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 *

108 related articles for article (PubMed ID: 34171756)

  • 21. CGMIM: automated text-mining of Online Mendelian Inheritance in Man (OMIM) to identify genetically-associated cancers and candidate genes.
    Bajdik CD; Kuo B; Rusaw S; Jones S; Brooks-Wilson A
    BMC Bioinformatics; 2005 Mar; 6():78. PubMed ID: 15796777
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Phenotypic and genotypic analyses of genetic skin disease through the Online Mendelian Inheritance in Man (OMIM) database.
    Feramisco JD; Sadreyev RI; Murray ML; Grishin NV; Tsao H
    J Invest Dermatol; 2009 Nov; 129(11):2628-36. PubMed ID: 19536140
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Online Mendelian Inheritance in Man (OMIM).
    Hamosh A; Scott AF; Amberger J; Valle D; McKusick VA
    Hum Mutat; 2000; 15(1):57-61. PubMed ID: 10612823
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Searching Online Mendelian Inheritance in Man (OMIM) for information on genetic loci involved in human disease.
    Baxevanis AD
    Curr Protoc Hum Genet; 2012 Apr; Chapter 9():9.13.1-9.13.10. PubMed ID: 22470145
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A Comprehensive Evaluation of Disease Phenotype Networks for Gene Prioritization.
    Li J; Lin X; Teng Y; Qi S; Xiao D; Zhang J; Kang Y
    PLoS One; 2016; 11(7):e0159457. PubMed ID: 27415759
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Co-expression network analysis identified hub genes critical to triglyceride and free fatty acid metabolism as key regulators of age-related vascular dysfunction in mice.
    Li H; Wang X; Lu X; Zhu H; Li S; Duan S; Zhao X; Zhang F; Alterovitz G; Wang F; Li Q; Tian XL; Xu M
    Aging (Albany NY); 2019 Sep; 11(18):7620-7638. PubMed ID: 31514170
    [No Abstract]   [Full Text] [Related]  

  • 28. Exploring Genes and Phenotypes Within Chromosomal Regions Using OMIM's GeneScout.
    Applegate CD; Schiettecatte F; Hamosh A; Amberger JS
    Curr Protoc; 2022 Sep; 2(9):e530. PubMed ID: 36130039
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Online Mendelian Inheritance in Man (OMIM) as a knowledgebase for human developmental disorders.
    Boyadjiev SA; Jabs EW
    Clin Genet; 2000 Apr; 57(4):253-66. PubMed ID: 10845565
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.
    Hartley T; Balcı TB; Rojas SK; Eaton A; Canada CR; Dyment DA; Boycott KM
    Am J Med Genet C Semin Med Genet; 2018 Dec; 178(4):458-463. PubMed ID: 30580481
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Phenome and genome based studies into human ageing and longevity: An overview.
    Eline Slagboom P; van den Berg N; Deelen J
    Biochim Biophys Acta Mol Basis Dis; 2018 Sep; 1864(9 Pt A):2742-2751. PubMed ID: 28951210
    [TBL] [Abstract][Full Text] [Related]  

  • 32. NET-GE: a novel NETwork-based Gene Enrichment for detecting biological processes associated to Mendelian diseases.
    Di Lena P; Martelli PL; Fariselli P; Casadio R
    BMC Genomics; 2015; 16 Suppl 8(Suppl 8):S6. PubMed ID: 26110971
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Searching Online Mendelian Inheritance in Man (OMIM) for information for genetic loci involved in human disease.
    Baxevanis AD
    Curr Protoc Hum Genet; 2003 Feb; Chapter 9():Unit9.13. PubMed ID: 18428346
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Application of Online Mendelian Inheritance in Man to medical genetics].
    Hu YA; Cui YX
    Zhonghua Nan Ke Xue; 2011 Jul; 17(7):639-43. PubMed ID: 21823350
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®).
    Amberger J; Bocchini C; Hamosh A
    Hum Mutat; 2011 May; 32(5):564-7. PubMed ID: 21472891
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Models to explore genetics of human aging.
    Karasik D; Newman A
    Adv Exp Med Biol; 2015; 847():141-61. PubMed ID: 25916590
    [TBL] [Abstract][Full Text] [Related]  

  • 37. PhenoMiner: from text to a database of phenotypes associated with OMIM diseases.
    Collier N; Groza T; Smedley D; Robinson PN; Oellrich A; Rebholz-Schuhmann D
    Database (Oxford); 2015; 2015():. PubMed ID: 26507285
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Prioritization of candidate disease genes by enlarging the seed set and fusing information of the network topology and gene expression.
    Zhang SW; Shao DD; Zhang SY; Wang YB
    Mol Biosyst; 2014 Jun; 10(6):1400-8. PubMed ID: 24695957
    [TBL] [Abstract][Full Text] [Related]  

  • 40. PhenOMIM: an OMIM-based secondary database purported for phenotypic comparison.
    van Triest HJ; Chen D; Ji X; Qi S; Li-Ling J
    Annu Int Conf IEEE Eng Med Biol Soc; 2011; 2011():3589-92. PubMed ID: 22255115
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.