BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 31872054)

  • 1. Identification of
    Wei L; Tian Y; Chen Y; Wei Q; Chen F; Cao B; Wu Y; Zhao B; Chen X; Xie C; Xi C; Yu X; Wang J; Lv X; Du J; Wang Y; Shen L; Wang X; Shen B; Guo Q; Guo L; Xia K; Xie P; Zhang X; Zuo X; Shang H; Wang K
    Neurol Genet; 2019 Dec; 5(6):e375. PubMed ID: 31872054
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels.
    Qi Q; Menzaghi C; Smith S; Liang L; de Rekeneire N; Garcia ME; Lohman KK; Miljkovic I; Strotmeyer ES; Cummings SR; Kanaya AM; Tylavsky FA; Satterfield S; Ding J; Rimm EB; Trischitta V; Hu FB; Liu Y; Qi L
    Hum Mol Genet; 2012 Nov; 21(21):4774-80. PubMed ID: 22843503
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4.
    Iacoangeli A; Fogh I; Selvackadunco S; Topp SD; Shatunov A; van Rheenen W; Al-Khleifat A; Opie-Martin S; Ratti A; Calvo A; ; Van Damme P; Robberecht W; Chio A; Dobson RJ; Hardiman O; Shaw CE; van den Berg LH; Andersen PM; Smith BN; Silani V; Veldink JH; Breen G; Troakes C; Al-Chalabi A; Jones AR
    Brain Commun; 2021; 3(4):fcab236. PubMed ID: 34708205
    [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. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study.
    Duan L; Wei L; Tian Y; Zhang Z; Hu P; Wei Q; Liu S; Zhang J; Wang Y; Li D; Yang W; Zong R; Xian P; Han C; Bao X; Zhao F; Feng J; Liu W; Cao W; Zhou G; Zhu C; Yu F; Yang W; Meng Y; Wang J; Chen X; Wang Y; Shen B; Zhao B; Wan J; Zhang F; Zhao G; Xu A; Zhang X; Liu J; Zuo X; Wang K
    Stroke; 2018 Jan; 49(1):11-18. PubMed ID: 29273593
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study.
    van Es MA; Van Vught PW; Blauw HM; Franke L; Saris CG; Andersen PM; Van Den Bosch L; de Jong SW; van 't Slot R; Birve A; Lemmens R; de Jong V; Baas F; Schelhaas HJ; Sleegers K; Van Broeckhoven C; Wokke JH; Wijmenga C; Robberecht W; Veldink JH; Ophoff RA; van den Berg LH
    Lancet Neurol; 2007 Oct; 6(10):869-77. PubMed ID: 17827064
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
    Chiò A; Schymick JC; Restagno G; Scholz SW; Lombardo F; Lai SL; Mora G; Fung HC; Britton A; Arepalli S; Gibbs JR; Nalls M; Berger S; Kwee LC; Oddone EZ; Ding J; Crews C; Rafferty I; Washecka N; Hernandez D; Ferrucci L; Bandinelli S; Guralnik J; Macciardi F; Torri F; Lupoli S; Chanock SJ; Thomas G; Hunter DJ; Gieger C; Wichmann HE; Calvo A; Mutani R; Battistini S; Giannini F; Caponnetto C; Mancardi GL; La Bella V; Valentino F; Monsurrò MR; Tedeschi G; Marinou K; Sabatelli M; Conte A; Mandrioli J; Sola P; Salvi F; Bartolomei I; Siciliano G; Carlesi C; Orrell RW; Talbot K; Simmons Z; Connor J; Pioro EP; Dunkley T; Stephan DA; Kasperaviciute D; Fisher EM; Jabonka S; Sendtner M; Beck M; Bruijn L; Rothstein J; Schmidt S; Singleton A; Hardy J; Traynor BJ
    Hum Mol Genet; 2009 Apr; 18(8):1524-32. PubMed ID: 19193627
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.
    Blauw HM; Veldink JH; van Es MA; van Vught PW; Saris CG; van der Zwaag B; Franke L; Burbach JP; Wokke JH; Ophoff RA; van den Berg LH
    Lancet Neurol; 2008 Apr; 7(4):319-26. PubMed ID: 18313986
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Integrated molecular landscape of amyotrophic lateral sclerosis provides insights into disease etiology.
    Klemann CJHM; Visser JE; Van Den Bosch L; Martens GJM; Poelmans G
    Brain Pathol; 2018 Mar; 28(2):203-211. PubMed ID: 28035716
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Type 2 Diabetes Mellitus and Amyotrophic Lateral Sclerosis: Genetic Overlap, Causality, and Mediation.
    Chen H; Zhang J; Wang T; Zhang S; Lai Q; Huang S; Zeng P
    J Clin Endocrinol Metab; 2021 Oct; 106(11):e4497-e4508. PubMed ID: 34171091
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.