ArticleJournal of the American Medical Informatics Association : JAMIA2015
Supporting interoperability of genetic data with LOINC.
Article in Journal of the American Medical Informatics Association : JAMIA, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
What it found
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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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
17 citing papers in PubMed.
- Article
- Creation of a structured molecular genomics report for Germany as a local adaption of HL7's Genomic Reporting Implementation Guide.Journal of the American Medical Informatics Association : JAMIA · 2023Article
- Pharmacogenomic testing and prescribing patterns for patients with cancer in a large national precision medicine cohort.Journal of medical genetics · 2023Observational
- Digital child health: opportunities and obstacles. A joint statement of European Academy of Paediatrics and European Confederation of Primary Care Paediatricians.Frontiers in pediatrics · 2023Review
- Harmonization and standardization of data for a pan-European cohort on SARS- CoV-2 pandemic.NPJ digital medicine · 2022Article
- Precision Medicine Landscape of Genomic Testing for Patients With Cancer in the National Institutes of Health All of Us Database Using Informatics Approaches.JCO clinical cancer informatics · 2022Observational
- Ethical Considerations on Pediatric Genetic Testing Results in Electronic Health Records.Applied clinical informatics · 2020Article
- Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2019Article
- Genomics and electronic health record systems.Human molecular genetics · 2018Review
- A computable pathology report for precision medicine: extending an observables ontology unifying SNOMED CT and LOINC.Journal of the American Medical Informatics Association : JAMIA · 2018Article
- The potential adoption benefits and challenges of LOINC codes in a laboratory department: a case study.Health information science and systems · 2017Article
- Assessing the readiness of precision medicine interoperabilty: An exploratory study of the National Institutes of Health genetic testing registry.Journal of innovation in health informatics · 2017Article
- Characterizing Pharmacogenomic-Guided Medication Use With a Clinical Data Repository.Clinical pharmacology and therapeutics · 2017Article
- Standardizing terms for clinical pharmacogenetic test results: consensus terms from the Clinical Pharmacogenetics Implementation Consortium (CPIC).Genetics in medicine : official journal of the American College of Medical Genetics · 2017Article
- Efficient Results in Semantic Interoperability for Health Care. Findings from the Section on Knowledge Representation and Management.Yearbook of medical informatics · 2016Article
- AMIA--Setting the Standard.Journal of the American Medical Informatics Association : JAMIA · 2015Article
- Health information technology data standards get down to business: maturation within domains and the emergence of interoperability.Journal of the American Medical Informatics Association : JAMIA · 2015Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Electronic reporting of genetic testing results is increasing, but they are often represented in diverse formats and naming conventions. Logical Observation Identifiers Names and Codes (LOINC) is a vocabulary standard that provides universal identifiers for laboratory tests and clinical observations. In genetics, LOINC provides codes to improve interoperability in the midst of reporting style transition, including codes for cytogenetic or mutation analysis tests, specific chromosomal alteration or mutation testing, and fully structured discrete genetic test reporting. LOINC terms follow the recommendations and nomenclature of other standards such as the Human Genome Organization Gene Nomenclature Committee's terminology for gene names. In addition to the narrative text they report now, we recommend that laboratories always report as discrete variables chromosome analysis results, genetic variation(s) found, and genetic variation(s) tested for. By adopting and implementing data standards like LOINC, information systems can help care providers and researchers unlock the potential of genetic information for delivering more personalized care.
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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.