Genetic databases and their potential in pharmacogenomics.
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Konstantinos Poulas | George P Patrinos | George Lagoumintzis | G. Patrinos | G. Lagoumintzis | K. Poulas | George Lagoumintzis
[1] D. Goldstein,et al. Will tomorrow's medicines work for everyone? , 2004, Nature Genetics.
[2] Alan F. Scott,et al. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders , 2004, Nucleic Acids Res..
[3] George P Patrinos,et al. National and ethnic mutation databases: recording populations' genography , 2006, Human mutation.
[4] G. Patrinos,et al. Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies , 2005, Human mutation.
[5] George P Patrinos,et al. DNA, diseases and databases: disastrously deficient. , 2005, Trends in genetics : TIG.
[6] Russ B Altman,et al. PharmGKB: the pharmacogenetics and pharmacogenomics knowledge base. , 2005, Methods in molecular biology.
[7] Gregory D. Schuler,et al. Database resources of the National Center for Biotechnology Information: update , 2004, Nucleic acids research.
[8] Ourania Horaitis,et al. Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases. , 2002, Genome research.
[9] R. G. H. Cotton,et al. The HUGO Mutation Database Initiative , 1998, Science.
[10] A. Davis,et al. Pharmacogenetics research network and knowledge base: 1st annual scientific meeting. , 2001, Pharmacogenomics.
[11] George P Patrinos,et al. Hellenic National Mutation Database: a prototype database for mutations leading to inherited disorders in the Hellenic population , 2005, Human mutation.
[12] Toshio Kojima,et al. Planning the Human Variome Project: The Spain report , 2009, Human mutation.
[13] Milan Macek,et al. FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide , 2006, Nucleic Acids Res..
[14] L. Stein. Creating a bioinformatics nation , 2002, Nature.
[15] P. Kwok,et al. Human Variome Project: an international collaboration to catalogue human genetic variation. , 2006, Pharmacogenomics.
[16] Debasis Dash,et al. HGVbaseG2P: a central genetic association database , 2008, Nucleic Acids Res..
[17] Joshua M. Stuart,et al. Integrating genotype and phenotype information: an overview of the PharmGKB project , 2001, The Pharmacogenomics Journal.
[18] Russ B. Altman,et al. PharmGKB: Understanding the Effects of Individual Genetic Variants , 2008, Drug metabolism reviews.
[19] Ourania Horaitis,et al. A database of locus-specific databases , 2007, Nature Genetics.
[20] Sue Povey,et al. Genew: the Human Gene Nomenclature Database, 2004 updates , 2004, Nucleic Acids Res..
[21] G. Patrinos,et al. Recording human globin gene variation. , 2004, Hemoglobin.
[22] Russ B. Altman,et al. PharmGKB and the International Warfarin Pharmacogenetics Consortium: the changing role for pharmacogenomic databases and single‐drug pharmacogenetics , 2008, Human mutation.
[23] P. Stenson,et al. Human Gene Mutation Database (HGMD®): 2003 update , 2003, Human mutation.
[24] R. A. George,et al. General mutation databases: analysis and review , 2007, Journal of Medical Genetics.
[25] B. Raby. Genetic mapping of pharmacogenetic regulatory variation. , 2009, Current pharmaceutical design.
[26] George P Patrinos,et al. HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server , 2002, Human mutation.
[27] H. L. Zhang,et al. PharmGED: pharmacogenetic effect database. , 2007, Clinical pharmacology and therapeutics.
[28] E. Petricoin,et al. A New Scientific Journal Linked to a Genetic Database: Towards a Novel Publication Modality , 2008, Human genomics and proteomics : HGP.
[29] Pertti Aula,et al. Database for the mutations of the Finnish disease heritage , 2002, Human mutation.
[30] Webb Miller,et al. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies , 2004, Nucleic Acids Res..
[31] R. Cotton,et al. A survey of locus-specific database curation , 2007, Journal of Medical Genetics.
[32] George P Patrinos,et al. The Cypriot and Iranian National Mutation Frequency Databases , 2006, Human mutation.