Evidence map›Paper›PMID 37625473›Full record

ArticleHeart rhythm2023

From founder to function: Can we unravel phenotype from genotype?

Chad S Weldy, Marco V Perez

Abstract readEditorialComment
PubMed Full text at PMC Publisher
In one paragraph

Article in Heart rhythm, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Chad S WeldyDivision of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California; Stanford Center for Inherited Cardiovascular Disease, Stanford, California.
Marco V PerezDivision of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California; Stanford Center for Inherited Cardiovascular Disease, Stanford, California. Electronic address: mvperez@stanford.edu.

Funding

Machine Learning in Atrial FibrillationR01HL149134 · NHLBI · STANFORD UNIVERSITY · PI NARAYAN, SANJIV M · 2020 to 2024
$3.8M
The WHI Strong and Healthy SilenT Atrial fibrillation Recording study (WHISH STAR)R01HL136390 · NHLBI · STANFORD UNIVERSITY · PI PEREZ, MARCO V · 2017 to 2021
$3.6M
ADAR mediated RNA editing is a causal mechanism in coronary artery diseaseK08HL167699 · NHLBI · STANFORD UNIVERSITY · PI Chad S Weldy · 2023 to 2026
$664k
A transcriptional network which governs smooth muscle transition is mediated by causal coronary artery disease gene PDGFDF32HL160067 · NHLBI · STANFORD UNIVERSITY · PI WELDY, CHAD S · 2021 to 2022
$135k
NHLBI NIH HHS F32 HL160067NHLBI NIH HHS K08 HL167699NHLBI NIH HHS L30 HL159413NHLBI NIH HHS R01 HL136390NHLBI NIH HHS R01 HL149134WHI NIH HHS HHSN268201100003C
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

GenotypeMutationPhenotype

Identifiers

PMID37625473
PMCPMC11182434

What OpenQuestion holds

Textmetadata
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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.