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Clinical assessment incorporating a personal genome

Clinical assessment incorporating a personal genome

http://www.wikidata.org/entity/Q24612653

about

Phased whole-genome genetic risk in a family quartet using a major allele reference sequence Sequencing and analysis of a South Asian-Indian personal genome Network-based analysis of comorbidities risk during an infection: SARS and HIV case studies Chapter 7: Pharmacogenomics Medical implications of technical accuracy in genome sequencing Clinical utility of sequence-based genotype compared with that derivable from genotyping arrays Multiplex meta-analysis of RNA expression to identify genes with variants associated with immune dysfunction Personalized medicine: hope or hype?Personal Genome Sequencing in Ostensibly Healthy Individuals and the PeopleSeq Consortium Implications of pleiotropy: challenges and opportunities for mining Big Data in biomedicine Exploring predisposition and treatment response--the promise of genomics Promise of personalized omics to precision medicine Teaching residents genomic pathology: a novel approach for new technology Pharmacogenetics and anaesthesia: the value of genetic profiling The Human Genome Project, and recent advances in personalized genomics Disease gene identification strategies for exome sequencing Annotating individual human genomes Transcriptomic biomarkers of cardiovascular disease Translational bioinformatics: linking the molecular world to the clinical world Treatment of Radiation Injury The emerging paradigm of network medicine in the study of human disease Personalized preventive medicine: genetics and the response to regular exercise in preventive interventions A public resource facilitating clinical use of genomes Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions Mining electronic health records: towards better research applications and clinical care Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease The coming age of data-driven medicine: translational bioinformatics' next frontier Translational bioinformatics: linking knowledge across biological and clinical realms Beyond base pairs to bedside: a population perspective on how genomics can improve health Predicting phenotypic severity of uncertain gene variants in the RET proto-oncogene Genetic background of patients from a university medical center in Manhattan: implications for personalized medicine Genotype-based ancestral background consistently predicts efficacy and side effects across treatments in CATIE and STAR*D PON-P2: prediction method for fast and reliable identification of harmful variants Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data Virtual Pharmacist: A Platform for Pharmacogenomics Translational bioinformatics in the era of real-time biomedical, health care and wellness data streams Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research Integrative network modeling approaches to personalized cancer medicine Progress towards the integration of pharmacogenomics in practice

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Clinical assessment incorporating a personal genome

http://www.wikidata.org/entity/Q24612653

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2010 nî lūn-bûn

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2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2010 թվականի մայիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年學術文章

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name

Clinical assessment incorporating a personal genome

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Clinical assessment incorporating a personal genome

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Clinical assessment incorporating a personal genome

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Clinical assessment incorporating a personal genome

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Clinical assessment incorporating a personal genome

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Clinical assessment incorporating a personal genome

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Clinical assessment incorporating a personal genome

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Clinical assessment incorporating a personal genome

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Abraham M Rosenbaum

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Aleksandra Pavlovic

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Alexander A Morgan

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Alexander Wait Zaranek

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Caroline F Thorn

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Dmitry Pushkarev

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Dorit S Berlin

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Euan A Ashley

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Frederick E Dewey

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Hersh Sagreiya

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P2860

The diploid genome sequence of an individual human

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

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

The complete genome of an individual by massively parallel DNA sequencing

Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy

Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Targeted capture and massively parallel sequencing of 12 human exomes

Massively parallel sequencing: the next big thing in genetic medicine

Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

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