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Human genome epidemiology : building the evidence for using genetic information to improve health and prevent disease
Khoury, Muin J, Oxford Scholarship Online Public Health and Epidemiology · Oxford New York : Oxford University Press, 2010
- Publisher
- Oxford New York : Oxford University Press, 2010
- ISBN
- 0195398440 (cloth : alk. paper);9780195398441 (cloth : alk. paper)
- Dewey classification
- 616
- Subjects
- Genetic disorders--EpidemiologyGenomicsMedical genetics--MethodologyGenetics, Medical--methodsGenetic Diseases, Inborn--epidemiologyGenetic Predisposition to Disease--epidemiologyGenetic TestingGenome, HumanGenomicsElectronic books
- Language
- English
Digital copy
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Catalogue record
| Field | Value |
|---|---|
| 001Control number | 20061 |
| 003Control number identifier | WaSeSS |
| 005Date and time of latest transaction | 9 Jul 2010, 13:44 |
| 006Fixed-length data elements – additional material characteristics | m d |
| 007Physical description fixed field | cr n |
| 008Fixed-length data elements | 090505s2010 enka sb 001 0 eng d |
| 010Library of Congress control number | 2009018899 |
| 016National bibliographic agency control number | 101504140 DNLM |
| 020International Standard Book Number (ISBN) |
|
| 035System control number |
|
| 040Cataloging source | DNLM/DLC DLC NLM C#P YDXCP VAM DLC WaSeSS |
| 041Language code | eng |
| 042Authentication code | pcc |
| 082Dewey Decimal call number | 616 22 |
| 245Title statement | Human genome epidemiology [electronic resource] : building the evidence for using genetic information to improve health and prevent disease / edited by Muin J. Khoury ... [et al.]. |
| 250Edition statement | 2nd ed. |
| 260Publication, distribution, etc. (imprint) | Oxford ; New York : Oxford University Press, 2010 |
| 504Bibliography, etc. note | Includes bibliographical references and index. |
| 505Formatted contents note | 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. |
| 506Restrictions on access note | Access limited to La Trobe staff and students. |
| 650Subject added entry – topical term |
|
| 655Index term – genre/form | Electronic books. |
| 700Added entry – personal name | Khoury, Muin J. |
| 710Added entry – corporate name | Oxford Scholarship Online Public Health and Epidemiology. |
| 999Collection | Downloads |
=001 20061=003 WaSeSS=005 20100709134437.0=006 m d=007 cr n=008 090505s2010 enka sb 001 0 eng d=010 ##$a2009018899=016 7\$a101504140 $2DNLM=020 ##$a0195398440 (cloth : alk. paper)=020 ##$a9780195398441 (cloth : alk. paper)=035 ##$a(WaSeSS)ssib004877762=035 ##$b25810406=040 ##$aDNLM/DLC $cDLC $dNLM $dC#P $dYDXCP $dVAM $dDLC $dWaSeSS=041 0#$aeng=042 ##$apcc=082 00$a616 $222=245 00$aHuman genome epidemiology $h[electronic resource] : $bbuilding the evidence for using genetic information to improve health and prevent disease / $cedited by Muin J. Khoury ... [et al.].=250 ##$a2nd ed.=260 ##$aOxford ; $aNew York : $bOxford University Press, $c2010=504 ##$aIncludes bibliographical references and index.=505 0#$aHuman 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.=506 ##$aAccess limited to La Trobe staff and students.=509 ##$aSerials Solutions eBook record.=650 #0$aGenetic disorders $xEpidemiology.=650 #0$aGenomics.=650 #0$aMedical genetics $xMethodology.=650 12$aGenetics, Medical $xmethods.=650 22$aGenetic Diseases, Inborn $xepidemiology.=650 22$aGenetic Predisposition to Disease $xepidemiology.=650 22$aGenetic Testing.=650 22$aGenome, Human.=650 22$aGenomics.=655 #0$aElectronic books.=700 1#$aKhoury, Muin J.=710 2#$aOxford Scholarship Online Public Health and Epidemiology.=LDR 03842nam a22004814a 4500