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Journal Abstract Search

719 related items for PubMed ID: 12955713

  • 1. Approaches to identify genes for complex human diseases: lessons from Mendelian disorders.
    Dean M.
    Hum Mutat; 2003 Oct; 22(4):261-74. PubMed ID: 12955713
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  • 5. The search for complex disease genes: fault by linkage or fault by association?
    Baron M.
    Mol Psychiatry; 2001 Mar; 6(2):143-9. PubMed ID: 11317215
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  • 7. DNA variation and the future of human genetics.
    Schafer AJ, Hawkins JR.
    Nat Biotechnol; 1998 Jan; 16(1):33-9. PubMed ID: 9447590
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  • 9. Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.
    Beckmann JS, Estivill X, Antonarakis SE.
    Nat Rev Genet; 2007 Aug; 8(8):639-46. PubMed ID: 17637735
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  • 10. Statistical tools for linkage analysis and genetic association studies.
    Forabosco P, Falchi M, Devoto M.
    Expert Rev Mol Diagn; 2005 Sep; 5(5):781-96. PubMed ID: 16149880
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  • 11. Teaching molecular genetics: chapter 4-positional cloning of genetic disorders.
    Puliti A, Caridi G, Ravazzolo R, Ghiggeri GM.
    Pediatr Nephrol; 2007 Dec; 22(12):2023-9. PubMed ID: 17661092
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  • 12. Mechanisms of disease: The genetic basis of coronary heart disease.
    Kullo IJ, Ding K.
    Nat Clin Pract Cardiovasc Med; 2007 Oct; 4(10):558-69. PubMed ID: 17893684
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  • 13. Modifier genes in humans: strategies for identification.
    Houlston RS, Tomlinson IP.
    Eur J Hum Genet; 1998 Jan; 6(1):80-8. PubMed ID: 9781018
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  • 14. The common variants/multiple disease hypothesis of common complex genetic disorders.
    Becker KG.
    Med Hypotheses; 2004 Jan; 62(2):309-17. PubMed ID: 14962646
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  • 15. Detecting susceptibility genes in case-control studies using set association.
    Kim S, Zhang K, Sun F.
    BMC Genet; 2003 Dec 31; 4 Suppl 1(Suppl 1):S9. PubMed ID: 14975077
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  • 16. Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
    McCarthy MI, Abecasis GR, Cardon LR, Goldstein DB, Little J, Ioannidis JP, Hirschhorn JN.
    Nat Rev Genet; 2008 May 31; 9(5):356-69. PubMed ID: 18398418
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  • 17. Singapore Human Mutation/Polymorphism Database: a country-specific database for mutations and polymorphisms in inherited disorders and candidate gene association studies.
    Tan EC, Loh M, Chuon D, Lim YP.
    Hum Mutat; 2006 Mar 31; 27(3):232-5. PubMed ID: 16429432
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  • 18. Is there a paradigm shift in genetics? Lessons from the study of human diseases.
    Weiss KM.
    Mol Phylogenet Evol; 1996 Feb 31; 5(1):259-65. PubMed ID: 8673294
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