Genomic Biomarkers in Human Population Studies

作者: Jacqueline S. Danik , Nina P. Paynter , Paul M. Ridker

DOI: 10.1016/B978-0-12-382227-7.00021-5

关键词:

摘要: The pace of discovery genetic determinants complex disease has accelerated with the availability gene chips that allow scientists to conduct large-scale genome-wide association studies. In this chapter, we address in three parts use single nucleotide polymorphisms (SNPs) as biomarkers for population-based research. first section, studies (GWAS) discover intermediate phenotypes interest process is examined. second concept using individual SNPs and multi-loci SNP panels potential predictors incident disease. Finally, review genomic evolving field pharmacogenomics. Throughout examples from cardiovascular medicine a template discussing utility limitations biomarker data population

参考文章(118)
SLCO1B1 variants and statin-induced myopathy--a genomewide study The New England Journal of Medicine. ,vol. 359, pp. 789- 799 ,(2008) , 10.1056/NEJMOA0801936
Marina Marketos, The top 200 generic drugs in 2003 (by units) Formulary. ,(2004)
Jean-Pierre Hugot, Mathias Chamaillard, Habib Zouali, Suzanne Lesage, Jean-Pierre Cézard, Jacques Belaiche, Sven Almer, Curt Tysk, Colm A. O'Morain, Miquel Gassull, Vibeke Binder, Yigael Finkel, Antoine Cortot, Robert Modigliani, Pierre Laurent-Puig, Corine Gower-Rousseau, Jeanne Macry, Jean-Frédéric Colombel, Mourad Sahbatou, Gilles Thomas, Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease Nature. ,vol. 411, pp. 599- 603 ,(2001) , 10.1038/35079107
Yasunori Ogura, Denise K. Bonen, Naohiro Inohara, Dan L. Nicolae, Felicia F. Chen, Richard Ramos, Heidi Britton, Thomas Moran, Reda Karaliuskas, Richard H. Duerr, Jean-Paul Achkar, Steven R. Brant, Theodore M. Bayless, Barbara S. Kirschner, Stephen B. Hanauer, Gabriel Nuñez, Judy H. Cho, A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease Nature. ,vol. 411, pp. 603- 606 ,(2001) , 10.1038/35079114
Terho Lehtimäki, Carita Eklund, Tanja Pessi, Mikko Hurme, Farhana Jahan, Interleukin 1B gene polymorphism is associated with baseline C‐reactive protein levels in healthy individuals European Cytokine Network. ,vol. 14, pp. 168- 171 ,(2003)
Qi Zhang, Xiao-feng Wang, Shuang-shuang Cheng, Xin-hong Wan, Fei-fei Cao, Lei Li, Xing-dong Chen, Wen-juan Liu, Xin-chun Yang, Li Jin, None, Three SNPs on chromosome 9p21 confer increased risk of myocardial infarction in Chinese subjects Atherosclerosis. ,vol. 207, pp. 26- 28 ,(2009) , 10.1016/J.ATHEROSCLEROSIS.2009.04.017
Matti Mänttäri, Vesa Manninen, Timo Palosuo, Christian Ehnholm, Apolipoprotein E polymorphism and C-reactive protein in dyslipidemic middle-aged men. Atherosclerosis. ,vol. 156, pp. 237- 238 ,(2001) , 10.1016/S0021-9150(01)00480-4
Stefan Kiechl, Eva Lorenz, Markus Reindl, Christian J. Wiedermann, Friedrich Oberhollenzer, Enzo Bonora, Johann Willeit, David A. Schwartz, Toll-like Receptor 4 Polymorphisms and Atherogenesis The New England Journal of Medicine. ,vol. 347, pp. 185- 192 ,(2002) , 10.1056/NEJMOA012673
H Jacqueline Suk, Paul M Ridker, Nancy R Cook, Robert YL Zee, None, Relation of polymorphism within the C-reactive protein gene and plasma CRP levels Atherosclerosis. ,vol. 178, pp. 139- 145 ,(2005) , 10.1016/J.ATHEROSCLEROSIS.2004.07.033
B Puthothu, M Krueger, M Bernhardt, A Heinzmann, None, ICAM1 amino-acid variant K469E is associated with paediatric bronchial asthma and elevated sICAM1 levels. Genes and Immunity. ,vol. 7, pp. 322- 326 ,(2006) , 10.1038/SJ.GENE.6364302