Evidence map›Paper›PMID 35839129›Full record

ArticleAnnals of the American Thoracic Society2022

Phenotypic Features of Cystic Lung Disease in Proteus Syndrome: A Clinical Trial.

Kim M Keppler-Noreuil, Jasmine Burton-Akright, David E Kleiner, Julie C Sapp, Marjorie J Lindhurst, Chen G Han, Leslie G Biesecker, Bernadette R Gochuico

Open access · greenAbstract read
In one paragraph

Article in Annals of the American Thoracic Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Quantification of Proteus syndrome-associated lung disease.Orphanet journal of rare diseases · 2024
    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

8 authors at 3 institutions in 2 countries.

Kim M Keppler-NoreuilMedical Genomics and Metabolic Genetics Branch.
Jasmine Burton-AkrightMedical Genomics and Metabolic Genetics Branch.
David E KleinerLaboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Julie C SappCenter for Precision Health Research, and.
Marjorie J LindhurstCenter for Precision Health Research, and.
Chen G HanMedical Genetics Branch, National Human Genome Research Institute, and.
Leslie G BieseckerCenter for Precision Health Research, and.
Bernadette R GochuicoMedical Genetics Branch, National Human Genome Research Institute, and.
Institut thématique Génétique, génomique et bioinformatique · FRNational Human Genome Research Institute · USNational Institutes of Health · US

Funding

Rare & Mosaic Disorders - Clinical ResearchZIAHG200388 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI BIESECKER, LESLIE · 2013 to 2025
$17.3M
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CystsLung DiseasesProteus SyndromePulmonary EmphysemaHumansPhenotypeRetrospective StudiesAKT1bullous lung diseaseemphysemascoliosisvascular malformations

Identifiers

PMID35839129
PMCPMC9667804
OpenAlexW4285493283

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.