BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

274 related articles for article (PubMed ID: 29170628)

  • 1. Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype.
    Cooper-Knock J; Robins H; Niedermoser I; Wyles M; Heath PR; Higginbottom A; Walsh T; Kazoka M; ; Ince PG; Hautbergue GM; McDermott CJ; Kirby J; Shaw PJ
    Front Mol Neurosci; 2017; 10():370. PubMed ID: 29170628
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.
    Giannoccaro MP; Bartoletti-Stella A; Piras S; Pession A; De Massis P; Oppi F; Stanzani-Maserati M; Pasini E; Baiardi S; Avoni P; Parchi P; Liguori R; Capellari S
    J Neurol; 2017 Jul; 264(7):1426-1433. PubMed ID: 28620717
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetics screening in an Italian cohort of patients with Amyotrophic Lateral Sclerosis: the importance of early testing and its implication.
    Libonati L; Cambieri C; Colavito D; Moret F; D'Andrea E; Del Giudice E; Leon A; Inghilleri M; Ceccanti M
    J Neurol; 2024 Apr; 271(4):1921-1936. PubMed ID: 38112783
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype.
    Cooper-Knock J; Shaw PJ; Kirby J
    Acta Neuropathol; 2014 Mar; 127(3):333-45. PubMed ID: 24493408
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Modelling C9ORF72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis and frontotemporal dementia.
    Stepto A; Gallo JM; Shaw CE; Hirth F
    Acta Neuropathol; 2014 Mar; 127(3):377-89. PubMed ID: 24366528
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic variability in sporadic amyotrophic lateral sclerosis.
    Van Daele SH; Moisse M; van Vugt JJFA; Zwamborn RAJ; van der Spek R; van Rheenen W; Van Eijk K; Kenna K; Corcia P; Vourc'h P; Couratier P; Hardiman O; McLaughin R; Gotkine M; Drory V; Ticozzi N; Silani V; Ratti A; de Carvalho M; Mora Pardina JS; Povedano M; Andersen PM; Weber M; Başak NA; Shaw C; Shaw PJ; Morrison KE; Landers JE; Glass JD; van Es MA; van den Berg LH; Al-Chalabi A; Veldink J; Van Damme P
    Brain; 2023 Sep; 146(9):3760-3769. PubMed ID: 37043475
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rare variants in MYH15 modify amyotrophic lateral sclerosis risk.
    Kim H; Lim J; Bao H; Jiao B; Canon SM; Epstein MP; Xu K; Jiang J; Parameswaran J; Li Y; Moberg KH; Landers JE; Fournier C; Allen EG; Glass JD; Wingo TS; Jin P
    Hum Mol Genet; 2019 Jul; 28(14):2309-2318. PubMed ID: 30985904
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci.
    He F; Jones JM; Figueroa-Romero C; Zhang D; Feldman EL; Goutman SA; Meisler MH; Callaghan BC; Todd PK
    Neurol Genet; 2016 Jun; 2(3):e71. PubMed ID: 27274540
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter.
    Gijselinck I; Van Mossevelde S; van der Zee J; Sieben A; Engelborghs S; De Bleecker J; Ivanoiu A; Deryck O; Edbauer D; Zhang M; Heeman B; Bäumer V; Van den Broeck M; Mattheijssens M; Peeters K; Rogaeva E; De Jonghe P; Cras P; Martin JJ; de Deyn PP; Cruts M; Van Broeckhoven C
    Mol Psychiatry; 2016 Aug; 21(8):1112-24. PubMed ID: 26481318
    [TBL] [Abstract][Full Text] [Related]  

  • 11. C9orf72 hexanucleotide repeat expansion in Indian patients with ALS: a common founder and its geographical predilection.
    Shamim U; Ambawat S; Singh J; Thomas A; Pradeep-Chandra-Reddy C; Suroliya V; Uppilli B; Parveen S; Sharma P; Chanchal S; Nashi S; Preethish-Kumar V; Vengalil S; Polavarapu K; Keerthipriya M; Mahajan NP; Reddy N; Thomas PT; Sadasivan A; Warrier M; Seth M; Zahra S; Mathur A; Vibha D; Srivastava AK; Nalini A; Faruq M
    Neurobiol Aging; 2020 Apr; 88():156.e1-156.e9. PubMed ID: 32035847
    [TBL] [Abstract][Full Text] [Related]  

  • 12. OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia.
    Farhan SMK; Gendron TF; Petrucelli L; Hegele RA; Strong MJ
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jan; 177(1):75-85. PubMed ID: 29080331
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort.
    Tripolszki K; Gampawar P; Schmidt H; Nagy ZF; Nagy D; Klivényi P; Engelhardt JI; Széll M
    Front Genet; 2019; 10():732. PubMed ID: 31475037
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Physical exercise is a risk factor for amyotrophic lateral sclerosis: Convergent evidence from Mendelian randomisation, transcriptomics and risk genotypes.
    Julian TH; Glascow N; Barry ADF; Moll T; Harvey C; Klimentidis YC; Newell M; Zhang S; Snyder MP; Cooper-Knock J; Shaw PJ
    EBioMedicine; 2021 Jun; 68():103397. PubMed ID: 34051439
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
    Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
    J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort.
    Krüger S; Battke F; Sprecher A; Munz M; Synofzik M; Schöls L; Gasser T; Grehl T; Prudlo J; Biskup S
    Front Mol Neurosci; 2016; 9():92. PubMed ID: 27790088
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis.
    Ruf WP; Boros M; Freischmidt A; Brenner D; Grozdanov V; de Meirelles J; Meyer T; Grehl T; Petri S; Grosskreutz J; Weyen U; Guenther R; Regensburger M; Hagenacker T; Koch JC; Emmer A; Roediger A; Steinbach R; Wolf J; Weishaupt JH; Lingor P; Deschauer M; Cordts I; Klopstock T; Reilich P; Schoeberl F; Schrank B; Zeller D; Hermann A; Knehr A; Günther K; Dorst J; Schuster J; Siebert R; Ludolph AC; Müller K
    Brain Commun; 2023; 5(3):fcad152. PubMed ID: 37223130
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The evolving genetic risk for sporadic ALS.
    Gibson SB; Downie JM; Tsetsou S; Feusier JE; Figueroa KP; Bromberg MB; Jorde LB; Pulst SM
    Neurology; 2017 Jul; 89(3):226-233. PubMed ID: 28642336
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Poly(GP) proteins are a useful pharmacodynamic marker for
    Gendron TF; Chew J; Stankowski JN; Hayes LR; Zhang YJ; Prudencio M; Carlomagno Y; Daughrity LM; Jansen-West K; Perkerson EA; O'Raw A; Cook C; Pregent L; Belzil V; van Blitterswijk M; Tabassian LJ; Lee CW; Yue M; Tong J; Song Y; Castanedes-Casey M; Rousseau L; Phillips V; Dickson DW; Rademakers R; Fryer JD; Rush BK; Pedraza O; Caputo AM; Desaro P; Palmucci C; Robertson A; Heckman MG; Diehl NN; Wiggs E; Tierney M; Braun L; Farren J; Lacomis D; Ladha S; Fournier CN; McCluskey LF; Elman LB; Toledo JB; McBride JD; Tiloca C; Morelli C; Poletti B; Solca F; Prelle A; Wuu J; Jockel-Balsarotti J; Rigo F; Ambrose C; Datta A; Yang W; Raitcheva D; Antognetti G; McCampbell A; Van Swieten JC; Miller BL; Boxer AL; Brown RH; Bowser R; Miller TM; Trojanowski JQ; Grossman M; Berry JD; Hu WT; Ratti A; Traynor BJ; Disney MD; Benatar M; Silani V; Glass JD; Floeter MK; Rothstein JD; Boylan KB; Petrucelli L
    Sci Transl Med; 2017 Mar; 9(383):. PubMed ID: 28356511
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.