ArticleGenetics in medicine : official journal of the American College of Medical Genetics2016
Your DNA is not your diagnosis: getting diagnoses right following secondary genomic findings.
Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.
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
14 citing papers in PubMed, 1 synthesis or guideline pooled it.
- International policies guiding the selection, analysis, and clinical management of secondary findings from genomic sequencing: A systematic review.American journal of human genetics · 2024Pooled it
- Genetics Visit Uptake Among Individuals Receiving Clinically Actionable Genomic Screening Results.JAMA network open · 2024Article
- Ready or not, genomic screening of fetuses is already here.Genetics in medicine : official journal of the American College of Medical Genetics · 2024Article
- From the patient to the population: Use of genomics for population screening.Frontiers in genetics · 2022Article
- Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first.Journal of genetic counseling · 2021Article
- DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG).Genetics in medicine : official journal of the American College of Medical Genetics · 2021Article
- Bringing monogenic disease screening to the clinic.Nature medicine · 2020Article
- Management of Secondary Genomic Findings.American journal of human genetics · 2020Review
- Genome-first findings require precision phenotyping.Genetics in medicine : official journal of the American College of Medical Genetics · 2018Article
- Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.JAMA network open · 2018Article
- A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.American journal of human genetics · 2018Article
- Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.Genetics in medicine : official journal of the American College of Medical Genetics · 2018Article
- Interpretation of genomic sequencing: variants should be considered uncertain until proven guilty.Genetics in medicine : official journal of the American College of Medical Genetics · 2018Article
- Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.Genetics in medicine : official journal of the American College of Medical Genetics · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
26447529What 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.