These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

295 related articles for article (PubMed ID: 12508258)

  • 21. A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations.
    Zhang C; Bailey DK; Awad T; Liu G; Xing G; Cao M; Valmeekam V; Retief J; Matsuzaki H; Taub M; Seielstad M; Kennedy GC
    Bioinformatics; 2006 Sep; 22(17):2122-8. PubMed ID: 16845142
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Estimation of relative allele frequencies of single-nucleotide polymorphisms in different populations by microarray hybridization of pooled DNA.
    Bang-Ce Y; Peng Z; Bincheng Y; Songyang L
    Anal Biochem; 2004 Oct; 333(1):72-8. PubMed ID: 15351282
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Quantifying the amount of missing information in genetic association studies.
    Nicolae DL
    Genet Epidemiol; 2006 Dec; 30(8):703-17. PubMed ID: 16986163
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Preliminary analysis of a KIR haplotype estimation algorithm: a simulation study.
    Gourraud PA; Gagne K; Bignon JD; Cambon-Thomsen A; Middleton D
    Tissue Antigens; 2007 Apr; 69 Suppl 1():96-100. PubMed ID: 17445177
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Simple estimates of haplotype relative risks in case-control data.
    French B; Lumley T; Monks SA; Rice KM; Hindorff LA; Reiner AP; Psaty BM
    Genet Epidemiol; 2006 Sep; 30(6):485-94. PubMed ID: 16755519
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Power of direct vs. indirect haplotyping in association studies.
    Thomas S; Porteous D; Visscher PM
    Genet Epidemiol; 2004 Feb; 26(2):116-24. PubMed ID: 14748011
    [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 haplotype map of the human genome.
    Olivier M
    Physiol Genomics; 2003 Mar; 13(1):3-9. PubMed ID: 12644628
    [No Abstract]   [Full Text] [Related]  

  • 29. Maximum likelihood estimates of allele frequencies and error rates from samples of related individuals by gene counting.
    Thomas A; Camp NJ
    Bioinformatics; 2006 Mar; 22(6):771-2. PubMed ID: 16410318
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Accounting for haplotype uncertainty in matched association studies: a comparison of simple and flexible techniques.
    Kraft P; Cox DG; Paynter RA; Hunter D; De Vivo I
    Genet Epidemiol; 2005 Apr; 28(3):261-72. PubMed ID: 15637718
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Haplotype inference for population data with genotyping errors.
    Zhu W; Kuk AY; Guo J
    Biom J; 2009 Aug; 51(4):644-58. PubMed ID: 19688759
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Efficiency of DNA pooling to estimate joint allele frequencies and measure linkage disequilibrium.
    Pfeiffer RM; Rutter JL; Gail MH; Struewing J; Gastwirth JL
    Genet Epidemiol; 2002 Jan; 22(1):94-102. PubMed ID: 11754476
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of disease causing loci using an array-based genotyping approach on pooled DNA.
    Craig DW; Huentelman MJ; Hu-Lince D; Zismann VL; Kruer MC; Lee AM; Puffenberger EG; Pearson JM; Stephan DA
    BMC Genomics; 2005 Sep; 6():138. PubMed ID: 16197552
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Bayesian method for gene detection and mapping, using a case and control design and DNA pooling.
    Johnson T
    Biostatistics; 2007 Jul; 8(3):546-65. PubMed ID: 16984977
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Algorithms for inferring haplotypes.
    Niu T
    Genet Epidemiol; 2004 Dec; 27(4):334-47. PubMed ID: 15368348
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Conditional likelihood methods for haplotype-based association analysis using matched case-control data.
    Chen J; Rodriguez C
    Biometrics; 2007 Dec; 63(4):1099-107. PubMed ID: 18078481
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Optimal selection strategies for QTL mapping using pooled DNA samples.
    Jawaid A; Bader JS; Purcell S; Cherny SS; Sham P
    Eur J Hum Genet; 2002 Feb; 10(2):125-32. PubMed ID: 11938443
    [TBL] [Abstract][Full Text] [Related]  

  • 38. DNA pooling: a comprehensive, multi-stage association analysis of ACSL6 and SIRT5 polymorphisms in schizophrenia.
    Chowdari KV; Northup A; Pless L; Wood J; Joo YH; Mirnics K; Lewis DA; Levitt PR; Bacanu SA; Nimgaonkar VL
    Genes Brain Behav; 2007 Apr; 6(3):229-39. PubMed ID: 16827919
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Two-Stage sampling designs for gene association studies.
    Thomas D; Xie R; Gebregziabher M
    Genet Epidemiol; 2004 Dec; 27(4):401-14. PubMed ID: 15543639
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Estimating haplotype relative risks in complex disease from unphased SNPs data in families using a likelihood adjusted for ascertainment.
    Carayol J; Philippi A; Tores F
    Genet Epidemiol; 2006 Dec; 30(8):666-76. PubMed ID: 16917928
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.