The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop. - Wikidata - wikimedia - TriplyDB

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.

http://www.wikidata.org/entity/Q34113976

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Finding the missing heritability of complex diseases Cardiovascular epidemiology in a changing world--challenges to investigators and the National Heart, Lung, and Blood Institute Genetic data and electronic health records: a discussion of ethical, logistical and technological considerations Perspectives on pharmacogenomics of antiretroviral medications and HIV-associated comorbidities Beyond base pairs to bedside: a population perspective on how genomics can improve health Using lifetime risk estimates in personal genomic profiles: estimation of uncertainty Concerns about unintended negative consequences of informing the public about multifactorial risks may be premature for young adult smokers An Empirical Evaluation of Normalization Methods for MicroRNA Arrays in a Liposarcoma Study Direct-to-Consumer Genetic and Genomic Testing: Preparing Nurse Practitioners for Genomic Healthcare.Implementing an Internet-Delivered Skin Cancer Genetic Testing Intervention to Improve Sun Protection Behavior in a Diverse Population: Protocol for a Randomized Controlled Trial.Cancer screening and genetics: a tale of two paradigms Translating colorectal cancer prevention through the guanylyl cyclase C signaling axis.A survey of UK public interest in internet-based personal genome testing.Parents' preferences for return of results in pediatric genomic research.Clinical and public health implications of emerging genetic technologies.Genetics of focal segmental glomerulosclerosis and human immunodeficiency virus-associated collapsing glomerulopathy: the role of MYH9 genetic variation.A compendium of genome-wide associations for cancer: critical synopsis and reappraisal.Personal genome testing: test characteristics to clarify the discourse on ethical, legal and societal issues Only connect: personal genomics and the future of American medicine.A community standard for immunogenomic data reporting and analysis: proposal for a STrengthening the REporting of Immunogenomic Studies statement.Overview of a chemoresponse assay in ovarian cancer The emergence of translational epidemiology: from scientific discovery to population health impact.Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record.The rules remain the same for genomic medicine: the case against "reverse genetic exceptionalism".Early identification of cardiovascular risk using genomics and proteomics.Regional differences in awareness and attitudes regarding genetic testing for disease risk and ancestry.Genome-wide association studies of cancer.Attitudes on DNA ancestry tests.From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.How the electronic health record will change the future of health care.How can polygenic inheritance be used in population screening for common diseases?An epidemiological perspective on the future of direct-to-consumer personal genome testing.Role of genomics in cardiovascular medicine.Translational research in cancer genetics: the road less traveled Health system implications of direct-to-consumer personal genome testing Genetics and primary care: where are we headed?Development of a communication protocol for telephone disclosure of genetic test results for cancer predisposition Genome Medicine: past, present and future.Primary care patient willingness for genetic testing for salt-sensitive hypertension: a cross sectional study Personalized medicine: new genomics, old lessons

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The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.

http://www.wikidata.org/entity/Q34113976

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2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2009 թվականի օգոստոսին հրատարակված գիտական հոդված

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P2860

Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers

Meta-analysis in genome-wide association studies

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

Blazing a trail: a public health research agenda in genomics and chronic disease

Letting the genome out of the bottle--will we get our wish?

Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology

General cardiovascular risk profile for use in primary care: the Framingham Heart Study

Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond

A HapMap harvest of insights into the genetics of common disease

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Stephen Chanock

George M. Church

Francis Collins

Rebekah Rasooly

Jay M. Bernhardt

Michael S Lauer

Centers for Disease Control and Prevention

A. Cecile Janssens

John P. A. Ioannidis

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