Evidence map›Paper›PMID 29656336›Full record

ArticleJournal of clinical immunology2018

Combined Immunodeficiency with Ring Chromosome 21.

Melissa Norman, Brynn Wainstein, Antoinette Anazodo, Anne Turner, Cindy Ma, Kathryn Payne, Stuart G Tangye, Paul Gray

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Journal of clinical immunology, 2018. 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. [Ring chromosome 21 syndrome: report of 2 cases].Revista medica del Instituto Mexicano del Seguro Social · 2025
    Article
  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

8 authors.

Melissa NormanDepartment of Immunology, Sydney Children's Hospital, Sydney, NSW, 2031, Australia. melissa.norman28@gmail.com.ORCID 0000-0002-9648-9861
Brynn WainsteinDepartment of Immunology, Sydney Children's Hospital, Sydney, NSW, 2031, Australia.
Antoinette AnazodoSchool of Women and Children's Health, Faculty of Medicine, UNSW, Sydney, NSW, 2052, Australia.
Anne TurnerUniversity of New South Wales, Sydney, NSW, 2052, Australia.
Cindy MaImmunology Division, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Kathryn PayneImmunology Division, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Stuart G TangyeImmunology Division, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
Paul GrayDepartment of Immunology, Sydney Children's Hospital, Sydney, NSW, 2031, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

BiomarkersChild, PreschoolChromosomes, Human, Pair 21FaciesFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansImmunologic Deficiency SyndromesInfectionsIn Situ Hybridization, FluorescenceKaryotypingPhenotypeRing ChromosomesUltrasonographyBiomarkers

Identifiers

PMID29656336

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.