Human genome variation and pharmacogenetics Export

@article{citeulike:6083610, abstract = {A recent HGVS-sponsored symposium has examined, for the first time, the possible effects of the discovery of very large and widespread amounts of human genome variation on the emerging fields of pharmacogenetics and pharmacogenomics. This article discusses the effects of the resultant paradigm shifts and raises a number of important questions that need to be considered in order to truly advance the field in a meaningful and significant way. Hum Mutat 29(4):453-455, 2008. {\copyright} 2008 Wiley-Liss, Inc.}, address = {Lady Davis Institute for Medical Research, Sir Mortimer B. Davis-Jewish General Hospital, Montreal, Quebec, Canada; Department of Human Genetics, McGill University, Montreal, Quebec, Canada; Department of Biology, John Abbott College, Ste Anne de Bellvue, Quebec, Canada}, author = {Gottlieb, Bruce}, citeulike-article-id = {6083610}, citeulike-linkout-0 = {http://dx.doi.org/10.1002/humu.20728}, citeulike-linkout-1 = {http://www3.interscience.wiley.com/cgi-bin/abstract/117932826/ABSTRACT}, doi = {10.1002/humu.20728}, issn = {1098-1004}, journal = {Human Mutation}, keywords = {cancer, cnv, genome, pharmacogenetics, variation}, number = {4}, pages = {453--455}, posted-at = {2009-11-08 02:17:31}, priority = {2}, title = {Human genome variation and pharmacogenetics}, url = {http://dx.doi.org/10.1002/humu.20728}, volume = {29}, year = {2008} }

TY - JOUR ID - citeulike:6083610 L3 - citeulike-article-id:6083610 N2 - A recent HGVS-sponsored symposium has examined, for the first time, the possible effects of the discovery of very large and widespread amounts of human genome variation on the emerging fields of pharmacogenetics and pharmacogenomics. This article discusses the effects of the resultant paradigm shifts and raises a number of important questions that need to be considered in order to truly advance the field in a meaningful and significant way. Hum Mutat 29(4):453-455, 2008. © 2008 Wiley-Liss, Inc. IS - 4 JF - Human Mutation SN - 1098-1004 AD - Lady Davis Institute for Medical Research, Sir Mortimer B. Davis-Jewish General Hospital, Montreal, Quebec, Canada; Department of Human Genetics, McGill University, Montreal, Quebec, Canada; Department of Biology, John Abbott College, Ste Anne de Bellvue, Quebec, Canada EP - 455 TI - Human genome variation and pharmacogenetics VL - 29 SP - 453 KW - cancer KW - cnv KW - genome KW - pharmacogenetics KW - variation AU - Gottlieb, Bruce PY - 2008/// UR - http://dx.doi.org/10.1002/humu.20728 ER -