connor DT; Zhang K; Crook R; Ryberg H; Hutton M; Katz J; Simpson EP; Mitsumoto H; Bowser R; Miller RG; Appel SH; Stephan DA
    N Engl J Med; 2007 Aug; 357(8):775-88. PubMed ID: 17671248
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.