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Results: 1 to 20 of 129

1.

Haplotype-based methods for detecting uncommon causal variants with common SNPs.

Lin WY, Yi N, Zhi D, Zhang K, Gao G, Tiwari HK, Liu N.

Genet Epidemiol. 2012 Sep;36(6):572-82. doi: 10.1002/gepi.21650. Epub 2012 Jun 15.

PMID:
22706849
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.

Lin WY, Yi N, Lou XY, Zhi D, Zhang K, Gao G, Tiwari HK, Liu N.

Genet Epidemiol. 2013 Sep;37(6):560-70. doi: 10.1002/gepi.21740. Epub 2013 Jun 5.

PMID:
23740760
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia.

Wason JM, Dudbridge F.

BMC Genet. 2010 Sep 9;11:80. doi: 10.1186/1471-2156-11-80.

PMID:
20828390
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Similarity in recombination rate and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene regions among Europeans indicates signs of selection and no advantage of using tagSNPs in population isolates.

Pimenoff VN, Laval G, Comas D, Palo JU, Gut I, Cann H, Excoffier L, Sajantila A.

Pharmacogenet Genomics. 2012 Dec;22(12):846-57. doi: 10.1097/FPC.0b013e32835a3a6d.

PMID:
23089684
[PubMed - indexed for MEDLINE]
5.

Similarity-based multimarker association tests for continuous traits.

Lin WY, Tiwari HK, Gao G, Zhang K, Arcaroli JJ, Abraham E, Liu N.

Ann Hum Genet. 2012 May;76(3):246-60. doi: 10.1111/j.1469-1809.2012.00706.x.

PMID:
22497480
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed with haplotype-tagging SNPs.

Kamatani N, Sekine A, Kitamoto T, Iida A, Saito S, Kogame A, Inoue E, Kawamoto M, Harigai M, Nakamura Y.

Am J Hum Genet. 2004 Aug;75(2):190-203. Epub 2004 Jun 16.

PMID:
15202072
[PubMed - indexed for MEDLINE]
Free PMC Article
7.
8.

Comparison of linkage disequilibrium patterns and haplotype structure of eight single nucleotide polymorphisms across the CYP1A2 gene between the Korean, and other populations registered in the International HapMap database.

Woo SW, Kang TS, Park HJ, Lee JE, Roh J.

J Clin Pharm Ther. 2009 Aug;34(4):429-36. doi: 10.1111/j.1365-2710.2008.01011.x.

PMID:
19583676
[PubMed - indexed for MEDLINE]
9.

Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test.

Abad-Grau MM, Medina-Medina N, Montes-Soldado R, Moreno-Ortega J, Matesanz F.

Hum Genet. 2010 Sep;128(3):325-44. doi: 10.1007/s00439-010-0854-z. Epub 2010 Jul 6.

PMID:
20603721
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity.

Liu Y, Li YJ, Satten GA, Allen AS, Tzeng JY.

Ann Hum Genet. 2009 Sep;73(Pt 5):520-6. doi: 10.1111/j.1469-1809.2009.00536.x. Epub 2009 Jul 20.

PMID:
19622101
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Incorporating single-locus tests into haplotype cladistic analysis in case-control studies.

Liu J, Papasian C, Deng HW.

PLoS Genet. 2007 Mar 23;3(3):e46.

PMID:
17381242
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

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. Epub 2004 Apr 12.

PMID:
15078859
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Multipoint linkage-disequilibrium mapping with haplotype-block structure.

Zheng M, McPeek MS.

Am J Hum Genet. 2007 Jan;80(1):112-25. Epub 2006 Nov 30.

PMID:
17160899
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Improved power by use of a weighted score test for linkage disequilibrium mapping.

Wang T, Elston RC.

Am J Hum Genet. 2007 Feb;80(2):353-60. Epub 2006 Dec 21.

PMID:
17236140
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Screening for recently selected alleles by analysis of human haplotype similarity.

Hanchard NA, Rockett KA, Spencer C, Coop G, Pinder M, Jallow M, Kimber M, McVean G, Mott R, Kwiatkowski DP.

Am J Hum Genet. 2006 Jan;78(1):153-9. Epub 2005 Nov 16.

PMID:
16385459
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Asymptotic tests of association with multiple SNPs in linkage disequilibrium.

Pan W.

Genet Epidemiol. 2009 Sep;33(6):497-507. doi: 10.1002/gepi.20402.

PMID:
19170135
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

SNP identification, linkage disequilibrium, and haplotype analysis for a 200-kb genomic region in a Korean population.

Kim KJ, Lee HJ, Park MH, Cha SH, Kim KS, Kim HT, Kimm K, Oh B, Lee JY.

Genomics. 2006 Nov;88(5):535-40. Epub 2006 Aug 17.

PMID:
16919420
[PubMed - indexed for MEDLINE]
Free Article
18.

A systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure.

Yang Y, Li SS, Chien JW, Andriesen J, Zhao LP.

BMC Genet. 2008 Dec 22;9:90. doi: 10.1186/1471-2156-9-90.

PMID:
19102730
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Haplotype sharing analysis with SNPs in candidate genes: the Genetic Analysis Workshop 12 example.

Fischer C, Beckmann L, Majoram P, te Meerman G, Chang-Claude J.

Genet Epidemiol. 2003 Jan;24(1):68-73.

PMID:
12508257
[PubMed - indexed for MEDLINE]
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