Evidence map›Paper›PMID 38884753›Full record

ReviewAdvances in experimental medicine and biology2024

Human Genetics of Truncus Arteriosus.

Hiroyuki Yamagishi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

1 author.

Hiroyuki YamagishiDivision of Pediatric Cardiology, Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan. hyamag@keio.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Integrated human genetics and molecular/developmental biology studies have revealed that truncus arteriosus is highly associated with 22q11.2 deletion syndrome. Other congenital malformation syndromes and variants in genes encoding TBX, GATA, and NKX transcription factors and some signaling proteins have also been reported as its etiology.

Indexed as

Truncus Arteriosus, PersistentDiGeorge SyndromeGenetic Predisposition to DiseaseHumansT-Box Domain ProteinsTranscription FactorsTruncus ArteriosusT-Box Domain ProteinsTranscription Factors22q11.2 deletion syndromeCHARGE syndromeCHD7Congenital heart diseaseDiabetic motherDiGeorge syndromeGATA4GATA binding protein (GATA)GATA4GATA6GATA binding protein (GATA)GATA6GATA transcription factorsNeural crest cellsNKX2-5NKX2-6NKX transcription factorsPLXNA2Second heart fieldSEMA3CSemaphorin (SEMA)SEMA3CTBX1TBX transcriptTetralogy of FallotVACTERL syndrome

Identifiers

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.