ArticleExpert review of molecular diagnostics2016
Toward clinical genomics in everyday medicine: perspectives and recommendations.
Article in Expert review of molecular diagnostics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03713333 (Implementation of High Definition Screening Using Handheld Imaging and Digital Health Technologies Within a Learning Health System to Identify Cardiovascular Disease at the Point-of-care), which is not on this map. Cited by 25 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Implementation of High Definition Screening Using Handheld Imaging and Digital Health Technologies Within a Learning Health System to Identify Cardiovascular Disease at the Point-of-care: The ASE-INNOVATE Program
Who cites it
25 citing papers in PubMed.
- Physician weight influences responses to a public health message about the genetics of obesity.Patient education and counseling · 2023Trial
- Prospective on Imaging Mass Spectrometry in Clinical Diagnostics.Molecular & cellular proteomics : MCP · 2023Review
- Landscape of genetic variants in sporadic meningiomas captured with clinical genomics.Acta neurochirurgica · 2022Article
- Engaging community stakeholders in research on best practices for clinical genomic sequencing.Personalized medicine · 2020Article
- Estimating the costs of genomic sequencing in cancer control.BMC health services research · 2020Article
- Rethinking the ethical principles of genomic medicine services.European journal of human genetics : EJHG · 2020Article
- Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease.NPJ genomic medicine · 2020Review
- Applying Mental Model Methods to Characterize Understanding of Gene-Environment Influences: The Case of Podoconiosis in Ethiopia.Critical public health · 2019Article
- Seave: a comprehensive web platform for storing and interrogating human genomic variation.Bioinformatics (Oxford, England) · 2019Article
- Cost Analyses of Genomic Sequencing: Lessons Learned from the MedSeq Project.Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research · 2018Article
- DNA.Land is a framework to collect genomes and phenomes in the era of abundant genetic information.Nature genetics · 2018Article
- Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results.Journal of community genetics · 2018Article
- Genetic testing for exercise prescription and injury prevention: AIS-Athlome consortium-FIMS joint statement.BMC genomics · 2017Article
- High-Definition Medicine.Cell · 2017Review
- Successful Application of Whole Genome Sequencing in a Medical Genetics Clinic.Journal of pediatric genetics · 2017Article
- Experience with precision genomics and tumor board, indicates frequent target identification, but barriers to delivery.Oncotarget · 2017Article
- Cardiac development: from current understanding to new regenerative concepts.Journal of thoracic disease · 2017Article
- Examining for an association between candidate gene polymorphisms in the metabolic syndrome components on excess weight and adiposity measures in youth: a cross-sectional study.Genes & nutrition · 2017Article
- Versatile ion S5XL sequencer for targeted next generation sequencing of solid tumors in a clinical laboratory.PloS one · 2017Article
- Aggregate penetrance of genomic variants for actionable disorders in European and African Americans.Science translational medicine · 2016Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
45 authors.
Funding
Abstract
Precision or personalized medicine through clinical genome and exome sequencing has been described by some as a revolution that could transform healthcare delivery, yet it is currently used in only a small fraction of patients, principally for the diagnosis of suspected Mendelian conditions and for targeting cancer treatments. Given the burden of illness in our society, it is of interest to ask how clinical genome and exome sequencing can be constructively integrated more broadly into the routine practice of medicine for the betterment of public health. In November 2014, 46 experts from academia, industry, policy and patient advocacy gathered in a conference sponsored by Illumina, Inc. to discuss this question, share viewpoints and propose recommendations. This perspective summarizes that work and identifies some of the obstacles and opportunities that must be considered in translating advances in genomics more widely into the practice of medicine.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.