Evidence map›Paper›PMID 30288645›Full record

ArticleJournal of clinical immunology2018

Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis.

Tamar S Rubin, Cheryl Rockman-Greenberg, Paul Van Caeseele, Geoffrey D E Cuvelier, Luvinia Kwan, Marlis L Schroeder

Abstract readLetter
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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Clinical Significance of IKBKB Mutations:Saudi medical journal · 2026
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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

6 authors at 2 institutions in 1 country.

Tamar S RubinDepartment of Pediatrics & Child Health, University of Manitoba, 840 Sherbrook Street, Winnipeg, Manitoba, R3A 1S1, Canada. trubin@manitoba-physicians.ca.
Cheryl Rockman-GreenbergDepartment of Pediatrics & Child Health, University of Manitoba, 840 Sherbrook Street, Winnipeg, Manitoba, R3A 1S1, Canada.
Paul Van CaeseeleDepartment of Pediatrics & Child Health, University of Manitoba, 840 Sherbrook Street, Winnipeg, Manitoba, R3A 1S1, Canada.
Geoffrey D E CuvelierDepartment of Pediatrics & Child Health, University of Manitoba, 840 Sherbrook Street, Winnipeg, Manitoba, R3A 1S1, Canada.
Luvinia KwanHLA laboratory, CancerCare Manitoba, 820 Sherbrook Street, Winnipeg, Manitoba, R3A 1R9, Canada.
Marlis L SchroederDepartment of Pediatrics & Child Health, University of Manitoba, 840 Sherbrook Street, Winnipeg, Manitoba, R3A 1S1, Canada.
University of Manitoba · CACancerCare Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAllelesDNA Mutational AnalysisGenotypeHumansI-kappa B KinaseInfant, NewbornMutationNeonatal ScreeningPhenotypeSevere Combined ImmunodeficiencyI-kappa B KinaseIKBKB protein, human

Identifiers

PMID30288645
OpenAlexW2894991436

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.