« Previous
Seminars in Orthodontics
Volume 14, Issue 2
, Pages 166-171
, June 2008
Personalized Orthodontics, The Future of Genetics in Practice
References
- . 2025: the practice of neurology: back from the future. Arch Neurol. 2001;58:1766–1767
- . Pharmacogenetics/genomics and personalized medicine. Hum Mol Genet. 2005;14:R207–R214
- Familial hypercholesterolemia and coronary heart disease: a HuGE Association review. Am J Epidemiol. 2004;160:421–429
- . Personalized medicine progresses. Nat Med. 2006;12:510–511
- . Personalized medicine: elusive dream or imminent reality?. Clin Pharmacol Ther. 2007;81:807–816
- . Systems biology, proteomics, and the future of health care: toward predictive, preventative, and personalized medicine. J Proteome Res. 2004;3:179–196
- . BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping. Biotechniques. 2002;32(6(Suppl)):56–5860-61
- Illumina, Inc., http://www.illumina.com (accessed 23 September 2007)
- International Human Genome Consortium: Initial sequencing and analysis of the human genome. Nature. 2001;409:860–921
- . The sequence of the human genome. Science. 2001;291:1304–1351
- . To a future of genetic medicine. Nature. 2001;409:822–823
- . International Human Genome Sequencing Consortium (Initial sequencing and analysis of the human genome). Nature. 2001;409:860–921
- The International HapMap Consortium: a haplotype map of the human genome. Nature. 2005;437:1299–1320
- . Genetic structure in human populations: implications for the personalized medicine value chain. Personalized Med. 2006;3:1–7
- The Genographic Project of the National Genographic Society. https://www3.nationalgeographic.com/genographic/(accessed 23 September 2007)
- Altshuler D, Lander E: A Haplotype Map of the Human Genome. 2001 HapMap Meeting Outline. http://www.genome.gov/page.cfm?pageID=10001682 (accessed 23 September 2007)
- A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science. 2006;314:1461–1463
- A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region. Nat Genet. 2006;38:617–619
- A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature. 2007;445:881–885
- Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. Hum Mol Genet. 2007;16:865–873
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007;447:661–678
- Genome-wide association study in esophageal cancer using GeneChip mapping 10K array. Cancer Res. 2005;65:2542–2546
- . Novel genes identified in a high-density genome wide association study for nicotine dependence. Hum Mol Genet. 2007;16:24–35
- . Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nat Genet. 2007;39:989–994
- Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol. 2006;11:911–916
- Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science. 2007;317:1397–1400
- Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature. 2007;448:470–473
- A whole-genome association study of major determinants for host control of HIV-1. Science. 2007;317:944–947
- Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature. 2007;448:353–357
- A genetic risk factor for periodic limb movements in sleep. N Engl J Med. 2007;357:639–647
- A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet. 2007;39:870–874
- Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet. 2007;39:865–869
- A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007;316:1491–1493
- Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. Nat Genet. 2007;39:631–637
- Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol. 2007;6:322–328
- Variation in the gene encoding the serotonin 2A receptor is associated with outcome of antidepressant treatment. Am J Hum Genet. 2006;78:804–814
- PRKCA and multiple sclerosis: association in two independent populations. PLoS Genet. 2006;2:e42
- . Personalized medicine: elusive dream or imminent reality?: a commentary. Clin Pharmacol Ther. 2007;81:801–805
- Successful genome-wide scan in paired blood and buccal samples. Cancer Epidemiol Biomarkers Prev. 2007;16:1023–1025
- . Genome-wide association studies for common diseases and complex traits. Nat Rev Genet. 2005;6:95–108
- National Human Genome Research Institute Educational Resource on Genome Wide-Association Studies. http://www.genome.gov/20019523 (accessed 24 September 2007)
PII: S1073-8746(08)00013-3
doi: 10.1053/j.sodo.2008.02.007
© 2008 Elsevier Inc. All rights reserved.
« Previous
Seminars in Orthodontics
Volume 14, Issue 2
, Pages 166-171
, June 2008
