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Human genome epidemiology :building ...

Khoury, Muin J.

Human genome epidemiology :building the evidence for using genetic information to improve health and prevent disease /

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Human genome epidemiology :/ edited by Muin J. Khoury ... [et al.].
Reminder of title:	building the evidence for using genetic information to improve health and prevent disease /
other author:	Khoury, Muin J.
Published:	Oxford ;Oxford University Press, : 2010.,
[NT 15000922]:	2nd ed.
Description:	xxiii, 676 p. :ill. ; : 25 cm.;
Subject:	Genetic disorders - Epidemiology. -
Online resource:	Oxford Scholarship Online
ISBN:	9780195398441 (hard) :

Human genome epidemiology :building the evidence for using genetic information to improve health and prevent disease /
Human genome epidemiology :building the evidence for using genetic information to improve health and prevent disease /edited by Muin J. Khoury ... [et al.]. - 2nd ed. - Oxford ;Oxford University Press,2010. - xxiii, 676 p. :ill. ;25 cm.

Includes bibliographical references and index.

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.

ISBN: 9780195398441 (hard) :NT2099

LCCN: 2009018899

Nat. Bib. Agency Control No.: 101504140DNLMSubjects--Topical Terms:

248232
Genetic disorders
--Epidemiology.

LC Class. No.: RB155.5 / .H86 2010

Dewey Class. No.: 616/.042

National Library of Medicine Call No.: QZ 50 / H91674 2010

Human genome epidemiology :building the evidence for using genetic information to improve health and prevent disease /
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245 0 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.
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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 $2 96060 $a Genetic disorders $x Epidemiology. $3 248232
650 0 $2 96060 $a Medical genetics $x Methodology. $3 248233
650 0 $2 96060 $a Genomics. $3 232799
650 1 2 $2 96060 $a Genetics, Medical $x methods. $3 248234
650 2 2 $2 96060 $a Genetic Diseases, Inborn $x epidemiology. $3 248236
650 2 2 $2 96060 $a Genetic Predisposition to Disease $x epidemiology. $3 248237
650 2 2 $a Genetic Testing. $3 336891
650 2 2 $2 96060 $a Genome, Human. $3 221223
700 1 $2 97000 $a Khoury, Muin J. $3 208075
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