Evidence map›Paper›PMID 42410704›Full record

ArticleJournal of Yeungnam medical science2026

Evolution of fragile X syndrome and neurodevelopmental disorders research: a Scopus-based bibliometric analysis.

Wan Nur Amalina Zakaria, Nazihah Mohd Yunus, Aziati Azwari Annuar, Ahmad Aizat Abd Aziz, Nurfadhlina Musa, Maruzairi Husain, Rowani Mohd Rawi

Abstract read
In one paragraph

Article in Journal of Yeungnam medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Wan Nur Amalina ZakariaHuman Genome Centre, School of Medical Sciences, Health Campus, Hospital Pakar Universiti Sains Malaysia, Kota Bharu, Malaysia. dr_amalina@usm.my.
Nazihah Mohd YunusHuman Genome Centre, School of Medical Sciences, Health Campus, Hospital Pakar Universiti Sains Malaysia, Kota Bharu, Malaysia.
Aziati Azwari AnnuarHuman Genome Centre, School of Medical Sciences, Health Campus, Hospital Pakar Universiti Sains Malaysia, Kota Bharu, Malaysia.
Ahmad Aizat Abd AzizHuman Genome Centre, School of Medical Sciences, Health Campus, Hospital Pakar Universiti Sains Malaysia, Kota Bharu, Malaysia.
Nurfadhlina MusaHuman Genome Centre, School of Medical Sciences, Health Campus, Hospital Pakar Universiti Sains Malaysia, Kota Bharu, Malaysia.
Maruzairi HusainDepartment of Psychiatry, School of Medical Sciences, Health Campus, Hospital Pakar Universiti Sains Malaysia, Kota Bharu, Malaysia.
Rowani Mohd RawiDepartment of Paediatrics, School of Medical Sciences, Health Campus, Hospital Pakar Universiti Sains Malaysia, Kota Bharu, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodevelopmental disorders (NDD), including intellectual disability, autism spectrum disorder, attention-deficit hyperactivity disorder, and specific learning disorder, are closely linked to fragile X syndrome (FXS). This study employed a bibliometric analysis to explore trends and shifts in research focusing on FXS and NDD. We extracted publication data related to FXS and NDD from the Scopus database and conducted a bibliometric analysis. This involved assessing cumulative publication trends over time, most prolific authors, geographic distribution, and co-occurrence of author keywords to identify the dominant research themes. The number of publications on FXS and NDD has steadily increased over the past decades. The United States emerged as the leading contributor, while China is becoming an important player in the field. An analysis of author keywords revealed a significant shift in research focus from molecular mechanisms to translational and clinical research. This analysis provides critical insights into the evolving research landscapes of FXS and NDD. These findings can inform future research directions, facilitate collaboration, and optimize resource allocation. Additionally, they underscore the necessity for ongoing research to deepen our understanding of these disorders and enhance treatment options for affected individuals.

Indexed as

Autistic disorderBibliometricsFragile X syndromeNeurodevelopmental disorders

Identifiers

PMID42410704
PMCPMC13681062

What OpenQuestion holds

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Registered trials

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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.