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 *

94 related articles for article (PubMed ID: 27168365)

  • 1. Disease-Phenotype Deconvolution in Genetic Eye Diseases Using Online Mendelian Inheritance in Man.
    Pandey P; Acharya M
    Invest Ophthalmol Vis Sci; 2016 May; 57(6):2895–2904. PubMed ID: 27168365
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Searching Online Mendelian Inheritance in Man (OMIM) for information on genetic loci involved in human disease.
    Borate B; Baxevanis AD
    Curr Protoc Bioinformatics; 2009 Sep; Chapter 1():Unit 1.2. PubMed ID: 19728286
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Searching Online Mendelian Inheritance in Man (OMIM): A Knowledgebase of Human Genes and Genetic Phenotypes.
    Amberger JS; Hamosh A
    Curr Protoc Bioinformatics; 2017 Jun; 58():1.2.1-1.2.12. PubMed ID: 28654725
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. McKusick's Online Mendelian Inheritance in Man (OMIM).
    Amberger J; Bocchini CA; Scott AF; Hamosh A
    Nucleic Acids Res; 2009 Jan; 37(Database issue):D793-6. PubMed ID: 18842627
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A text-mining analysis of the human phenome.
    van Driel MA; Bruggeman J; Vriend G; Brunner HG; Leunissen JA
    Eur J Hum Genet; 2006 May; 14(5):535-42. PubMed ID: 16493445
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Global Single Clustering of Phenotype-Associated Human Aging Genes in the Co-Expression and Physical Interaction Networks: An OMIM-Based Investigative Review.
    M R; M A; H B; M O
    Arch Gerontol Geriatr; 2021; 96():104461. PubMed ID: 34171756
    [TBL] [Abstract][Full Text] [Related]  

  • 9. OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders.
    Amberger JS; Bocchini CA; Schiettecatte F; Scott AF; Hamosh A
    Nucleic Acids Res; 2015 Jan; 43(Database issue):D789-98. PubMed ID: 25428349
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Review on the research progress of mining of OMIM data].
    Li J; Li Z; Kang Y; Li L
    Sheng Wu Yi Xue Gong Cheng Xue Za Zhi; 2014 Dec; 31(6):1400-4. PubMed ID: 25868267
    [TBL] [Abstract][Full Text] [Related]  

  • 11. KMeyeDB: a graphical database of mutations in genes that cause eye diseases.
    Kawamura T; Ohtsubo M; Mitsuyama S; Ohno-Nakamura S; Shimizu N; Minoshima S
    Hum Mutat; 2010 Jun; 31(6):667-74. PubMed ID: 20232414
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ocular manifestations in Wolf-Hirschhorn syndrome.
    Dickmann A; Parrilla R; Salerni A; Savino G; Vasta I; Zollino M; Petroni S; Zampino G
    J AAPOS; 2009 Jun; 13(3):264-7. PubMed ID: 19541266
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Application of genetic approaches to ocular disease.
    Ruttum MS; Reis LM; Semina EV
    Pediatr Clin North Am; 2006 Aug; 53(4):751-65. PubMed ID: 16873003
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotype-phenotype variations in five Spanish families with Norrie disease or X-linked FEVR.
    Riveiro-Alvarez R; Trujillo-Tiebas MJ; Gimenez-Pardo A; Garcia-Hoyos M; Cantalapiedra D; Lorda-Sanchez I; Rodriguez de Alba M; Ramos C; Ayuso C
    Mol Vis; 2005 Sep; 11():705-12. PubMed ID: 16163268
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Towards prediction and prioritization of disease genes by the modularity of human phenome-genome assembled network.
    Jiang JQ; Dress AW; Chen M
    J Integr Bioinform; 2010 Nov; 7(2):. PubMed ID: 21098881
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. The bipolar disorder phenome database: a resource for genetic studies.
    Potash JB; Toolan J; Steele J; Miller EB; Pearl J; Zandi PP; Schulze TG; Kassem L; Simpson SG; Lopez V; ; MacKinnon DF; McMahon FJ
    Am J Psychiatry; 2007 Aug; 164(8):1229-37. PubMed ID: 17671286
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. OMIA (Online Mendelian Inheritance in Animals): an enhanced platform and integration into the Entrez search interface at NCBI.
    Lenffer J; Nicholas FW; Castle K; Rao A; Gregory S; Poidinger M; Mailman MD; Ranganathan S
    Nucleic Acids Res; 2006 Jan; 34(Database issue):D599-601. PubMed ID: 16381939
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Marfan syndrome: ocular findings and novel mutations-in pursuit of genotype-phenotype associations.
    Latasiewicz M; Fontecilla C; Millá E; Sánchez A
    Can J Ophthalmol; 2016 Apr; 51(2):113-8. PubMed ID: 27085269
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.