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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 /

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Human genome epidemiology :/ edited by Muin J. Khoury ... [et al.].
其他題名:	building the evidence for using genetic information to improve health and prevent disease /
其他作者:	Khoury, Muin J.
出版者:	Oxford ;Oxford University Press, : 2010.,
版本:	2nd ed.
面頁冊數:	xxiii, 676 p. :ill. ; : 25 cm.;
標題:	Genetic disorders - Epidemiology. -
電子資源:	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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