ArticleJournal of the American Medical Informatics Association : JAMIA
Design of Genetics Home Reference: a new NLM consumer health resource.
Article in Journal of the American Medical Informatics Association : JAMIA. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
12 citing papers in PubMed.
- An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases.Nature communications · 2022Article
- The multiple dimensions of expanded access to health information: Don Lindberg and the U.S. National Library of Medicine.Information services & use · 2022Article
- Knowledge bases and software support for variant interpretation in precision oncology.Briefings in bioinformatics · 2021Article
- Optimizing genetics online resources for diverse readers.Genetics in medicine : official journal of the American College of Medical Genetics · 2020Article
- Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies.Molecular cytogenetics · 2018Review
- Online Patient Education for Chronic Disease Management: Consumer Perspectives.Journal of medical systems · 2016Article
- Electronic medical records and personalized medicine.Human genetics · 2011Article
- Biomedical text summarization to support genetic database curation: using Semantic MEDLINE to create a secondary database of genetic information.Journal of the Medical Library Association : JMLA · 2010Article
- Current Challenge in Consumer Health Informatics: Bridging the Gap between Access to Information and Information Understanding.Biomedical informatics insights · 2009Article
- Challenges and strategies of the Genetics Home Reference.Journal of the Medical Library Association : JMLA · 2006Article
- Argument-predicate distance as a filter for enhancing precision in extracting predications on the genetic etiology of disease.BMC bioinformatics · 2006Article
- Infobuttons at Intermountain Healthcare: utilization and infrastructure.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2006Article
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
No grant is acknowledged in the PubMed record.
Abstract
The authors have developed the Genetics Home Reference, a consumer resource that addresses the health implications of the Human Genome Project. The research results made possible by the Human Genome Project are being made available increasingly in scientific databases on the Internet, but, because of the often highly technical nature of these databases, they are not readily accessible to the lay public. The authors' goal is to provide a bridge between the clinical questions of the public and the richness of the data emanating from the Human Genome Project. The Genetics Home Reference currently focuses on single gene or polygenic conditions that are also topics on MEDLINEplus, the National Library of Medicine's primary consumer health site. As knowledge of genetics expands, the interrelationships between genes and diseases will continue to unfold, and the site will reflect these developments.
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.