ArticlePharmacogenomics and personalized medicine2023
Novel
Article in Pharmacogenomics and personalized medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 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
9 citing papers in PubMed, 6 citations in OpenAlex.
- Are clinical trajectories in obstructive hypertrophic cardiomyopathy mutation-specific? A systematic review and meta-analysis ofFrontiers in cardiovascular medicine · 2026Review
- Downregulation of miR-214 promotes dilated Cardiomyopathy Progression through PDE5A-Mediated cGMP regulation.Scientific reports · 2024Article
- Hypertrophic Obstructive Cardiomyopathy: A Brief Account.International journal of applied & basic medical researchArticle
- Results of comprehensive genetic testing in patients presenting to a multidisciplinary inherited heart disease clinic in India.Indian heart journalArticle
- Genetic testing of cardiomyopathies: Position statement of the Cardiological Society of India.Indian heart journalArticle
- India-specific cardiogenetic aspects: Focus on cardiomyopathies and inherited arrhythmia syndromes.Indian pacing and electrophysiology journalReview
- Biallelic truncating variants in the myosin-binding protein C3 result in a fatal form of cardiomyopathy in Indian infants.Annals of pediatric cardiologyArticle
- Inherited cardiomyopathies: Contemporary genetics for clinical practice.Indian pacing and electrophysiology journalReview
- Cardiogenetics: Closing the knowledge gap in India.Indian pacing and electrophysiology journalArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors at 4 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Mutations in Myosin Binding Protein C ( Methods: We carried out targeted direct sequencing of Results: We detected 34 single nucleotide variations in Conclusion: The present comprehensive study on
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.