Evidence map›Paper›PMID 41789055›Full record

ReviewClinical, cosmetic and investigational dermatology2026

Genetics of Vitiligo: A Review.

Honghao He, Rina Su, Fang Liu

Abstract readReview
In one paragraph

Review in Clinical, cosmetic and investigational dermatology, 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

3 authors.

Honghao He *Department of Dermatology, Venereology and Medicine, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, People's Republic of China.
Rina Su *Department of Dermatology, Venereology and Medicine, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, People's Republic of China.
Fang LiuDepartment of Dermatology, Venereology and Medicine, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, People's Republic of China.ORCID 0000-0003-3456-160X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitiligo is a common acquired depigmentation skin disease with obvious family aggregation. About 25-50% of patients have positive family history, which belongs to polygenetic disease. In recent years, through candidate genes and genome-wide association studies, multiple susceptibility gene loci have been found, and studies also show that there is genetic heterogeneity among different populations. Environmental factors can also interact with genetic factors to trigger diseases through various mechanisms. The risk assessment model based on genetic and environmental factors provides a new direction for early screening and personalized prevention and treatment. In the future, we need to combine single cell sequencing and other multi omics technologies to explore the mechanism, develop targeted treatment strategies, and strengthen the application of genetic counseling and preventive measures in high-risk populations.

Indexed as

autoimmunegeneticsgenomevitiligo

Identifiers

PMID41789055
PMCPMC12957958

What OpenQuestion holds

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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.