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03706cam a22004334a 4500 001 3D2A323E62A311DFAF3CE96BC41A358D 003 SILO 005 20100519080509 008 090505s2010 enka b 001 0 eng 010 $a 2009018899 020 $a 0195398440 (cloth : alk. paper) 020 $a 9780195398441 (cloth : alk. paper) 035 $a (OCoLC)320493100 040 $a DNLM/DLC $c DLC $d SILO $d C#P $d YDXCP $d VAM $d IWO $d SILO 042 $a pcc 050 00 $a RB155.5 $b .H86 2010 060 00 $a 2010 A-853 060 10 $a QZ 50 $b H91674 2010 082 00 $a 616/.042 $2 22 245 0 $a Human genome epidemiology : $b building the evidence for using genetic information to improve health and prevent disease / $c edited by Muin J. Khoury ... [et al.]. 250 $a 2nd ed. 260 $a New York : $b Oxford University Press, $c 2010. 300 $a xxiii, 676 p. : $b ill. ; $c 25 cm. 504 $a Includes bibliographical references and index. 505 0 $a Human genome epidemiology: the road map revisited -- Principles of analysis of germline genetics -- The public health genomics enterprise -- Navigating the evolving knowledge of human genetic variation in health and disease -- The global emergence of epidemiological biobanks: opportunities and challenges -- Case-control and cohort studies in the age of genome-wide associations -- The emergence of networks in human genome epidemiology: challenges and opportunities -- Design and analysis issues in genome-wide association studies -- The challenge of assessing complex gene-environment and gene-gene interactions -- STrengthening the REporting of genetic association studies (STREGA)-an extension of the STROBE statement -- Integration of the evidence on gene-disease associations: methods of HuGE reviews -- Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases -- Colorectal cancer -- Childhood leukemias -- Bladder cancer -- Type 2 diabetes -- Osteoporosis -- Preterm birth -- Coronary heart disease -- Schizophrenia -- Mendelian randomization: the contribution of genetic epidemiology to elucidating environmentally modifiable causes of disease -- Evaluation of predictive genetic tests for common diseases: bridging epidemiological, clinical, and public health measures -- The evaluation of genomic applications in practice and prevention (EGAPP) initiative: methods of the EGAPP working group -- Rapid, evidence-based reviews of genetic tests -- Role of social and behavioral research in assessing the utility of genetic information -- Assessing the evidence for clinical utility in newborn screening -- The role of epidemiology in assessing the potential clinical impact of pharmacogenomics -- The human epigenome and cancer -- The use of family history in public health practice: the epidemiologic view -- Cytochrome P450 testing in the treatment of depression -- A rapid-ACCE review of CYP2CP and VKORC1 allele testing to inform warfarin dosing in adults at elevated risk for thrombotic events to avoid serious bleeding -- Hereditary hemochromatosis: population screening for gene mutations. 650 0 $a Genetic disorders $x Epidemiology. 650 0 $a Medical genetics $x Methodology. 650 0 $a Genomics. 650 12 $a Genetics, Medical $x methods. 650 22 $a Genetic Diseases, Inborn $x epidemiology. 650 22 $a Genetic Predisposition to Disease $x epidemiology. 650 22 $a Genetic Testing. 650 22 $a Genome, Human. 650 22 $a Genomics. 700 1 $a Khoury, Muin J. 941 $a 1 952 $l USUX851 $d 20171003034526.0 956 $a http://locator.silo.lib.ia.us/search.cgi?index_0=id&term_0=3D2A323E62A311DFAF3CE96BC41A358D 994 $a 02 $b IWOInitiate Another SILO Locator Search