# Trends in Mendelian randomization in neurological disease research: a bibliometric analysis

**Authors:** Shengnan Yin, Kudelati Zakeer, Zekun Ma, Miaomiao Zhao, Aierpati Maimaiti, Zengliang Wang

PMC · DOI: 10.3389/fneur.2025.1525481 · Frontiers in Neurology · 2025-07-17

## TL;DR

This study analyzes trends in using Mendelian randomization to understand neurological diseases, showing growing interest and international collaboration.

## Contribution

The study provides a bibliometric overview of MR in neurological research, identifying key themes and collaborative patterns.

## Key findings

- Stroke, cardiovascular disease, and genome-wide association studies are prominent research hotspots in MR for neurological diseases.
- China, the UK, and the US lead international collaborative efforts in MR research.
- MR is highlighted as a valuable method for uncovering causal genetic relationships in neurological disorders.

## Abstract

Bibliometric analysis (BA) was used in this study to examine the current state and trends of Mendelian randomization (MR) in neurological disease research. The Web of Science database was searched between 1 January 2014 and 1 September 2024 to retrieve relevant literature. The volume of publications, research themes, collaborative networks, and geographical distribution were studied quantitatively. A keyword co-occurrence analysis identified prominent research hotspots, including stroke, cardiovascular disease, and genome-wide association studies. Furthermore, highly cited literature underscored the potential of MR to elucidate causal relationships between genetic variants and health outcomes. International collaborative networks indicate that China, the United Kingdom, and the United States are the most engaged in collaborative efforts within this domain. The findings suggest that MR methods hold significant potential for applications in the investigation of neurological disorders, highlighting the necessity of international collaboration to foster scientific advancement. Future research should prioritize enhancing interdisciplinary collaboration and conducting comprehensive explorations of disease mechanisms to aid in prevention and treatment.

## Linked entities

- **Diseases:** stroke (MONDO:0005098), cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** PSME1 (proteasome activator subunit 1) [NCBI Gene 5720] {aka HEL-S-129m, IFI5111, PA28A, PA28alpha, REGalpha}, CD33 (CD33 molecule) [NCBI Gene 945] {aka CD33rSiglec, SIGLEC-3, SIGLEC3, p67}, GNAI3 (G protein subunit alpha i3) [NCBI Gene 2773] {aka 87U6, ARCND1, ARCODS, HG1A}, VPS29 (VPS29 retromer complex component) [NCBI Gene 51699] {aka DC15, DC7, PEP11}, TBCA (tubulin folding cofactor A) [NCBI Gene 6902]
- **Diseases:** CNS disease (MESH:D002493), orbital inflammation (MESH:D007249), migraine (MESH:D008881), Neurological Disorders (MESH:D009461), Parkinson's (MESH:D010300), ischemic stroke (MESH:D002544), Alzheimer disease (MESH:D000544), coronary heart disease (MESH:D003327), brain tumors (MESH:D001932), cerebral palsy (MESH:D002547), brain injury (MESH:D001930), neurological disease (MESH:D020271), stroke (MESH:D020521), hyperlipidemia (MESH:D006949), cardiovascular and metabolic diseases (MESH:D002318), cerebrovascular diseases (MESH:D002561), AF (MESH:D001281), dementias (MESH:D003704), acute ischemic stroke (MESH:D000083242), WOS (MESH:C563636), brain disorder (MESH:D001927), CNS disorder (MESH:D002494), head trauma (MESH:D006259), traumatic brain injury (MESH:D000070642), neurodegenerative diseases (MESH:D019636), HF (MESH:D006333), traumatic disorders of the nervous system (MESH:D009422), spinal cord injury (MESH:D013119), MR (MESH:C562757), diabetes mellitus (MESH:D003920), GBM (MESH:D005909), hypertension (MESH:D006973), multiple sclerosis (MESH:D009103), Epilepsy (MESH:D004827), CAD (MESH:D003324), malnutrition (MESH:D044342), myocardial infarction (MESH:D009203), acquired brain injury (MESH:D001928), headache disorders (MESH:D020773), neurodevelopmental disorders (MESH:D002658)
- **Chemicals:** vitamin D (MESH:D014807), MR (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12312639/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12312639/full.md

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Source: https://tomesphere.com/paper/PMC12312639