BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

336 related articles for article (PubMed ID: 18325640)

  • 21. Genes on bovine chromosome 18 associated with bilateral convergent strabismus with exophthalmos in German Brown cattle.
    Fink S; Mömke S; Wöhlke A; Distl O
    Mol Vis; 2008 Sep; 14():1737-51. PubMed ID: 18836565
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Testing association between disease and multiple SNPs in a candidate gene.
    Gauderman WJ; Murcray C; Gilliland F; Conti DV
    Genet Epidemiol; 2007 Jul; 31(5):383-95. PubMed ID: 17410554
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Universal false discovery rate estimation methodology for genome-wide association studies.
    Forner K; Lamarine M; Guedj M; Dauvillier J; Wojcik J
    Hum Hered; 2008; 65(4):183-94. PubMed ID: 18073488
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease.
    Evangelou E; Maraganore DM; Ioannidis JP
    PLoS One; 2007 Feb; 2(2):e196. PubMed ID: 17332845
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Advances in high-density whole genome-wide single nucleotide polymorphism array in cancer research].
    Zeng ZY; Xiong W; Zhou YH; Li XL; Li GY
    Ai Zheng; 2006 Nov; 25(11):1454-8. PubMed ID: 17094921
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The patterns of natural variation in human genes.
    Crawford DC; Akey DT; Nickerson DA
    Annu Rev Genomics Hum Genet; 2005; 6():287-312. PubMed ID: 16124863
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence.
    Taudien S; Galgoczy P; Huse K; Reichwald K; Schilhabel M; Szafranski K; Shimizu A; Asakawa S; Frankish A; Loncarevic IF; Shimizu N; Siddiqui R; Platzer M
    BMC Genomics; 2004 Dec; 5(1):92. PubMed ID: 15588320
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Primer: SNP-associated studies and what they can teach us.
    Yamada R
    Nat Clin Pract Rheumatol; 2008 Apr; 4(4):210-7. PubMed ID: 18319711
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Bioinformatics tools for single nucleotide polymorphism discovery and analysis.
    Clifford RJ; Edmonson MN; Nguyen C; Scherpbier T; Hu Y; Buetow KH
    Ann N Y Acad Sci; 2004 May; 1020():101-9. PubMed ID: 15208187
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians.
    Gragnoli C
    J Cell Physiol; 2008 Nov; 217(2):291-5. PubMed ID: 18680108
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Integrating genetic, functional genomic, and bioinformatics data in a systems biology approach to complex diseases: application to schizophrenia.
    Middleton FA; Rosenow C; Vailaya A; Kuchinsky A; Pato MT; Pato CN
    Methods Mol Biol; 2007; 401():337-64. PubMed ID: 18368374
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic association studies of complex traits: design and analysis issues.
    Newton-Cheh C; Hirschhorn JN
    Mutat Res; 2005 Jun; 573(1-2):54-69. PubMed ID: 15829237
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Innate immunity genes as candidate genes: searching for relevant natural polymorphisms in databases and assessing family-based association of polymorphisms with human diseases.
    Rihet P
    Methods Mol Biol; 2008; 415():17-48. PubMed ID: 18370146
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fine mapping of disease genes using tagging SNPs.
    Sjölander A; Hössjer O; Hartman LW; Humphreys K
    Ann Hum Genet; 2007 Nov; 71(Pt 6):815-27. PubMed ID: 17587339
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Targeted screening of cis-regulatory variation in human haplotypes.
    Verlaan DJ; Ge B; Grundberg E; Hoberman R; Lam KC; Koka V; Dias J; Gurd S; Martin NW; Mallmin H; Nilsson O; Harmsen E; Dewar K; Kwan T; Pastinen T
    Genome Res; 2009 Jan; 19(1):118-27. PubMed ID: 18971308
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Comparison of family based haplotype methods using intragenic SNPs in candidate genes.
    Bourgain C; Genin E; Clerget-Darpoux F
    Eur J Hum Genet; 2002 May; 10(5):313-9. PubMed ID: 12082506
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Genome-wide association studies].
    Feenstra B; Boyd HA; Melbye M
    Ugeskr Laeger; 2008 Oct; 170(41):3216-20. PubMed ID: 18940150
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Detrimental effects of mannose-binding lectin (MBL2) promoter genotype XA/XA on HIV-1 vertical transmission and AIDS progression.
    Mangano A; Rocco C; Marino SM; Mecikovsky D; Genre F; Aulicino P; Bologna R; Sen L
    J Infect Dis; 2008 Sep; 198(5):694-700. PubMed ID: 18637753
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic studies to identify hepatic fibrosis genes and SNPs in human populations.
    Day CP
    Methods Mol Med; 2005; 117():315-31. PubMed ID: 16118460
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Singleton SNPs in the human genome and implications for genome-wide association studies.
    Ke X; Taylor MS; Cardon LR
    Eur J Hum Genet; 2008 Apr; 16(4):506-15. PubMed ID: 18197193
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.