Evidence map›Paper›PMID 30800050›Full record

ArticleMolecular syndromology2019

8p 11 Microduplication Is Associated with Neonatal Stridor.

Surasak Puvabanditsin, Natalie Gengel, Christina Botti, Marianne Jacob, Maaz Jalil, Kenya Cabrera, Rajeev Mehta

Open access · bronzeAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular syndromology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Clinical and genomic characterization of 8p cytogenomic disorders.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
  3. Frontiers in pediatrics · 2020
    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

7 authors at 1 institution in 1 country.

Surasak PuvabanditsinDepartment of Pediatrics, NJ, USA.
Natalie GengelDepartment of Pediatrics, NJ, USA.
Christina BottiDivision of Medical Genetics, Rutgers Robert Wood Johnson Medical School (RWJMS), New Brunswick, NJ, USA.
Marianne JacobDepartment of Pediatrics, NJ, USA.
Maaz JalilDepartment of Pediatrics, NJ, USA.
Kenya CabreraDepartment of Pediatrics, NJ, USA.
Rajeev MehtaDepartment of Pediatrics, NJ, USA.
Johnson University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a term male infant with congenital stridor secondary to tracheomalacia and a mild coarctation of the aorta. Developmental delay was noted upon follow-up. Whole genome SNP microarray analysis showed an ∼846-kb interstitial duplication of the short arm of chromosome 8 (8p11.21p11.1). We report novel clinical findings of this rare genetic condition.

Indexed as

8p11.21 microduplicationChromosomal microduplicationCongenital anomalyDevelopmental delayNeonatal stridor

Identifiers

PMID30800050
PMCPMC6381896
OpenAlexW2901119907

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.