These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 33924139)

  • 1. The Increasing Impact of Translational Research in the Molecular Diagnostics of Neuromuscular Diseases.
    Yubero D; Natera-de Benito D; Pijuan J; Armstrong J; Martorell L; Fernàndez G; Maynou J; Jou C; Roldan M; Ortez C; Nascimento A; Hoenicka J; Palau F
    Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33924139
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The rapid evolution of molecular genetic diagnostics in neuromuscular diseases.
    Volk AE; Kubisch C
    Curr Opin Neurol; 2017 Oct; 30(5):523-528. PubMed ID: 28665809
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service.
    Westra D; Schouten MI; Stunnenberg BC; Kusters B; Saris CGJ; Erasmus CE; van Engelen BG; Bulk S; Verschuuren-Bemelmans CC; Gerkes EH; de Geus C; van der Zwaag PA; Chan S; Chung B; Barge-Schaapveld DQCM; Kriek M; Sznajer Y; van Spaendonck-Zwarts K; van der Kooi AJ; Krause A; Schönewolf-Greulich B; de Die-Smulders C; Sallevelt SCEH; Krapels IPC; Rasmussen M; Maystadt I; Kievit AJA; Witting N; Pennings M; Meijer R; Gillissen C; Kamsteeg EJ; Voermans NC
    J Neuromuscul Dis; 2019; 6(2):241-258. PubMed ID: 31127727
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield.
    Ankala A; da Silva C; Gualandi F; Ferlini A; Bean LJ; Collins C; Tanner AK; Hegde MR
    Ann Neurol; 2015 Feb; 77(2):206-14. PubMed ID: 25380242
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi-omic pipelines.
    Alston CL; Stenton SL; Hudson G; Prokisch H; Taylor RW
    J Pathol; 2021 Jul; 254(4):430-442. PubMed ID: 33586140
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Increasing phenotypic annotation improves the diagnostic rate of exome sequencing in a rare neuromuscular disorder.
    Thompson R; Papakonstantinou Ntalis A; Beltran S; Töpf A; de Paula Estephan E; Polavarapu K; 't Hoen PAC; Missier P; Lochmüller H
    Hum Mutat; 2019 Oct; 40(10):1797-1812. PubMed ID: 31231902
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnostic value of whole-exome sequencing in Chinese pediatric-onset neuromuscular patients.
    Tsang MHY; Chiu ATG; Kwong BMH; Liang R; Yu MHC; Yeung KS; Ho WHL; Mak CCY; Leung GKC; Pei SLC; Fung JLF; Wong VCN; Muntoni F; Chung BHY; Chan SHS
    Mol Genet Genomic Med; 2020 May; 8(5):e1205. PubMed ID: 32154989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Intersection of Proteomics and Genomics to "Solve the Unsolved" in Rare Disorders such as Neurodegenerative and Neuromuscular Diseases.
    Roos A; Thompson R; Horvath R; Lochmüller H; Sickmann A
    Proteomics Clin Appl; 2018 Mar; 12(2):. PubMed ID: 29059504
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Translational Diagnostics: An In-House Pipeline to Validate Genetic Variants in Children with Undiagnosed and Rare Diseases.
    Pijuan J; Rodríguez-Sanz M; Natera-de Benito D; Ortez C; Altimir A; Osuna-López M; Roura M; Ugalde M; Van de Vondel L; Reina-Castillón J; Fons C; Benítez R; Nascimento A; Hoenicka J; Palau F
    J Mol Diagn; 2021 Jan; 23(1):71-90. PubMed ID: 33223419
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genomics and proteomics in the research of neuromuscular diseases].
    Gangfuß A; Schara-Schmidt U; Roos A
    Nervenarzt; 2022 Feb; 93(2):114-121. PubMed ID: 34622318
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Next-generation sequencing in neuromuscular diseases.
    Efthymiou S; Manole A; Houlden H
    Curr Opin Neurol; 2016 Oct; 29(5):527-36. PubMed ID: 27588584
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Detailed Catalogue of Multi-Omics Methodologies for Identification of Putative Biomarkers and Causal Molecular Networks in Translational Cancer Research.
    Vlachavas EI; Bohn J; Ückert F; Nürnberg S
    Int J Mol Sci; 2021 Mar; 22(6):. PubMed ID: 33802234
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Omics-Based Investigations of Breast Cancer.
    Neagu AN; Whitham D; Bruno P; Morrissiey H; Darie CA; Darie CC
    Molecules; 2023 Jun; 28(12):. PubMed ID: 37375323
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genomic medicine and risk prediction across the disease spectrum.
    Kotze MJ; Lückhoff HK; Peeters AV; Baatjes K; Schoeman M; van der Merwe L; Grant KA; Fisher LR; van der Merwe N; Pretorius J; van Velden DP; Myburgh EJ; Pienaar FM; van Rensburg SJ; Yako YY; September AV; Moremi KE; Cronje FJ; Tiffin N; Bouwens CS; Bezuidenhout J; Apffelstaedt JP; Hough FS; Erasmus RT; Schneider JW
    Crit Rev Clin Lab Sci; 2015; 52(3):120-37. PubMed ID: 25597499
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Target resequencing of neuromuscular disease-related genes using next-generation sequencing for patients with undiagnosed early-onset neuromuscular disorders.
    Kitamura Y; Kondo E; Urano M; Aoki R; Saito K
    J Hum Genet; 2016 Nov; 61(11):931-942. PubMed ID: 27357428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Impact of integrated translational research on clinical exome sequencing.
    Klee EW; Cousin MA; Pinto E Vairo F; Morales-Rosado JA; Macke EL; Jenkinson WG; Ferrer A; Schultz-Rogers LE; Olson RJ; Oliver GR; Sigafoos AN; Schwab TL; Zimmermann MT; Urrutia RA; Kaiwar C; Gupta A; Blackburn PR; Boczek NJ; Prochnow CA; Lowy RJ; Mulvihill LA; McAllister TM; Aoudia SL; Kruisselbrink TM; Gunderson LB; Kemppainen JL; Fisher LJ; Tarnowski JM; Hager MM; Kroc SA; Bertsch NL; Agre KE; Jackson JL; Macklin-Mantia SK; Murphree MI; Rust LM; Summer Bolster JM; Beck SA; Atwal PS; Ellingson MS; Barnett SS; Rasmussen KJ; Lahner CA; Niu Z; Hasadsri L; Ferber MJ; Marcou CA; Clark KJ; Pichurin PN; Deyle DR; Morava-Kozicz E; Gavrilova RH; Dhamija R; Wierenga KJ; Lanpher BC; Babovic-Vuksanovic D; Farrugia G; Schimmenti LA; Stewart AK; Lazaridis KN
    Genet Med; 2021 Mar; 23(3):498-507. PubMed ID: 33144682
    [TBL] [Abstract][Full Text] [Related]  

  • 17. "Transcriptomics": molecular diagnosis of inborn errors of metabolism via RNA-sequencing.
    Kremer LS; Wortmann SB; Prokisch H
    J Inherit Metab Dis; 2018 May; 41(3):525-532. PubMed ID: 29372369
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomics.
    Ravenscroft G; Clayton JS; Faiz F; Sivadorai P; Milnes D; Cincotta R; Moon P; Kamien B; Edwards M; Delatycki M; Lamont PJ; Chan SH; Colley A; Ma A; Collins F; Hennington L; Zhao T; McGillivray G; Ghedia S; Chao K; O'Donnell-Luria A; Laing NG; Davis MR
    J Med Genet; 2021 Sep; 58(9):609-618. PubMed ID: 33060286
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Natural History, Trial Readiness and Gene Discovery: Advances in Patient Registries for Neuromuscular Disease.
    Thompson R; Robertson A; Lochmüller H
    Adv Exp Med Biol; 2017; 1031():97-124. PubMed ID: 29214567
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.