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 *

164 related articles for article (PubMed ID: 37100502)

  • 41. Patient Representation From Structured Electronic Medical Records Based on Embedding Technique: Development and Validation Study.
    Huang Y; Wang N; Zhang Z; Liu H; Fei X; Wei L; Chen H
    JMIR Med Inform; 2021 Jul; 9(7):e19905. PubMed ID: 34297000
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Calculating phenotypic similarity between genes using hierarchical structure data based on semantic similarity.
    Zhang S; Chang Z; Li Z; DuanMu H; Li Z; Li K; Liu Y; Qiu F; Xu Y
    Gene; 2012 Apr; 497(1):58-65. PubMed ID: 22305981
    [TBL] [Abstract][Full Text] [Related]  

  • 43. MKGE: Knowledge graph embedding with molecular structure information.
    Zhang Y; Li Z; Duan B; Qin L; Peng J
    Comput Biol Chem; 2022 Oct; 100():107730. PubMed ID: 35945150
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Towards similarity-based differential diagnostics for common diseases.
    Slater K; Karwath A; Williams JA; Russell S; Makepeace S; Carberry A; Hoehndorf R; Gkoutos GV
    Comput Biol Med; 2021 Jun; 133():104360. PubMed ID: 33836447
    [TBL] [Abstract][Full Text] [Related]  

  • 45. HPOSim: an R package for phenotypic similarity measure and enrichment analysis based on the human phenotype ontology.
    Deng Y; Gao L; Wang B; Guo X
    PLoS One; 2015; 10(2):e0115692. PubMed ID: 25664462
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Phen2Disease: a phenotype-driven model for disease and gene prioritization by bidirectional maximum matching semantic similarities.
    Zhai W; Huang X; Shen N; Zhu S
    Brief Bioinform; 2023 Jul; 24(4):. PubMed ID: 37248747
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A Topic Recognition Method of News Text Based on Word Embedding Enhancement.
    Du Q; Li N; Liu W; Sun D; Yang S; Yue F
    Comput Intell Neurosci; 2022; 2022():4582480. PubMed ID: 35222628
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Biomedical ontology alignment: an approach based on representation learning.
    Kolyvakis P; Kalousis A; Smith B; Kiritsis D
    J Biomed Semantics; 2018 Aug; 9(1):21. PubMed ID: 30111369
    [TBL] [Abstract][Full Text] [Related]  

  • 49. PhenoBERT: A Combined Deep Learning Method for Automated Recognition of Human Phenotype Ontology.
    Feng Y; Qi L; Tian W
    IEEE/ACM Trans Comput Biol Bioinform; 2023; 20(2):1269-1277. PubMed ID: 35471885
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Clinical Phenotypic Spectrum of 4095 Individuals with Down Syndrome from Text Mining of Electronic Health Records.
    Havrilla JM; Zhao M; Liu C; Weng C; Helbig I; Bhoj E; Wang K
    Genes (Basel); 2021 Jul; 12(8):. PubMed ID: 34440331
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Comparative effectiveness of medical concept embedding for feature engineering in phenotyping.
    Lee J; Liu C; Kim JH; Butler A; Shang N; Pang C; Natarajan K; Ryan P; Ta C; Weng C
    JAMIA Open; 2021 Apr; 4(2):ooab028. PubMed ID: 34142015
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Termviewer - A Web Application for Streamlined Human Phenotype Ontology (HPO) Tagging and Document Annotation.
    Nixon A; Fang L; Havrilla JM; Wang K
    Chem Biodivers; 2022 Dec; 19(12):e202200805. PubMed ID: 36328766
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Evolving knowledge graph similarity for supervised learning in complex biomedical domains.
    Sousa RT; Silva S; Pesquita C
    BMC Bioinformatics; 2020 Jan; 21(1):6. PubMed ID: 31900127
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Deep Phenotyping of Chinese Electronic Health Records by Recognizing Linguistic Patterns of Phenotypic Narratives With a Sequence Motif Discovery Tool: Algorithm Development and Validation.
    Li S; Deng L; Zhang X; Chen L; Yang T; Qi Y; Jiang T
    J Med Internet Res; 2022 Jun; 24(6):e37213. PubMed ID: 35657661
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology.
    Dhombres F; Morgan P; Chaudhari BP; Filges I; Sparks TN; Lapunzina P; Roscioli T; Agarwal U; Aggarwal S; Beneteau C; Cacheiro P; Carmody LC; Collardeau-Frachon S; Dempsey EA; Dufke A; Duyzend MH; El Ghosh M; Giordano JL; Glad R; Grinfelde I; Iliescu DG; Ladewig MS; Munoz-Torres MC; Pollazzon M; Radio FC; Rodo C; Silva RG; Smedley D; Sundaramurthi JC; Toro S; Valenzuela I; Vasilevsky NA; Wapner RJ; Zemet R; Haendel MA; Robinson PN
    Am J Med Genet C Semin Med Genet; 2022 Jun; 190(2):231-242. PubMed ID: 35872606
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Querying phenotype-genotype relationships on patient datasets using semantic web technology: the example of Cerebrotendinous xanthomatosis.
    Taboada M; Martínez D; Pilo B; Jiménez-Escrig A; Robinson PN; Sobrido MJ
    BMC Med Inform Decis Mak; 2012 Jul; 12():78. PubMed ID: 22849591
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Cross-platform binary code similarity detection based on NMT and graph embedding.
    Zhu X; Jiang L; Chen Z
    Math Biosci Eng; 2021 May; 18(4):4528-4551. PubMed ID: 34198452
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Ontology-driven and weakly supervised rare disease identification from clinical notes.
    Dong H; Suárez-Paniagua V; Zhang H; Wang M; Casey A; Davidson E; Chen J; Alex B; Whiteley W; Wu H
    BMC Med Inform Decis Mak; 2023 May; 23(1):86. PubMed ID: 37147628
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Anc2vec: embedding gene ontology terms by preserving ancestors relationships.
    Edera AA; Milone DH; Stegmayer G
    Brief Bioinform; 2022 Mar; 23(2):. PubMed ID: 35136916
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease.
    Groza T; Köhler S; Moldenhauer D; Vasilevsky N; Baynam G; Zemojtel T; Schriml LM; Kibbe WA; Schofield PN; Beck T; Vasant D; Brookes AJ; Zankl A; Washington NL; Mungall CJ; Lewis SE; Haendel MA; Parkinson H; Robinson PN
    Am J Hum Genet; 2015 Jul; 97(1):111-24. PubMed ID: 26119816
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.