ReviewCirculation. Cardiovascular genetics2013
A clinical approach to inherited hypertrophy: the use of family history in diagnosis, risk assessment, and management.
Review in Circulation. Cardiovascular genetics, 2013. 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.
- 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families.Heart rhythm · 2021Guideline
- Sudden Cardiac Death in Young Individuals: A Current Review of Evaluation, Screening and Prevention.Journal of clinical medicine research · 2023Review
- Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation.Orphanet journal of rare diseases · 2021Article
- Sudden Death in Adults: A Practical Flow Chart for Pathologist Guidance.Healthcare (Basel, Switzerland) · 2021Review
- 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families.Journal of arrhythmia · 2021Article
- Loperamide Toxicity Revealing Apical Hypertrophic Cardiomyopathy.Methodist DeBakey cardiovascular journal · 2021Article
- Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes.EBioMedicine · 2020Article
- Familial occurrence of mitral regurgitation in patients with mitral valve prolapse undergoing mitral valve surgery.European journal of preventive cardiology · 2020Article
- Morphomechanic phenotypic variability of sarcomeric cardiomyopathies: A multifactorial polygenic perspective.Journal of molecular and cellular cardiology · 2019Review
- Letter to the Editor: Contemporary Screening and Treatment of Hypertrophic Cardiomyopathy.Ochsner journal · 2018Article
- Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.Genetics in medicine : official journal of the American College of Medical Genetics · 2017Article
- Provision of cardiovascular genetic counseling services: current practice and future directions.Journal of genetic counseling · 2014Article
- Inpatient detection of cardiac-inherited disease: the impact of improving family history taking.Open heartArticle
- A Case for Inclusion of Genetic Counselors in Cardiac Care.Cardiology in reviewReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
PubMed holds no abstract for this paper.
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.