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 *

417 related articles for article (PubMed ID: 38344397)

  • 21. Added Value of Reanalysis of Whole Exome- and Whole Genome Sequencing Data From Patients Suspected of Primary Immune Deficiency Using an Extended Gene Panel and Structural Variation Calling.
    Mørup SB; Nazaryan-Petersen L; Gabrielaite M; Reekie J; Marquart HV; Hartling HJ; Marvig RL; Katzenstein TL; Masmas TN; Lundgren J; Murray DD; Helleberg M; Borgwardt L
    Front Immunol; 2022; 13():906328. PubMed ID: 35874679
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical relevance of cancer genome sequencing.
    Ku CS; Cooper DN; Roukos DH
    World J Gastroenterol; 2013 Apr; 19(13):2011-8. PubMed ID: 23599619
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical sequencing: From raw data to diagnosis with lifetime value.
    Caspar SM; Dubacher N; Kopps AM; Meienberg J; Henggeler C; Matyas G
    Clin Genet; 2018 Mar; 93(3):508-519. PubMed ID: 29206278
    [TBL] [Abstract][Full Text] [Related]  

  • 24. JWES: a new pipeline for whole genome/exome sequence data processing, management, and gene-variant discovery, annotation, prediction, and genotyping.
    Ahmed Z; Renart EG; Mishra D; Zeeshan S
    FEBS Open Bio; 2021 Sep; 11(9):2441-2452. PubMed ID: 34370400
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Using the Sankey diagram to visualize article features on the topics of whole-exome sequencing (WES) and whole-genome sequencing (WGS) since 2012: Bibliometric analysis.
    Li MJ; Chien TW; Liao KW; Lai FJ
    Medicine (Baltimore); 2022 Sep; 101(38):e30682. PubMed ID: 36197161
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Using human genetics to discover new therapeutic targets for plasma lipids.
    Cohen JC
    J Intern Med; 2016 Nov; 280(5):487-495. PubMed ID: 27739219
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Reporting results from whole-genome and whole-exome sequencing in clinical practice: a proposal for Canada?
    Zawati MH; Parry D; Thorogood A; Nguyen MT; Boycott KM; Rosenblatt D; Knoppers BM
    J Med Genet; 2014 Jan; 51(1):68-70. PubMed ID: 24078715
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.
    Wilfert AB; Sulovari A; Turner TN; Coe BP; Eichler EE
    Genome Med; 2017 Nov; 9(1):101. PubMed ID: 29179772
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Integration of Real-World Data and Genetics to Support Target Identification and Validation.
    Davitte JM; Stott-Miller M; Ehm MG; Cunnington MC; Reynolds RF
    Clin Pharmacol Ther; 2022 Jan; 111(1):63-76. PubMed ID: 34818443
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.
    Bomba L; Walter K; Guo Q; Surendran P; Kundu K; Nongmaithem S; Karim MA; Stewart ID; Langenberg C; Danesh J; Di Angelantonio E; Roberts DJ; Ouwehand WH; ; Dunham I; Butterworth AS; Soranzo N
    Am J Hum Genet; 2022 Jun; 109(6):1038-1054. PubMed ID: 35568032
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Whole-Exome Sequencing of Metastatic Cancer and Biomarkers of Treatment Response.
    Beltran H; Eng K; Mosquera JM; Sigaras A; Romanel A; Rennert H; Kossai M; Pauli C; Faltas B; Fontugne J; Park K; Banfelder J; Prandi D; Madhukar N; Zhang T; Padilla J; Greco N; McNary TJ; Herrscher E; Wilkes D; MacDonald TY; Xue H; Vacic V; Emde AK; Oschwald D; Tan AY; Chen Z; Collins C; Gleave ME; Wang Y; Chakravarty D; Schiffman M; Kim R; Campagne F; Robinson BD; Nanus DM; Tagawa ST; Xiang JZ; Smogorzewska A; Demichelis F; Rickman DS; Sboner A; Elemento O; Rubin MA
    JAMA Oncol; 2015 Jul; 1(4):466-74. PubMed ID: 26181256
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing.
    Alfares A; Aloraini T; Subaie LA; Alissa A; Qudsi AA; Alahmad A; Mutairi FA; Alswaid A; Alothaim A; Eyaid W; Albalwi M; Alturki S; Alfadhel M
    Genet Med; 2018 Nov; 20(11):1328-1333. PubMed ID: 29565419
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Use of whole exome and genome sequencing in the identification of genetic causes of primary immunodeficiencies.
    Chou J; Ohsumi TK; Geha RS
    Curr Opin Allergy Clin Immunol; 2012 Dec; 12(6):623-8. PubMed ID: 23095910
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Human genetics and genomics a decade after the release of the draft sequence of the human genome.
    Naidoo N; Pawitan Y; Soong R; Cooper DN; Ku CS
    Hum Genomics; 2011 Oct; 5(6):577-622. PubMed ID: 22155605
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Preconception genome medicine: current state and future perspectives to improve infertility diagnosis and reproductive and health outcomes based on individual genomic data.
    Capalbo A; Poli M; Riera-Escamilla A; Shukla V; Kudo Høffding M; Krausz C; Hoffmann ER; Simon C
    Hum Reprod Update; 2021 Feb; 27(2):254-279. PubMed ID: 33197264
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Whole exome sequencing and whole genome sequencing in undiagnosed disease: of value for certain patient populations].
    Linthorst GE; Hollak CEM
    Ned Tijdschr Geneeskd; 2019 May; 163():. PubMed ID: 31120221
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An evaluation of copy number variation detection tools from whole-exome sequencing data.
    Tan R; Wang Y; Kleinstein SE; Liu Y; Zhu X; Guo H; Jiang Q; Allen AS; Zhu M
    Hum Mutat; 2014 Jul; 35(7):899-907. PubMed ID: 24599517
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Organizational Aspects of the Implementation and Use of Whole Genome Sequencing and Whole Exome Sequencing in the Pediatric Population in Italy: Results of a Survey.
    Nurchis MC; Raspolini GM; Heidar Alizadeh A; Altamura G; Radio FC; Tartaglia M; Dallapiccola B; Damiani G
    J Pers Med; 2023 May; 13(6):. PubMed ID: 37373888
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetics of primary ovarian insufficiency: new developments and opportunities.
    Qin Y; Jiao X; Simpson JL; Chen ZJ
    Hum Reprod Update; 2015; 21(6):787-808. PubMed ID: 26243799
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cost-Effectiveness of Whole-Genome vs Whole-Exome Sequencing Among Children With Suspected Genetic Disorders.
    Nurchis MC; Radio FC; Salmasi L; Heidar Alizadeh A; Raspolini GM; Altamura G; Tartaglia M; Dallapiccola B; Pizzo E; Gianino MM; Damiani G
    JAMA Netw Open; 2024 Jan; 7(1):e2353514. PubMed ID: 38277144
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.