Evidence map›Paper›PMID 38223010›Full record

ArticleIndian journal of clinical biochemistry : IJCB2024

A Novel

Prabodh Kumar, Ganesh Paramasivam, Tom Devasia, Mukund Prabhu, Maneesh K Rai, K Prakashini, Sandeep Mallya, Dinesh Reghunathan, A Megha, Krishnananda Nayak and 1 more

Open access · greenAbstract readCase Reports
In one paragraph

Article in Indian journal of clinical biochemistry : IJCB, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 52% of its field
1 · What the graph read from 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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Prabodh KumarDepartment of Cell and Molecular Biology, Manipal School of Life Sciences, Manipal Academy of Higher Education (MAHE), Planetarium Complex, Madhav Nagar, Manipal, 576104 Karnataka India.
Ganesh ParamasivamDepartment of Cardiology, Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Manipal, 576104 Karnataka India.
Tom DevasiaDepartment of Cardiology, Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Manipal, 576104 Karnataka India.
Mukund PrabhuDepartment of Cardiology, Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Manipal, 576104 Karnataka India.
Maneesh K RaiDepartment of Cardiology, Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Mangalore, 575001 Karnataka India.
K PrakashiniDepartment of Radiodiagnosis and Imaging, Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Manipal, 576104 Karnataka India.
Sandeep MallyaDepartment of Bioinformatics, Manipal School of Life Sciences, Manipal Academy of Higher Education (MAHE), Manipal, 576104 Karnataka India.
Dinesh ReghunathanDepartment of Cell and Molecular Biology, Manipal School of Life Sciences, Manipal Academy of Higher Education (MAHE), Planetarium Complex, Madhav Nagar, Manipal, 576104 Karnataka India.
A MeghaDepartment of Cardiovascular Technology, Manipal College of Health Profession, Manipal Academy of Higher Education (Manipal), Manipal, 576104 Karnataka India.
Krishnananda NayakDepartment of Cardiovascular Technology, Manipal College of Health Profession, Manipal Academy of Higher Education (Manipal), Manipal, 576104 Karnataka India.
Rajasekhar MokaDepartment of Cell and Molecular Biology, Manipal School of Life Sciences, Manipal Academy of Higher Education (MAHE), Planetarium Complex, Madhav Nagar, Manipal, 576104 Karnataka India.
Manipal Academy of Higher Education · INKasturba Medical College, Manipal · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac disorder characterised by unexplained left ventricular hypertrophy in the absence of abnormal loading conditions. The global prevalence of HCM is estimated to be 1 in 250 in the general population. It is caused due to mutations in genes coding for sarcomeric proteins. α-tropomyosin

Indexed as

Familial hypertrophic cardiomyopathyLeft ventricular hypertrophyTPM1 geneα-Tropomyosin mutation

Identifiers

PMID38223010
PMCPMC10784234
OpenAlexW4223485523

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.