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adult-type hypolactasia. Nat Genet 2002;30:233–7.
12. Tishkoff SA, Verrelli BC. Patterns of human genetic
diversity: implications for human evolutionary history
and disease. Annu Rev Genomics Hum Genet
2003;4:293–340.
13. Guttmacher AE, Collins FS. Genomic medicine—A
primer. N Engl J Med 2002;347:1512–20.
14. Venter JC, Adams MD, Myers EW, et al. The sequence
of the human genome. Science 2001;291:1304–51.
15. Tishkoff SA, Kidd KK. Implications of biogeography of
human populations for ‘race’ and medicine. Nat Genet
2004;36(11 suppl):S21–7.
16. Nachman MW, Crowell SL. Estimate of the mutation rate
per nucleotide in humans. Genetics 2000;156:297–304.
17. Wall JD, Pritchard JK. Haplotype blocks and linkage
disequilibrium in the human genome. Nat Rev Genet
2003;4:587–97.
18. Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy
J, Blumenstiel B, Higgins J, DeFelice M, Lochner A,
Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A,
Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D.
The structure of haplotype blocks in the human genome.
Science 2002;296:2225–9.
19. Crawford DC, Nickerson DA. Definition and clinical
importance of haplotypes. Annu Rev Med 2005;56:
303–20.
20. Van Blerkom LM. Role of viruses in human evolution.
Am J Phys Anthropol 2003;suppl 37:14–46.
21. Brookfield JF. Mobile DNAs: The poacher turned gamekeeper.
Curr Biol 2003;13:R846–7.
22. Batzer MA, Deininger PL. Alu repeats and human
genomic diversity. Nat Rev Genet 2002;3:370–9.
23. Bamshad M, Wooding SP. Signatures of natural selection
in the human genome. Nat Rev Genet 2003;4:99–111.
24. Waterland RA, Jirtle RL. Transposable elements: Targets
for early nutritional effects on epigenetic gene regulation.
Mol Cell Biol 2003;23:5293–300.
25. Friso S, Choi SW. Gene-nutrient interactions and DNA
methylation. J Nutr 2002;132(8 suppl):2382S–7S.
26. Friso S, Choi SW, Dolnikowski GG, Selhub J. A method
to assess genomic DNA methylation using high-performance
liquid chromatography/electrospray ionization
mass spectrometry. Anal Chem 2002;74:4526–31.
27. Waterland RA, Garza C. Potential mechanisms of metabolic
imprinting that lead to chronic disease. Am J Clin
Nutr 1999;69:179–97.
28. Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt
RA, Wang G, Wickramasinghe SN, Everson RB, Ames
BN. Folate deficiency causes uracil misincorporation
into human DNA and chromosome breakage: Implications
for cancer and neuronal damage. Proc Natl Acad
Sci USA 1997;94:3290–5.
29. Fenech M. Micronutrients and genomic stability: A new
paradigm for recommended dietary allowances (RDAs).
Food Chem Toxicol 2002;40:1113–7.
30. Fenech M. Genome health nutrigenomics: Nutrition and
the science of optimal genome maintenance. Asia Pac J
Clin Nutr 2004;13(suppl):S15.
31. Fenech M. Chromosomal biomarkers of genomic
instability relevant to cancer. Drug Discov Today
2002;7:1128–37.
32. Fenech M. Recommended dietary allowances (RDAs)
for genomic stability. Mutat Res 2001;480–481:51–4.
P. J. Stover
33. Mishra HN, Das C. A review on biological control and
metabolism of aflatoxin. Crit Rev Food Sci Nutr 2003;
43:245–64.
34. Ames BN. DNA damage from micronutrient deficiencies
is likely to be a major cause of cancer. Mutat Res
2001;475:7–20.
35. Goswami T, Rolfs A, Hediger MA. Iron transport:
Emerging roles in health and disease. Biochem Cell Biol
2002;80:679–89.
36. Hediger MA, Rolfs A, Goswami T. Iron transport and
hemochromatosis. J Investig Med 2002;50:239S–46S.
37. Wolfe KH, Li WH. Molecular evolution meets the
genomics revolution. Nat Genet 2003;33 suppl:255–65.
38. Cooper DN, Krawczak M. Cytosine methylation and the
fate of CpG dinucleotides in vertebrate genomes. Hum
Genet 1989;83:181–8.
39. Kimura M. Evolutionary rate at the molecular level.
Nature 1968;217:624–6.
40. King JL, Jukes TH. Non-Darwinian evolution. Science
1969;164:788–98.
41. Akey JM, Zhang G, Zhang K, Jin L, Shriver MD. Interrogating
a high-density SNP map for signatures of natural
selection. Genome Res 2002;12:1805–14.
42. Akey JM, Eberle MA, Rieder MJ, Carlson CS, Shriver
MD, Nickerson DA, Kruglyak L. Population history and
natural selection shape patterns of genetic variation in
132 genes. PLoS Biol 2004;2:e286.
43. Wooding S. Natural selection: Sign, sign, everywhere a
sign. Curr Biol 2004;14:R700–1.
44. Collins FS. What we do and don’t know about ‘race’,
‘ethnicity’, genetics and health at the dawn of the genome
era. Nat Genet 2004;36(11 suppl):S13–5.
45. Chakravarti A. To a future of genetic medicine. Nature
2001;409:822–3.
46. Reich DE, Lander ES. On the allelic spectrum of human
disease. Trends Genet 2001;17:502–10.
47. Pritchard JK. Are rare variants responsible for susceptibility
to complex diseases? Am J Hum Genet
2001;69:124–37.
48. Pritchard JK, Cox NJ. The allelic architecture of human
disease genes: Common disease-common variant…or
not? Hum Mol Genet 2002;11:2417–23.
49. Jorde LB, Watkins WS, Bamshad MJ. Population genomics:
A bridge from evolutionary history to genetic medicine.
Hum Mol Genet 2001;10:2199–207.
50. Jorde LB, Watkins WS, Bamshad MJ, Dixon ME, Ricker
CE, Seielstad MT, Batzer MA. The distribution of
human genetic diversity: A comparison of mitochondrial,
autosomal, and Y-chromosome data. Am J Hum
Genet 2000;66:979–88.
51. Jorde LB, Wooding SP. Genetic variation, classification
and ‘race’. Nat Genet 2004;36(11 suppl):S28–33.
52. Bersaglieri T, Sabeti PC, Patterson N, Vanderploeg
T, Schaffner SF, Drake JA, Rhodes M, Reich DE, Hirschhorn
JN. Genetic signatures of strong recent positive
selection at the lactase gene. Am J Hum Genet 2004;
74:1111–20.
53. Poulter M, Hollox E, Harvey CB, Mulcare C, Peuhkuri
K, Kajander K, Sarner M, Korpela R, Swallow DM. The
causal element for the lactase persistence/non-persistence
polymorphism is located in a 1 Mb region of
linkage disequilibrium in Europeans. Ann Hum Genet
2003;67(pt 4):298–311.