Similar articles for PMID: 12502794

Year	Number of Results
1998	3
1999	2
2000	1
2001	3
2002	7
2003	1
2004	6
2005	3
2006	2
2007	2
2008	3
2013	3
2014	3
2015	5
2016	1
2023	1
2024	0

1

Sequence variations in the public human genome data reflect a bottlenecked population history.

Marth G, Schuler G, Yeh R, Davenport R, Agarwala R, Church D, Wheelan S, Baker J, Ward M, Kholodov M, Phan L, Czabarka E, Murvai J, Cutler D, Wooding S, Rogers A, Chakravarti A, Harpending HC, Kwok PY, Sherry ST. Marth G, et al. Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):376-81. doi: 10.1073/pnas.222673099. Epub 2002 Dec 26. Proc Natl Acad Sci U S A. 2003. PMID: 12502794 Free PMC article.

2

[Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].

Zhang DL, Ji L, Li YD. Zhang DL, et al. Yi Chuan Xue Bao. 2004 May;31(5):431-43. Yi Chuan Xue Bao. 2004. PMID: 15478601 Chinese.

3

Increased gene coverage and Alu frequency in large linkage disequilibrium blocks of the human genome.

Wang Y, Fong PY, Leung FC, Mak W, Sham PC. Wang Y, et al. Genet Mol Res. 2007 Dec 11;6(4):1131-41. Genet Mol Res. 2007. PMID: 18273807 Free article.

4

New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies.

De La Vega FM, Dailey D, Ziegle J, Williams J, Madden D, Gilbert DA. De La Vega FM, et al. Biotechniques. 2002 Jun;Suppl:48-50, 52, 54. Biotechniques. 2002. PMID: 12083398

5

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.

Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, Mullikin JC, Mortimore BJ, Willey DL, Hunt SE, Cole CG, Coggill PC, Rice CM, Ning Z, Rogers J, Bentley DR, Kwok PY, Mardis ER, Yeh RT, Schultz B, Cook L, Davenport R, Dante M, Fulton L, Hillier L, Waterston RH, McPherson JD, Gilman B, Schaffner S, Van Etten WJ, Reich D, Higgins J, Daly MJ, Blumenstiel B, Baldwin J, Stange-Thomann N, Zody MC, Linton L, Lander ES, Altshuler D; International SNP Map Working Group. Sachidanandam R, et al. Nature. 2001 Feb 15;409(6822):928-33. doi: 10.1038/35057149. Nature. 2001. PMID: 11237013

6

Introduction to SNPs: discovery of markers for disease.

Weiner MP, Hudson TJ. Weiner MP, et al. Biotechniques. 2002 Jun;Suppl:4-7, 10, 12-3. Biotechniques. 2002. PMID: 12083396 No abstract available.

7

The relative power of SNPs and haplotype as genetic markers for association tests.

Bader JS. Bader JS. Pharmacogenomics. 2001 Feb;2(1):11-24. doi: 10.1517/14622416.2.1.11. Pharmacogenomics. 2001. PMID: 11258193

8

Construction and characterization of a genomic BAC library for the Mus m. musculus mouse subspecies (PWD/Ph inbred strain).

Jansa P, Divina P, Forejt J. Jansa P, et al. BMC Genomics. 2005 Nov 16;6:161. doi: 10.1186/1471-2164-6-161. BMC Genomics. 2005. PMID: 16288658 Free PMC article.

9

Identity by descent genome segmentation based on single nucleotide polymorphism distributions.

Blackwell TW, Rouchka E, States DJ. Blackwell TW, et al. Proc Int Conf Intell Syst Mol Biol. 1999:54-9. Proc Int Conf Intell Syst Mol Biol. 1999. PMID: 10786286

10

Detecting SNP combinations discriminating human populations from HapMap data.

Ding X, Li M, Gu H, Peng X, Zhang Z, Wu F. Ding X, et al. IEEE Trans Nanobioscience. 2015 Mar;14(2):220-8. doi: 10.1109/TNB.2015.2391134. Epub 2015 Jan 13. IEEE Trans Nanobioscience. 2015. PMID: 25594978

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