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    Results: 1 to 20 of 101

    1.

    Protein interactions in human genetic diseases.

    Schuster-Böckler B, Bateman A.

    Genome Biol. 2008 Jan 16;9(1):R9.

    PMID:
    18199329
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.

    Hamosh A, Scott AF, Amberger JS, Bocchini CA, McKusick VA.

    Nucleic Acids Res. 2005 Jan 1;33(Database issue):D514-7.

    PMID:
    15608251
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    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.

    PMID:
    18428346
    [PubMed - indexed for MEDLINE]
    4.

    Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.

    Hamosh A, Scott AF, Amberger J, Bocchini C, Valle D, McKusick VA.

    Nucleic Acids Res. 2002 Jan 1;30(1):52-5.

    PMID:
    11752252
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    5.

    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.

    PMID:
    19728286
    [PubMed - indexed for MEDLINE]
    6.

    Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.

    Capriotti E, Calabrese R, Casadio R.

    Bioinformatics. 2006 Nov 15;22(22):2729-34. Epub 2006 Aug 7.

    PMID:
    16895930
    [PubMed - indexed for MEDLINE]
    Free Article
    7.

    The cypriot and Iranian National Mutation Frequency Databases.

    Kleanthous M, Patsalis PC, Drousiotou A, Motazacker M, Christodoulou K, Cariolou M, Baysal E, Khrizi K, Moghimi B, Pourfarzad F, van Baal S, Deltas C, Najmabadi H, Patrinos GP.

    Hum Mutat. 2006 Jun;27(6):598-9.

    PMID:
    16705699
    [PubMed - indexed for MEDLINE]
    8.

    Discovering disease-genes by topological features in human protein-protein interaction network.

    Xu J, Li Y.

    Bioinformatics. 2006 Nov 15;22(22):2800-5. Epub 2006 Sep 5.

    PMID:
    16954137
    [PubMed - indexed for MEDLINE]
    Free Article
    9.

    Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.

    Patrinos GP, van Baal S, Petersen MB, Papadakis MN.

    Hum Mutat. 2005 Apr;25(4):327-33.

    PMID:
    15776445
    [PubMed - indexed for MEDLINE]
    10.
    11.

    Sequence-based prediction of pathological mutations.

    Ferrer-Costa C, Orozco M, de la Cruz X.

    Proteins. 2004 Dec 1;57(4):811-9.

    PMID:
    15390262
    [PubMed - indexed for MEDLINE]
    12.

    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 29;6:78.

    PMID:
    15796777
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    13.

    FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide.

    van Baal S, Kaimakis P, Phommarinh M, Koumbi D, Cuppens H, Riccardino F, Macek M Jr, Scriver CR, Patrinos GP.

    Nucleic Acids Res. 2007 Jan;35(Database issue):D690-5. Epub 2006 Nov 28.

    PMID:
    17135191
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    14.

    [Integrated database for mutations in disease genes: MutationView/KMDB].

    Ohtsubo M, Shibuya K, Kudoh J, Minoshima S, Shimizu N.

    Tanpakushitsu Kakusan Koso. 2003 May;48(6):762-9. Review. Japanese. No abstract available.

    PMID:
    12816011
    [PubMed - indexed for MEDLINE]
    15.

    Thailand mutation and variation database (ThaiMUT).

    Ruangrit U, Srikummool M, Assawamakin A, Ngamphiw C, Chuechote S, Thaiprasarnsup V, Agavatpanitch G, Pasomsab E, Yenchitsomanus PT, Mahasirimongkol S, Chantratita W, Palittapongarnpim P, Uyyanonvara B, Limwongse C, Tongsima S.

    Hum Mutat. 2008 Aug;29(8):E68-75.

    PMID:
    18484585
    [PubMed - indexed for MEDLINE]
    16.

    Arab genetic disease database (AGDDB): a population-specific clinical and mutation database.

    Teebi AS, Teebi SA, Porter CJ, Cuticchia AJ.

    Hum Mutat. 2002 Jun;19(6):615-21.

    PMID:
    12007218
    [PubMed - indexed for MEDLINE]
    17.

    Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database.

    Zlotogora J, van Baal S, Patrinos GP.

    Hum Mutat. 2007 Oct;28(10):944-9.

    PMID:
    17492749
    [PubMed - indexed for MEDLINE]
    18.

    The GDB Human Genome Data Base: a source of integrated genetic mapping and disease data.

    Brandt KA.

    Bull Med Libr Assoc. 1993 Jul;81(3):285-92.

    PMID:
    8374584
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    19.

    Protein-protein interactions and disease: use of S. cerevisiae as a model system.

    Hsu WT, Pang CN, Sheetal J, Wilkins MR.

    Biochim Biophys Acta. 2007 Jul;1774(7):838-47. Epub 2007 May 5.

    PMID:
    17560182
    [PubMed - indexed for MEDLINE]
    20.

    General mutation databases: analysis and review.

    George RA, Smith TD, Callaghan S, Hardman L, Pierides C, Horaitis O, Wouters MA, Cotton RG.

    J Med Genet. 2008 Feb;45(2):65-70. Epub 2007 Sep 24. Review.

    PMID:
    17893115
    [PubMed - indexed for MEDLINE]
    Free Article

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