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 *

197 related articles for article (PubMed ID: 23800157)

  • 1. Prediction of gene-phenotype associations in humans, mice, and plants using phenologs.
    Woods JO; Singh-Blom UM; Laurent JM; McGary KL; Marcotte EM
    BMC Bioinformatics; 2013 Jun; 14():203. PubMed ID: 23800157
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linking human diseases to animal models using ontology-based phenotype annotation.
    Washington NL; Haendel MA; Mungall CJ; Ashburner M; Westerfield M; Lewis SE
    PLoS Biol; 2009 Nov; 7(11):e1000247. PubMed ID: 19956802
    [TBL] [Abstract][Full Text] [Related]  

  • 3. From phenologs to silent suppressors: Identifying potential therapeutic targets for human disease.
    Golden A
    Mol Reprod Dev; 2017 Nov; 84(11):1118-1132. PubMed ID: 28834577
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish.
    Doelken SC; Köhler S; Mungall CJ; Gkoutos GV; Ruef BJ; Smith C; Smedley D; Bauer S; Klopocki E; Schofield PN; Westerfield M; Robinson PN; Lewis SE
    Dis Model Mech; 2013 Mar; 6(2):358-72. PubMed ID: 23104991
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inferring disease and gene set associations with rank coherence in networks.
    Hwang T; Zhang W; Xie M; Liu J; Kuang R
    Bioinformatics; 2011 Oct; 27(19):2692-9. PubMed ID: 21824970
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Signalogs: orthology-based identification of novel signaling pathway components in three metazoans.
    Korcsmáros T; Szalay MS; Rovó P; Palotai R; Fazekas D; Lenti K; Farkas IJ; Csermely P; Vellai T
    PLoS One; 2011 May; 6(5):e19240. PubMed ID: 21559328
    [TBL] [Abstract][Full Text] [Related]  

  • 7. OrthoDisease: a database of human disease orthologs.
    O'Brien KP; Westerlund I; Sonnhammer EL
    Hum Mutat; 2004 Aug; 24(2):112-9. PubMed ID: 15241792
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparative analysis of function and interaction of transcription factors in nematodes: extensive conservation of orthology coupled to rapid sequence evolution.
    Haerty W; Artieri C; Khezri N; Singh RS; Gupta BP
    BMC Genomics; 2008 Aug; 9():399. PubMed ID: 18752680
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Integration of anatomy ontology data with protein-protein interaction networks improves the candidate gene prediction accuracy for anatomical entities.
    Fernando PC; Mabee PM; Zeng E
    BMC Bioinformatics; 2020 Oct; 21(1):442. PubMed ID: 33028186
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Systematic discovery of nonobvious human disease models through orthologous phenotypes.
    McGary KL; Park TJ; Woods JO; Cha HJ; Wallingford JB; Marcotte EM
    Proc Natl Acad Sci U S A; 2010 Apr; 107(14):6544-9. PubMed ID: 20308572
    [TBL] [Abstract][Full Text] [Related]  

  • 11. OrthoList 2: A New Comparative Genomic Analysis of Human and
    Kim W; Underwood RS; Greenwald I; Shaye DD
    Genetics; 2018 Oct; 210(2):445-461. PubMed ID: 30120140
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transfer learning across ontologies for phenome-genome association prediction.
    Petegrosso R; Park S; Hwang TH; Kuang R
    Bioinformatics; 2017 Feb; 33(4):529-536. PubMed ID: 27797759
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Experimental-confirmation and functional-annotation of predicted proteins in the chicken genome.
    Buza TJ; McCarthy FM; Burgess SC
    BMC Genomics; 2007 Nov; 8():425. PubMed ID: 18021451
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide modeling of complex phenotypes in Caenorhabditis elegans and Drosophila melanogaster.
    De S; Zhang Y; Wolkow CA; Zou S; Goldberg I; Becker KG
    BMC Genomics; 2013 Aug; 14():580. PubMed ID: 23984798
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Functional genomics complements quantitative genetics in identifying disease-gene associations.
    Guan Y; Ackert-Bicknell CL; Kell B; Troyanskaya OG; Hibbs MA
    PLoS Comput Biol; 2010 Nov; 6(11):e1000991. PubMed ID: 21085640
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inference of gene-phenotype associations via protein-protein interaction and orthology.
    Wang P; Lai WF; Li MJ; Xu F; Yalamanchili HK; Lovell-Badge R; Wang J
    PLoS One; 2013; 8(10):e77478. PubMed ID: 24194887
    [TBL] [Abstract][Full Text] [Related]  

  • 17. HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich node embeddings for the Human Phenotype Ontology.
    Shen F; Peng S; Fan Y; Wen A; Liu S; Wang Y; Wang L; Liu H
    J Biomed Inform; 2019 Aug; 96():103246. PubMed ID: 31255713
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An integrative modular approach to systematically predict gene-phenotype associations.
    Mehan MR; Nunez-Iglesias J; Dai C; Waterman MS; Zhou XJ
    BMC Bioinformatics; 2010 Jan; 11 Suppl 1(Suppl 1):S62. PubMed ID: 20122238
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Co-clustering phenome-genome for phenotype classification and disease gene discovery.
    Hwang T; Atluri G; Xie M; Dey S; Hong C; Kumar V; Kuang R
    Nucleic Acids Res; 2012 Oct; 40(19):e146. PubMed ID: 22735708
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DeepPheno: Predicting single gene loss-of-function phenotypes using an ontology-aware hierarchical classifier.
    Kulmanov M; Hoehndorf R
    PLoS Comput Biol; 2020 Nov; 16(11):e1008453. PubMed ID: 33206638
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.