The Locator -- [(subject = "Genome Human")]

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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 IWO

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