BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

581 related articles for article (PubMed ID: 15372618)

  • 21. Further investigation of linkage disequilibrium SNPs and their ability to identify associated susceptibility loci.
    North BV; Curtis D; Martin ER; Lai EH; Roses AD; Sham PC
    Ann Hum Genet; 2004 May; 68(Pt 3):240-8. PubMed ID: 15180704
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests.
    Liu W; Zhao W; Chase GA
    Hum Hered; 2006; 61(1):31-44. PubMed ID: 16557026
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis.
    Suzuki S; Yoshimura M; Nakayama M; Abe K; Yamamuro M; Nagayoshi Y; Kojima S; Kaikita K; Sugiyama S; Yasue H; Ogawa H
    Pharmacogenet Genomics; 2007 Nov; 17(11):919-30. PubMed ID: 18075462
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Tag SNP selection in genotype data for maximizing SNP prediction accuracy.
    Halperin E; Kimmel G; Shamir R
    Bioinformatics; 2005 Jun; 21 Suppl 1():i195-203. PubMed ID: 15961458
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The role of haplotypes in candidate gene studies.
    Clark AG
    Genet Epidemiol; 2004 Dec; 27(4):321-33. PubMed ID: 15368617
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies.
    Zhang K; Qin ZS; Liu JS; Chen T; Waterman MS; Sun F
    Genome Res; 2004 May; 14(5):908-16. PubMed ID: 15078859
    [TBL] [Abstract][Full Text] [Related]  

  • 27. High density linkage disequilibrium mapping using models of haplotype block variation.
    Greenspan G; Geiger D
    Bioinformatics; 2004 Aug; 20 Suppl 1():i137-44. PubMed ID: 15262792
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A new multimarker test for family-based association studies.
    Rakovski CS; Xu X; Lazarus R; Blacker D; Laird NM
    Genet Epidemiol; 2007 Jan; 31(1):9-17. PubMed ID: 17086514
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Haplotype tagging for the identification of common disease genes.
    Johnson GC; Esposito L; Barratt BJ; Smith AN; Heward J; Di Genova G; Ueda H; Cordell HJ; Eaves IA; Dudbridge F; Twells RC; Payne F; Hughes W; Nutland S; Stevens H; Carr P; Tuomilehto-Wolf E; Tuomilehto J; Gough SC; Clayton DG; Todd JA
    Nat Genet; 2001 Oct; 29(2):233-7. PubMed ID: 11586306
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A haplotype analysis of HER-2 gene polymorphisms: association with breast cancer risk, HER-2 protein expression in the tumor, and disease recurrence in Korea.
    Han W; Kang D; Lee JE; Park IA; Choi JY; Lee KM; Bae JY; Kim S; Shin ES; Lee JE; Shin HJ; Kim SW; Kim SW; Noh DY
    Clin Cancer Res; 2005 Jul; 11(13):4775-8. PubMed ID: 16000574
    [TBL] [Abstract][Full Text] [Related]  

  • 31. On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles.
    Morris RW; Kaplan NL
    Genet Epidemiol; 2002 Oct; 23(3):221-33. PubMed ID: 12384975
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Optimal selection of SNP markers for disease association studies.
    Halldórsson BV; Istrail S; De La Vega FM
    Hum Hered; 2004; 58(3-4):190-202. PubMed ID: 15812176
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Tag SNPs chosen from HapMap perform well in several population isolates.
    Service S; ; Sabatti C; Freimer N
    Genet Epidemiol; 2007 Apr; 31(3):189-94. PubMed ID: 17323370
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome.
    Tsunoda T; Lathrop GM; Sekine A; Yamada R; Takahashi A; Ohnishi Y; Tanaka T; Nakamura Y
    Hum Mol Genet; 2004 Aug; 13(15):1623-32. PubMed ID: 15190013
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Linkage disequilibrium maps and disease-association mapping.
    Maniatis N
    Methods Mol Biol; 2007; 376():109-21. PubMed ID: 17984541
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Defining haplotype blocks and tag single-nucleotide polymorphisms in the human genome.
    Schulze TG; Zhang K; Chen YS; Akula N; Sun F; McMahon FJ
    Hum Mol Genet; 2004 Feb; 13(3):335-42. PubMed ID: 14681300
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Toward positional cloning with SNPs.
    Morton NE; Collins A
    Curr Opin Mol Ther; 2002 Jun; 4(3):259-64. PubMed ID: 12139312
    [TBL] [Abstract][Full Text] [Related]  

  • 39. MLR-tagging: informative SNP selection for unphased genotypes based on multiple linear regression.
    He J; Zelikovsky A
    Bioinformatics; 2006 Oct; 22(20):2558-61. PubMed ID: 16895924
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Selecting single-nucleotide polymorphisms for association studies with SNPbrowser software.
    De La Vega FM
    Methods Mol Biol; 2007; 376():177-93. PubMed ID: 17984546
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 30.