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 *

227 related articles for article (PubMed ID: 26888179)

  • 1. Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes.
    Pua CJ; Bhalshankar J; Miao K; Walsh R; John S; Lim SQ; Chow K; Buchan R; Soh BY; Lio PM; Lim J; Schafer S; Lim JQ; Tan P; Whiffin N; Barton PJ; Ware JS; Cook SA
    J Cardiovasc Transl Res; 2016 Feb; 9(1):3-11. PubMed ID: 26888179
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
    Belkadi A; Bolze A; Itan Y; Cobat A; Vincent QB; Antipenko A; Shang L; Boisson B; Casanova JL; Abel L
    Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5473-8. PubMed ID: 25827230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
    Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
    Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions.
    Lelieveld SH; Spielmann M; Mundlos S; Veltman JA; Gilissen C
    Hum Mutat; 2015 Aug; 36(8):815-22. PubMed ID: 25973577
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole exome sequencing combined with integrated variant annotation prediction identifies asymptomatic Tangier disease with compound heterozygous mutations in ABCA1 gene.
    Tada H; Kawashiri MA; Nohara A; Saito R; Tanaka Y; Nomura A; Konno T; Sakata K; Fujino N; Takamura T; Inazu A; Mabuchi H; Yamagishi M; Hayashi K
    Atherosclerosis; 2015 Jun; 240(2):324-9. PubMed ID: 25875382
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
    LaDuca H; Farwell KD; Vuong H; Lu HM; Mu W; Shahmirzadi L; Tang S; Chen J; Bhide S; Chao EC
    PLoS One; 2017; 12(2):e0170843. PubMed ID: 28152038
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
    LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V
    Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Rapid, High-Quality, Cost-Effective, Comprehensive and Expandable Targeted Next-Generation Sequencing Assay for Inherited Heart Diseases.
    Wilson KD; Shen P; Fung E; Karakikes I; Zhang A; InanlooRahatloo K; Odegaard J; Sallam K; Davis RW; Lui GK; Ashley EA; Scharfe C; Wu JC
    Circ Res; 2015 Sep; 117(7):603-11. PubMed ID: 26265630
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Semiconductor Whole Exome Sequencing for the Identification of Genetic Variants in Colombian Patients Clinically Diagnosed with Long QT Syndrome.
    Burgos M; Arenas A; Cabrera R
    Mol Diagn Ther; 2016 Aug; 20(4):353-62. PubMed ID: 27251404
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction.
    Hastings R; de Villiers CP; Hooper C; Ormondroyd L; Pagnamenta A; Lise S; Salatino S; Knight SJ; Taylor JC; Thomson KL; Arnold L; Chatziefthimiou SD; Konarev PV; Wilmanns M; Ehler E; Ghisleni A; Gautel M; Blair E; Watkins H; Gehmlich K
    Circ Cardiovasc Genet; 2016 Oct; 9(5):426-435. PubMed ID: 27625337
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches.
    Ware JS; John S; Roberts AM; Buchan R; Gong S; Peters NS; Robinson DO; Lucassen A; Behr ER; Cook SA
    J Cardiovasc Transl Res; 2013 Feb; 6(1):94-103. PubMed ID: 22956155
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Systematic comparison of germline variant calling pipelines cross multiple next-generation sequencers.
    Chen J; Li X; Zhong H; Meng Y; Du H
    Sci Rep; 2019 Jun; 9(1):9345. PubMed ID: 31249349
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic testing for inherited cardiac disease.
    Wilde AA; Behr ER
    Nat Rev Cardiol; 2013 Oct; 10(10):571-83. PubMed ID: 23900354
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in Adults.
    Seidelmann SB; Smith E; Subrahmanyan L; Dykas D; Abou Ziki MD; Azari B; Hannah-Shmouni F; Jiang Y; Akar JG; Marieb M; Jacoby D; Bale AE; Lifton RP; Mani A
    Circ Cardiovasc Genet; 2017 Feb; 10(1):. PubMed ID: 28087566
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders.
    Leo VC; Morgan NV; Bem D; Jones ML; Lowe GC; Lordkipanidzé M; Drake S; Simpson MA; Gissen P; Mumford A; Watson SP; Daly ME;
    J Thromb Haemost; 2015 Apr; 13(4):643-50. PubMed ID: 25556537
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
    Waldmüller S; Schroeder C; Sturm M; Scheffold T; Imbrich K; Junker S; Frische C; Hofbeck M; Bauer P; Bonin M; Gawaz M; Gramlich M
    Mol Cell Probes; 2015 Oct; 29(5):308-14. PubMed ID: 25979592
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations.
    Griffin HR; Pyle A; Blakely EL; Alston CL; Duff J; Hudson G; Horvath R; Wilson IJ; Santibanez-Koref M; Taylor RW; Chinnery PF
    Genet Med; 2014 Dec; 16(12):962-71. PubMed ID: 24901348
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data.
    Cherukuri PF; Maduro V; Fuentes-Fajardo KV; Lam K; ; Adams DR; Tifft CJ; Mullikin JC; Gahl WA; Boerkoel CF
    BMC Genomics; 2015 Nov; 16():998. PubMed ID: 26602380
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
    Zhang JX; Fu L; de Voer RM; Hahn MM; Jin P; Lv CX; Verwiel ET; Ligtenberg MJ; Hoogerbrugge N; Kuiper RP; Sheng JQ; Geurts van Kessel A
    World J Gastroenterol; 2015 Apr; 21(14):4136-49. PubMed ID: 25892863
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers.
    Li X; Buckton AJ; Wilkinson SL; John S; Walsh R; Novotny T; Valaskova I; Gupta M; Game L; Barton PJ; Cook SA; Ware JS
    PLoS One; 2013; 8(7):e67744. PubMed ID: 23861798
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.