Publications
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“Usefulness of direct sequencing of pooled DNA for SNP identification and allele-frequency determination compatible with a common disease/common variant hypothesis”, vol. 9, pp. 772-779, 2010.
, Altshuler D, Hirschhorn JN, Klannemark M, Lindgren CM, et al. (2000). The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat. Genet. 26: 76-80.
http://dx.doi.org/10.1038/79216
PMid:10973253
Anonymous (2003). The International HapMap Project. Nature 426: 789-796.
http://dx.doi.org/10.1038/nature02168
PMid:14685227
Anonymous (2004). Finishing the euchromatic sequence of the human genome. Nature 431: 931-945.
http://dx.doi.org/10.1038/nature03001
PMid:15496913
Bang-Ce Y, Peng Z, Bincheng Y and Songyang L (2004). Estimation of relative allele frequencies of single-nucleotide polymorphisms in different populations by microarray hybridization of pooled DNA. Anal. Biochem. 333: 72-78.
http://dx.doi.org/10.1016/j.ab.2004.05.016
PMid:15351282
Belmont JW and Gibbs RA (2004). Genome-wide linkage disequilibrium and haplotype maps. Am. J. Pharmacogenomics 4: 253-262.
http://dx.doi.org/10.2165/00129785-200404040-00005
PMid:15287819
Bertina RM, Koeleman BP, Koster T, Rosendaal FR, et al. (1994). Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 369: 64-67.
http://dx.doi.org/10.1038/369064a0
PMid:8164741
Chakravarti A (1999). Population genetics-making sense out of sequence. Nat. Genet. 21: 56-60.
http://dx.doi.org/10.1038/4482
PMid:9915503
Corder EH, Saunders AM, Strittmatter WJ, Schmechel DE, et al. (1993). Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science 261: 921-923.
http://dx.doi.org/10.1126/science.8346443
PMid:8346443
Fakhrai-Rad H, Zheng J, Willis TD, Wong K, et al. (2004). SNP discovery in pooled samples with mismatch repair detection. Genome Res. 14: 1404-1412.
http://dx.doi.org/10.1101/gr.2373904
PMid:15231755 PMCid:442157
Germer S, Holland MJ and Higuchi R (2000). High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR. Genome Res. 10: 258-266.
http://dx.doi.org/10.1101/gr.10.2.258
PMid:10673283 PMCid:310828
Goldstein DB, Ahmadi KR, Weale ME and Wood NW (2003). Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. Trends Genet. 19: 615-622.
http://dx.doi.org/10.1016/j.tig.2003.09.006
PMid:14585613
Jang SY, Kim MK, Lee KR, Park MS, et al. (2009). Gene-to-gene interaction between sodium channel-related genes in determining the risk of antiepileptic drug resistance. J. Korean Med. Sci. 24: 62-68.
http://dx.doi.org/10.3346/jkms.2009.24.1.62
PMid:19270815 PMCid:2650995
Judson R, Salisbury B, Schneider J, Windemuth A, et al. (2002). How many SNPs does a genome-wide haplotype map require? Pharmacogenomics 3: 379-391.
http://dx.doi.org/10.1517/14622416.3.3.379
PMid:12052145
Kim YO, Kim MK, Woo YJ, Lee MC, et al. (2006). Single nucleotide polymorphisms in the multidrug resistance 1 gene in Korean epileptics. Seizure 15: 67-72.
http://dx.doi.org/10.1016/j.seizure.2005.11.001
PMid:16386926
Kim YU, Kim SH, Jin H, Park YK, et al. (2008). The Korean HapMap Project Website. Genomics Inform. 6: 91-94.
http://dx.doi.org/10.5808/GI.2008.6.2.091
Kwok PY, Carlson C, Yager TD, Ankener W, et al. (1994). Comparative analysis of human DNA variations by fluorescence-based sequencing of PCR products. Genomics 23: 138-144.
http://dx.doi.org/10.1006/geno.1994.1469
PMid:7829062
Long AD and Langley CH (1999). The power of association studies to detect the contribution of candidate genetic loci to variation in complex traits. Genome Res. 9: 720-731.
PMid:10447507 PMCid:310800
Reich DE and Lander ES (2001). On the allelic spectrum of human disease. Trends Genet. 17: 502-510.
http://dx.doi.org/10.1016/S0168-9525(01)02410-6
Risch N and Merikangas K (1996). The future of genetic studies of complex human diseases. Science 273: 1516-1517.
http://dx.doi.org/10.1126/science.273.5281.1516
PMid:8801636
Roses AD (2000). Pharmacogenetics and the practice of medicine. Nature 405: 857-865.
http://dx.doi.org/10.1038/35015728
PMid:10866212
Salisbury BA, Pungliya M, Choi JY, Jiang R, et al. (2003). SNP and haplotype variation in the human genome. Mutat. Res. 526: 53-61.
http://dx.doi.org/10.1016/S0027-5107(03)00014-9
Schneider JA, Pungliya MS, Choi JY, Jiang R, et al. (2003). DNA variability of human genes. Mech. Ageing Dev. 124: 17-25.
http://dx.doi.org/10.1016/S0047-6374(02)00165-3
Stenson PD, Ball EV, Mort M, Phillips AD, et al. (2003). Human Gene Mutation Database (HGMD): 2003 update. Hum. Mutat. 21: 577-581.
http://dx.doi.org/10.1002/humu.10212
PMid:12754702
Suh Y and Vijg J (2005). SNP discovery in associating genetic variation with human disease phenotypes. Mutat. Res. 573: 41-53.
http://dx.doi.org/10.1016/j.mrfmmm.2005.01.005
PMid:15829236