Matches in Library of Congress for { <http://lccn.loc.gov/2009018899> ?p ?o. }
Showing items 1 to 29 of
29
with 100 items per page.
- 2009018899 contributor B11415376.
- 2009018899 created "2010.".
- 2009018899 date "2010".
- 2009018899 date "2010.".
- 2009018899 dateCopyrighted "2010.".
- 2009018899 description "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.".
- 2009018899 description "Includes bibliographical references and index.".
- 2009018899 extent "xxiii, 676 p. :".
- 2009018899 identifier "0195398440 (cloth : alk. paper)".
- 2009018899 identifier "9780195398441 (cloth : alk. paper)".
- 2009018899 issued "2010".
- 2009018899 issued "2010.".
- 2009018899 language "eng".
- 2009018899 publisher "Oxford ; New York : Oxford University Press,".
- 2009018899 subject "2010 A-853".
- 2009018899 subject "616/.042 22".
- 2009018899 subject "Genetic Diseases, Inborn epidemiology.".
- 2009018899 subject "Genetic Predisposition to Disease epidemiology.".
- 2009018899 subject "Genetic Testing.".
- 2009018899 subject "Genetic disorders Epidemiology.".
- 2009018899 subject "Genetics, Medical methods.".
- 2009018899 subject "Genome, Human.".
- 2009018899 subject "Genomics.".
- 2009018899 subject "Medical genetics Methodology.".
- 2009018899 subject "QZ 50 H91674 2010".
- 2009018899 subject "RB155.5 .H86 2010".
- 2009018899 tableOfContents "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.".
- 2009018899 title "Human genome epidemiology : building the evidence for using genetic information to improve health and prevent disease / edited by Muin J. Khoury ... [et al.].".
- 2009018899 type "text".