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.
89 related articles for article (PubMed ID: 12052145)
1. How many SNPs does a genome-wide haplotype map require? Judson R; Salisbury B; Schneider J; Windemuth A; Stephens JC Pharmacogenomics; 2002 May; 3(3):379-91. PubMed ID: 12052145 [TBL] [Abstract][Full Text] [Related]
2. Estimating haplotype frequencies and standard errors for multiple single nucleotide polymorphisms. Li SS; Khalid N; Carlson C; Zhao LP Biostatistics; 2003 Oct; 4(4):513-22. PubMed ID: 14557108 [TBL] [Abstract][Full Text] [Related]
3. On the use of DNA pooling to estimate haplotype frequencies. Wang S; Kidd KK; Zhao H Genet Epidemiol; 2003 Jan; 24(1):74-82. PubMed ID: 12508258 [TBL] [Abstract][Full Text] [Related]
4. Inference of missing SNPs and information quantity measurements for haplotype blocks. Su SC; Kuo CC; Chen T Bioinformatics; 2005 May; 21(9):2001-7. PubMed ID: 15699029 [TBL] [Abstract][Full Text] [Related]
5. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping. Maniatis N; Collins A; Morton NE Genet Epidemiol; 2007 Apr; 31(3):179-88. PubMed ID: 17285621 [TBL] [Abstract][Full Text] [Related]
6. The reliability of haplotyping inference in nuclear families: misassignment rates for SNPs and microsatellites. Lindholm E; Zhang J; Hodge SE; Greenberg DA Hum Hered; 2004; 57(3):117-27. PubMed ID: 15297805 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Patil N; Berno AJ; Hinds DA; Barrett WA; Doshi JM; Hacker CR; Kautzer CR; Lee DH; Marjoribanks C; McDonough DP; Nguyen BT; Norris MC; Sheehan JB; Shen N; Stern D; Stokowski RP; Thomas DJ; Trulson MO; Vyas KR; Frazer KA; Fodor SP; Cox DR Science; 2001 Nov; 294(5547):1719-23. PubMed ID: 11721056 [TBL] [Abstract][Full Text] [Related]
9. Zero-recombinant haplotyping: applications to fine mapping using SNPs. O'Connell JR Genet Epidemiol; 2000; 19 Suppl 1():S64-70. PubMed ID: 11055372 [TBL] [Abstract][Full Text] [Related]
10. Haplotype reconstruction from genotype data using Imperfect Phylogeny. Halperin E; Eskin E Bioinformatics; 2004 Aug; 20(12):1842-9. PubMed ID: 14988101 [TBL] [Abstract][Full Text] [Related]
11. Fine mapping of disease genes via haplotype clustering. Waldron ER; Whittaker JC; Balding DJ Genet Epidemiol; 2006 Feb; 30(2):170-9. PubMed ID: 16385468 [TBL] [Abstract][Full Text] [Related]
12. Genome scan linkage analysis comparing microsatellites and single-nucleotide polymorphisms markers for two measures of alcoholism in chromosomes 1, 4, and 7. Chen G; Adeyemo A; Zhou J; Yuan A; Chen Y; Rotimi C BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S4. PubMed ID: 16451650 [TBL] [Abstract][Full Text] [Related]
13. [Analysis and application of SNP and haplotype in the human genome]. Li J; Pan YC; Li YX; Shi TL Yi Chuan Xue Bao; 2005 Aug; 32(8):879-89. PubMed ID: 16231744 [TBL] [Abstract][Full Text] [Related]
14. Haplotype reconstruction from SNP fragments by minimum error correction. Wang RS; Wu LY; Li ZP; Zhang XS Bioinformatics; 2005 May; 21(10):2456-62. PubMed ID: 15731204 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes. Morris AP Genet Epidemiol; 2005 Sep; 29(2):91-107. PubMed ID: 15940704 [TBL] [Abstract][Full Text] [Related]
19. Fine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs. Cheng R; Ma JZ; Elston RC; Li MD Ann Hum Genet; 2005 Jan; 69(Pt 1):102-12. PubMed ID: 15638831 [TBL] [Abstract][Full Text] [Related]
20. Tag SNP selection for association studies. Stram DO Genet Epidemiol; 2004 Dec; 27(4):365-74. PubMed ID: 15372618 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]