Evidence map›Paper›PMID 38884747›Full record

ReviewAdvances in experimental medicine and biology2024

Human Genetics of Semilunar Valve and Aortic Arch Anomalies.

Matina Prapa, Siew Yen Ho

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. Perspectives on the Parathyroid-Thymus Interconnection-A Literature Review.International journal of molecular sciences · 2025
    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

2 authors.

Matina PrapaDepartment of Clinical Genetics, St George's University Hospitals NHS Foundation Trust, London, UK. s.prapa09@alumni.imperial.ac.uk.
Siew Yen HoCardiac Morphology, Royal Brompton & Harefield Hospitals, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lesions of the semilunar valve and the aortic arch can occur either in isolation or as part of well-described clinical syndromes. The polygenic cause of calcific aortic valve disease will be discussed including the key role of NOTCH1 mutations. In addition, the complex trait of bicuspid aortic valve disease will be outlined, both in sporadic/familial cases and in the context of associated syndromes, such as Alagille, Williams, and Kabuki syndromes. Aortic arch abnormalities particularly coarctation of the aorta and interrupted aortic arch, including their association with syndromes such as Turner and 22q11 deletion, respectively, are also discussed. Finally, the genetic basis of congenital pulmonary valve stenosis is summarized, with particular note to Ras-/mitogen-activated protein kinase (Ras/MAPK) pathway syndromes and other less common associations, such as Holt-Oram syndrome.

Indexed as

Aorta, ThoracicAortic ValveAbnormalities, MultipleAortic Valve DiseaseBicuspid Aortic Valve DiseaseCalcinosisHeart Defects, CongenitalHeart Valve DiseasesHematologic DiseasesHumansMutationPulmonary Valve StenosisReceptor, Notch1Vestibular DiseasesNOTCH1 protein, humanReceptor, Notch122q11 deletion syndromeAlagille syndromeAortic archAortic coarctationAortic valve stenosisBAVBicuspid aortic valveBMPCHD7Costello syndromeDiGeorge syndromeElastinELNGATA4Holt–Oram syndromeIAAInterrupted aortic archJAG1Kabuki syndromeMLL2NKX2–5Noonan syndromeNOTCH1PTPN11Pulmonary stenosisRas–MAPK pathwaySemilunar valveSMADSOS1Supravalvar aortic stenosisTBX1TBX5Turner syndromeVascular smooth muscle cellsVelocardiofacial syndromeWilliams syndrome

Identifiers

PMID38884747

What OpenQuestion holds

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Registered trials

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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.