Similar articles for PMID: 16385459

Year	Number of Results
2001	1
2002	8
2003	3
2004	11
2005	7
2006	6
2007	9
2008	4
2009	5
2010	11
2011	4
2012	6
2013	11
2014	5
2015	5
2016	2
2017	5
2018	2
2019	2
2021	1
2024	0

1

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. Hanchard NA, et al. Am J Hum Genet. 2006 Jan;78(1):153-9. doi: 10.1086/499252. Epub 2005 Nov 16. Am J Hum Genet. 2006. PMID: 16385459 Free PMC article.

2

[How about the uncertainty in the haplotypes in the population-based KORA studies?].

Heid IM, Lamina C, Bongardt F, Fischer G, Klopp N, Huth C, Küchenhoff H, Kronenberg F, Wichmann HE, Illig T. Heid IM, et al. Gesundheitswesen. 2005 Aug;67 Suppl 1:S132-6. doi: 10.1055/s-2005-858253. Gesundheitswesen. 2005. PMID: 16032531 German.

3

A hidden Markov model for investigating recent positive selection through haplotype structure.

Chen H, Hey J, Slatkin M. Chen H, et al. Theor Popul Biol. 2015 Feb;99:18-30. doi: 10.1016/j.tpb.2014.11.001. Epub 2014 Nov 13. Theor Popul Biol. 2015. PMID: 25446961 Free PMC article.

4

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. Lin WY, et al. Genet Epidemiol. 2012 Sep;36(6):572-82. doi: 10.1002/gepi.21650. Epub 2012 Jun 15. Genet Epidemiol. 2012. PMID: 22706849 Free PMC article.

5

Detecting recent positive selection in the human genome from haplotype structure.

Sabeti PC, Reich DE, Higgins JM, Levine HZ, Richter DJ, Schaffner SF, Gabriel SB, Platko JV, Patterson NJ, McDonald GJ, Ackerman HC, Campbell SJ, Altshuler D, Cooper R, Kwiatkowski D, Ward R, Lander ES. Sabeti PC, et al. Nature. 2002 Oct 24;419(6909):832-7. doi: 10.1038/nature01140. Epub 2002 Oct 9. Nature. 2002. PMID: 12397357

6

A powerful score test to detect positive selection in genome-wide scans.

Zhong M, Lange K, Papp JC, Fan R. Zhong M, et al. Eur J Hum Genet. 2010 Oct;18(10):1148-59. doi: 10.1038/ejhg.2010.60. Epub 2010 May 12. Eur J Hum Genet. 2010. PMID: 20461112 Free PMC article.

7

The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests.

Liu W, Zhao W, Chase GA. Liu W, et al. Hum Hered. 2006;61(1):31-44. doi: 10.1159/000092141. Epub 2006 Mar 23. Hum Hered. 2006. PMID: 16557026

8

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. Zhang K, et al. Genome Res. 2004 May;14(5):908-16. doi: 10.1101/gr.1837404. Epub 2004 Apr 12. Genome Res. 2004. PMID: 15078859 Free PMC article.

9

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. Fischer C, et al. Genet Epidemiol. 2003 Jan;24(1):68-73. doi: 10.1002/gepi.10207. Genet Epidemiol. 2003. PMID: 12508257

10

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

Liu J, Papasian C, Deng HW. Liu J, et al. PLoS Genet. 2007 Mar 23;3(3):e46. doi: 10.1371/journal.pgen.0030046. PLoS Genet. 2007. PMID: 17381242 Free PMC article.

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