Evidence map›Paper›PMID 35741713›Full record

ArticleGenes2022

Siti Waheeda Mohd-Zin, Amelia Cheng Wei Tan, Wahib M Atroosh, Meow-Keong Thong, Abu Bakar Azizi, Nicholas D E Greene, Noraishah Mydin Abdul-Aziz

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

Article in Genes, 2022. 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
0.2field-weighted citation impact, top 57% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. A "Smurf-Cap" head requiring total cranial vault reshaping. A novel syndromic presentation of craniofrontonasal dysplasia associated with spina bifida.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 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

7 authors at 3 institutions in 2 countries.

Siti Waheeda Mohd-ZinInvertebrate and Vertebrate Neurobiology Laboratory, Department of Parasitology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur 50603, Malaysia.
Amelia Cheng Wei TanInvertebrate and Vertebrate Neurobiology Laboratory, Department of Parasitology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur 50603, Malaysia.
Wahib M AtrooshDepartment of Parasitology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur 50603, Malaysia.
Meow-Keong ThongDepartment of Paediatrics, Faculty of Medicine, Universiti Malaya, Kuala Lumpur 50603, Malaysia.ORCID 0000-0002-7288-7910
Abu Bakar AziziNeurosurgery Unit, Department of Surgery, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras 56000, Malaysia.
Nicholas D E GreeneDevelopmental Biology and Cancer Department, Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.ORCID 0000-0002-4170-5248
Noraishah Mydin Abdul-AzizInvertebrate and Vertebrate Neurobiology Laboratory, Department of Parasitology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur 50603, Malaysia.ORCID 0000-0002-2447-3211
University of Malaya · MYGreat Ormond Street Hospital · GBNational University of Malaysia · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neural tube defects (NTDs) are common birth defects with a complex genetic etiology. Mouse genetic models have indicated a number of candidate genes, of which functional mutations in some have been found in human NTDs, usually in a heterozygous state. This study focuses on

Indexed as

EphrinsNeural Tube DefectsSpinal DysraphismAsian PeopleEphrin-B1GenotypeHumansMalaysiaReceptor, EphA2Receptors, Eph FamilyEFNB1 protein, humanEPHA2 protein, humanEPHB6 protein, humanEphrin-B1EphrinsReceptor, EphA2Receptors, Eph FamilyEFNB1EphEPHA2EPHB6ephrinsneural tube defectsspina bifida

Identifiers

PMID35741713
PMCPMC9222557
OpenAlexW4281632586

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.