Association and causal impact of TERT genetic variants on peripheral blood leukocyte telomere length and cerebral small vessel disease risk in a Chinese Han population: a mendelian randomization analysis

Multiple genetic models and MR results indicate that TERT gene SNPs may be related to an elevated risk of CSVD, and that shorter LTL may be causally linked to such CSVD risk.

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Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2024-08-23
DOI
https://doi.org/10.1186/s13023-024-03316-5
Primary Topic
Cerebrovascular and genetic disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Association and causal impact of TERT genetic variants on peripheral blood leukocyte telomere length and cerebral small vessel disease risk in a Chinese Han population: a mendelian randomization analysis

Jiuhan Zhao, Wanru Geng, Ying Song, Long Yin et al.
Orphanet Journal of Rare Diseases
Cerebrovascular and genetic disorders
article

Association and causal impact of TERT genetic variants on peripheral blood leukocyte telomere length and cerebral small vessel disease risk in a Chinese Han population: a mendelian randomization analysis

Jiuhan Zhao, Wanru Geng, Ying Song, Long Yin, Jialiang Xu, Jialu Wang
article en

Abstract

Multiple genetic models and MR results indicate that TERT gene SNPs may be related to an elevated risk of CSVD, and that shorter LTL may be causally linked to such CSVD risk.

Orphanet Journal of Rare DiseasesVol. 19(1)
First Affiliated Hospital of Liaoning Medical University (CN), Liaoning Provincial People's Hospital (CN), First Hospital of China Medical University (CN), China Medical University (CN)
Shenyang Science and Technology Bureau
Good health and well-being
Openalex Percentile: Top 78%
Cerebrovascular and genetic disorders
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Association and causal impact of TERT genetic variants on peripheral blood leukocyte telomere length and cerebral small vessel disease risk in a Chinese Han population: a mendelian randomization analysis — Jiuhan Zhao, Wanru Geng, et al. · Orphanet Journal of Rare Diseases (2024) | TGRS Research Map | TGRS