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Zongrui Shen

Observed name: Shen, Zongrui
ORCID: 0000-0002-6435-4874
Observed ORCID: 0000-0002-6435-4874
OpenAlex ID: A5084431051
Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis
2023 · Jianfan Chen, Xueqing Xu, et al. · International Journal of Oral Science · 14
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The molecular mechanism of Gaucher disease caused by compound heterozygous mutations in GBA1 gene
2023 · Qi Liu, Zongrui Shen, et al. · Frontiers in Pediatrics · 6
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Plasma-derived exosomal miRNA profiles reveal potential epigenetic pathogenesis of premature ovarian failure
2023 · Jiaqiong Lin, Zhihong Wu, et al. · Human Genetics · 5
Intravenous Administration of an AAV9 Vector Ubiquitously Expressing C1orf194 Gene Improved CMT-Like Neuropathy in C1orf194-/- Mice
2023 · Zongrui Shen, Meiyi Li, et al. · Neurotherapeutics · 3
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Molecular and phenotype characterization of an elongated β‐globin variant produced by HBB:C.313delA
2021 · Wanying Lin, Qianqian Zhang, et al. · International Journal of Laboratory Hematology · 2
HLA-A drives diabetic retinopathy pathogenesis: multi-omics integration reveals resveratrol’s therapeutic potential via immunomodulation
2025 · Jiaqiong Lin, Fangkeng Liang, et al. · Journal of Translational Medicine · 1
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Functional characterization of novel compound heterozygous SLC12A3 mutations in a patient with Gitelman syndrome
2026 · Zhongren Shen, Xiaoqun Liu, et al. · Orphanet Journal of Rare Diseases
TEAD 4 Drives SKCM Progression Through COL 1 A 2 Transcriptional Activation and Modulation of AKT /m TOR Signalling and Necroptosis‐Related Phenotypes
2026 · Jiaqiong Lin, Yingchun Zheng, et al. · Experimental Dermatology
ARID1B regulates sphingolipid metabolism and myelin development via STAG2: Mechanistic insights into ARID1B-related coffin–siris syndrome
2026 · Xingkun Yang, Zhongzhi Gan, et al. · Cellular Signalling
Molecular mechanism study of novel compound heterozygous EOGT mutations leading to Adams-Oliver syndrome type 4
2026 · Yufei He, Xiangyu Liu, et al. · Global Medical Genetics
Context-specific expression quantitative trait loci dynamics uncover genetic pleiotropy in schizophrenia
2025 · Linyan Ye, Zongrui Shen, et al. · Neurobiology of Disease
Identification of an IL17RC missense variant in a Chinese family with multiple osteochondromas and ankylosing spondylitis
2025 · Yingchun Zheng, Xuewu Wei, et al. · Journal of Human Genetics
Identification of a novel nonsense mutation in α-galactosidase A that causes Fabry disease in a Chinese family
2024 · Yushi Peng, Meize Pan, et al. · Renal Failure
Works count: 14
Citation count: 31
H-index: 3
I10-index: 1
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